# FewerJobs export - 100 curated jobs
Generated: 2026-08-16T10:15:25.555Z
Source: https://fewerjobs.com

## Filters applied
- **q**: Beam Therapeutics Inc
- **quality_floor**: default
- **match_401k_strict**: true
- **parental_strict**: true
- **non_birth_strict**: true
- **pto_strict**: true
- **include_older**: false
- **apply_url_verified**: false
- **page**: 2
- **per_page**: 100
- **sort**: relevance

## Jobs
### Senior/Executive Director, Health Economics & Outcomes Research (HEOR) - Viking Therapeutics
- Location: Viking Therapeutics, Inc. (unspecified)
- Salary: Not disclosed
- Posted: 2026-04-29
- Apply: https://recruiting.paylocity.com/Recruiting/Jobs/Details/4127771
- Excerpt: Senior/Executive Director, Health Economics & Outcomes Research (HEOR) Viking Therapeutics, Inc. Senior/Executive Director, Health Economics & Outcomes Research (HEOR)

### Strategic Partner Development Principal Lead, Beam Hardware Partnerships - Google
- Location: Mountain View, CA, USA (unspecified)
- Salary: $176K-$256K
- Posted: 2026-06-10
- Parental leave: 18 weeks (not source-backed)
- Non-birth-parent leave: 18 weeks (not source-backed)
- 401(k) match: listed (not source-backed)
- Apply: https://www.google.com/about/careers/applications/signin?jobId=CiUAL2FckQzmvD27qMJKCHESYMTxWzQtnhRF5_UYZ8p9L3PWwiMYEjsACxwdTDBW2bKLglrW6RAbnSibdpNXGt10pih4KdQ-9YzF94vZ0IMsVLzhb69lXQKXaWvJabO1LzlmDA%3D%3D_V2&loc=US&title=Strategic+Partner+Development+Principal+Lead
- Excerpt: Strategic Partner Development Principal Lead, Beam Hardware Partnerships Mountain View, CA, USA As a Strategic Partner Development Manager, you'll open doors with potential partners, lead exploratory discussions and evaluate/develop business opportunities. You will lead cross-functional teams, provide thought leadership and serve as a mentor to managers and associates. You are comfortable escalating and presenting business development strategies and key issues to senior management. You'll work closely with Google Product, Engineering, Legal and Sales teams on new product initiatives and key strategic relationships that support our online advertising business. In this role, you will be a primary driver in scaling the Google Beam hardware portfolio. You will have a focus on product and manufacturing, tasked with securing the long-term alliances necessary for next-generation Beam devices. You will lead the identification, recruitment, audit, and onboarding of Original Equipment Manufacturers (OEMs) and Joint Design Manufacturers (JDMs) to move Beam from a single-product offering to a portfolio of form factors. You will be expected to thrive in ambiguous environments, lead large cross-functional workstreams, and serve as a "go-to" expert for internal and external stakeholders in the video conferencing hardware and manufacturing industry. The Global Partnerships organization is responsible for exploring new opportunities with Google's partners. Google's Global Partnerships team works with a wide range of partners to bring the best of Google to power their business. The Global Partnerships team supports Google's own Product teams with essential partnerships to help Google's user experiences in advertising, Search, Assistant, Maps, Travel, Shopping, Payments and more. Teams

### Senior Project Manager - Definium Therapeutics
- Location: Remote (remote)
- Salary: $130K-$160K
- Posted: 2026-06-04
- Apply: https://job-boards.greenhouse.io/definiumtherapeutics/jobs/5836395004
- Excerpt: Senior Project Manager Remote Definium Therapeutics is a late-stage clinical biopharmaceutical company and our mission is to forge a new era of psychiatry by applying scientific rigor to psychedelics, with the goal of developing accessible treatments that unlock healing at scale. Our lead product candidate, lysergide tartrate (our proprietary orally disintegrating tablet form of lysergide (LSD) D-tartrate), represents a highly differentiated, potential best-in-class opportunity for patients suffering from generalized anxiety, major depressive disorder, and posttraumatic stress disorder. Our early stage pipeline includes DT402, the R-enantiomer of MDMA and is under development to target the core symptoms of autism spectrum disorder (ASD), specifically addressing social communication challenges. Guided by the recognition that patients deserve more than better, Definium is relentlessly advancing a new generation of therapeutics intended to address the underlying causes of psychiatric and neurological disorders. By turning evidence into impact, Definium aims to change the trajectory of today's mental health care crisis and enable a healthier future. Headquartered in New York, Definium Therapeutics trades on Nasdaq under the symbol DFTX. Together we are moving psychiatry forward-beyond better, into a boundless future. Join us! The ideal candidate enjoys working in a rapidly growing environment with strong focus on execution, navigating multiple stakeholders and priorities, and has an excellent understanding of formal project management methodologies, preferably including experience in using Planisware Enterprise. The Sr. Project Manager will lead the development of Project plan(s) to support functional areas or workstreams. Closely and proactively monitor the execution of the project plans and deliverables

### Senior Software Engineer, Head Tracking, Beam, AI/ML - Google
- Location: Seattle, WA, USA; +2 more (unspecified)
- Salary: $174K-$253K
- Posted: 2026-06-05
- Parental leave: 18 weeks (not source-backed)
- Non-birth-parent leave: 18 weeks (not source-backed)
- 401(k) match: listed (not source-backed)
- Apply: https://www.google.com/about/careers/applications/signin?jobId=CiUAL2FckV4GK2khnnAi4EYpVvTBhbJIGSWRyc6sllkqtwBAm0TAEjsACxwdTHmwc1KEkCRU5K2G7T54PQsUJiwfgKeUjEeuOJ9BJ-MuFixqMuQd2_2Nk73ym7vX6Jg8zMMXwA%3D%3D_V2&loc=US&title=Senior+Software+Engineer
- Excerpt: Senior Software Engineer, Head Tracking, Beam, AI/ML Seattle, WA, USA; +2 more Google's software engineers develop the next-generation technologies that change how billions of users connect, explore, and interact with information and one another. Our products need to handle information at massive scale, and extend well beyond web search. We're looking for engineers who bring fresh ideas from all areas, including information retrieval, distributed computing, large-scale system design, networking and data storage, security, artificial intelligence, natural language processing, UI design and mobile; the list goes on and is growing every day. As a software engineer, you will work on a specific project critical to Google's needs with opportunities to switch teams and projects as you and our fast-paced business grow and evolve. We need our engineers to be versatile, display leadership qualities and be enthusiastic to take on new problems across the full-stack as we continue to push technology forward. In this role, with your technical expertise you will manage project priorities, deadlines, and deliverables. You will design, develop, test, deploy, maintain, and enhance software solutions. Google Beam is a true-to-life new communication technology from Google that allows people to feel like they're having real face-to-face conversations, no matter the distance. Powered by realistic state-of-the-art 3D imaging and spatial audio and integrated with today's leading remote video platforms, Google Beam enables you to be immersed in the moment, together. As a part of the Google Beam team, you'll work with incredible teammates across all major functions in a fast-paced product-oriented

### Staff Software Engineer, Google Beam - Google
- Location: Mountain View, CA, USA (unspecified)
- Salary: $207K-$301K
- Posted: 2026-06-05
- Parental leave: 18 weeks (not source-backed)
- Non-birth-parent leave: 18 weeks (not source-backed)
- 401(k) match: listed (not source-backed)
- Apply: https://www.google.com/about/careers/applications/signin?jobId=CiUAL2FckYGIyoZcEcm5QyHNmjgBXNeZoPepwnRducDBKY6TRwRWEjsACxwdTFq1lLL0yLeKOHKNtnw4mC1EPSJLboLYSfOqA9BR0M-g6bjpFw8JGJjQcoagL8Zc1Upse2IeXw%3D%3D_V2&loc=US&title=Staff+Software+Engineer
- Excerpt: Staff Software Engineer, Google Beam Mountain View, CA, USA Google's software engineers develop the next-generation technologies that change how billions of users connect, explore, and interact with information and one another. Our products need to handle information at massive scale, and extend well beyond web search. We're looking for engineers who bring fresh ideas from all areas, including information retrieval, distributed computing, large-scale system design, networking and data storage, security, artificial intelligence, natural language processing, UI design and mobile; the list goes on and is growing every day. As a software engineer, you will work on a specific project critical to Google's needs with opportunities to switch teams and projects as you and our fast-paced business grow and evolve. We need our engineers to be versatile, display leadership qualities and be enthusiastic to take on new problems across the full-stack as we continue to push technology forward. Google Beam is a true-to-life new communication technology from Google that allows people to feel like they're having real face-to-face conversations, no matter the distance. Powered by realistic Three-Dimensional imaging and spatial audio and integrated with today's leading remote video platforms, Google Beam enables you to be immersed in the moment, together. As a part of the Google Beam team, you will work with incredible teammates across all major functions in a changing product-oriented environment. Your contributions will have an impact on the future of communications with Google products. You will apply technology to solve that really important problem that we often want

### Sr. Medical Director, Drug Safety and Pharmacovigilance - BridgeBio Pharma, Inc.
- Location: Remote - United States (remote)
- Salary: $325K-$370K
- Posted: 2025-09-29
- Apply: https://job-boards.greenhouse.io/bridgebio/jobs/4924366007
- Excerpt: Sr. Medical Director, Drug Safety and Pharmacovigilance Remote - United States Mavericks Wanted When was the last time you achieved the impossible? If that thought feels overwhelming, you might want to pause here, but if it sparks excitement...read on In 2015, we pioneered a “moneyball for biotech” approach, pooling projects and promising early-stage research from academia together under one financial umbrella to reduce risk and unleash innovation. This model allows science and small teams of experts to lead the way. We build bridges to groundbreaking advancements in rare disease, and develop life-changing medicines for patients with unmet needs as fast as humanly possible. Together we define white space, push boundaries, and empower people to solve problems. If you're someone who defies convention, join us and work alongside some of the most respected minds in the industry. Together, we'll ask "why not?" and help reengineer the future of biopharma. At BridgeBio, we value curiosity and experimentation-including the ethical & thoughtful use of AI to improve clarity, speed, and quality of work. Affiliate Overview Eidos Therapeutics, an affiliate within BridgeBio Pharma, is a commercial-stage biopharmaceutical company focused on Transthyretin Amyloid Cardiomyopathy (ATTR-CM). What You'll Do The Sr. Medical Director, Drug Safety and Pharmacovigilance, is responsible for the overall risk management and safety strategy of assigned products, including both internal and external engagement with key collaborators. - Oversight and understanding of all aspects of the assigned product's safety profile from clinical development to post-approval safety surveillance, including management of CROs and other partners

### Software Engineer, Google Beam, Full Stack - Google
- Location: Seattle, WA, USA; +1 more (unspecified)
- Salary: $147K-$211K
- Posted: 2026-06-05
- Parental leave: 18 weeks (not source-backed)
- Non-birth-parent leave: 18 weeks (not source-backed)
- 401(k) match: listed (not source-backed)
- Apply: https://www.google.com/about/careers/applications/signin?jobId=CiUAL2FckZKGCd6H5ixW4Ypiwdo0OQUE7MJnkM9x7VEXGv5SG44pEjoACxwdTOpZ33r4lJD_P7KnUaXtziByQXIAtn8bRtFVUua52mKBF-oFtP_AyUYxHv1StONdVtc_5vQp_V2&loc=US&title=Software+Engineer
- Excerpt: Software Engineer, Google Beam, Full Stack Seattle, WA, USA; +1 more Google's software engineers develop the next-generation technologies that change how billions of users connect, explore, and interact with information and one another. Our products need to handle information at massive scale, and extend well beyond web search. We're looking for engineers who bring fresh ideas from all areas, including information retrieval, distributed computing, large-scale system design, networking and data storage, security, artificial intelligence, natural language processing, UI design and mobile; the list goes on and is growing every day. As a software engineer, you will work on a specific project critical to Google's needs with opportunities to switch teams and projects as you and our fast-paced business grow and evolve. We need our engineers to be versatile, display leadership qualities and be enthusiastic to take on new problems across the full-stack as we continue to push technology forward.Google Beam is a true-to-life new communication technology from Google that allows people to feel like they're having real face-to-face conversations, no matter the distance. Powered by realistic state-of-the-art 3D imaging and spatial audio and integrated with today's leading remote video platforms, Google Beam enables you to be immersed in the moment, together. As a part of the Google Beam team, you'll work with incredible teammates across all major functions in a fast-paced product-oriented environment. Your contributions will have an impact on the future of communications with Google products. You will apply technology to solve that really important problem that we often

### Scientist, Downstream, Process Development and Manufacturing (PD/MFG) (Biologics) - Oruka Therapeutics Inc
- Location: Waltham, Massachusetts, United States (unspecified)
- Salary: $130K-$146K
- Posted: 2026-05-27
- Apply: https://job-boards.greenhouse.io/oruka/jobs/5232207008
- Excerpt: Scientist, Downstream, Process Development and Manufacturing (PD/MFG) (Biologics) Waltham, Massachusetts, United States About Us: Oruka Therapeutics (Nasdaq: ORKA) is developing novel biologics designed to set a new standard for the treatment of chronic skin diseases. Oruka's mission is to offer patients suffering from chronic skin diseases like plaque psoriasis the greatest possible freedom from their condition by achieving high rates of complete disease clearance with dosing as infrequently as once or twice per year. Oruka is advancing a proprietary portfolio of potentially best-in-class antibodies that were engineered by Paragon Therapeutics and target the core mechanisms underlying plaque psoriasis and other dermatologic and inflammatory diseases. For more information, visit www.orukatx.com As we build our core team, we're seeking top talent in different functional areas who are not just looking for a job, but an opportunity to be part of something bigger. Someone who is passionate about making a difference and eager to contribute to establishing an engaged, inclusive, and positive company culture. Job Title: Scientist, Downstream, Process Development and Manufacturing (PD/MFG) (Biologics) Location: Hybrid - Waltham, MA . Candidates will be required to be in-office 3 days/week. Role Overview: We are seeking a motivated Process Development individual to lead downstream pre-clinical to early stage enabling process development, optimization, scale-up and transfer of manufacturing activities. In this role, the ideal candidate will be responsible for early-stage process development, tox batch production, optimization, scale up to GMP and late stage pivotal development. The successful candidate will be involved in pre-clinical development to pre-pivotal

### Senior Software Engineer, Google Beam - Google
- Location: Mountain View, CA, USA (unspecified)
- Salary: $174K-$253K
- Posted: 2026-06-05
- Parental leave: 18 weeks (not source-backed)
- Non-birth-parent leave: 18 weeks (not source-backed)
- 401(k) match: listed (not source-backed)
- Apply: https://www.google.com/about/careers/applications/signin?jobId=CiUAL2FckU4aTrjD-oAzNnhDDcoq4dn0fKMXYz65KypLaatWzCX2EjsACxwdTHVsMKsWMvjB5rhKMFeYzQ8JvRjMSng_Dl31FYoQ-18pR-RfNvnG0Rh7cZt-7eD4L5qaeBF35Q%3D%3D_V2&loc=US&title=Senior+Software+Engineer
- Excerpt: Senior Software Engineer, Google Beam Mountain View, CA, USA Google's software engineers develop the next-generation technologies that change how billions of users connect, explore, and interact with information and one another. Our products need to handle information at massive scale, and extend well beyond web search. We're looking for engineers who bring fresh ideas from all areas, including information retrieval, distributed computing, large-scale system design, networking and data storage, security, artificial intelligence, natural language processing, UI design and mobile; the list goes on and is growing every day. As a software engineer, you will work on a specific project critical to Google's needs with opportunities to switch teams and projects as you and our fast-paced business grow and evolve. We need our engineers to be versatile, display leadership qualities and be enthusiastic to take on new problems across the full-stack as we continue to push technology forward. Google Beam is a true-to-life new communication technology from Google that allows people to feel like they're having real face-to-face conversations, no matter the distance. Powered by realistic 3D imaging and spatial audio and integrated with today's leading remote video platforms, Google Beam enables you to be immersed in the moment, together. As a part of the Google Beam team, you'll work with incredible teammates across all major functions in a changing product-oriented environment. Your contributions will have an impact on the future of communications with Google products. You will apply technology to solve that really important problem that we often want to

### Manager, Market Intelligence and Strategy - Entrada Therapeutics Inc
- Location: Boston, MA (unspecified)
- Salary: $127K-$166K
- Posted: 2026-05-08
- Parental leave: 0 weeks (not source-backed)
- 401(k) match: listed (not source-backed)
- Learning budget: yes (not source-backed)
- Apply: https://job-boards.greenhouse.io/entradatherapeutics/jobs/5132958007
- Excerpt: Manager, Market Intelligence and Strategy Boston, MA The Organization What's happening at Entrada Therapeutics? Entrada is a clinical-stage biopharmaceutical company aiming to transform the lives of patients by establishing a new class of medicines that engage intracellular targets that have long been considered inaccessible. Through proprietary and versatile approaches, Entrada is advancing a robust development portfolio of genetic medicines for the potential treatment of neuromuscular and inherited retinal diseases, among others. Our lead oligonucleotide programs are in development for the potential treatment of people living with Duchenne muscular dystrophy (DMD) who are exon 44, 45, 50 and 51 skipping amenable. Entrada has partnered with Vertex Pharmaceuticals to develop a clinical-stage program, VX-670, for myotonic dystrophy type 1 (DM1). 2026 represents a catalyst-rich period for Entrada. We expect multiple clinical data readouts as we advance several DMD programs across the U.K., EU, and U.S. By year-end 2026, we anticipate four clinical-stage programs in our DMD franchise (ENTR-601-44, ENTR-601-45, ENTR-601-50, and ENTR-601-51). These programs are complemented by the ongoing clinical progress of our DM1 collaboration with Vertex (VX-670). We are a tight-knit team of experts and leaders in both therapeutic development and rare diseases and are excited to grow and attract colleagues who are ready to join a high-energy, dedicated team that likes to get things done and dramatically improve the lives of patients and their families. The Perfect Addition to Our Team You are interested in working at the intersection of life sciences and business. You want to join a high

### Software Engineer, Beam Starcam - Google
- Location: San Francisco, CA, USA; +2 more (unspecified)
- Salary: $147K-$211K
- Posted: 2026-06-05
- Parental leave: 18 weeks (not source-backed)
- Non-birth-parent leave: 18 weeks (not source-backed)
- 401(k) match: listed (not source-backed)
- Apply: https://www.google.com/about/careers/applications/signin?jobId=CiUAL2FckepCyT4jdVn9BBaRIAa_p8zcUlwkoq9tyEE17WPTzqFsEjsACxwdTP30sDeNxEwLwfVRrMIYA0fjuVdzKwqaklK0R5SK70GtE6prm30SkFNqimG7o0hIgypNMn_HXA%3D%3D_V2&loc=US&title=Software+Engineer
- Excerpt: Software Engineer, Beam Starcam San Francisco, CA, USA; +2 more Google's software engineers develop the next-generation technologies that change how billions of users connect, explore, and interact with information and one another. Our products need to handle information at massive scale, and extend well beyond web search. We're looking for engineers who bring fresh ideas from all areas, including information retrieval, distributed computing, large-scale system design, networking and data storage, security, artificial intelligence, natural language processing, UI design and mobile; the list goes on and is growing every day. As a software engineer, you will work on a specific project critical to Google's needs with opportunities to switch teams and projects as you and our fast-paced business grow and evolve. We need our engineers to be versatile, display leadership qualities and be enthusiastic to take on new problems across the full-stack as we continue to push technology forward. With your technical expertise, you will manage project priorities, deadlines, and deliverables. You will design, develop, test, deploy, maintain, and enhance software solutions.Google Beam is a true-to-life new communication technology from Google that allows people to feel like they're having real face-to-face conversations, no matter the distance. Powered by realistic state-of-the-art 3D imaging and spatial audio and integrated with today's leading remote video platforms, Google Beam enables you to be immersed in the moment, together. As a part of the Google Beam team, you'll work with incredible teammates across all major functions in a fast-paced product-oriented environment. Your contributions will have an

