# FewerJobs export - 100 curated jobs Generated: 2026-08-13T06:14:23.818Z Source: https://fewerjobs.com ## Filters applied - **q**: Xenon Pharmaceuticals - **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**: 1 - **per_page**: 100 - **sort**: relevance ## Jobs ### Director, Regulatory Affairs, Commercial (Advertising & Promotion) - Xenon Pharmaceuticals - Location: Boston | [Hybrid] | Remote (hybrid) - Salary: Not disclosed - Posted: 2026-06-10 - Apply: https://jobs.ashbyhq.com/xenon/75abced6-0750-4a48-ac32-b86245a9c5e9 - Excerpt: Director, Regulatory Affairs, Commercial (Advertising & Promotion) Boston | [Hybrid] | Remote ### Senior Manager, Data Management - Xenon Pharmaceuticals - Location: Boston | [Hybrid] | Remote (hybrid) - Salary: Not disclosed - Posted: 2026-06-10 - Apply: https://jobs.ashbyhq.com/xenon/173400f9-4eb6-4f3b-ac54-b0d41c724943 - Excerpt: Senior Manager, Data Management Boston | [Hybrid] | Remote ### Director, Quality Assurance, GCP - Xenon Pharmaceuticals - Location: Boston | [Hybrid] | Remote (hybrid) - Salary: Not disclosed - Posted: 2026-06-10 - Apply: https://jobs.ashbyhq.com/xenon/166325d2-cf3d-4b81-bdb5-e8ee120e7f60 - Excerpt: Director, Quality Assurance, GCP Boston | [Hybrid] | Remote ### Senior Manager/Associate Director, Enterprise Integration & Data Engineering - Xenon Pharmaceuticals - Location: Boston | [Hybrid] | Remote (hybrid) - Salary: Not disclosed - Posted: 2026-06-10 - Apply: https://jobs.ashbyhq.com/xenon/1d0bfc68-b56c-4eda-8c80-aab4bdebc410 - Excerpt: Senior Manager/Associate Director, Enterprise Integration & Data Engineering Boston | [Hybrid] | Remote ### Director, Quality Assurance, GMP - Xenon Pharmaceuticals - Location: Boston | [Hybrid] | Remote (hybrid) - Salary: Not disclosed - Posted: 2026-06-10 - Apply: https://jobs.ashbyhq.com/xenon/0fd257c7-e773-44c3-b378-ee7da5f9e47f - Excerpt: Director, Quality Assurance, GMP Boston | [Hybrid] | Remote ### Executive Director, Total Rewards - Xenon Pharmaceuticals - Location: Vancouver | [Hybrid] | Remote (hybrid) - Salary: Not disclosed - Posted: 2026-06-10 - Apply: https://jobs.ashbyhq.com/xenon/66a87f03-02a8-427a-978a-93b0068eb238 - Excerpt: Executive Director, Total Rewards Vancouver | [Hybrid] | Remote ### Manager/Senior Manager, Trial Operations - Xenon Pharmaceuticals - Location: Boston | [Hybrid] | Remote (hybrid) - Salary: Not disclosed - Posted: 2026-06-10 - Apply: https://jobs.ashbyhq.com/xenon/b83ed917-f851-4a2a-bfed-8b2dd29babd3 - Excerpt: Manager/Senior Manager, Trial Operations Boston | [Hybrid] | Remote ### Director, Medical Affairs (Epilepsy) - Xenon Pharmaceuticals - Location: Boston | [Hybrid] | Remote (hybrid) - Salary: Not disclosed - Posted: 2026-06-10 - Apply: https://jobs.ashbyhq.com/xenon/a2530692-06d3-42a5-a24f-aae49229f5ba - Excerpt: Director, Medical Affairs (Epilepsy) Boston | [Hybrid] | Remote ### Principal/Senior Systems Engineer (Microsoft Copilot AI) - Xenon Pharmaceuticals - Location: Boston | [Hybrid] | Remote (hybrid) - Salary: Not disclosed - Posted: 2026-06-10 - Apply: https://jobs.ashbyhq.com/xenon/37a973b1-adb4-4493-afde-2181b16373e8 - Excerpt: Principal/Senior Systems Engineer (Microsoft Copilot AI) Boston | [Hybrid] | Remote ### AI in Residence - Xaira - Location: South San Francisco, California, United States (unspecified) - Salary: $10K-$15K/mo - Posted: 2026-03-25 - Apply: https://job-boards.greenhouse.io/xairatherapeutics/jobs/5089321007 - Excerpt: AI in Residence South San Francisco, California, United States About Xaira Therapeutics Xaira is an innovative biotech startup focused on leveraging AI to transform drug discovery and development. The company is leading the development of generative AI models to design protein and antibody therapeutics, enabling the creation of medicines against historically hard-to-drug molecular targets. It is also developing foundation models for biology and disease to enable better target elucidation and patient stratification. Collectively, these technologies aim to continually enable the identification of novel therapies and to improve success in drug development. Xaira is headquartered in the San Francisco Bay Area, Seattle, and London. AI in Residence AI in Residence is a highly selective role at the intersection of frontier machine learning and drug discovery. Designed as an industry alternative to a traditional postdoctoral position, the program is for exceptional researchers and engineers who want to apply advanced AI to real biomedical problems end to end, from data to deployed systems. Residents join a small cohort working on high-impact AI efforts across Xaira. You'll collaborate closely with AI scientists, research engineers, and drug discovery teams to design, build, and ship machine learning capabilities that directly influence therapeutic programs. This is hands-on, system-level work with real scientific consequence. We're looking for candidates with technical depth, intellectual independence, strong research judgment, and evidence of delivering high-quality work-whether through publications, open-source, or production systems. What You'll Do - Develop and advance ML models for biological, preclinical, and translational datasets (e.g., multimodal omics, imaging, text, ### Senior Research Associate/Associate Scientist, Display Technology (Contract) - Xaira - Location: South San Francisco, California, United States (unspecified) - Salary: $45-$60/hr - Posted: 2026-03-04 - Apply: https://job-boards.greenhouse.io/xairatherapeutics/jobs/5068166007 - Excerpt: Senior Research Associate/Associate Scientist, Display Technology (Contract) South San Francisco, California, United States About Xaira Therapeutics Xaira is an innovative biotech startup focused on leveraging AI to transform drug discovery and development. The company is leading the development of generative AI models to design protein and antibody therapeutics, enabling the creation of medicines against historically hard-to-drug molecular targets. It is also developing foundation models for biology and disease to enable better target elucidation and patient stratification. Collectively, these technologies aim to continually enable the identification of novel therapies and to improve success in drug development. Xaira is headquartered in the San Francisco Bay Area, Seattle, and London. About the Role You are an enthusiastic protein biochemist who takes pride in your bench execution skills. Your passion lies in display technology, drug discovery and developing novel treatments for patients. You are conscientious, detail-oriented, and organized. Collaboration comes naturally to you, and you thrive in a fast-paced environment where pushing the boundaries of what is possible is the norm. Responsibilities - Build, adapt, and automate display systems to facilitate AI antibody design. - Establish, develop, and/or optimize cutting edge technologies to enable data generation at scale for AI model training or evaluation - Design and apply multiple innovative selection techniques to provide data at scale based on ML training needs. - Design, setup, optimize, and use automation to characterize affinity and function at the clonal level. - Contribute to the preparation of technical reports and presentations. Qualifications - Significant hands-on experience with ### Pharmaceutical Sciences, Technology & Innovation Lead (Sr. Director) - Takeda Pharmaceutical Company Limited - Location: Boston, MA (unspecified) - Salary: Not disclosed - Posted: 2026-06-11 - 401(k) match: listed (not source-backed) - Apply: https://takeda.wd3.myworkdayjobs.com/External/job/Boston-MA/Pharmaceutical-Sciences--Technology---Innovation-Lead--Sr-Director-_R0178501-1 - Excerpt: Pharmaceutical Sciences, Technology & Innovation Lead (Sr. Director) Boston, MA posted: Posted Yesterday ### Software Engineer, X-Scientist - Xaira - Location: South San Francisco, California, United States (unspecified) - Salary: $140K-$215K - Posted: 2026-06-11 - Apply: https://job-boards.greenhouse.io/xairatherapeutics/jobs/5161853007 - Excerpt: Software Engineer, X-Scientist South San Francisco, California, United States About Xaira Therapeutics Xaira is an innovative biotech startup focused on leveraging AI to transform drug discovery and development. The company is leading the development of generative AI models to design protein and antibody therapeutics, enabling the creation of medicines against historically hard-to-drug molecular targets. It is also developing foundation models for biology and disease to enable better target elucidation and patient stratification. Collectively, these technologies aim to continually enable the identification of novel therapies and to improve success in drug development. Xaira is headquartered in the San Francisco Bay Area, Seattle, and London. About the Role Xaira is pioneering an AI-native approach to discovering and developing the next generation of life-changing medicines. We are building predictive and agentic AI systems across drug discovery, and the X-Scientist team accelerates this mission by making AI-assisted science reliable, usable, and scalable across drug discovery workflows. On the X-Scientist team, you will work at