### Associate Director, Biostatistics - Definium Therapeutics
- Location: Remote (remote)
- Salary: $184K-$209K
- Posted: 2026-06-04
- Apply: https://job-boards.greenhouse.io/definiumtherapeutics/jobs/5848284004
- Excerpt: Associate Director, Biostatistics Remote Definium Therapeutics is a late-stage clinical biopharmaceutical company and our mission is to forge a new era of psychiatry by applying scientific rigor to psychedelics, with the goal of developing accessible treatments that unlock healing at scale. Our lead product candidate, lysergide tartrate (our proprietary orally disintegrating tablet form of lysergide (LSD) D-tartrate), represents a highly differentiated, potential best-in-class opportunity for patients suffering from generalized anxiety, major depressive disorder, and posttraumatic stress disorder. Our early stage pipeline includes DT402, the R-enantiomer of MDMA and is under development to target the core symptoms of autism spectrum disorder (ASD), specifically addressing social communication challenges. Guided by the recognition that patients deserve more than better, Definium is relentlessly advancing a new generation of therapeutics intended to address the underlying causes of psychiatric and neurological disorders. By turning evidence into impact, Definium aims to change the trajectory of today's mental health care crisis and enable a healthier future. Headquartered in New York, Definium Therapeutics trades on Nasdaq under the symbol DFTX. Together we are moving psychiatry forward-beyond better, into a boundless future. Join us! As an Associate Director, Biostatistics this person will provide statistical support for pipeline compounds' clinical development, regulatory filing, and commercialization. Reporting to Vice President, Head of Biometrics and Data Science, the successful candidate will serve as the biostatistician for assigned clinical trials to provide statistical leadership from trial design, data analysis, to results interpretation and dissemination. This role will also provide statistical support to regulatory filing

### Director, Product and Pipeline Communications (Endocrinology and Metabolic) - Corcept Therapeutics
- Location: Redwood City, California, United States (unspecified)
- Salary: $239K-$281K
- Posted: 2026-06-10
- 401(k) match: listed (not source-backed)
- Apply: https://www.corcept.com/careers/current-opportunities/?gh_jid=6019134004
- Excerpt: Director, Product and Pipeline Communications (Endocrinology and Metabolic) Redwood City, California, United States For more than 25 years, Corcept has been singularly focused on the science of cortisol, a powerful hormone that when unregulated, can play a role in a broad range of diseases. Our commercial portfolio includes treatments for hypercortisolism and oncology, and the company has discovered more than 1,000 proprietary selective cortisol modulators and glucocorticoid receptor antagonists. With advanced clinical trials in patients with hypercortisolism, solid tumors, ALS and liver disease, Corcept is unlocking the power of cortisol modulation to help address some of the most devastating diseases patients face today. Corcept is headquartered in Redwood City, California. To learn more, visit www.corcept.com . The Director of Product and Pipeline Communications will drive product communications initiatives and activities across a growing roster of therapeutic areas for our Endocrinology business and metabolic disease program. Reporting to the Senior Director of Corporate Communications, the Director of Product and Pipeline Communications will drive initiatives that support increased product awareness and bolster Corcept's corporate reputation, developing approaches to communication that improve engagement with external stakeholders and meet the evolving business needs of the organization. Responsibilities: - Partner with leaders throughout the organization to plan and execute strategic communications activities to raise visibility of our products and pipeline - Develop and implement communications plans leveraging earned media, sponsored content, social media and owned media channels to engage and inform media, investors, employees, healthcare professionals, consumers, policymakers, advocacy partners and other external stakeholders -

### Equipment Maintenance Engineer (m/f/d) - TE Connectivity
- Location: Job Country Germany (unspecified)
- Salary: Not disclosed
- Posted: 2026-06-12
- 401(k) match: listed (not source-backed)
- Apply: https://careers.te.com/job/Berlin-Equipment-Maintenance-Engineer-%28mfd%29-BE-12459/149347-en_US/
- Excerpt: Equipment Maintenance Engineer (m/f/d) Job Country Germany At TE, you will unleash your potential working with people from diverse backgrounds and industries to create a safer, sustainable and more connected world. Job Overview We are seeking a highly motivated Equipment Maintenance Engineer (m/f/d) responsible for maintaining the reliability, availability, and optimal performance of semiconductor front-end processing equipment used in metallization and plasma-based processes. The role emphasizes the implementation of preventive and predictive maintenance strategies, advanced troubleshooting, root cause analysis, and continuous improvement initiatives to support high-volume semiconductor manufacturing. The engineer will collaborate closely with Process Engineering, Production, Facilities, and equipment vendors to ensure stable tool operation, minimize downtime, improve yield, and maintain strict compliance with cleanroom protocols and contamination control standards. Job Requirements Equipment Reliability & Maintenance Engineering Develop and improve preventive/predictive maintenance programs for metallization and plasma tools (PVD, E-Beam, Ion Beam Etch, PECVD) Lead advanced troubleshooting and root cause investigations across vacuum, RF/DC plasma, electrical, mechanical, thermal, and robotic subsystems Analyze fault logs and system data to identify degradation trends and implement corrective actions Support rapid tool recovery to restore production capability Oversee critical maintenance including chamber rebuilds, target replaceme

### Electron Beam Welder (Raptor Combustion Devices) - SpaceX
- Location: Hawthorne, CA (unspecified)
- Salary: $23-$27/hr
- Posted: 2026-05-28
- Parental leave: 0 weeks (not source-backed)
- Apply: https://boards.greenhouse.io/spacex/jobs/8569299002?gh_jid=8569299002
- Excerpt: Electron Beam Welder (Raptor Combustion Devices) Hawthorne, CA SpaceX was founded under the belief that a future where humanity is out exploring the stars is fundamentally more exciting than one where we are not. Today SpaceX is actively developing the technologies to make this possible, with the ultimate goal of enabling human life on Mars. ELECTRON BEAM WELDER (RAPTOR COMBUSTION DEVICES) RESPONSIBILITIES: - EB weld, assemble, and fabricate all combustion device hardware (Raptor V3 Fuel Stack) - Assist engineering in development of new weld schedules and optimization of existing tooling - Complete machine preventative maintenance and provide subject matter expertise to troubleshoot issues - Use precision calibrated tools - torque wrenches, micrometers and calipers - Perform work according to procedures, specifications and test instructions - Read and interpret technical drawings, and follow detailed work instructions - Use various mechanical tools without instruction - Perform other related duties for the purpose of ensuring an efficient and effective work environment - Operate forklifts, cranes and heavy equipment BASIC QUALIFICATIONS: - High school diploma or equivalency certificate - 2+ years of experience in EB welding, TIG Welding, CNC machine operation, and/or mechanical assembly PREFERRED SKILLS AND EXPERIENCE: - 5+ years of experience in welding with one or more of the following materials: stainless steel, inconel, aluminum or titanium - Experience with aerospace electron beam welding - Experience with aerospace TIG welding - Knowledge of weld assembly tolerances and pre-weld cleanliness requirements - Proficient in blue print reading and lay out - Knowledge and

### Senior Principal Engineer/Associate Director, Drug Product MSAT - Summit Therapeutics
- Location: Princeton, NJ (unspecified)
- Salary: $180K-$195K
- Posted: 2026-04-27
- Apply: https://job-boards.greenhouse.io/summittherapeutics/jobs/4232801009
- Excerpt: Senior Principal Engineer/Associate Director, Drug Product MSAT Princeton, NJ About Summit: Summit Therapeutics Inc. is a biopharmaceutical oncology company with a mission focused on improving quality of life, increasing potential duration of life, and resolving serious unmet medical needs. At Summit, we believe in building a team of world class professionals who are passionate about this mission, and it is our people who drive this mission to reality. Summit's core values include integrity, passion for excellence, purposeful urgency, collaboration, and our commitment to people. Our employees are truly the heart and soul of our culture, and they are invaluable in shaping our journey toward excellence. Summit's team is inspired to touch and help change lives through Summit's clinical studies in the field of oncology. Summit has multiple global Phase 3 clinical studies, including: Non-small Cell Lung Cancer (NSCLC) - HARMONi: Phase 3 clinical study which was intended to evaluate ivonescimab combined with chemotherapy compared to placebo plus chemotherapy in patients with EGFR-mutated, locally advanced or metastatic non-squamous NSCLC who were previously treated with a 3rd generation EGFR TKI. - HARMONi-3: Phase 3 clinical study which is intended to evaluate ivonescimab combined with chemotherapy compared to pembrolizumab combined with chemotherapy in patients with first-line metastatic NSCLC. - HARMONi-7: Phase 3 clinical study which is intended to evaluate ivonescimab monotherapy compared to pembrolizumab monotherapy in patients with first-line metastatic NSCLC. Colorectal Cancer (CRC) - HARMONi-GI3: Phase 3 clinical study intended to evaluate ivonescimab in combination with chemotherapy compared with bevacizumab plus chemotherapy.

### GNC Engineer, Beam Planning (Starshield) - SpaceX
- Location: Hawthorne, CA (unspecified)
- Salary: $125K-$150K
- Posted: 2026-05-26
- Parental leave: 0 weeks (not source-backed)
- Apply: https://boards.greenhouse.io/spacex/jobs/8564124002?gh_jid=8564124002
- Excerpt: GNC Engineer, Beam Planning (Starshield) Hawthorne, CA SpaceX was founded under the belief that a future where humanity is out exploring the stars is fundamentally more exciting than one where we are not. Today SpaceX is actively developing the technologies to make this possible, with the ultimate goal of enabling human life on Mars. GNC ENGINEER, BEAM PLANNING (STARSHIELD) Starshield leverages SpaceX's Starlink technology and launch capability to support national security efforts. While Starlink is designed for consumer and commercial use, Starshield is designed for government use, with an initial focus on earth observation, communications, and hosted payloads. As a GNC engineer on this team, you will bring a passion and expertise in areas like state estimation, spacecraft systems design, optimization, and software development to join the Starshield GNC team. Engineers on this team support various payloads through initial conception to on-orbit operation, with a focus on beam planning and algorithm development. You will be driving future hardware design and optimizing current payload performance through modeling and simulation. We are looking for engineers who enjoy solving complex problems, can work effectively in a fast-paced environment, and are passionate about advancing the space industry. RESPONSIBILITIES: - Develop highly reliable and performant GNC algorithms, flight software, simulations, tools, and services using C++ or Python - Conduct analyses, recommend designs, and write GNC software that balances competing requirements - Build software tools and construct scenarios to analyze system performance - Write high-quality technical documentation of programs, algorithms, or analysis - Develop software models

### Associate Director, Medicinal Chemistry - Maplight Therapeutics Inc
- Location: Remote (remote)
- Salary: $180K-$205K
- Posted: 2026-05-04
- Apply: https://job-boards.greenhouse.io/maplighttherapeutics/jobs/5209830008
- Excerpt: Associate Director, Medicinal Chemistry Remote Who We Are: MapLight Therapeutics is a clinical stage biotech company that focuses on drug discovery for central nervous system disorders. We combine cutting-edge technologies including optogenetics, in vivo physiology, and spatial transcriptomics to identify novel drug targets and develop effective therapies to address psychiatric symptoms. What You'll Do: We are searching for a highly motivated Medicinal Chemist to join our drug discovery team at the Associate Director level. Reporting to the Executive Director of Chemistry, the candidate will be expected to co-lead, or lead, preclinical medicinal chemistry programs from hit to candidate nomination. A highly qualified candidate will have experience in CNS drug discovery and an in-depth understanding of designing efficacious and safe brain-penetrant small molecules. While MapLight has in-house laboratories for pre-clinical research, many activities like chemical synthesis are outsourced to external vendors. Experience managing remote CRO teams, logistics across multiple partners, and coordinating internal drug discovery activities across different time zones is essential. This is a fantastic opportunity to join a small medicinal chemistry team and have a significant impact in addressing unmet patient needs by advancing MapLight's pipeline. Responsibilities: - Co-lead, or lead, preclinical medicinal chemistry programs from hit to candidate nomination. - Design and execute successful medicinal chemistry strategies to meet project and corporate goals. - Conduct multi-parameter optimization to deliver orally bioavailable, brain-penetrant candidates without secondary pharmacology, ADME, or safety concerns of initial hits. - Apply structure-based drug design principles utilizing in-house resources and external computational partners. - Manage

### Clinical Supply Manager - Tango Therapeutics Inc
- Location: Boston, MA (unspecified)
- Salary: $131K-$197K
- Posted: 2026-05-06
- 401(k) match: listed (not source-backed)
- Apply: https://job-boards.greenhouse.io/tangotherapeutics/jobs/7723999003
- Excerpt: Clinical Supply Manager Boston, MA Company Overview Tango Therapeutics is a biotechnology company dedicated to discovering novel drug targets and delivering the next generation of precision medicine for the treatment of cancer. Using an approach that starts and ends with patients, Tango leverages the genetic principle of synthetic lethality to discover and develop therapies that take aim at critical targets in cancer. This includes expanding the universe of precision oncology targets into novel areas such as tumor suppressor gene loss and their contribution to the ability of cancer cells to evade immune cell killing. Tango's labs and offices are located at 201 Brookline Avenue, in the vibrant Fenway area of Boston, Massachusetts Summary We are seeking a Clinical Supply Manager (CSM) to lead the end-to-end clinical supply management process of our growing clinical portfolio. This role will serve as the primary sponsor contact for external vendors managing the packaging and labeling, storage, distribution, and return/ destruction of clinical supplies. In a fast-paced, small biotech environment, the CSM will plan, execute and oversee clinical supplies in alignment with trial timelines, budget, regulatory requirements and internal standards. This individual will play a key role in enabling clinical trial start, patient enrollment, and continuous supply as per trial requirements, proactively identifying and mitigating risks, and ensuring compliance of clinical supply with applicable regulations and internal standards. The ideal candidate is highly collaborative, detail-oriented, and comfortable operating in a hands-on environment, with a focus on building scalable processes, tools, and best practices to support

### Sr. Welding Engineer - SpaceX
- Location: Hawthorne, CA (unspecified)
- Salary: $130K-$180K
- Posted: 2025-12-16
- Parental leave: 0 weeks (not source-backed)
- Apply: https://boards.greenhouse.io/spacex/jobs/8341264002?gh_jid=8341264002
- Excerpt: Sr. Welding Engineer Hawthorne, CA SpaceX was founded under the belief that a future where humanity is out exploring the stars is fundamentally more exciting than one where we are not. Today SpaceX is actively developing the technologies to make this possible, with the ultimate goal of enabling human life on Mars. SR. WELDING ENGINEER This position will support manufacturing and development of SpaceX's Falcon 9 and Starship launch vehicles, Dragon spacecraft, and Starlink satellites alongside a strong group of design and build engineers. The person in this position will help develop, qualify, and optimize welding designs and processes including but not limited to; electron beam welding, laser beam welding, gas tungsten arc welding, orbital tube welding, resistance welding, gas metal arc welding, and plasma arc welding. The welding engineer in this role will interface daily with design and manufacturing engineers to make welding judgment calls and improvements and will enforce standardized practices and procedures on multiple welded assemblies. RESPONSIBILITIES: - Develop, optimize, and qualify weld processes and parameters for multiple welding processes including but not limited to: electron beam welding, laser beam welding, gas tungsten arc welding, orbital tube welding, resistance welding, gas metal arc welding, friction stir welding, and plasma arc welding - Support production operations on full scale welded assemblies, providing direction to manufacturing engineers and welders on correct techniques in a fast paced manufacturing environment - Support design, manufacturing, and materials engineering with root cause analysis - Work closely with design, tooling, automation, and development engineers

### Patient Access Navigator - Cogent Biosciences Inc
- Location: Waltham, Massachusetts, United States (unspecified)
- Salary: $170K-$200K
- Posted: 2026-03-02
- Parental leave: 12 weeks (not source-backed)
- 401(k) match: listed (not source-backed)
- Learning budget: yes (not source-backed)
- Apply: https://job-boards.greenhouse.io/cogentbiosciences/jobs/4163457009
- Excerpt: Patient Access Navigator Waltham, Massachusetts, United States Who We Are: Cogent Biosciences is a publicly traded biotechnology company focused on developing novel precision therapies to treat a broad range of patients with unmet medical needs. Cogent's lead program, bezuclastinib, is designed to selectively and potently inhibit exon 17 mutations found within the KIT receptor tyrosine kinase, including KIT D816V. KIT D816V is responsible for driving a rare and serious condition called Systemic Mastocytosis, and exon 17 mutations are also found in patients with gastrointestinal stromal tumors (GIST), a type of cancer with strong dependence on oncogenic KIT signaling. Bezuclastinib has exhibited promising initial data across all three trials: APEX in AdvSM, SUMMIT in NonAdvSM and PEAK in GIST, including an encouraging safety profile across 600+ patients in single agent and combination dosing. The Role: Cogent Biosciences is searching for compassionate and highly motivated Patient Access Navigators to establish the inaugural Patient Services team. The Patient Access Navigators will be responsible for delivering a high-touch, patient-centered access experience across the prescription fulfillment journey. The Patient Access Navigator will own the end-to-end patient experience within an assigned geographic region and partners closely with patients, caregivers, healthcare providers (HCPs), specialty pharmacies, internal field teams, and external patient services partners to ensure timely access to therapy and continuity of care. While primarily remote/office-based (depending on location), the Patient Access Navigator will support limited non-promotional on-site visits to HCP offices, when appropriate, to support complex access, reimbursement or care coordination needs. The successful candidate will

### Sr. Software Engineer, Beam Planning (Starlink) - SpaceX
- Location: Redmond, WA (unspecified)
- Salary: $160K-$225K
- Posted: 2026-03-25
- Apply: https://boards.greenhouse.io/spacex/jobs/8478512002?gh_jid=8478512002
- Excerpt: Sr. Software Engineer, Beam Planning (Starlink) Redmond, WA SpaceX was founded under the belief that a future where humanity is out exploring the stars is fundamentally more exciting than one where we are not. Today SpaceX is actively developing the technologies to make this possible, with the ultimate goal of enabling human life on Mars. SR. SOFTWARE ENGINEER, BEAM PLANNING (STARLINK) At SpaceX we're leveraging our experience in building rockets and spacecraft to deploy Starlink, the world's most advanced broadband internet system. Starlink is the world's largest satellite constellation and is providing fast, reliable internet to millions of users worldwide. We design, build, test, and operate all parts of the system - thousands of satellites, consumer receivers that allow users to connect within minutes of unboxing, and the software that brings it all together. We've only begun to scratch the surface of Starlink's potential global impact and are looking for the world's best engineers to help maximize Starlink's utility for communities and businesses around the globe. As a Beam Planning Software Engineer on the Starlink program, you will be solving challenges that improve our ability to fully utilize the hardware we have deployed. Our goal is to provide customers with the best possible satellite internet experience, often providing under-served communities with affordable, life-changing broadband internet access. Our software engineers are responsible for the complete lifecycle of the software they create, including development, testing, and support. We expect our engineers to close the feedback loop between software design and real-world performance.