the intersection of AI, software engineering, and therapeutic discovery. You will collaborate closely with AI scientists, engineers, platform teams, and drug discovery experts to build systems that connect AI models, biological tools, datasets, and scientific workflows. This role spans backend systems, APIs, tool-calling infrastructure, workflow orchestration, developer-facing SDKs and CLIs, and agentic interfaces that help scientists run analyses, inspect intermediate steps, and iterate on results. What You'll Do - Backend systems and APIs that connect AI models to scientific tools, datasets, and analysis workflows - Tool-calling infrastructure, CLIs, SDKs, and ### Vice President, Information Technology - Xaira - Location: South San Francisco, California, United States (unspecified) - Salary: $300K-$325K - Posted: 2026-04-13 - Apply: https://job-boards.greenhouse.io/xairatherapeutics/jobs/5107095007 - Excerpt: Vice President, Information Technology South San Francisco, California, United States About Xaira Therapeutics Xaira is an innovative biotech startup focused on leveraging AI to transform drug discovery and development. The company is leading the development of generative AI models to design protein and antibody therapeutics, enabling the creation of medicines against historically hard-to-drug molecular targets. It is also developing foundation models for biology and disease to enable better target elucidation and patient stratification. Collectively, these technologies aim to continually enable the identification of novel therapies and to improve success in drug development. Xaira is headquartered in the San Francisco Bay Area, Seattle, and London. About the Role We are a technology-driven biotechnology company using AI to compress the timelines of drug discovery and development. At Xaira, we believe that becoming a truly AI-native organization is not a future ambition. It is a present imperative. The way we build our infrastructure, adopt our tools, and lead our technology function will determine how fast we can move and how far we can go.The optimal candidate is energized and enthused to push the frontier of what an enterprise can do with all available and evolving AI tools. We are seeking a VP of Information Technology to serve as the senior-most IT leader and AI evangelist on the team. The optimal candidate is energized and enthused to push the frontier of what an enterprise can do with all available and evolving AI tools.This role will own the full scope of IT: strategy, security, infrastructure, ### Director, Drug Product Development - Apogee Therapeutics Inc - Location: Remote (remote) - Salary: $210K-$235K - Posted: 2026-01-12 - 401(k) match: listed (not source-backed) - Apply: https://job-boards.greenhouse.io/apogeetherapeutics/jobs/5021986007 - Excerpt: Director, Drug Product Development 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, Drug Product Development to develop protein drug product presentations and ### Pharmaceutical Sciences, Operations & Performance Lead (Sr. Director) - Takeda Pharmaceutical Company Limited - Location: Boston, MA (unspecified) - Salary: Not disclosed - Posted: 2026-05-12 - 401(k) match: listed (not source-backed) - Apply: https://takeda.wd3.myworkdayjobs.com/External/job/Boston-MA/Pharmaceutical-Sciences--Strategy---Operations-Lead--Sr-Director-_R0178498 - Excerpt: Pharmaceutical Sciences, Operations & Performance Lead (Sr. Director) Boston, MA posted: Posted 30+ Days Ago ### Pharmaceutical Technician II - Thermo Fisher Scientific - Location: Singapore, Singapore (unspecified) - Salary: Not disclosed - Posted: 2026-06-11 - 401(k) match: listed (not source-backed) - Apply: https://thermofisher.wd5.myworkdayjobs.com/ThermoFisherCareers/job/Singapore-Singapore/Pharmaceutical-Technician-II_R-01340680-1/apply - Excerpt: Pharmaceutical Technician II Singapore, Singapore Embrace the opportunity to become a Pharmaceutical Technician II and play a vital role in sterile pharmaceutical production. Operate advanced equipment, ensure GMP compliance, and contribute to quality manufacturing. If you have hands-on experience in pharma production and a passion for safety and precision, this is your opportunity to make a difference. ### Pharmaceutical Technician II - Thermo Fisher Scientific - Location: Singapore, Singapore (unspecified) - Salary: Not disclosed - Posted: 2026-06-11 - 401(k) match: listed (not source-backed) - Apply: https://thermofisher.wd5.myworkdayjobs.com/ThermoFisherCareers/job/Singapore-Singapore/Pharmaceutical-Technician-II_R-01354187/apply - Excerpt: Pharmaceutical