### Technician Maintenance E-Beam - Vishay Precision Group INC
- Location: 2 Locations (unspecified)
- Salary: Not disclosed
- Posted: 2026-05-12
- 401(k) match: listed (not source-backed)
- Apply: https://vishay.wd3.myworkdayjobs.com/VishayCareers/job/Durango-MX/Technician-Maintenance-E-Beam_JR-4959
- Excerpt: Technician Maintenance E-Beam 2 Locations Garantiza que las instalaciones y la maquinaria utilizados para producir materiales y bienes nuevos y existentes funcionen con su máxima eficiencia y rendimiento, liderando a un grupo de técnicos de mantenimiento asignados en piso de producción. Incluye actividades de mantenimiento predictivo, mantenimiento preventivo total, la gestión de averías de equipos mecánicos, eléctricos y electrónicos (incluida la programación de software). Educación: TSU o Ingeniería en mecatrónica, eléctrica, mecánica o electrónica. Experiencia: 3 a 5 años de experiencia en actividades de mantenimiento a equipo de manufactura. Estas actividades incluyen trabajos de naturaleza mecánica, eléctrica y electrónica. Requisitos: Bilingüe, buen dominio del idioma inglés. Importante: Visa vigente y disponibilidad de viaje cuando se disponga.

### Senior Director, Medical Affairs Operations and Strategy - Definium Therapeutics
- Location: Remote (remote)
- Salary: $269K-$295K
- Posted: 2026-06-04
- Apply: https://job-boards.greenhouse.io/definiumtherapeutics/jobs/5973783004
- Excerpt: Senior Director, Medical Affairs Operations and Strategy Remote Definium Therapeutics is a late-stage clinical biopharmaceutical company and our mission is to forge a new era of psychiatry by applying scientific rigor to psychedelics, with the goal of developing accessible treatments that unlock healing at scale. Our lead product candidate, lysergide tartrate (our proprietary orally disintegrating tablet form of lysergide (LSD) D-tartrate), represents a highly differentiated, potential best-in-class opportunity for patients suffering from generalized anxiety, major depressive disorder, and posttraumatic stress disorder. Our early stage pipeline includes DT402, the R-enantiomer of MDMA and is under development to target the core symptoms of autism spectrum disorder (ASD), specifically addressing social communication challenges. Guided by the recognition that patients deserve more than better, Definium is relentlessly advancing a new generation of therapeutics intended to address the underlying causes of psychiatric and neurological disorders. By turning evidence into impact, Definium aims to change the trajectory of today's mental health care crisis and enable a healthier future. Headquartered in New York, Definium Therapeutics trades on Nasdaq under the symbol DFTX. Together we are moving psychiatry forward-beyond better, into a boundless future. Join us! Responsibilities: In collaboration with Medical Affairs leadership, develop, operationalize, and continuously refine the Medical Affairs strategy, helping to translate strategic objectives into actionable project plans, KPIs and timelines Oversee and ensure the quality of the departmental strategic planning processes, including operations tasks, and other activities related to pipeline compounds Leads organization, updating and communication of strategic plans to internal and external stakeholders

### Senior Manager/Associate Director, Marketing Operations - Cogent Biosciences Inc
- Location: Waltham, Massachusetts, United States (unspecified)
- Salary: $175K-$200K
- Posted: 2026-05-01
- 401(k) match: listed (not source-backed)
- Learning budget: yes (not source-backed)
- Apply: https://job-boards.greenhouse.io/cogentbiosciences/jobs/4238109009
- Excerpt: Senior Manager/Associate Director, Marketing Operations Waltham, Massachusetts, United States Who We Are: Cogent Biosciences is a publicly traded biotechnology company focused on developing novel precision therapies to treat a broad range of patients with unmet medical needs. Cogent's lead program, bezuclastinib, is designed to selectively and potently inhibit exon 17 mutations found within the KIT receptor tyrosine kinase, including KIT D816V. KIT D816V is responsible for driving a rare and serious condition called Systemic Mastocytosis, and exon 17 mutations are also found in patients with gastrointestinal stromal tumors (GIST), a type of cancer with strong dependence on oncogenic KIT signaling. Bezuclastinib has exhibited promising initial data across all three trials: APEX in AdvSM, SUMMIT in NonAdvSM and PEAK in GIST, including an encouraging safety profile across 600+ patients in single agent and combination dosing. The Role: This critical role will manage the tactical execution of marketing operations supporting the launch of bezuclastinib, Cogent Biosciences' key pipeline asset. This role ensures compliant, efficient, and impactful delivery of promotional content, omnichannel campaigns, key marketing KPI's. This role is critical to implementing. evolving and advancing our organization's omnichannel capabilities. The Senior Manager partners closely with brand leads to unify personal and non-personal promotional activities into a seamless customer experience that drives brand performance goals and commercial growth. Responsibilities: - Omnichannel Campaign Orchestration - Work with marketing to ensure the execution of complex customer engagement plans into high-performing omnichannel campaigns across HCP, patient, and caregiver audiences. - Collaborate with analytics teams to integrate insights

### Overhead Crane Operator - Arcosa Inc
- Location: Clinton, IL (unspecified)
- Salary: Not disclosed
- Posted: 2026-06-05
- 401(k) match: listed (not source-backed)
- Apply: https://recruiting2.ultipro.com/ARC1026ARCOI/JobBoard/2af23579-6cf8-4926-be1a-3bc74872c197/OpportunityDetail?opportunityId=21897c8c-9373-49d6-b95f-ba0cc2da403a
- Excerpt: Overhead Crane Operator Clinton, IL Meyer Utility Structures is searching for Overhead Crane Operators for our Clinton, IL location. As an Overhead Crane Operator, you'll be responsible for the safe and precise operation of an overhead crane to lift, move, and position heavy materials, such as steel plates, beams, and components, within a fabrication environment. This role is critical to maintaining production workflow and ensuring all safety protocols are strictly followed.

### Cell Therapy Account Management - Michigan - Iovance Biotherapeutics Inc
- Location: Michigan (unspecified)
- Salary: $200K-$220K
- Posted: 2026-05-27
- 401(k) match: listed (not source-backed)
- Apply: https://job-boards.greenhouse.io/iovancebiotherapeutics/jobs/5231791008
- Excerpt: Cell Therapy Account Management - Michigan Michigan Iovance Biotherapeutics aims to be the global leader in innovating, developing and delivering tumor infiltrating lymphocyte (TIL) therapy for people with cancer. We are pioneering a transformational approach to treating cancer by harnessing the ability of the human immune system to recognize and attack diverse cancer cells in each patient. The Iovance TIL platform has demonstrated promising clinical data across multiple solid tumors. We are committed to continuous innovation in cell therapy, including gene-edited cell therapy, which may be a promising option for patients with cancer. Overview Amtagvi™ is the best-in-class cell therapy treatment for advanced melanoma. The Cell Therapy Account Management (CTAM) will be responsible for driving Amtagvi demand by building a robust referral network between community practices and academic centers; enable early patient identification and streamline referral pathways; and collaborate with internal teams to enhance scientific and operational excellence in cell therapy account management. To succeed in this role, you will use prior experience to optimize territory strategy in the oncology rare disease space and have demonstrated experience influencing others and building relationships. Additional competencies include experience with immunotherapy and solid tumor cancer, as well as prior launch experience, demonstrated ability to drive demand, pull through, and sustain the growth of Amtagvi™. Essential Functions and Responsibilities: - Drive Amtagvi TM demand and appropriate pull-through at targeted ATCs and serve as a liaison between community oncology practices and internal stakeholders to align initiatives with business and medical objectives. - Serve as the

### Sr. Quality Engineering Manager, Amazon Devices, Quality & Lean - Amazon
- Location: Bellevue, Washington, USA (unspecified)
- Salary: $137K-$186K
- Posted: 2026-05-04
- Parental leave: 6 weeks (not source-backed)
- Non-birth-parent leave: 6 weeks (not source-backed)
- 401(k) match: listed (not source-backed)
- Fertility benefits: yes (not source-backed)
- Adoption assistance: yes (not source-backed)
- Mental health support: yes (not source-backed)
- Childcare support: yes (not source-backed)
- Apply: https://www.amazon.jobs/en/jobs/10410621/sr-quality-engineering-manager-amazon-devices-quality-lean
- Excerpt: Sr. Quality Engineering Manager, Amazon Devices, Quality & Lean Bellevue, Washington, USA Amazon Lab126 is an inventive research and development company that designs and engineers high-profile consumer electronics. Lab126 began in 2004 as a subsidiary of Amazon.com, Inc., originally creating the best-selling Kindle family of products. Since then, we have produced groundbreaking devices like Fire Tablets, Fire TV, Amazon Echo and E-reader products. What will you help us create? The Role: The Sr. Hardware Quality Engineering Manager (QEM) is responsible for ensuring that our products are designed for quality. As early as the concept phase of the product, the QEM will develop a risk assessment utilizing the NUD process (New, Unique, Different). This risk assessment will be comprehensive of lessons learned on previous products, along with technological, manufacturing and operational risks to the current design. The successful candidate will establish quality goals and monitor performance, investigate the full suite of failure analysis leading to root cause determination and subsequent closed loop corrective action. Conduct quality lessons learned and institutes remedies to prevent re-occurrence of quality issues and possess a high sense of urgency when managing critical issues. This position also needs to onsite support NPI builds and drive build issues to closure with RCCA/8D. The candidate must be able to influence engineering teams for design improvements, with an emphasis on delivering robust RF & antenna solutions essential to beam forming, beam pointing, and beam steering. In addition to the work done in the New Product Introduction (NPI) and Early Sustaining

### Pointing and Precision Engineer - Aetherflux
- Location: San Carlos, California, United States (unspecified)
- Salary: Not disclosed
- Posted: 2024-10-08
- Apply: https://aetherflux.recruitee.com/o/pointing-and-precision-engineer
- Excerpt: Pointing and Precision Engineer San Carlos, California, United States As a Precision, Pointing, and Tracking Engineer at Aetherflux, you will be responsible for the design, development, and optimization of satellite systems to achieve precise laser pointing and alignment. This role focuses on ensuring accurate positioning and stability of laser beams, which are critical for successful energy transmission from space to Earth. You will collaborate with multidisciplinary teams, including optical, mechanical, and systems engineers, to develop control algorithms, fine-tune system precision, and validate the pointing accuracy of our satellite platforms. Key Responsibilities: - Pointing Control System Design: Develop and implement pointing and control algorithms to achieve high-precision laser beam steering and alignment in space environments. - Hardware and Software Integration: Work closely with electrical, optical, and software engineers to integrate pointing control systems with satellite platforms, ensuring seamless coordination between hardware and control software. - Precision Alignment: Design and test systems that ensure precise alignment of laser beams with ground-based receivers, taking into account environmental factors such as satellite motion, atmospheric distortion, and thermal effects. - System Testing and Validation: Lead system-level testing and validation efforts, including lab simulations and in-orbit tests, to verify the pointing accuracy and stability of satellite laser systems. - Performance Optimization: Conduct analysis to optimize system performance, improving beam precision and pointing accuracy while minimizing energy loss during transmission. - Risk Management: Identify potential risks related to pointing precision, such as system misalignment or external disturbances, and implement mitigation strategies. - Cross-functional Collaboration: Collaborate with optical,

### Senior Manager, Trade and Distribution - Cogent Biosciences Inc
- Location: Waltham, Massachusetts, United States (unspecified)
- Salary: $175K-$205K
- Posted: 2026-03-25
- 401(k) match: listed (not source-backed)
- Learning budget: yes (not source-backed)
- Apply: https://job-boards.greenhouse.io/cogentbiosciences/jobs/4195598009
- Excerpt: Senior Manager, Trade and Distribution Waltham, Massachusetts, United States Who We Are: Cogent Biosciences is a publicly traded biotechnology company focused on developing novel precision therapies to treat a broad range of patients with unmet medical needs. Cogent's lead program, bezuclastinib, is designed to selectively and potently inhibit exon 17 mutations found within the KIT receptor tyrosine kinase, including KIT D816V. KIT D816V is responsible for driving a rare and serious condition called Systemic Mastocytosis, and exon 17 mutations are also found in patients with gastrointestinal stromal tumors (GIST), a type of cancer with strong dependence on oncogenic KIT signaling. Bezuclastinib has exhibited promising initial data across all three trials: APEX in AdvSM, SUMMIT in NonAdvSM and PEAK in GIST, including an encouraging safety profile across 600+ patients in single agent and combination dosing. The Role: The Senior Manager of Trade and Distribution will be responsible for management of Cogent Bioscience's network of Specialty Distributor accounts. The Key responsibilities will be to oversee the physical and financial flow of the Cogent Biosciences portfolio beginning with the launch of Bezuclastinib. The candidate will be the primary for Specialty Distributor customers tasked with maintaining relationships and growing Cogent Biosciences business while contributing to the evolving channel strategy for products. This candidate will oversee all aspects of business operations within assigned customers including inventory management, product fulfillment, data flow and management of returns. The individual will report to the Executive Director Trade & Distribution within the Market Access team and work closely with

### Principal Scientist, Peptide Therapeutics - Genentech, Inc.
- Location: South San Francisco, California, United States of America (unspecified)
- Salary: Not disclosed
- Posted: 2026-02-24
- 401(k) match: listed (not source-backed)
- Apply: https://roche.wd3.myworkdayjobs.com/ROG-A2O-GENE/job/South-San-Francisco/Principal-Scientist--Peptide-Therapeutics_202602-103654/apply
- Excerpt: Principal Scientist, Peptide Therapeutics South San Francisco, California, United States of America This is a primarily lab-based, technical leadership position within the Peptide Therapeutics department. In this lab-based leadership role, you will combine hands-on synthetic expertise with strategic...

### Software Engineer, Android Platform, Google Beam - Google
- Location: Mountain View, CA, USA; +2 more (unspecified)
- Salary: $147K-$211K
- Posted: 2026-06-05
- Parental leave: 18 weeks (not source-backed)
- Non-birth-parent leave: 18 weeks (not source-backed)
- 401(k) match: listed (not source-backed)
- Apply: https://www.google.com/about/careers/applications/signin?jobId=CiUAL2FckTq_5x7d8_y6yD4tdGQB0ePBs0tZ7HC9EwrDPb-zJv7jEjsACxwdTLy6h7pJDpCiUF5MmAL-HZbwCqKTm8eDSZwz8N54Or19o_45164tb1ikI8942_GuplAAm1PA5w%3D%3D_V2&loc=US&title=Software+Engineer
- Excerpt: Software Engineer, Android Platform, Google Beam Mountain View, CA, USA; +2 more Google's software engineers develop the next-generation technologies that change how billions of users connect, explore, and interact with information and one another. Our products need to handle information at massive scale, and extend well beyond web search. We're looking for engineers who bring fresh ideas from all areas, including information retrieval, distributed computing, large-scale system design, networking and data storage, security, artificial intelligence, natural language processing, UI design and mobile; the list goes on and is growing every day. As a software engineer, you will work on a specific project critical to Google's needs with opportunities to switch teams and projects as you and our fast-paced business grow and evolve. We need our engineers to be versatile, display leadership qualities and be enthusiastic to take on new problems across the full-stack as we continue to push technology forward. Beam is redefining the boundaries of human connection through three-dimensional video technology. By creating immersive, life-sized communication experiences, we are making the distance between people disappear. As a Software Engineer on the Beam team, you will sit at the intersection of innovative three-dimensional computer goals and the android ecosystem. This role presents unique engineering issues that go beyond standard application development. You will be tasked with optimizing the android operating system to manage high-bandwidth, low-latency three-dimensional video streams. This involves deep-stack systems programming, custom networking configurations, and fine-tuning hardware abstraction layers to ensure a seamless, "being there" experience. You will

### Frontend Engineer, Product - Grow Therapy
- Location: New York City, New York, United States, San Francisco, Seattle (unspecified)
- Salary: $166K-$250K
- Posted: 2026-06-05
- Parental leave: 18 weeks (not source-backed)
- Mental health support: yes (not source-backed)
- Apply: https://jobs.ashbyhq.com/grow-therapy/0cda95fe-87c9-45f0-943f-a6d340bc2f03
- Excerpt: Frontend Engineer, Product New York City, New York, United States, San Francisco, Seattle Grow Therapy is on a mission to serve as the trusted partner for therapists growing their practice, and patients accessing high-quality care. Powered by technology, we are a three-sided marketplace that empowers providers, augments insurance payors, and serves patients. Following the mass increase in depression and anxiety, the need for accessibility is more important than ever. To make our vision for mental healthcare a reality, we're building a team of entrepreneurs and mission-driven go-getters. Since launching in February 2021, we've empowered more than ten thousand therapists and hundreds of thousands of clients across the country and insurance landscape. We've raised more than $328Mm in funding, including our Series D, at a $3B valuation from Sequoia Capital, Transformation Capital, TCV, SignalFire, Menlo Ventures, Goldman Sachs Alternatives, and others. The Opportunity We're looking for a product-focused Frontend Engineer to raise the bar on how we deliver experiences across Grow's marketplace - the search, matching, and booking surfaces that every client and provider touches first. This role sits at the intersection of design and engineering: you'll work directly with designers and product to ship new experiences that feel crafted, consistent, and human. You'll join a product team and own high-impact work from ideation through launch - owning the implementation layer and the polish in everything we ship. Beyond new feature development, you'll proactively close gaps in product quality by partnering with design and product teams and raising the UI bar

### Therapeutic Area Lead Vaccines & Infectious Diseases - Merck & Co., Inc.
- Location: POL - Mazowieckie Wojewodztwo - Warsaw (Trade Center) (unspecified)
- Salary: Not disclosed
- Posted: 2026-06-10
- 401(k) match: listed (not source-backed)
- Apply: https://msd.wd5.myworkdayjobs.com/SearchJobs/job/POL---Mazowieckie-Wojewodztwo---Warsaw-Trade-Center/Therapeutic-Area-Lead-Vaccines---Infectious-Diseases_R397207-1
- Excerpt: Therapeutic Area Lead Vaccines & Infectious Diseases POL - Mazowieckie Wojewodztwo - Warsaw (Trade Center) posted: Posted 2 Days Ago

### Sr. Manager / Associate Director, Drug Substance; Hypopara - BridgeBio Pharma, Inc.
- Location: San Francisco - 1800 Owens (unspecified)
- Salary: $175K-$185K
- Posted: 2026-04-22
- Apply: https://job-boards.greenhouse.io/bridgebio/jobs/5106746007
- Excerpt: Sr. Manager / Associate Director, Drug Substance; Hypopara San Francisco - 1800 Owens Mavericks Wanted When was the last time you achieved the impossible? If that thought feels overwhelming, you might want to pause here, but if it sparks excitement...read on In 2015, we pioneered a “moneyball for biotech” approach, pooling projects and promising early-stage research from academia together under one financial umbrella to reduce risk and unleash innovation. This model allows science and small teams of experts to lead the way. We build bridges to groundbreaking advancements in rare disease, and develop life-changing medicines for patients with unmet needs as fast as humanly possible. Together we define white space, push boundaries, and empower people to solve problems. If you're someone who defies convention, join us and work alongside some of the most respected minds in the industry. Together, we'll ask "why not?" and help reengineer the future of biopharma. At BridgeBio, we value curiosity and experimentation-including the ethical & thoughtful use of AI to improve clarity, speed, and quality of work. What You'll Do Senior Scientist / Associate Director, Drug Substance Development and Manufacturing will support Calcilytix Therapeutics, a subsidiary of BridgeBio Pharma. This position will be responsible for managing outsourced drug substance process development and manufacturing activities at contract suppliers, including manufacture of raw materials and drug substance for clinical studies, process validation, commercial launch, and tech transfer to new vendors to build and maintain the commercial supply chain throughout product lifecycle. The position will also support submission

### Associate Director, Drug Substance Development & Manufacturing - Entrada Therapeutics Inc
- Location: Boston, MA (unspecified)
- Salary: $172K-$202K
- Posted: 2026-02-27
- 401(k) match: listed (not source-backed)
- Learning budget: yes (not source-backed)
- Apply: https://job-boards.greenhouse.io/entradatherapeutics/jobs/5062031007
- Excerpt: Associate Director, Drug Substance Development & Manufacturing Boston, MA The Organization What's happening at Entrada Therapeutics? Entrada is a clinical-stage biopharmaceutical company aiming to transform the lives of patients by establishing a new class of medicines that engage intracellular targets that have long been considered inaccessible. Through proprietary and versatile approaches, Entrada is advancing a robust development portfolio of genetic medicines for the potential treatment of neuromuscular and inherited retinal diseases, among others. Our lead oligonucleotide programs are in development for the potential treatment of people living with Duchenne muscular dystrophy (DMD) who are exon 44, 45, 50 and 51 skipping amenable. Entrada has partnered with Vertex Pharmaceuticals to develop a clinical-stage program, VX-670, for myotonic dystrophy type 1 (DM1). 2026 represents a catalyst-rich period for Entrada. We expect multiple clinical data readouts as we advance several DMD programs across the U.K., EU, and U.S. By year-end 2026, we anticipate four clinical-stage programs in our DMD franchise (ENTR-601-44, ENTR-601-45, ENTR-601-50, and ENTR-601-51). These programs are complemented by the ongoing clinical progress of our DM1 collaboration with Vertex (VX-670). We are a tight-knit team of experts and leaders in both therapeutic development and rare diseases and are excited to grow and attract colleagues who are ready to join a high-energy, dedicated team that likes to get things done and dramatically improve the lives of patients and their families. The Perfect Addition to Our Team You are a motivated, resourceful, and enthusiastic Drug Substance Development & Manufacturing expert excited to support the

### Associate Therapeutic Development Manager - Merck & Co., Inc.
- Location: HKG - Hong Kong Island - Hong Kong (Lee Garden Two) (unspecified)
- Salary: Not disclosed
- Posted: 2026-05-27
- 401(k) match: listed (not source-backed)
- Apply: https://msd.wd5.myworkdayjobs.com/SearchJobs/job/HKG---Hong-Kong-Island---Hong-Kong-Lee-Garden-Two/Associate-Therapeutic-Development-Manager_R400021
- Excerpt: Associate Therapeutic Development Manager HKG - Hong Kong Island - Hong Kong (Lee Garden Two) posted: Posted 16 Days Ago

### Therapeutic Area Head – Respiratory - Apogee Therapeutics Inc
- Location: Remote (remote)
- Salary: $395K-$425K
- Posted: 2026-06-11
- 401(k) match: listed (not source-backed)
- Apply: https://job-boards.greenhouse.io/apogeetherapeutics/jobs/5160938007
- Excerpt: Therapeutic Area Head – Respiratory Remote About Apogee Therapeutics Founded in 2022, Apogee Therapeutics, Inc. (Ticker: APGE) is a well-funded, Nasdaq listed company that offers the opportunity to work in a fast-paced, highly dynamic environment. At Apogee, you can actively contribute to shaping the company culture, take on various roles and responsibilities, and grow professionally. Apogee Therapeutics is a clinical-stage biotechnology company advancing novel biologics with potential for differentiated efficacy and dosing in the largest I&I markets, Apogee's antibody programs are designed to overcome limitations of existing therapies by targeting well-established mechanisms of action and incorporating advanced antibody engineering to optimize half-life and other properties. Zumilokibart (APG777), the company's most advanced program, is being initially developed for the treatment of atopic dermatitis (AD), which is the largest and one of the least penetrated I&I markets, as well as asthma. With four validated targets in its portfolio, Apogee is seeking to achieve best-in-class efficacy and dosing through monotherapies and combinations of its novel antibodies. Based on a broad pipeline and depth of leadership and expertise, the company believes it can deliver value and meaningful benefit to patients underserved by today's standard of care. We are a fast-paced company committed to building an exceptional culture, founded on our C.O.R.E. values: C aring, O riginal, R esilient and E goless and a commitment to refusing to stop at “good enough”. If this sounds like you, keep reading! Role Summary We are seeking a Therapeutic Area (TA) Head, Respiratory - Clinical Development. In this

### Marketing Manager I - Rheumatology - AbbVie Inc.
- Location: Florham Park, NJ, United States (unspecified)
- Salary: Not disclosed
- Posted: 2026-06-10
- Parental leave: 12 weeks (not source-backed)
- Non-birth-parent leave: 12 weeks (not source-backed)
- 401(k) match: listed (not source-backed)
- Apply: https://jobs.smartrecruiters.com/AbbVie/3743990013522486-marketing-manager-i-rheumatology
- Excerpt: Marketing Manager I - Rheumatology Florham Park, NJ, United States Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: The Associate Director, Operations and Communications will work directly with the Rheumatology franchise VP, senior staff and employees across sales, marketing and IBT to ensure strategic and tactical imperatives are communicated clearly and operating effectively and efficiently to advance the business, inspire internal stakeholders and elevate employee engagement and culture. Effectiveness in role includes day-to-day planning and execution of a strategic communications & operational plan as well as seeking opportunities to close gaps and elevate agility and engagement. The role also includes strategic projects to advance Rheumatology commercial or IBT organization as needs are identified. Responsibilities: Integrate marketing, sales, and IBT strategies to enhance overall communication, execution and engagement. Manage scope, project plan, logistics and schedule of strategic and tactical initiatives. Establish strong organizational tools to drive project progress, ensure deadlines and project goals are met, identify and resolve issues, identify and close gaps as needed. Work cross-functionally with internal stakeholders to create, socialize, optimize and implement commercial

### Therapeutic Area Policy Director - Genentech, Inc.
- Location: South San Francisco, California, United States of America (unspecified)
- Salary: Not disclosed
- Posted: 2026-06-01
- 401(k) match: listed (not source-backed)
- Apply: https://roche.wd3.myworkdayjobs.com/ROG-A2O-GENE/job/South-San-Francisco/Therapeutic-Area-Policy-Director_202605-112975-1/apply
- Excerpt: Therapeutic Area Policy Director South San Francisco, California, United States of America Exciting opportunity for a strategic policy director to shape healthcare policy and optimize patient access across diverse therapeutic areas. Lead cross-functional teams, influence policy at the highest levels, and drive strategic readiness for innovative therapies. Join us to make a significant impact on patient outcomes and healthcare innovation.

### Associate Director, Bioanalytical Development - Formation Bio
- Location: New York, NY; Boston, MA (unspecified)
- Salary: $178K-$232K
- Posted: 2026-03-03
- Apply: https://job-boards.greenhouse.io/formationbio/jobs/7530453
- Excerpt: Associate Director, Bioanalytical Development New York, NY; Boston, MA About Formation Bio Formation Bio is a tech and AI driven pharma company differentiated by radically more efficient drug development. Advancements in AI and drug discovery are creating more candidate drugs than the industry can progress because of the high cost and time of clinical trials. Recognizing that this development bottleneck may ultimately limit the number of new medicines that can reach patients, Formation Bio, founded in 2016 as TrialSpark Inc., has built technology platforms, processes, and capabilities to accelerate all aspects of drug development and clinical trials. Formation Bio partners, acquires, or in-licenses drugs from pharma companies, research organizations, and biotechs to develop programs past clinical proof of concept and beyond, ultimately helping to bring new medicines to patients. The company is backed by investors across pharma and tech, including a16z, Sequoia, Sanofi, Thrive Capital, John Doerr, Spark Capital, SV Angel Growth, and others. You can read more at the following links: - Our Vision for AI in Pharma - Our Current Drug Portfolio - Our Technology & Platform At Formation Bio, our values are the driving force behind our mission to revolutionize the pharma industry. Every team and individual at the company shares these same values, and every team and individual plays a key part in our mission to bring new treatments to patients faster and more efficiently. About the Position The Associate Director, Bioanalytical will lead bioanalytical strategy and delivery for assigned programs, working across nonclinical and clinical

### Therapeutic Area Manager (TAM), Breast - Pennsylvania Ecosystem - Genentech, Inc.
- Location: Wilmington, Delaware, United States of America (unspecified)
- Salary: Not disclosed
- Posted: 2026-06-04
- 401(k) match: listed (not source-backed)
- Apply: https://roche.wd3.myworkdayjobs.com/ROG-A2O-GENE/job/Delaware/Therapeutic-Area-Manager--TAM---Breast---Pennsylvania-Ecosystem_202606-114052/apply
- Excerpt: Therapeutic Area Manager (TAM), Breast - Pennsylvania Ecosystem Wilmington, Delaware, United States of America Embrace the opportunity to become a Therapeutic Area Manager, Breast, and drive impactful patient outcomes in the Pennsylvania ecosystem. Leverage your expertise in healthcare sales, account management, and cross-functional collaboration to optimize product access and support innovative treatments. Make a difference in the rare disease community with Genentech.

### Executive Director of Protein Engineering and Chemistry - Shasqi
- Location: United States | Remote | Remote - United States (remote)
- Salary: Not disclosed
- Posted: 2026-06-10
- Apply: https://jobs.ashbyhq.com/shasqi/fc93e119-7bf1-44cf-9eaa-5e9be635478a
- Excerpt: Executive Director of Protein Engineering and Chemistry United States | Remote | Remote - United States What if cancer drugs could find the tumor - and go nowhere else? What if this meant you could get potent therapy directly to the tumor, sparing healthy cells? That's the future we're building at Shasqi, using Nobel Prize-winning science to unleash powerful therapies only where they're needed. We're a small, driven team encompassing broad backgrounds and experiences, united by a single mission: make cancer treatments more effective with minimal side effects. OUR OPERATING PRINCIPLES - We move fast because speed matters to cancer patients. - We aim to communicate openly and challenge ideas regardless of job title. - We are bold, take risks, and push boundaries being led by science. - We operate with humble confidence: meaning we can balance our sense of capability and conviction without ego, while being humble to seek advice and learn from our mistakes. If that fires you up, come build the future of cancer therapy with us! YOU'RE THE RIGHT FIT FOR SHASQI IF YOU.. - Are mission driven and eager to do the best work of your career, developing novel therapies that will transform cancer treatment. - Can balance scientific rigor with a fast-paced environment. - Are comfortable with ambiguity and making decisions in the face of uncertainty. - Operate with a strong sense of agency and invite feedback and advice. - Can challenge convention and think of creative solutions that meet the needs of the

### Executive Director, Therapeutic Strategy Leader, APAC - Fortrea Holdings Inc
- Location: Shanghai, China (unspecified)
- Salary: Not disclosed
- Posted: 2026-05-12
- 401(k) match: listed (not source-backed)
- Apply: https://fortrea.wd1.myworkdayjobs.com/Fortrea/job/Shanghai/ED--Therapeutic-Strategy-Leader--APAC_261967/apply
- Excerpt: Executive Director, Therapeutic Strategy Leader, APAC Shanghai, China This role is for upcoming future opportunities that may arise at Fortrea. Fortrea is excited to connect with talented individuals for future opportunities. If you meet the job requirements, we'll i...

### Finance Enterprise Partner - Therapeutic Area - Genentech, Inc.
- Location: South San Francisco, California, United States of America (unspecified)
- Salary: Not disclosed
- Posted: 2026-05-08
- 401(k) match: listed (not source-backed)
- Apply: https://roche.wd3.myworkdayjobs.com/ROG-A2O-GENE/job/South-San-Francisco/Finance-Enterprise-Partner---Therapeutic-Area_202603-108237-1/apply
- Excerpt: Finance Enterprise Partner - Therapeutic Area South San Francisco, California, United States of America Embrace the role of a Finance Enterprise Partner - Therapeutic Area and drive strategic financial decisions in a dynamic pharmaceutical environment. Collaborate with cross-functional leaders, lead financial planning, and optimize portfolio performance. Shape the future of healthcare finance while supporting commercial, medical, and market access initiatives. Grow your career with us!

### Staff Software Engineer - ML Platform - Grow Therapy
- Location: San Francisco, California, United States (unspecified)
- Salary: $217K-$288K
- Posted: 2026-06-03
- Parental leave: 18 weeks (not source-backed)
- Mental health support: yes (not source-backed)
- Apply: https://jobs.ashbyhq.com/grow-therapy/3a1a8a10-c120-4a1a-b516-762fbcdb701f
- Excerpt: Staff Software Engineer - ML Platform San Francisco, California, United States Grow Therapy is on a mission to serve as the trusted partner for therapists growing their practice, and patients accessing high-quality care. Powered by technology, we are a three-sided marketplace that empowers providers, augments insurance payors, and serves patients. Following the mass increase in depression and anxiety, the need for accessibility is more important than ever. To make our vision for mental healthcare a reality, we're building a team of entrepreneurs and mission-driven go-getters. Since launching in February 2021, we've empowered more than ten thousand therapists and hundreds of thousands of clients across the country and insurance landscape. We've raised more than $328Mm in funding, including our Series D, at a $3B valuation from Sequoia Capital, Transformation Capital, TCV, SignalFire, Menlo Ventures, Goldman Sachs Alternatives, and others. The Opportunity We're hiring a Staff ML Platform Engineer to drive the technical vision and execution of Grow Therapy's Machine Learning Platform. In this role, you'll design, build, and scale the real-time ML systems that power core product experiences, starting with patient-provider matching and define the architecture that will carry the platform through the next several years of growth. You'll operate as a de facto technical decision-maker, partnering closely with Data Science, Product and Engineering to translate business goals into robust platform capabilities and setting the bar for what excellent ML infrastructure looks like at Grow. Why This Role Matters Matching a client to the right therapist is one of the most

### Project Director, Peptide API - AbbVie Inc.
- Location: North Chicago, IL, United States (unspecified)
- Salary: Not disclosed
- Posted: 2026-06-10
- Parental leave: 12 weeks (not source-backed)
- Non-birth-parent leave: 12 weeks (not source-backed)
- 401(k) match: listed (not source-backed)
- Apply: https://jobs.smartrecruiters.com/AbbVie/3743990012905596-project-director-peptide-api
- Excerpt: Project Director, Peptide API North Chicago, IL, United States Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: Purpose: The Project Director will drive transformational performance in delivery of Peptide API projects in the United States through adoption of best-in-class technology, cross-functional alignment with Operations and external functions, seamless execution and delivery of projects with manufacturing sites and reduce overall project timeline to deliver products to patients. Adoption of first-time process technologies and modality with a change readiness mindset is critical to this role. This role requires cross-functional collaboration with other functions during all phases of the development of strategic projects. The incumbent will provide key technical inputs to business development activities involving external pipeline and new modalities, in addition to ensuring manufacturing capacity for product growth and internal pipeline. The incumbent will report to VP, Strategic Capital Deployment in the Operations Transformation organization. Responsibilities: Lead a team of professionals to achieve the charter, priorities and milestones of strategic peptide manufacturing project within the US. Lead and manage complex and strategically critical capital projects to ensure timely

### Therapeutic Area Analytics & Insights Director - Respiratory - Genentech, Inc.
- Location: South San Francisco, California, United States of America (unspecified)
- Salary: Not disclosed
- Posted: 2026-06-02
- 401(k) match: listed (not source-backed)
- Apply: https://roche.wd3.myworkdayjobs.com/ROG-A2O-GENE/job/South-San-Francisco/Therapeutic-Area-Analytics---Insights-Director---Respiratory_202605-113485-1/apply
- Excerpt: Therapeutic Area Analytics & Insights Director - Respiratory South San Francisco, California, United States of America Join our team as Director, Therapeutic Area Analytics & Insights - Respiratory and drive high-impact, data-driven strategies for a leading healthcare portfolio. Leverage your expertise in analytics, stakeholder management, and respiratory expertise to shape business outcomes, collaborate with cross-functional teams, and deliver actionable insights that improve patient care and outcomes.

### Executive Director, Therapeutic Area Lead, CVRM - Genentech, Inc.
- Location: South San Francisco, California, United States of America (unspecified)
- Salary: Not disclosed
- Posted: 2025-12-17
- 401(k) match: listed (not source-backed)
- Apply: https://roche.wd3.myworkdayjobs.com/ROG-A2O-GENE/job/South-San-Francisco/Executive-Director--Therapeutic-Area-Lead--CVRM_202512-132040-1/apply
- Excerpt: Executive Director, Therapeutic Area Lead, CVRM South San Francisco, California, United States of America Exciting opportunity for an Executive Director, Therapeutic Area Lead and drive medical strategy, innovation, and leadership in a dynamic healthcare environment. Lead high-impact teams, shape clinical trials, and collaborate across functions to advance patient outcomes. If you have deep medical expertise and proven people management skills, this is your next career-defining opportunity.

### Executive Director, US Market Access Strategy - Summit Therapeutics
- Location: Princeton, NJ (unspecified)
- Salary: $245K-$307K
- Posted: 2026-04-17
- Apply: https://job-boards.greenhouse.io/summittherapeutics/jobs/4224815009
- Excerpt: Executive Director, US Market Access Strategy Princeton, NJ About Summit: Summit Therapeutics Inc. is a biopharmaceutical oncology company with a mission focused on improving quality of life, increasing potential duration of life, and resolving serious unmet medical needs. At Summit, we believe in building a team of world class professionals who are passionate about this mission, and it is our people who drive this mission to reality. Summit's core values include integrity, passion for excellence, purposeful urgency, collaboration, and our commitment to people. Our employees are truly the heart and soul of our culture, and they are invaluable in shaping our journey toward excellence. Summit's team is inspired to touch and help change lives through Summit's clinical studies in the field of oncology. Summit has multiple global Phase 3 clinical studies, including: Non-small Cell Lung Cancer (NSCLC) - HARMONi: Phase 3 clinical study which was intended to evaluate ivonescimab combined with chemotherapy compared to placebo plus chemotherapy in patients with EGFR-mutated, locally advanced or metastatic non-squamous NSCLC who were previously treated with a 3rd generation EGFR TKI. - HARMONi-3: Phase 3 clinical study which is intended to evaluate ivonescimab combined with chemotherapy compared to pembrolizumab combined with chemotherapy in patients with first-line metastatic NSCLC. - HARMONi-7: Phase 3 clinical study which is intended to evaluate ivonescimab monotherapy compared to pembrolizumab monotherapy in patients with first-line metastatic NSCLC. Colorectal Cancer (CRC) - HARMONi-GI3: Phase 3 clinical study intended to evaluate ivonescimab in combination with chemotherapy compared with bevacizumab plus chemotherapy. Ivonescimab

### Principal Product Leader, Therapeutics Discovery - Genentech, Inc.
- Location: South San Francisco, California, United States of America (unspecified)
- Salary: Not disclosed
- Posted: 2026-06-11
- 401(k) match: listed (not source-backed)
- Apply: https://roche.wd3.myworkdayjobs.com/ROG-A2O-GENE/job/South-San-Francisco/Principal-Product-Leader--Therapeutics-Discovery_202606-114878-1/apply
- Excerpt: Principal Product Leader, Therapeutics Discovery South San Francisco, California, United States of America Exciting opportunity for a Principal Product Leader in Therapeutics Discovery, driving strategy and innovation for cutting-edge products in drug discovery. Collaborate with top scientists, shape product vision, and accelerate impactful solutions in a dynamic, data-driven environment. Make a difference in advancing life-changing therapies and scientific discovery at the forefront of biotechnology.

### Executive Director / Vice President, Corporate and Internal Communications - BioPharma - Dianthus Therapeutics
- Location: Remote (remote)
- Salary: Not disclosed
- Posted: 2026-06-04
- Apply: https://job-boards.greenhouse.io/dianthustherapeutics/jobs/4679135005
- Excerpt: Executive Director / Vice President, Corporate and Internal Communications - BioPharma Remote About Us We are developing potentially best in class therapies for patients living with severe autoimmune diseases. Our lead antibody, claseprubart (DNTH103), is purposefully engineered with extended half-life, improved potency, and high selectivity for only the active C1s complement protein that drives disease pathology - enabling less frequent and more convenient self-administered subcutaneous injections. Our second clinical candidate, DNTH212 is a first and potentially best in class, bifunctional inhibitor that targets clinically validated and complementary disease modifying mechanisms, Type 1 IFN suppression and B cell modulation - enabling potential for improved clinical outcomes and patient friendly convenient, self-administered subcutaneous injections. To learn more, please visit www.dianthustx.com and follow us on LinkedIn . About the Role BioPharma Experience is required. We are seeking a strategic, creative, and execution-oriented ED / VP, Corporate & Internal Communications to build and lead a modern, high-impact communications function in a fast-growing biotech company. This role sits at the intersection of people, corporate brand, and business strategy-responsible for shaping how we communicate internally and externally, strengthening employee engagement, elevating our corporate brand, and ensuring a consistent and compelling company narrative across all audiences, while operating as predominantly a remote company. You will serve as a trusted advisor to senior leadership and partner closely with the VP of Marketing and VP of Investor Relations to ensure alignment across corporate and internal communications. We are building a culture of individuals who hold our core principles at

### Senior Product Quality Manager (Peptide Technology) - AbbVie Inc.
- Location: North Chicago, IL, United States (unspecified)
- Salary: Not disclosed
- Posted: 2026-06-10
- Parental leave: 12 weeks (not source-backed)
- Non-birth-parent leave: 12 weeks (not source-backed)
- 401(k) match: listed (not source-backed)
- Apply: https://jobs.smartrecruiters.com/AbbVie/3743990013423956-senior-product-quality-manager-peptide-technology-
- Excerpt: Senior Product Quality Manager (Peptide Technology) North Chicago, IL, United States Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: Responsible for quality of assigned new product introduction programs to ensure business objectives are met with regards to on time deliverables of program development while assuring compliance with local, divisional, and corporate policies and external agency regulations worldwide. Products include regulatory starting materials, Active Pharmaceutical Ingredients (API), and Drug Products produced by AbbVie plants or by third-party manufacturers, in Licensing relationships, or Co-Marketing relationships. Develop in concert with the appropriate regulatory strategies set forth by the governance processes. AbbVie Operations Quality Assurance is seeking a Product Quality Manager to lead quality deliverables for late-stage development and commercialization of Peptides, from registration through commercialization. We are seeking a highly motivated candidate with a proven track record of accomplishment in the field of peptide manufacturing development, to work in a multi-functional team environment at our North Chicago, IL location. Leads the development and implementation of global Product Quality Assurance strategy to support New Product Introduction (NPI) programs for the

### GNC Engineer, Device Navigation and Beam Pointing (Starlink) - SpaceX
- Location: Redmond, WA (unspecified)
- Salary: $125K-$145K
- Posted: 2026-02-03
- Parental leave: 0 weeks (not source-backed)
- Apply: https://boards.greenhouse.io/spacex/jobs/8395371002?gh_jid=8395371002
- Excerpt: GNC Engineer, Device Navigation and Beam Pointing (Starlink) Redmond, WA SpaceX was founded under the belief that a future where humanity is out exploring the stars is fundamentally more exciting than one where we are not. Today SpaceX is actively developing the technologies to make this possible, with the ultimate goal of enabling human life on Mars. GNC ENGINEER, DEVICE NAVIGATION AND BEAM POINTING (STARLINK) At SpaceX we're leveraging our experience in building rockets and spacecraft to deploy Starlink, the world's most advanced broadband internet system. Starlink is the world's largest satellite constellation and is providing fast, reliable internet to 10M+ users worldwide. We design, build, test, and operate all parts of the system - thousands of satellites, consumer receivers that allow users to connect within minutes of unboxing, and the software that brings it all together. We've only begun to scratch the surface of Starlink's potential global impact and are looking for best-in-class engineers to help maximize Starlink's utility for communities and businesses around the globe. As an engineer on this team, you will bring a passion and expertise in areas like control theory, state estimation, orbital mechanics, spacecraft systems design, optimization, and software development to join the Starlink guidance, navigation, and control (GNC). Come help us write the autopilot algorithms for thousands of satellites (the world's largest constellation!) and more than one million user terminals, enabling access to high-speed broadband internet in all corners of the world. RESPONSIBILITIES: - Design and analysis of GNC logic for consumer and

### Contract Process Development Associate II - Keros Therapeutics Inc
- Location: Lexington, Massachusetts, United States (unspecified)
- Salary: $53-$62/hr
- Posted: 2026-05-28
- 401(k) match: listed (not source-backed)
- Apply: https://kerostx.com/current-opportunities?gh_jid=4699788005
- Excerpt: Contract Process Development Associate II Lexington, Massachusetts, United States At Keros, our mission is to deliver significant clinical benefit to a wide range of patients with disorders that are linked to dysfunctional signaling of the transforming growth factor-beta (TGF-ß) family of proteins. With a focus on developing differentiated product candidates that are designed to alter TGF-β signaling, we aim to target the pathways critical for the growth, repair and maintenance of blood cells and a number of tissues, including bone, skeletal muscle, adipose and heart tissue. We believe our product candidates have the potential to unlock the full therapeutic benefits of modulating the TGF-β superfamily and provide disease-modifying benefit to patients. This role is responsible for providing overall support in early stages of process development and acting as an interface with the Research and CMC organizations. This person will be responsible for executing and developing stage appropriate downstream processes for novel protein therapeutics. Developing downstream purification processes for expression scales that range from shake flasks to pilot scale bioreactors. Theis person will also be involved in providing and analyzing data and relevant information for reports supporting tech transfer activities for external manufacturing. Responsibilities: - Hands-on execution, and optimization of protein purification processes including primary recovery unit operations (centrifugation, homogenization, flocculation, tangential-flow filtration (TFF), and depth filtration), chromatography (ion-exchange, affinity, hydrophobic interaction), and pre-formulation (TFF, dialysis) - Generate and analyze process and analytical data supporting key documents such as development reports, regulatory submissions, and technology transfer packages - Execute routine scale

### Senior Site Reliability Engineer - Super
- Location: Netherlands (unspecified)
- Salary: Not disclosed
- Posted: 2026-06-12
- Apply: https://job-boards.eu.greenhouse.io/super/jobs/4860916101
- Excerpt: Senior Site Reliability Engineer Netherlands We are on a mission to pioneer the world's next era of play. As we grow across Europe and Latin America, we're building The Playstack - the technology powering the next generation of sports, gaming, and fan experiences. Join us, and help make it the most widely used platform in the world! From operations, to marketing, to product, we are looking for talented people who will shape how millions of customers play, watch, and connect every day. We are looking for a Senior DevOps/SRE Engineer with hands-on experience in the Erlang and/or Elixir ecosystem to join our Release Engineering team. You will own the build, test, and release pipelines for our BEAM-based services, ensuring our delivery practices meet the same standard as the rest of the platform. This is a high-impact role at the heart of our operations, with full ownership of reliability and delivery for a stack that is central to what we do. What the role involves Own and evolve CI/CD pipelines for Erlang and Elixir services - from build through to production deployment - using tools such as Betler and Argo Workflows. Build and maintain base Docker images, release packaging, and deployment automation for BEAM-based applications. Collaborate with application teams to define and enforce release standards, quality gates, and rollback strategies for Erlang/Elixir services. Improve observability and reliability of the BEAM stack, including monitoring, deployment health checks, and incident response tooling. Contribute to migration and modernisation efforts as we consolidate delivery infrastructure

### Software Engineer, Beam Planning (Starlink) - SpaceX
- Location: Redmond, WA (unspecified)
- Salary: $125K-$145K
- Posted: 2026-03-13
- Apply: https://boards.greenhouse.io/spacex/jobs/8450082002?gh_jid=8450082002
- Excerpt: Software Engineer, Beam Planning (Starlink) Redmond, WA SpaceX was founded under the belief that a future where humanity is out exploring the stars is fundamentally more exciting than one where we are not. Today SpaceX is actively developing the technologies to make this possible, with the ultimate goal of enabling human life on Mars. SOFTWARE ENGINEER, BEAM PLANNING (STARLINK) At SpaceX we're leveraging our experience in building rockets and spacecraft to deploy Starlink, the world's most advanced broadband internet system. Starlink is the world's largest satellite constellation and is providing fast, reliable internet to millions of users worldwide. We design, build, test, and operate all parts of the system - thousands of satellites, consumer receivers that allow users to connect within minutes of unboxing, and the software that brings it all together. We've only begun to scratch the surface of Starlink's potential global impact and are looking for the world's best engineers to help maximize Starlink's utility for communities and businesses around the globe. As a Software Engineer on the Starlink program, you will be solving challenges that improve our ability to fully utilize the hardware we have deployed. Our goal is to provide customers with the best possible satellite internet experience, often providing under-served communities with affordable, life-changing broadband internet access. Our software engineers are responsible for the complete lifecycle of the software they create, including development, testing, and support. We expect our engineers to close the feedback loop between software design and real-world performance. In this role, your

### Associate Director, Digital & Commercial Analytics - Corcept Therapeutics
- Location: Redwood City, California, United States (unspecified)
- Salary: $215K-$253K
- Posted: 2026-04-29
- 401(k) match: listed (not source-backed)
- Apply: https://www.corcept.com/careers/current-opportunities/?gh_jid=5983868004
- Excerpt: Associate Director, Digital & Commercial Analytics Redwood City, California, United States For more than 25 years, Corcept has been singularly focused on the science of cortisol, a powerful hormone that when unregulated, can play a role in a broad range of diseases. Our commercial portfolio includes treatments for hypercortisolism and oncology, and the company has discovered more than 1,000 proprietary selective cortisol modulators and glucocorticoid receptor antagonists. With advanced clinical trials in patients with hypercortisolism, solid tumors, ALS and liver disease, Corcept is unlocking the power of cortisol modulation to help address some of the most devastating diseases patients face today. Corcept is headquartered in Redwood City, California. To learn more, visit www.corcept.com . Corcept Oncology is seeking an experienced and collaborative Associate Director, Digital & Commercial Analytics to lead next best action (NBA) orchestration and advanced analytics across marketing, and market access domains. This individual will co-lead the design, deployment, and monitoring of next best action (NBA) orchestration and deliver high-impact analytics across marketing performance, digital engagement, and market access. This role will work in close partnership with Digital Marketing, Commercial Operations, Market Access, IT, and external partners. The ideal candidate brings strong experience in data-driven decisioning and orchestration platforms (e.g., Salesforce Marketing Cloud, CRM) and has operated in complex, matrixed commercial environments. While pharmaceutical experience is preferred, we are open to candidates from other industries with demonstrated expertise in decision sciences, personalization, and digital analytics. Responsibilities: Next Best Action (NBA) Strategy & Orchestration - Co-lead the design, implementation,

### Senior Scientist II / Principal Scientist I, Biologics Drug Product Development - AbbVie Inc.
- Location: North Chicago, IL, United States (unspecified)
- Salary: Not disclosed
- Posted: 2026-06-10
- Parental leave: 12 weeks (not source-backed)
- Non-birth-parent leave: 12 weeks (not source-backed)
- 401(k) match: listed (not source-backed)
- Apply: https://jobs.smartrecruiters.com/AbbVie/3743990013490176-senior-scientist-ii-principal-scientist-i-biologics-drug-product-development
- Excerpt: Senior Scientist II / Principal Scientist I, Biologics Drug Product Development North Chicago, IL, United States Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: Description: Biologics Drug Product Development (Bio DPD), a part of Development Sciences within AbbVie's R&D, is a global organization that is responsible for drug product formulation and process development, and definition of the product presentation for biologics (proteins, conjugates, peptides, neurotoxins etc.) and genetic medicine (AAV, LNPs, Cell Therapy). AbbVie is seeking a highly motivated candidate for the position of Senior Scientist II / Principal Scientist I, located in North Chicago, IL. We are seeking an accomplished scientist with a proven track record in biologics drug product formulation and process development, scale-up and tech transfer. This position will be an integral part of the product development and CMC teams and will have strong collaborations with several stakeholders, including discovery research, analytical research and development, bioprocess development, combination products development, product development science and technology, pilot plants and third-party manufacturers. Key Responsibilities: Represent Bio DPD in the cross-functional Product Presentation and Device Strategy

### Senior Principal Scientist, Peptide Therapeutics - Genentech, Inc.
- Location: South San Francisco, California, United States of America (unspecified)
- Salary: Not disclosed
- Posted: 2026-01-08
- 401(k) match: listed (not source-backed)
- Apply: https://roche.wd3.myworkdayjobs.com/ROG-A2O-GENE/job/South-San-Francisco/Senior-Principal-Scientist--Peptide-Therapeutics_202510-126773/apply
- Excerpt: Senior Principal Scientist, Peptide Therapeutics South San Francisco, California, United States of America You will lead the Medicinal Chemistry efforts for a highly integrated and collaborative team, applying your deep scientific expertise to solve complex drug discovery challenges and drive projects forw...

### Senior Manager, Marketing Analytics - Rheumatology - AbbVie Inc.
- Location: Mettawa, IL, United States (unspecified)
- Salary: Not disclosed
- Posted: 2026-06-10
- Parental leave: 12 weeks (not source-backed)
- Non-birth-parent leave: 12 weeks (not source-backed)
- 401(k) match: listed (not source-backed)
- Apply: https://jobs.smartrecruiters.com/AbbVie/3743990013002176-senior-manager-marketing-analytics-rheumatology-
- Excerpt: Senior Manager, Marketing Analytics - Rheumatology Mettawa, IL, United States Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: AbbVie's Rheumatology Franchise is looking for a strong Senior Manager, Marketing Analytical candidate to join a high-performing team supporting Sales and Marketing initiatives. In this role, you'll be responsible for delivering analysis, insights, and recommendations to Marketing leaders in support of brand strategy. You'll use your analytics expertise and relevant data to identify trends in performance and build a narrative around appropriate strategic and tactical adjustments to drive increased business performance. You will be expected to partner with Brand and Sales Leadership to align Marketing strategies and key priorities while supporting the current and future portfolio. A successful candidate must be able to meaningfully communicate insights and information to a broad group of stakeholders through exceptional oral and written communication. Major Responsibilities: Develop fact-based promotional investment strategies and guide investment decisions from marketing mix/business optimization and other analysis to optimize performance, influence business growth & inform the annual financial forecasting and brand planning process Develop near-term KPIs and

### Information Security Lead - Click Therapeutics
- Location: New York, NY (unspecified)
- Salary: $130K-$200K
- Posted: 2026-02-25
- 401(k) match: listed (not source-backed)
- Fertility benefits: yes (not source-backed)
- Learning budget: yes (not source-backed)
- Apply: https://job-boards.greenhouse.io/clicktherapeutics/jobs/8414783002
- Excerpt: Information Security Lead New York, NY Who We Are: Click Therapeutics, Inc., develops, validates, and commercializes software as prescription medical treatments for people with unmet medical needs. As a leading innovator of Digital Therapeutics™, Click delivers accessible, clinically proven, FDA-regulated prescription treatments to the smartphone in your hand. Click's treatments are defined by a commitment to applying technical and scientific rigor and patient-centric design to the development process. This results in uniquely engaging experiences that achieve compelling clinical outcomes for patients seeking new treatment options. Click Therapeutics continuously expands and refines its platform with novel cognitive, behavioral and neuromodulatory mechanisms of action and advanced data-driven tools such as artificial intelligence and machine learning. The digital therapeutics under development on Click's platform address diverse areas of therapeutic need, including indications in psychiatry, neurology, oncology, immunology, and cardiometabolic diseases. Consistently named a best place to work, Click fosters an inclusive, diverse workforce of innovators, clinicians, scientists, researchers, designers, technologists, engineers and more, united in a common mission to provide patients everywhere access to safe and effective prescription digital therapeutics. For more information, visit www.clicktherapeutics.com and connect with us on LinkedIn. About the Role: As Information Security Lead, you'll be at the forefront of safeguarding our groundbreaking digital therapeutics. We're seeking an individual with deep technical expertise in information security in the healthcare sector, ready to tackle complex challenges and pioneer innovative solutions. This isn't just a role; it's an opportunity to build, mentor, and inspire a high-performing team, while strategically collaborating across

### Clinical Trial Leader - Tango Therapeutics Inc
- Location: Boston, MA (unspecified)
- Salary: $160K-$241K
- Posted: 2026-05-06
- 401(k) match: listed (not source-backed)
- Apply: https://job-boards.greenhouse.io/tangotherapeutics/jobs/7723892003
- Excerpt: Clinical Trial Leader Boston, MA Company Overview Tango Therapeutics is a biotechnology company dedicated to discovering novel drug targets and delivering the next generation of precision medicine for the treatment of cancer. Using an approach that starts and ends with patients, Tango leverages the genetic principle of synthetic lethality to discover and develop therapies that take aim at critical targets in cancer. This includes expanding the universe of precision oncology targets into novel areas such as tumor suppressor gene loss and their contribution to the ability of cancer cells to evade immune cell killing. The Tango labs and offices are located at 201 Brookline Avenue, in the Fenway area of Boston, Massachusetts. Summary We are seeking a Clinical Trial Leader (CTL) to lead cross-functional clinical trial teams (CTTs) in the execution of clinical trials of Tango's portfolio. This role will chair the CTT and represent the cross-functional team to internal governance bodies. The CTL will be an internal escalation point for other CTT members. In a fast-paced, small biotech environment, the CTL will operationally lead the set-up, conduct and reporting of clinical trials as per approved timelines, budget, regulatory requirements, and internal standards. This individual will play a key role in the execution and delivery of clinical trial objectives. The ideal candidate is highly collaborative, detail-oriented, and comfortable operating in a hands-on environment, with a focus on building scalable processes, tools, and best practices to support efficient and compliant clinical trial execution. Your role - Lead cross-functional Clinical Trial Team

### Laser System Operator - Lawrence Livermore National Laboratory
- Location: Livermore, CA, United States (unspecified)
- Salary: $43.55-$53.36/hr
- Posted: 2026-06-10
- Learning budget: yes (not source-backed)
- Apply: https://jobs.smartrecruiters.com/LLNL/3743990013239066-laser-system-operator
- Excerpt: Laser System Operator Livermore, CA, United States Company Description: Join us and make YOUR mark on the World! Lawrence Livermore National Laboratory (LLNL) has turned bold ideas into world-changing impact advancing science and technology to strengthen U.S. security and promote global stability. Our mission spans four critical national security areas nuclear deterrence, threat preparedness, energy security, and multi-domain defense empowering teams to take on the toughest challenges of today and tomorrow. With a culture built on innovation and operational excellence, LLNL is a place where your expertise can make a real impact. Job Description: We have multiple openings for NIF Laser System Operators supporting the Beam Control System (BCS) and Injection Laser System (ILS) in the NIF Control Room. You will be a vital member of the operations team at the National Ignition Facility (NIF), supporting the world's most energetic laser system. It is an exciting time to join the team that achieved fusion ignition in December 2022, a historic moment in science, opening new physics regimes and setting the stage for new fusion energy possibilities. As a Control Room Operator, you will work in a multidisciplinary team to develop, deploy and maintain complex laser systems while ensuring the reliable and safe functioning of the beam control and injection laser subsystems, which are essential for the precision and performance of NIF's experimental campaigns. A NIF Laser System Operator is responsible for overseeing the real-time operation of laser beam control and injection systems, ensuring precise alignment, timing, and pulse shaping for

### Frontend Engineer, Platform - Grow Therapy
- Location: San Francisco, California, United States, Seattle, New York City (unspecified)
- Salary: $182K-$250K
- Posted: 2026-06-05
- Parental leave: 18 weeks (not source-backed)
- Mental health support: yes (not source-backed)
- Apply: https://jobs.ashbyhq.com/grow-therapy/e7aea8ac-7c44-4182-ae5f-9c21e510d952
- Excerpt: Frontend Engineer, Platform San Francisco, California, United States, Seattle, New York City Grow Therapy is on a mission to serve as the trusted partner for therapists growing their practice, and patients accessing high-quality care. Powered by technology, we are a three-sided marketplace that empowers providers, augments insurance payors, and serves patients. Following the mass increase in depression and anxiety, the need for accessibility is more important than ever. To make our vision for mental healthcare a reality, we're building a team of entrepreneurs and mission-driven go-getters. Since launching in February 2021, we've empowered more than ten thousand therapists and hundreds of thousands of clients across the country and insurance landscape. We've raised more than $328Mm in funding, including our Series D, at a $3B valuation from Sequoia Capital, Transformation Capital, TCV, SignalFire, Menlo Ventures, Goldman Sachs Alternatives, and others. The Opportunity We're building a dedicated Frontend Platform team, and we're looking for a Frontend Engineer who loves working on the systems that every product team builds on. You'll own the design system and the horizontal web foundation - the shared components, patterns, architecture, and tooling that let every team ship consistent, high-quality experiences without reinventing the basics. This is the engineering layer underneath Grow's product surface. As we consolidate into a modern Next.js architecture and launch a major new consumer brand, the platform you build is what makes everyone else faster - and what keeps the experience cohesive as we scale. It's a foundational role on a new team, with

### Senior Medical Director, Oncology - Corcept Therapeutics
- Location: Redwood City, California, United States (unspecified)
- Salary: $298K-$351K
- Posted: 2026-03-06
- 401(k) match: listed (not source-backed)
- Apply: https://www.corcept.com/careers/current-opportunities/?gh_jid=5821320004
- Excerpt: Senior Medical Director, Oncology Redwood City, California, United States For more than 25 years, Corcept has been singularly focused on the science of cortisol, a powerful hormone that when unregulated, can play a role in a broad range of diseases. Our commercial portfolio includes treatments for hypercortisolism and oncology, and the company has discovered more than 1,000 proprietary selective cortisol modulators and glucocorticoid receptor antagonists. With advanced clinical trials in patients with hypercortisolism, solid tumors, ALS and liver disease, Corcept is unlocking the power of cortisol modulation to help address some of the most devastating diseases patients face today. Corcept is headquartered in Redwood City, California. To learn more, visit www.corcept.com . Responsibilities: - Design and implement Phase I to III clinical studies - Develop and participate in the writing and review of protocols, investigator brochures, study reports and other clinical and regulatory documents - Provide scientific oversight for Company operational staff, CROs, and clinical trial sites in all areas related to the therapeutic programs - Act as a clinical subject matter expert for both Company team members and for external contacts related to the assigned therapeutic programs - Establish and approve scientific methods for design and implementation of applicable clinical protocols, data collection systems and final reports - Act to provide medical oversight and safety monitoring for ongoing clinical trials including participation in SAE reporting and serving on the safety committee - Play a key role in the analysis, interpretation and delivery of high-quality clinical data - Interact with

### CEFIB and TEM Engineer - Renesas Electronics
- Location: Palm Bay, Florida, United States (unspecified)
- Salary: Not disclosed
- Posted: 2026-06-10
- 401(k) match: listed (not source-backed)
- Apply: https://jobs.smartrecruiters.com/RenesasElectronics/744000124722100-cefib-and-tem-engineer
- Excerpt: CEFIB and TEM Engineer Palm Bay, Florida, United States Company Description: Job Description: Applicants for this position must be currently authorized to work in the United States on a full-time basis. Renesas is unable to sponsor applicants for work visas for this position now or in the future. This includes anyone on F1/OPT. Our Global Quality Assurance Lab (QAL) Team is looking for an experienced CEFIB and TEM Engineer to join our Palm Bay, Florida office. We are seeking an enthusiastic, initiative-taking, fast-learning individual who will focus on managing and supporting the design and failure analysis teams with CEFIB and TEM support. A successful candidate would have knowledge or experience in the following: Experience using Circuit Edit Focused Ion Beam (CE-FIB), Transmission Electron Microscopy (TEM) and other SEM based tools. Familiar with Thermofisher (FEI) V400ACE and Helios Dual Beam. Ability to read and interpret electrical schematics and layouts using various CAD tools, like Cadence virtuoso. Understanding on use and interpretation of Elemental Dispersive Spectroscopy (EDS) Knowledge and experience with failure analysis techniques. An understanding of Semiconductor fabrication and packaging which include wet chemistry, polishing, plasma deprocessing techniques Qualifications: Applicants for this position must be currently authorized to work in the United States on a full-time basis. Renesas is unable to sponsor applicants for work visas for this position now or in the future. This includes anyone on F1/OPT. MUST HAVE - 10 to 15 years of experience using Circuit Edit Focused Ion Beam (CE-FIB), Transmission Electron Microscopy (TEM) and other

### Wireless Systems Engineer (Starlink Mobile) - SpaceX
- Location: Sunnyvale, CA (unspecified)
- Salary: $135K-$155K
- Posted: 2026-05-13
- Apply: https://boards.greenhouse.io/spacex/jobs/8546717002?gh_jid=8546717002
- Excerpt: Wireless Systems Engineer (Starlink Mobile) Sunnyvale, CA SpaceX was founded under the belief that a future where humanity is out exploring the stars is fundamentally more exciting than one where we are not. Today SpaceX is actively developing the technologies to make this possible, with the ultimate goal of enabling human life on Mars. WIRELESS SYSTEMS ENGINEER (STARLINK MOBILE) As a Wireless Systems Engineer for Starlink Mobile you will design and develop wireless communications algorithms that maximize system performance for the Starlink Mobile satellite constellation and future networks. The ideal candidate will have deep technical expertise in wireless communication systems, strong knowledge of 3GPP RAN protocols (4G/5G/6G), and an interest in building production algorithms that get deployed at global scale. RESPONSIBILITIES: - Design and optimize wireless systems algorithms at the MAC and PHY layer for link adaptation, power control, timing advance, and doppler tracking. - Design and simulate complex MAC layer scheduling algorithms that support joint scheduling of users across multiple beams subject to Quality of Service (QoS) and latency constraints. - Analyze inter-cell and inter-beam interference on both uplink and downlink, identify issues on-orbit, and propose solutions through beam planning optimizations, MAC layer scheduling improvements, or advanced signal processing techniques. - Run link level simulations and system level simulations to compare performance of different algorithms at all layers of the protocol stack. - Work directly with software engineers to implement algorithms and deploy to orbit. - Qualify algorithm performance in production through aggregate KPI analysis, high rate per TTI

### Associate Director/Director, Biology (Oncology Drug Discovery) - Iambic Therapeutics
- Location: San Diego HQ, San Diego, California, United States (unspecified)
- Salary: Not disclosed
- Posted: 2026-04-15
- Apply: https://jobs.ashbyhq.com/iambic-therapeutics/8be25b14-d0a4-41ea-8c1b-b8745d139751
- Excerpt: Associate Director/Director, Biology (Oncology Drug Discovery) San Diego HQ, San Diego, California, United States JOB SUMMARY Iambic Therapeutics is seeking a highly motivated and experienced Associate Director or Director to lead oncology drug discovery efforts and advance our core mission of accelerating small molecule drug discovery through the integration of experimental and AI/ML-driven approaches. The successful candidate will have a proven track record of driving oncology drug discovery programs and will lead project teams with a deep understanding of the progression of drug candidates from hit identification to IND submission. This role will set scientific direction and drive cross-functional collaboration with Chemistry, DMPK, Safety, and Computational teams. This position is based at our San Diego headquarters. IMPACT & SCOPE - Partner with Iambic's computational and ML scientists to incorporate AI/ML-based tools and models that accelerate data interpretation, hypothesis generation, and decision-making across biology workflows. - This is a high-impact role that influences portfolio strategy and progression. KEY RESPONSIBILITIES - Program leadership: Initiate, direct, and execute biology plans that support medicinal chemistry and translational goals across discovery stages (hit-to-lead, LO, candidate selection, IND-enabling). - Cross-functional integration: Chair or co-lead cross-functional workstreams; align assay strategy with SAR hypotheses, DMPK/PD needs, and safety/translational biomarkers. - Collaboration leadership: Lead or co-lead key scientific collaborations with internal and external partners, driving integration of data and strategy toward shared objectives. - Assay strategy & data integrity: Conceptualize and oversee the design and validation of in vitro and ex vivo assays (signaling, binding, trafficking, imaging, and mechanism

### Associate Director/Director, Technical Operations - Drug Substance (Small Molecules) - Axsome Therapeutics
- Location: New York, NY (unspecified)
- Salary: $175K-$215K
- Posted: 2026-06-04
- Apply: https://job-boards.greenhouse.io/axsometherapeutics/jobs/5980968004
- Excerpt: Associate Director/Director, Technical Operations - Drug Substance (Small Molecules) New York, NY Axsome Therapeutics is a biopharmaceutical company leading a new era in the treatment of central nervous system (CNS) conditions. We deliver scientific breakthroughs by identifying critical gaps in care and develop differentiated products with a focus on novel mechanisms of action that enable meaningful advancements in patient outcomes. Our industry-leading neuroscience portfolio includes FDA-approved treatments for major depressive disorder, excessive daytime sleepiness associated with narcolepsy and obstructive sleep apnea, and migraine, and multiple late-stage development programs addressing a broad range of serious neurological and psychiatric conditions that impact over 150 million people in the United States. Together, we are on a mission to solve some of the brain's biggest problems so patients and their loved ones can flourish. For more information, please visit us at www.axsome.com and follow us on LinkedIn and X . About This Role: Axsome Therapeutics is seeking an Associate Director/Director, Technical Operations - Drug Substance (Small Molecules) to provide technical leadership across the development and commercial lifecycle of small‑molecule drug substance programs. This role is responsible for supporting and overseeing drug substance manufacturing activities, including technology transfer, process validation, continued process verification (CPV), and post‑approval process changes at internal and external manufacturing sites. The successful candidate will serve as a key technical leader within CMC, partnering closely with external CDMOs and internal cross‑functional teams (QA, QC, Regulatory, R&D, and Supply Chain) to ensure robust, compliant, and efficient manufacturing operations. This position reports into senior

### Associate Director, Clinical Development (Clinical Science) – Immunology - Apogee Therapeutics Inc
- Location: Remote (remote)
- Salary: $180K-$210K
- Posted: 2026-05-28
- 401(k) match: listed (not source-backed)
- Apply: https://job-boards.greenhouse.io/apogeetherapeutics/jobs/5146485007
- Excerpt: Associate Director, Clinical Development (Clinical Science) – Immunology Remote About Apogee Therapeutics Founded in 2022, Apogee Therapeutics, Inc. (Ticker: APGE) is a well-funded, Nasdaq listed company that offers the opportunity to work in a fast-paced, highly dynamic environment. At Apogee, you can actively contribute to shaping the company culture, take on various roles and responsibilities, and grow professionally. Apogee Therapeutics is a clinical-stage biotechnology company advancing novel biologics with potential for differentiated efficacy and dosing in the largest I&I markets, Apogee's antibody programs are designed to overcome limitations of existing therapies by targeting well-established mechanisms of action and incorporating advanced antibody engineering to optimize half-life and other properties. Zumilokibart (APG777), the company's most advanced program, is being initially developed for the treatment of atopic dermatitis (AD), which is the largest and one of the least penetrated I&I markets, as well as asthma. With four validated targets in its portfolio, Apogee is seeking to achieve best-in-class efficacy and dosing through monotherapies and combinations of its novel antibodies. Based on a broad pipeline and depth of leadership and expertise, the company believes it can deliver value and meaningful benefit to patients underserved by today's standard of care. We are a fast-paced company committed to building an exceptional culture, founded on our C.O.R.E. values: C aring, O riginal, R esilient and E goless and a commitment to refusing to stop at “good enough”. If this sounds like you, keep reading! Role Summary Apogee Therapeutics is seeking an experienced Clinical Scientist for an Associate

### Scientist/Senior Scientist, Upstream, Process Development & Manufacturing (Biologics) - Oruka Therapeutics Inc
- Location: Remote; Waltham, Massachusetts, United States (remote)
- Salary: $130K-$208K
- Posted: 2026-04-17
- Hires in: MA
- Apply: https://job-boards.greenhouse.io/oruka/jobs/5192663008
- Excerpt: Scientist/Senior Scientist, Upstream, Process Development & Manufacturing (Biologics) Remote; Waltham, Massachusetts, United States About Us: Oruka Therapeutics (Nasdaq: ORKA) is developing novel biologics designed to set a new standard for the treatment of chronic skin diseases. Oruka's mission is to offer patients suffering from chronic skin diseases like plaque psoriasis the greatest possible freedom from their condition by achieving high rates of complete disease clearance with dosing as infrequently as once or twice per year. Oruka is advancing a proprietary portfolio of potentially best-in-class antibodies that were engineered by Paragon Therapeutics and target the core mechanisms underlying plaque psoriasis and other dermatologic and inflammatory diseases. For more information, visit www.orukatx.com As we build our core team, we're seeking top talent in different functional areas who are not just looking for a job, but an opportunity to be part of something bigger. Someone who is passionate about making a difference and eager to contribute to establishing an engaged, inclusive, and positive company culture. Job Title: Scientist / Senior Scientist, Upstream, Process Development & Manufacturing (Biologics) Location: Hybrid - Waltham, MA required to be in-office 3 days/week -OR- Remote Position Overview: We are seeking an experienced and motivated Scientist/Senior Scientist to support upstream manufacturing activities. This role will be instrumental in contributing to process development and delivery of clinical trial material at CDMOs. The ideal candidate will collaborate cross-functionally within the CMC team including downstream, analytical, and drug product and other stakeholders such as QA, regulatory, and program management. The successful candidate

### Senior Field Applications Engineer - PDF Solutions INC
- Location: Boise, Idaho (unspecified)
- Salary: $110K-$110K
- Posted: 2026-04-24
- 401(k) match: listed (not source-backed)
- Apply: https://careers-pdf.icims.com/jobs/1476/login
- Excerpt: Senior Field Applications Engineer Boise, Idaho Overview PDF Solutions Inc is seeking a Field Applications Engineer to join the field team to work on PDF's e-beam inspection tool for Design-For-Inspection used for enhancing yield in state-of-art 300mm semiconductor fabs. The Applications Engineer must be an organized and highly motivated team player with strong initiative and communication skills and possesses the drive to deliver quality results on time in a dynamic, multi-discipline, intensive and highly productive small team environment. Responsibilities Work in 300mm fab and write inspection recipes on PDF's e-beam tools. Drive wafer inspection and perform analysis reduce yield loss on some of the world's most advanced ICs. Oversee the data pipeline from measurement and monitor data quality and health of tool. Perform R&D and experiments for improving and optimizing recipes based on data analysis Lead complex engineering projects and drive continuous business process improvement and automation Qualifications Job Requirements: Minimum Master's degree or minimum 2 years of field experience Degree in Electrical Engineering, Applied Physics, Materials Science or similar engineering field Experience working with inspection tools, including optical, voltage-contract or spectroscopy Ability to work in production environment and respond to customer promptly requests with high standard results Preferred Skills: Experience in semiconductor industry (preferably sub-20nm FIN-fet technology) Statistical data analysis in NumPy, JMP, Tableau, or MATLAB Python or other programming experience (Java, C#, C++, Ruby, Perl, etc.) Ability to interact with RD teams of different disciplines to resolve issues or drive improvement Pay Range USD $110,000.00 - USD $150,000.00

### Senior Clinical Trial Associate (CONTRACT) - Entrada Therapeutics Inc
- Location: Boston, MA (unspecified)
- Salary: Not disclosed
- Posted: 2026-06-04
- 401(k) match: listed (not source-backed)
- Apply: https://job-boards.greenhouse.io/entradatherapeutics/jobs/5155427007
- Excerpt: Senior Clinical Trial Associate (CONTRACT) Boston, MA The Organization What's happening at Entrada Therapeutics? Entrada is a clinical-stage biopharmaceutical company aiming to transform the lives of patients by establishing a new class of medicines that engage intracellular targets that have long been considered inaccessible. Through proprietary and versatile approaches, Entrada is advancing a robust development portfolio of genetic medicines for the potential treatment of neuromuscular and inherited retinal diseases, among others. Our lead oligonucleotide programs are in development for the potential treatment of people living with Duchenne muscular dystrophy (DMD) who are exon 44, 45, 50 and 51 skipping amenable. Entrada has partnered with Vertex Pharmaceuticals to develop a clinical-stage program, VX-670, for myotonic dystrophy type 1 (DM1). 2026 represents a catalyst-rich period for Entrada. We expect multiple clinical data readouts as we advance several DMD programs across the U.K., EU, and U.S. By year-end 2026, we anticipate four clinical-stage programs in our DMD franchise (ENTR-601-44, ENTR-601-45, ENTR-601-50, and ENTR-601-51). These programs are complemented by the ongoing clinical progress of our DM1 collaboration with Vertex (VX-670). We are a tight-knit team of experts and leaders in both therapeutic development and rare diseases and are excited to grow and attract colleagues who are ready to join a high-energy, dedicated team that likes to get things done and dramatically improve the lives of patients and their families. The Perfect Addition to Our Team You are patient focused and excited about the opportunity to help support and develop the Clinical Operations organization at

### Director, Process Engineering (Peptides) - AbbVie Inc.
- Location: North Chicago, IL, United States (unspecified)
- Salary: Not disclosed
- Posted: 2026-06-10
- Parental leave: 12 weeks (not source-backed)
- Non-birth-parent leave: 12 weeks (not source-backed)
- 401(k) match: listed (not source-backed)
- Apply: https://jobs.smartrecruiters.com/AbbVie/3743990012925336-director-process-engineering-peptides-
- Excerpt: Director, Process Engineering (Peptides) North Chicago, IL, United States Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: Purpose: The Director of Process Engineering will lead the process engineering effort for multiple strategic projects. This role serves as the owner-side Design Authority for process engineering on major biopharmaceutical capital programs. This role provides strategic leadership, technical governance, and oversight of all process engineering activities supporting large-scale manufacturing facility projects. The incumbent is responsible for ensuring that process systems are designed, integrated, and implemented in alignment with corporate engineering standards, regulatory expectations, and operational requirements. The role provides technical oversight of A&E contractor engineering activities and ensures that core process engineering deliverables-including process flow diagrams (PFDs), piping and instrumentation diagrams (P&IDs), cause and effect diagrams, process schematics, and operations philosophy documentation-meet the technical, safety, and operational standards required for pharmaceutical manufacturing facilities. As part of the project leadership team, the Director ensures effective integration of process design with utilities, automation, commissioning, qualification, and operational readiness activities. The role also supports corporate capital governance stage-gate processes, process safety management,

### Senior Director, Clinical Operations - Jade Biosciences Inc
- Location: Boston; Chicago; San Francisco; Seattle (unspecified)
- Salary: $255K-$280K
- Posted: 2026-02-28
- Apply: https://job-boards.greenhouse.io/jadebiosciences/jobs/5136907008
- Excerpt: Senior Director, Clinical Operations Boston; Chicago; San Francisco; Seattle About Jade Biosciences Jade Biosciences is a clinical-stage biotechnology company focused on developing best-in-class therapies that address critical unmet needs in autoimmune diseases. Jade's lead candidate, JADE101, targets the cytokine APRIL, and is currently being evaluated in a Phase 1 clinical trial for the treatment of immunoglobulin A nephropathy. Jade's pipeline also includes JADE201, an afucosylated anti-BAFF-R monoclonal antibody, as well as JADE301, an undisclosed antibody candidate, both currently in preclinical development. Jade was launched based on assets licensed from Paragon Therapeutics, an antibody discovery engine founded by Fairmount. For more information, visit JadeBiosciences.com and follow the Company on LinkedIn . Role Overview The Senior Director, Clinical Operations is responsible for directing the strategy, management, and oversight of clinical program(s) and functional activities as assigned. Key Responsibilities - Acts as Clinical Operations program lead for assigned program(s) - R epresent Clinical Operations at the Clinical Development Team and /or Global Program Team - Develops and executes program operational strategy - Partners closely and effectively with other functions and functional heads to drive program forward - Provides strategic and technical recommendations to senior leadership - Directs the selection of CROs and other vendors ( IxRS , Central Lab, ancillary/tech vendors) - Acts as an escalation point for CRO/vendor issues - Directs development of vendor Scopes of Work (SOW), scope changes, budgets, and vendor payments - Partners with CRO and other vendors to deliver on study execution - Creates and tracks clinical program

### AI Product Engineer - Iovance Biotherapeutics Inc
- Location: Remote (remote)
- Salary: $100K-$125K
- Posted: 2026-05-31
- 401(k) match: listed (not source-backed)
- Apply: https://job-boards.greenhouse.io/iovancebiotherapeutics/jobs/5234974008
- Excerpt: AI Product Engineer Remote Iovance Biotherapeutics aims to be the global leader in innovating, developing and delivering tumor infiltrating lymphocyte (TIL) therapy for people with cancer. We are pioneering a transformational approach to treating cancer by harnessing the ability of the human immune system to recognize and attack diverse cancer cells in each patient. The Iovance TIL platform has demonstrated promising clinical data across multiple solid tumors. We are committed to continuous innovation in cell therapy, including gene-edited cell therapy, which may be a promising option for patients with cancer. Overview Iovance Biotherapeutics is a commercial-stage cell therapy company focused on developing life-saving cancer immunotherapies. We are building an internal AI Strategy & Operations function to drive measurable cost savings and operational efficiency across every department in the company. We are hiring an AI Full-Stack Product Engineer to build the first generation of internal AI-enabled tools at Iovance. This is a hands-on full-stack JavaScript engineering role for someone who uses AI-assisted development to ship faster without compromising code quality, security, or maintainability. You will design, build, and deploy micro-applications and workflow automations that solve real business problems. You will work directly with stakeholders across Commercial, Regulatory, Quality, Manufacturing, and R&D to turn validated use cases into tools people use every day. The foundation of this role is engineering. The multiplier is AI fluency. You should be using tools like Claude, Cursor, Copilot to dramatically accelerate your workflow. We want a skilled engineer who produces significantly more output because of how

### Associate Director, Analytical Development & QC - Formation Bio
- Location: New York, NY; Boston, MA (unspecified)
- Salary: $178K-$232K
- Posted: 2026-03-03
- Apply: https://job-boards.greenhouse.io/formationbio/jobs/7529162
- Excerpt: Associate Director, Analytical Development & QC New York, NY; Boston, MA About Formation Bio Formation Bio is a tech and AI driven pharma company differentiated by radically more efficient drug development. Advancements in AI and drug discovery are creating more candidate drugs than the industry can progress because of the high cost and time of clinical trials. Recognizing that this development bottleneck may ultimately limit the number of new medicines that can reach patients, Formation Bio, founded in 2016 as TrialSpark Inc., has built technology platforms, processes, and capabilities to accelerate all aspects of drug development and clinical trials. Formation Bio partners, acquires, or in-licenses drugs from pharma companies, research organizations, and biotechs to develop programs past clinical proof of concept and beyond, ultimately helping to bring new medicines to patients. The company is backed by investors across pharma and tech, including a16z, Sequoia, Sanofi, Thrive Capital, John Doerr, Spark Capital, SV Angel Growth, and others. You can read more at the following links: - Our Vision for AI in Pharma - Our Current Drug Portfolio - Our Technology & Platform At Formation Bio, our values are the driving force behind our mission to revolutionize the pharma industry. Every team and individual at the company shares these same values, and every team and individual plays a key part in our mission to bring new treatments to patients faster and more efficiently. About the Position We are seeking a highly motivated, self-driven and detail-oriented Associate Director of Analytical Development and Quality

### Senior Director, Clinical Development - Dianthus Therapeutics
- Location: Remote (remote)
- Salary: Not disclosed
- Posted: 2026-06-04
- Apply: https://job-boards.greenhouse.io/dianthustherapeutics/jobs/4683188005
- Excerpt: Senior Director, Clinical Development Remote About Us We are developing potentially best in class therapies for patients living with severe autoimmune diseases. Our lead antibody, claseprubart (DNTH103), is purposefully engineered with extended half-life, improved potency, and high selectivity for only the active C1s complement protein that drives disease pathology - enabling less frequent and more convenient self-administered subcutaneous injections. Our second clinical candidate, DNTH212 is a first and potentially best in class, bifunctional inhibitor that targets clinically validated and complementary disease modifying mechanisms, Type 1 IFN suppression and B cell modulation - enabling potential for improved clinical outcomes and patient friendly convenient, self-administered subcutaneous injections. To learn more, please visit www.dianthustx.com and follow us on LinkedIn . About the Role The Senior Medical Director, Clinical Development will be the clinical and medical strategic lead of one or more clinical trials for DNTH212. Reporting to the SVP, Clinical Development, you will steer the preparation, review and execution of clinical study synopses and protocols, investigator brochures, and clinical study reports; review SAPs and TLF shells, guide the evaluation of emerging clinical trial data, oversee/guide the data interpretation and data mining, and ensure assigned studies are conducted according to GCPs and SOPs. You will act as a the medical monitor in close collaboration with the CRO medical and clinical monitors, ensure timely recruitment in collaboration with clinical operations, oversee/guide in conducting literature searches and reviews, meta-analyses, and publishing data. You must have experience with Rare Diseases or Rheumatology within the biotechnology or pharmaceutical

### Associate Director, Patient Services Marketing - Rheumatology - AbbVie Inc.
- Location: Mettawa, IL, United States (unspecified)
- Salary: Not disclosed
- Posted: 2026-06-10
- Parental leave: 12 weeks (not source-backed)
- Non-birth-parent leave: 12 weeks (not source-backed)
- 401(k) match: listed (not source-backed)
- Apply: https://jobs.smartrecruiters.com/AbbVie/3743990013348764-associate-director-patient-services-marketing-rheumatology
- Excerpt: Associate Director, Patient Services Marketing - Rheumatology Mettawa, IL, United States Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: The Associate Director of Patient Services Marketing will lead the strategic direction and execution of integrated patient access marketing initiatives for the RINVOQ Rheumatology franchise across APS provider and patient workstreams. This role serves as a subject matter expert in provider and patient access strategy, translating care model priorities into actionable plans while driving cross-functional alignment and communication across a highly matrixed organization, including brand, market access, legal, finance, and communications partners. Responsibilities: Lead integrated rheumatology access strategies and plans that translate care model priorities into effective marketing execution. Serve as a subject matter expert for provider access strategy, patient journey planning, segmentation, and resource development. Partner closely with the rheumatology brand team, Field Reimbursement Managers (FRMs), and key stakeholders to advance access priorities, align messaging, and support efficient resource utilization. Develop rheumatology-specific messaging and educational strategies that enhance provider engagement and patient understanding. Guide digital and content initiatives that strengthen the provider and patient experience across

### Therapeutic Specialist, Vision Care, Southwestern Ontario and Niagara - AbbVie Inc.
- Location: Remote | London, ON, Canada (remote)
- Salary: Not disclosed
- Posted: 2026-06-10
- Parental leave: 12 weeks (not source-backed)
- Non-birth-parent leave: 12 weeks (not source-backed)
- 401(k) match: listed (not source-backed)
- Apply: https://jobs.smartrecruiters.com/AbbVie/3743990013455576-therapeutic-specialist-vision-care-southwestern-ontario-and-niagara
- Excerpt: Therapeutic Specialist, Vision Care, Southwestern Ontario and Niagara Remote | London, ON, Canada Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. When choosing your career path, choose to be remarkable. Job Description: We are presently recruiting for the role of Therapeutic Specialist - Vision Care for Southwestern Ontario and Niagara , reporting to Lisa Culley, District Sales Manager in Ontario for Vision Care. The candidate will be responsible for managing and leading business development in some of our largest customer key accounts in Southwestern Ontario and Niagara. The product portfolio includes dry eye prescription and OTC products. The Therapeutic Specialist - Vision Care for Southwestern Ontario and Niagara is intended to be the face of AbbVie to identified Key Accounts to continue to build on and develop the long-term customer relationships across the vision care portfolio. Position Overview and Role Description: The successful candidate will be responsible for cultivating relationships with existing customers and expanding awareness and use of focused AbbVie Vision Care products in the Dry Eye portfolio. The Therapeutic Specialist - Vision Care for Southwestern Ontario

### Central Operations Head (COH) - Tango Therapeutics Inc
- Location: Boston, MA (unspecified)
- Salary: $187K-$281K
- Posted: 2026-05-08
- 401(k) match: listed (not source-backed)
- Apply: https://job-boards.greenhouse.io/tangotherapeutics/jobs/7726623003
- Excerpt: Central Operations Head (COH) Boston, MA Company Overview Tango Therapeutics is a biotechnology company dedicated to discovering novel drug targets and delivering the next generation of precision medicine for the treatment of cancer. Using an approach that starts and ends with patients, Tango leverages the genetic principle of synthetic lethality to discover and develop therapies that take aim at critical targets in cancer. This includes expanding the universe of precision oncology targets into novel areas such as tumor suppressor gene loss and their contribution to the ability of cancer cells to evade immune cell killing. The Tango labs and offices are located at 201 Brookline Avenue, in the Fenway area of Boston, Massachusetts. Summary We are seeking a Central Operations Head (COH) to provide strategic leadership across clinical drug supply, Clinical Trial Agreement (CTA), and eTMF management to support global clinical development programs. This role partners cross-functionally with Clinical, Regulatory, Legal, Technical Operations, and Operational Excellence to ensure alignment on trial needs, risk management, and execution priorities. You will oversee end-to-end delivery across trials, define outsourcing and vendor strategies, and ensure performance through KPIs, KRIs, and governance. This role is accountable for driving operational excellence, ensuring inspection readiness, and maintaining compliance with global regulations and internal standards. As a leader, you will build and develop a high-performing team, establish scalable processes and best practices, and foster a culture of accountability, innovation, and continuous improvement in a fast-paced biotech environment. Your role - Provide strategic direction for clinical drug supply management,

### Medical Advisor, Gastro - AbbVie Inc.
- Location: Seoul, Seoul, Korea, republic of (unspecified)
- Salary: Not disclosed
- Posted: 2026-06-10
- Parental leave: 12 weeks (not source-backed)
- Non-birth-parent leave: 12 weeks (not source-backed)
- 401(k) match: listed (not source-backed)
- Apply: https://jobs.smartrecruiters.com/AbbVie/3743990013290166-medical-advisor-gastro
- Excerpt: Medical Advisor, Gastro Seoul, Seoul, Korea, republic of Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: PRIMARY FUNCTION/OBJECTIVE To lead medical team and activities in responsible therapeutic areas. Set and execute Medical Affairs strategies for the responsible therapeutic areas. To set and deliver medical affairs strategies which generate, evaluate and communicate scientific evidence to support the needs of health care professionals and patients in covered therapeutic areas, in line with the strategic priorities of the brand and company, and all prevailing governance requirements. To make recommendations regarding staffing levels and structure for the team, and to plan and manage budget within prevailing finance guidance. To support the Korea Medical Director to build the organisation, ensuring the medical department is fully integrated to support the strategy and affiliate business, while being functionally independent and operating within a culture of ethical and compliant behaviour. Main responsibilities: Fulfill the responsibilities of a Medical Advisor in the Gastroenterology therapeutic area. Develop and execute the annual medical affairs strategy and plans, and contribute to long-range strategic plans for the assigned therapeutic

### Associate Director, Oncology Digital and Omnichannel Marketing - Corcept Therapeutics
- Location: Remote (remote)
- Salary: $172K-$228K
- Posted: 2026-06-03
- 401(k) match: listed (not source-backed)
- Apply: https://www.corcept.com/careers/current-opportunities/?gh_jid=6013629004
- Excerpt: Associate Director, Oncology Digital and Omnichannel Marketing Remote For more than 25 years, Corcept has been singularly focused on the science of cortisol, a powerful hormone that when unregulated, can play a role in a broad range of diseases. Our commercial portfolio includes treatments for hypercortisolism and oncology, and the company has discovered more than 1,000 proprietary selective cortisol modulators and glucocorticoid receptor antagonists. With advanced clinical trials in patients with hypercortisolism, solid tumors, ALS and liver disease, Corcept is unlocking the power of cortisol modulation to help address some of the most devastating diseases patients face today. Corcept is headquartered in Redwood City, California. To learn more, visit www.corcept.com . The Associate Director, Oncology Digital and Omnichannel Marketing will play a critical leadership role in shaping and executing the digital and omnichannel marketing plan for Corcept's first oncology product, Lifyorli, in platinum-resistant ovarian cancer. Reporting to the Senior Director of Oncology Marketing, this individual will be responsible for operationalizing Corcept's omnichannel engagement model, driving seamless, data-driven customer engagement across HCP and Patient audiences. This role will drive successful execution of digital and media plans for Lifyorli, collaborating closely with Marketing, Market Access, Insights & Analytics, and IT, ensuring campaigns are measurable and continuously optimized to deliver against brand objectives. This role requires a self-starter who can effectively navigate ambiguity, brings structure to complex initiatives and proactively partners cross-functionally to translate strategy into disciplined execution. Responsibilities: Omnichannel Planning & Implementation - Collaborate on the development and execution of the operational

### Optical Engineer - Cowboy Space Corporation
- Location: San Carlos, California, San Carlos, California, United States (unspecified)
- Salary: $120K-$200K
- Posted: 2026-05-12
- Apply: https://jobs.ashbyhq.com/cowboyspace/3fb88f42-b125-4415-8354-e47d8ea4f2d3
- Excerpt: Optical Engineer San Carlos, California, San Carlos, California, United States Optical Engineer About Cowboy Space Corp: Cowboy Space Corp. is building the infrastructure to power and connect the orbital economy. Our satellites operate in Low Earth Orbit to collect sunlight and enable a new class of capabilities-from powering on-orbit compute, to transmitting energy via infrared lasers (space-to-earth and space-to-space), powering on-orbit compute to delivering secure, high-bandwidth optical data. By rethinking how energy and data are generated and distributed in space, we're unlocking entirely new ways to operate both in orbit and on Earth. Founded in 2024 by Baiju Bhatt (co-founder of Robinhood), Cowboy Space Corp. is backed by leading investors and built by a team from top aerospace and defense organizations. We're moving quickly to solve complex technical challenges and build a new category of space infrastructure. About the Role : The Lasers & Optics team is looking for an Optical Engineer to design and build the free-space optical path for our next generation laser communications system. This role spans the transmitter beam path, the ground receive telescope, and beam diagnostic systems. You will work closely with laser, mechanical, and systems engineers to deliver a working end-to-end optical link. Responsibilities: - Design and optimize free-space optical assemblies including beam expanders, collimators, and telescope interfaces. - Build and maintain optical system models using Zemax or Code V, including tolerance and stray light analyses. - Define optical interface specifications for mechanical and opto-mechanical design. - Specify optical components, coatings, and filters, and

### Senior Scientist, Cellular Pharmacology - Genentech, Inc.
- Location: South San Francisco, California, United States of America (unspecified)
- Salary: Not disclosed
- Posted: 2026-06-10
- 401(k) match: listed (not source-backed)
- Apply: https://roche.wd3.myworkdayjobs.com/ROG-A2O-GENE/job/South-San-Francisco/Senior-Scientist--Cellular-Pharmacology_202606-114286/apply
- Excerpt: Senior Scientist, Cellular Pharmacology South San Francisco, California, United States of America Join our team as a Senior Scientist in Cellular Pharmacology and drive innovation in drug discovery for diverse therapeutic areas. Lead advanced pharmacology assays, collaborate with multidisciplinary teams, and shape the future of cell-based therapies. If you have expertise in iPSCs, CRISPR gene editing, and ophthalmology/neuroscience therapeutics, we want to hear from you!

### Contract Research Associate II, Protein Science - Keros Therapeutics Inc
- Location: Lexington, Massachusetts, United States (unspecified)
- Salary: Not disclosed
- Posted: 2026-03-16
- 401(k) match: listed (not source-backed)
- Apply: https://kerostx.com/current-opportunities?gh_jid=4673674005
- Excerpt: Contract Research Associate II, Protein Science Lexington, Massachusetts, United States At Keros, our mission is to deliver significant clinical benefit to a wide range of patients with disorders that are linked to dysfunctional signaling of the transforming growth factor-beta (TGF-ß) family of proteins. With a focus on developing differentiated product candidates that are designed to alter TGF-β signaling, we aim to target the pathways critical for the growth, repair and maintenance of blood cells and a number of tissues, including bone, skeletal muscle, adipose and heart tissue. We believe our product candidates have the potential to unlock the full therapeutic benefits of modulating the TGF-β superfamily and provide disease-modifying benefit to patients. Keros Therapeutics is seeking a highly motivated and collaborative individual to join our protein biochemistry group within our Research Department. Our group exploits multidisciplinary approaches in protein sciences and protein engineering, to better the understanding of the biochemical, biophysical, and structural functional properties of the biomolecules within the TGF-β superfamily that drive the signaling pathway. Our efforts greatly contribute to advance innovative research and drug discovery and heavily support our discovery pipeline. You will have the opportunity to learn about and contribute to early-stage drug discovery from a protein chemistry perspective as well as through internal and external collaboration with other departments. You will play an important role supporting in vivo and in vitro studies crucial for the progress of our therapeutic research programs by generating high-quality proteins and other reagents in this hands-on laboratory position. The successful

### Director, Head of Product Management – AI-Enabled Precision Medicine (Therapeutics & Innovations) - Natera, Inc.
- Location: US Remote (remote)
- Salary: $185K-$231K
- Posted: 2026-05-15
- 401(k) match: listed (not source-backed)
- Fertility benefits: yes (not source-backed)
- Apply: https://job-boards.greenhouse.io/natera/jobs/5994721004
- Excerpt: Director, Head of Product Management – AI-Enabled Precision Medicine (Therapeutics & Innovations) US Remote Director, Head of Product Management - AI-Enabled Precision Medicine (Therapeutics & Innovations) About Us We are redefining the future of precision medicine by integrating AI with healthcare to create next-generation, precision treatment modalities. Our multidisciplinary team is building products at the intersection of clinical data, multi-omics, and machine learning-unlocking entirely new approaches to drug development and patient care. Within the Therapeutics & Innovations Business Unit, we are developing a new category that bridges diagnostics and therapeutics. Our platform combines deep scientific expertise with proprietary datasets to power AI-enabled solutions that can transform how therapies are discovered, developed, and deployed. We are looking for a product leader who can translate this potential into real, scalable products-owning the strategy, roadmap, and execution to bring these innovations to market. The Role We are seeking a Director / Head of Product Management to lead product strategy and execution for our AI-enabled therapeutics platform. This is a highly cross-functional leadership role at the center of science, engineering, clinical development, and commercial strategy. You will define what we build, why it matters, and how it creates value-for biopharma partners, clinicians, and ultimately patients. You will own the product lifecycle end-to-end: from concept and validation through development, launch, and iteration. This role requires a rare blend of scientific fluency, product rigor, and commercial instinct . You will work closely with R&D, AI, medical, business development, and marketing to ensure our products are scientifically

### Manager, MHI Business Analytics - AbbVie Inc.
- Location: North Chicago, IL, United States (unspecified)
- Salary: Not disclosed
- Posted: 2026-06-10
- Parental leave: 12 weeks (not source-backed)
- Non-birth-parent leave: 12 weeks (not source-backed)
- 401(k) match: listed (not source-backed)
- Apply: https://jobs.smartrecruiters.com/AbbVie/3743990013473367-manager-mhi-business-analytics
- Excerpt: Manager, MHI Business Analytics North Chicago, IL, United States Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: Purpose: The ME (Medical Engagement) team within MHI (Medical Affairs + Health Impact) plays an instrumental role in supporting Therapeutic Area (TA) strategy and informing tactical execution for AbbVie's therapeutic areas globally. As Manager, Business Analytics on the Medical Engagement team you will execute standard and ad-hoc analytic delivery. Analytic output will be used to inform strategic opportunities, provide recommendations, elevate organizational data maturation, and develop sustainable, automated analytic processes. This role requires strong data analytic capabilities across various data ecosystems. Responsibilities: Perform and lead analytics projects across the various AbbVie therapeutic areas and the MHI organization through claims and business data analysis by leveraging both internal and external datasets including big data sources to shape utilization of strategic insight opportunities. Demonstrate strong understanding of the U.S. healthcare landscape and key AbbVie Therapeutic areas to identify and proactively address opportunities and threats. Build collaborative relationships with internal stakeholders (e.g., HEOR, RWD/E teams, therapeutic area teams, operations, and BTS/IR to

### Associate Director, Patient Services - Axsome Therapeutics
- Location: New York, NY (unspecified)
- Salary: $155K-$185K
- Posted: 2026-06-04
- Apply: https://job-boards.greenhouse.io/axsometherapeutics/jobs/5779343004
- Excerpt: Associate Director, Patient Services New York, NY Axsome Therapeutics is a biopharmaceutical company leading a new era in the treatment of central nervous system (CNS) conditions. We deliver scientific breakthroughs by identifying critical gaps in care and develop differentiated products with a focus on novel mechanisms of action that enable meaningful advancements in patient outcomes. Our industry-leading neuroscience portfolio includes FDA-approved treatments for major depressive disorder, excessive daytime sleepiness associated with narcolepsy and obstructive sleep apnea, and migraine, and multiple late-stage development programs addressing a broad range of serious neurological and psychiatric conditions that impact over 150 million people in the United States. Together, we are on a mission to solve some of the brain's biggest problems so patients and their loved ones can flourish. For more information, please visit us at www.axsome.com and follow us on LinkedIn and X . About This Role Axsome Therapeutics is seeking an Associate Director, Patient Services to lead the establishment and growth of a new Patient Services Hub. This role will work closely with the Director, Patient Services for developing, implementing, and overseeing all aspects of the Hub's operations, ensuring efficient and seamless patient access to therapies and support services. This role requires a strong leader to build and manage the hub team, foster collaborative relationships, and drive continuous improvement within a fast-paced environment. This role will have close collaboration among, and provide ad hoc support to, Field Access and Patient Service functions within the Market Access team, as related to the HUB.

### Associate Director, Statistical Programming - Apogee Therapeutics Inc
- Location: Remote (remote)
- Salary: $190K-$210K
- Posted: 2026-04-02
- 401(k) match: listed (not source-backed)
- Apply: https://job-boards.greenhouse.io/apogeetherapeutics/jobs/5097750007
- Excerpt: Associate Director, Statistical Programming Remote About Apogee Therapeutics Founded in 2022, Apogee Therapeutics, Inc. (Ticker: APGE) is a well-funded, Nasdaq listed company that offers the opportunity to work in a fast-paced, highly dynamic environment. At Apogee, you can actively contribute to shaping the company culture, take on various roles and responsibilities, and grow professionally. Apogee Therapeutics is a clinical-stage biotechnology company advancing novel biologics with potential for differentiated efficacy and dosing in the largest I&I markets, Apogee's antibody programs are designed to overcome limitations of existing therapies by targeting well-established mechanisms of action and incorporating advanced antibody engineering to optimize half-life and other properties. Zumilokibart (APG777), the company's most advanced program, is being initially developed for the treatment of atopic dermatitis (AD), which is the largest and one of the least penetrated I&I markets, as well as asthma. With four validated targets in its portfolio, Apogee is seeking to achieve best-in-class efficacy and dosing through monotherapies and combinations of its novel antibodies. Based on a broad pipeline and depth of leadership and expertise, the company believes it can deliver value and meaningful benefit to patients underserved by today's standard of care. We are a fast-paced company committed to building an exceptional culture, founded on our C.O.R.E. values: C aring, O riginal, R esilient and E goless and a commitment to refusing to stop at “good enough”. If this sounds like you, keep reading! Role Summary We are seeking an Associate Director of Statistical Programming. In this position you will be

### Sr. Medical Director, Pharmacovigilance - Maplight Therapeutics Inc
- Location: Remote (remote)
- Salary: $319K-$361K
- Posted: 2025-12-09
- Apply: https://job-boards.greenhouse.io/maplighttherapeutics/jobs/5025985008
- Excerpt: Sr. Medical Director, Pharmacovigilance Remote Who We Are: MapLight Therapeutics is a clinical stage biotech company that focuses on drug discovery for central nervous system disorders. We combine cutting-edge technologies including optogenetics, in vivo physiology, and spatial transcriptomics to identify novel drug targets and develop effective therapies to address psychiatric symptoms. What You'll Do: The Senior Medical Director, Pharmacovigilance will lead the medical safety evaluation and benefit-risk assessment for products throughout their lifecycle with focus on patient well-being and compliance and applicable regulatory requirements. This person will lead cross-functional safety management team (SMT) and collaborate with other members Clinical Development and Medical Affairs (CDMA), contract research organizations (CROs), and drug development collaborators/partners to ensure that all clinical safety and benefit-risk assessment is performed adequately for assigned products. Reporting to the Vice President, Pharmacovigilance, the Senior Medical Director will oversee cross-functional teams and may have direct reports Responsibilities: - Lead product safety surveillance and oversee evolving safety and benefit-risk profiles for assigned products. - Lead cross-functional safety management team (SMT) for assigned products, and responsible for the on-going assessment of benefit-risk profiles and related actions during the product life cycle. - Review safety data from various sources (e.g. pre-clinical, clinical trial data, post-marketing, literature) throughout the development process as well as post marketing for assigned products. - Responsible for conducting signal detection activities, monitoring, evaluation, interpretation and appropriate management and communication of safety information - Represent pharmacovigilance on cross-functional product/project teams including review of safety sections of protocols, investigator brochures, informed

### Senior Manager, Clinical Biomarker Operations - Apogee Therapeutics Inc
- Location: Remote (remote)
- Salary: $150K-$170K
- Posted: 2026-04-22
- 401(k) match: listed (not source-backed)
- Apply: https://job-boards.greenhouse.io/apogeetherapeutics/jobs/5117623007
- Excerpt: Senior Manager, Clinical Biomarker Operations Remote About Apogee Therapeutics Founded in 2022, Apogee Therapeutics, Inc. (Ticker: APGE) is a well-funded, Nasdaq listed company that offers the opportunity to work in a fast-paced, highly dynamic environment. At Apogee, you can actively contribute to shaping the company culture, take on various roles and responsibilities, and grow professionally. Apogee Therapeutics is a clinical-stage biotechnology company advancing novel biologics with potential for differentiated efficacy and dosing in the largest I&I markets, Apogee's antibody programs are designed to overcome limitations of existing therapies by targeting well-established mechanisms of action and incorporating advanced antibody engineering to optimize half-life and other properties. Zumilokibart (APG777), the company's most advanced program, is being initially developed for the treatment of atopic dermatitis (AD), which is the largest and one of the least penetrated I&I markets, as well as asthma. With four validated targets in its portfolio, Apogee is seeking to achieve best-in-class efficacy and dosing through monotherapies and combinations of its novel antibodies. Based on a broad pipeline and depth of leadership and expertise, the company believes it can deliver value and meaningful benefit to patients underserved by today's standard of care. We are a fast-paced company committed to building an exceptional culture, founded on our C.O.R.E. values: C aring, O riginal, R esilient and E goless and a commitment to refusing to stop at “good enough”. If this sounds like you, keep reading! Role Summary The Department of Research and Translational Medicine is seeking a Clinical Biomarker Operations Sr.

### Vice President, Engineering - Formation Bio
- Location: NYC, NY; Boston MA (unspecified)
- Salary: $347K-$435K
- Posted: 2026-01-14
- Apply: https://job-boards.greenhouse.io/formationbio/jobs/7472161
- Excerpt: Vice President, Engineering NYC, NY; Boston MA About Formation Bio Formation Bio is a tech and AI driven pharma company differentiated by radically more efficient drug development. Advancements in AI and drug discovery are creating more candidate drugs than the industry can progress because of the high cost and time of clinical trials. Recognizing that this development bottleneck may ultimately limit the number of new medicines that can reach patients, Formation Bio, founded in 2016 as TrialSpark Inc., has built technology platforms, processes, and capabilities to accelerate all aspects of drug development and clinical trials. Formation Bio partners, acquires, or in-licenses drugs from pharma companies, research organizations, and biotechs to develop programs past clinical proof of concept and beyond, ultimately helping to bring new medicines to patients. The company is backed by investors across pharma and tech, including a16z, Sequoia, Sanofi, Thrive Capital, John Doerr, Spark Capital, SV Angel Growth, and others. You can read more at the following links: - Our Vision for AI in Pharma - Our Current Drug Portfolio - Our Technology & Platform At Formation Bio, our values are the driving force behind our mission to revolutionize the pharma industry. Every team and individual at the company shares these same values, and every team and individual plays a key part in our mission to bring new treatments to patients faster and more efficiently. About the Position We're looking for a Vice President of Engineering to lead and grow the team that builds the AI-native software platform

### Director, Clinical Development (Clinical Science) - Apogee Therapeutics Inc
- Location: Remote (remote)
- Salary: $230K-$260K
- Posted: 2026-05-15
- 401(k) match: listed (not source-backed)
- Apply: https://job-boards.greenhouse.io/apogeetherapeutics/jobs/5138987007
- Excerpt: Director, Clinical Development (Clinical Science) Remote About Apogee Therapeutics Founded in 2022, Apogee Therapeutics, Inc. (Ticker: APGE) is a well-funded, Nasdaq listed company that offers the opportunity to work in a fast-paced, highly dynamic environment. At Apogee, you can actively contribute to shaping the company culture, take on various roles and responsibilities, and grow professionally. Apogee Therapeutics is a clinical-stage biotechnology company advancing novel biologics with potential for differentiated efficacy and dosing in the largest I&I markets, Apogee's antibody programs are designed to overcome limitations of existing therapies by targeting well-established mechanisms of action and incorporating advanced antibody engineering to optimize half-life and other properties. Zumilokibart (APG777), the company's most advanced program, is being initially developed for the treatment of atopic dermatitis (AD), which is the largest and one of the least penetrated I&I markets, as well as asthma. With four validated targets in its portfolio, Apogee is seeking to achieve best-in-class efficacy and dosing through monotherapies and combinations of its novel antibodies. Based on a broad pipeline and depth of leadership and expertise, the company believes it can deliver value and meaningful benefit to patients underserved by today's standard of care. We are a fast-paced company committed to building an exceptional culture, founded on our C.O.R.E. values: C aring, O riginal, R esilient and E goless and a commitment to refusing to stop at “good enough”. If this sounds like you, keep reading! Role Summary We are seeking an experienced non-MD Clinical Scientist. As a Director in Clinical Development,

### Site Management Leader (SML) - Tango Therapeutics Inc
- Location: Boston, MA (unspecified)
- Salary: $128K-$192K
- Posted: 2026-05-08
- 401(k) match: listed (not source-backed)
- Apply: https://job-boards.greenhouse.io/tangotherapeutics/jobs/7725413003
- Excerpt: Site Management Leader (SML) Boston, MA Company Overview Tango Therapeutics is a biotechnology company dedicated to discovering novel drug targets and delivering the next generation of precision medicine for the treatment of cancer. Using an approach that starts and ends with patients, Tango leverages the genetic principle of synthetic lethality to discover and develop therapies that take aim at critical targets in cancer. This includes expanding the universe of precision oncology targets into novel areas such as tumor suppressor gene loss and their contribution to the ability of cancer cells to evade immune cell killing. The Tango labs and offices are located at 201 Brookline Avenue, in the Fenway area of Boston, Massachusetts. Summary We are seeking a Site Management Leader (SML) to oversee all site management and monitoring activities conducted by the CRO in a clinical trial. This role will be assigned to critical clinical trials of the Tango portfolio and serve as the primary contact between sponsor and CRO for site management aspects. In a fast-paced, small biotech environment, the SML will operationally oversee and manage the end-to-end site management activities as per approved timelines, budget, regulatory requirements, and internal standards. This individual will play a key role in the execution and delivery of clinical trial objectives. The ideal candidate is highly collaborative, detail-oriented, and comfortable operating in a hands-on environment, with a focus on building scalable processes, tools, and best practices to support efficient and compliant clinical trial execution. Your role - Serve as the primary liaison

### SRA DNA Encoded Library Technology - (Brisbane, CA) - Nurix Therapeutics Inc
- Location: Brisbane, CA (unspecified)
- Salary: $129K-$147K
- Posted: 2026-05-18
- 401(k) match: listed (not source-backed)
- Apply: https://job-boards.greenhouse.io/nurix/jobs/8553710002
- Excerpt: SRA DNA Encoded Library Technology - (Brisbane, CA) Brisbane, CA Company Nurix Therapeutics is a clinical stage biopharmaceutical company focused on the discovery, development, and commercialization of targeted protein degradation medicines, the next frontier in innovative drug design aimed at improving treatment options for patients with cancer and inflammatory diseases. Powered by a fully AI-integrated discovery engine capable of tackling any protein class, and coupled with unparalleled ligase expertise, Nurix's dedicated team has built a formidable advantage in translating the science of targeted protein degradation into clinical advancements. Nurix aims to establish degrader-based treatments at the forefront of patient care, writing medicine's next chapter with a new script to outmatch disease. Research Associate III/Scientist I, DNA Encoded Library Technology - Nurix Brisbane Position We are seeking a talented and motivated chemist to join our Discovery Chemistry team and contribute to the design and synthesis of DNA-encoded libraries (DELs). This hands-on position offers the opportunity to shape Nurix's DEL-based lead discovery platform, working at the interface of chemistry, biology, and automation. Key responsibilities: - Design and validate novel DEL library builds. - Develop and bring in new DNA-compatible chemical transformations that can widen the DEL chemical space. - Construct DEL libraries to support the in-house library production efforts. - Work with external partners to support our DEL synthesis and hit follow up strategies. - Engage in cross-functional team discussions that support DEL screening, data analysis, machine learning and hit-optimization. - Contribute to platform automation and technology development efforts. - Present results,

### Clinical Trial Manager - Apogee Therapeutics Inc
- Location: Remote (remote)
- Salary: $145K-$160K
- Posted: 2026-04-02
- 401(k) match: listed (not source-backed)
- Apply: https://job-boards.greenhouse.io/apogeetherapeutics/jobs/5098120007
- Excerpt: Clinical Trial Manager Remote About Apogee Therapeutics Founded in 2022, Apogee Therapeutics, Inc. (Ticker: APGE) is a well-funded, Nasdaq listed company that offers the opportunity to work in a fast-paced, highly dynamic environment. At Apogee, you can actively contribute to shaping the company culture, take on various roles and responsibilities, and grow professionally. Apogee Therapeutics is a clinical-stage biotechnology company advancing novel biologics with potential for differentiated efficacy and dosing in the largest I&I markets, Apogee's antibody programs are designed to overcome limitations of existing therapies by targeting well-established mechanisms of action and incorporating advanced antibody engineering to optimize half-life and other properties. Zumilokibart (APG777), the company's most advanced program, is being initially developed for the treatment of atopic dermatitis (AD), which is the largest and one of the least penetrated I&I markets, as well as asthma. With four validated targets in its portfolio, Apogee is seeking to achieve best-in-class efficacy and dosing through monotherapies and combinations of its novel antibodies. Based on a broad pipeline and depth of leadership and expertise, the company believes it can deliver value and meaningful benefit to patients underserved by today's standard of care. We are a fast-paced company committed to building an exceptional culture, founded on our C.O.R.E. values: C aring, O riginal, R esilient and E goless and a commitment to refusing to stop at “good enough”. If this sounds like you, keep reading! Role Summary We are seeking a Clinical Trial Manger (CTM) to join our growing Clinical Operations team! In

### Director, AI Enablement - Apogee Therapeutics Inc
- Location: Remote (remote)
- Salary: $225K-$250K
- Posted: 2026-05-19
- 401(k) match: listed (not source-backed)
- Apply: https://job-boards.greenhouse.io/apogeetherapeutics/jobs/5141496007
- Excerpt: Director, AI Enablement Remote About Apogee Therapeutics Founded in 2022, Apogee Therapeutics, Inc. (Ticker: APGE) is a well-funded, Nasdaq listed company that offers the opportunity to work in a fast-paced, highly dynamic environment. At Apogee, you can actively contribute to shaping the company culture, take on various roles and responsibilities, and grow professionally. Apogee Therapeutics is a clinical-stage biotechnology company advancing novel biologics with potential for differentiated efficacy and dosing in the largest I&I markets, Apogee's antibody programs are designed to overcome limitations of existing therapies by targeting well-established mechanisms of action and incorporating advanced antibody engineering to optimize half-life and other properties. Zumilokibart (APG777), the company's most advanced program, is being initially developed for the treatment of atopic dermatitis (AD), which is the largest and one of the least penetrated I&I markets, as well as asthma. With four validated targets in its portfolio, Apogee is seeking to achieve best-in-class efficacy and dosing through monotherapies and combinations of its novel antibodies. Based on a broad pipeline and depth of leadership and expertise, the company believes it can deliver value and meaningful benefit to patients underserved by today's standard of care. We are a fast-paced company committed to building an exceptional culture, founded on our C.O.R.E. values: C aring, O riginal, R esilient and E goless and a commitment to refusing to stop at “good enough”. If this sounds like you, keep reading! Role Summary We are seeking a Director, IT - AI Enablement . In this newly created role, you

### Engineering Manager - Pelago
- Location: New York, NY (unspecified)
- Salary: $225K-$235K
- Posted: 2026-02-11
- Apply: https://job-boards.greenhouse.io/pelago/jobs/5045362007
- Excerpt: Engineering Manager New York, NY Pelago is the world's leading virtual clinic for Substance Use Management. Our program provides guidance, support and treatment for members seeking to overcome their tobacco, alcohol and opioid use. From unhealthy habits to active substance use disorders, Pelago delivers a personalized solution based on individual health, habits, genetics, and goals, providing care for members wherever they might be on the substance use spectrum. Pelago's suite of virtual services ranges from education, to cognitive behavioral therapy (CBT) to comprehensive medication-assisted treatment (MAT). Pelago enables employers and health plans to deliver accessible, affordable, and effective treatment for substance misuse. Pelago has scaled to helping hundreds of employers and health plans and has already helped more than 750,000 members manage their substance use better. We have recently closed our Series C and raised over $151m from leading global investors. If you are passionate about making an impact on the health of others, join us and make it happen! About Pelago Engineering: Our engineering team operates as empowered, outcome-oriented problem solvers, working in close partnership with product, design, and clinical teams to improve member outcomes at scale. As AI transforms how software is built, we are intentionally evolving our development lifecycle so we spend less time on mechanical implementation and more time on system design, judgment, and impact. How We Work: - Outcome-driven: Engineers are given problems to solve, not just features to build. Success is measured by learning, impact, and outcomes-not velocity alone - AI-native: We use AI

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Source-backed benefit claims include source links; other benefit values are labeled separately.