Technician II Singapore, Singapore Embrace the role of a Pharmaceutical Technician II and play a vital role in sterile pharmaceutical production. Operate advanced equipment, ensure GMP compliance, and support quality manufacturing processes. If you have hands-on experience in pharmaceutical manufacturing and a passion for safety and precision, this is your opportunity to make an impact. ### Pharmaceutical Technician II - Thermo Fisher Scientific - Location: Singapore, Singapore (unspecified) - Salary: Not disclosed - Posted: 2026-06-11 - 401(k) match: listed (not source-backed) - Apply: https://thermofisher.wd5.myworkdayjobs.com/ThermoFisherCareers/job/Singapore-Singapore/Pharmaceutical-Technician-II_R-01349946-1/apply - Excerpt: Pharmaceutical Technician II Singapore, Singapore Embrace the role of a Pharmaceutical Technician II and play a vital role in sterile pharmaceutical production. Operate advanced equipment, ensure GMP compliance, and support quality manufacturing processes. Ideal for candidates with 1-5 years' experience in pharma, this role offers hands-on work in a dynamic, safety-focused environment. Grow your career in pharmaceutical manufacturing today! ### Pharmaceutical Technician II - Thermo Fisher Scientific - Location: Singapore, Singapore (unspecified) - Salary: Not disclosed - Posted: 2026-06-11 - 401(k) match: listed (not source-backed) - Apply: https://thermofisher.wd5.myworkdayjobs.com/ThermoFisherCareers/job/Singapore-Singapore/Pharmaceutical-Technician-II_R-01340678/apply - Excerpt: Pharmaceutical Technician II Singapore, Singapore Embrace the role of a Pharmaceutical Technician II and play a vital role in sterile pharmaceutical production. Operate advanced equipment, ensure GMP compliance, and contribute to quality manufacturing. If you have hands-on experience in pharma production and a passion for safety and precision, this is your opportunity to make a difference. ### Principal or Associate Scientist, Analytical Development Japan, Pharmaceutical Sciences - Takeda Pharmaceutical Company Limited - Location: Fujisawa, Japan (unspecified) - Salary: Not disclosed - Posted: 2026-05-12 - 401(k) match: listed (not source-backed) - Apply: https://takeda.wd3.myworkdayjobs.com/External/job/Fujisawa-Japan/Principal-or-Associate-Scientist--Analytical-Development-Japan--Pharmaceutical-Sciences_R0177837-1 - Excerpt: Principal or Associate Scientist, Analytical Development Japan, Pharmaceutical Sciences Fujisawa, Japan posted: Posted 30+ Days Ago ### Associate Director or Principal Scientist, Facility Operations, Pharmaceutical Sciences - Takeda Pharmaceutical Company Limited - Location: Fujisawa, Japan (unspecified) - Salary: Not disclosed - Posted: 2026-05-12 - 401(k) match: listed (not source-backed) - Apply: https://takeda.wd3.myworkdayjobs.com/External/job/Fujisawa-Japan/Associate-Director-or-Principal-Scientist--Facility-Operations--Pharmaceutical-Sciences_R0178525-1 - Excerpt: Associate Director or Principal Scientist, Facility Operations, Pharmaceutical Sciences Fujisawa, Japan posted: Posted 30+ Days Ago ### Principal or Associate Scientist, Analytical Development Japan (Late Stage), Pharmaceutical Sciences - Takeda Pharmaceutical Company Limited - Location: Fujisawa, Japan (unspecified) - Salary: Not disclosed - Posted: 2026-06-12 - 401(k) match: listed (not source-backed) - Apply: https://takeda.wd3.myworkdayjobs.com/External/job/Fujisawa-Japan/Principal-or-Associate-Scientist--Analytical-Development-Japan--Late-Stage---Pharmaceutical-Sciences_R0181177-1 - Excerpt: Principal or Associate Scientist, Analytical Development Japan (Late Stage), Pharmaceutical Sciences Fujisawa, Japan posted: Posted Today ### Senior Director, Strategic Sourcing and Contracts - Xaira - Location: South San Francisco, California, United States (unspecified) - Salary: $215K-$280K - Posted: 2026-04-24 - Apply: https://job-boards.greenhouse.io/xairatherapeutics/jobs/5036679007 - Excerpt: Senior Director, Strategic Sourcing and Contracts South San Francisco, California, United States About Xaira Therapeutics Xaira is an innovative biotech startup focused on leveraging AI to transform drug discovery and development. The company is leading the development of generative AI models to design protein and antibody therapeutics, enabling the creation of medicines against historically hard-to-drug molecular targets. It is also developing foundation models for biology and disease to enable better target elucidation and patient stratification. Collectively, these technologies aim to continually enable the identification of novel therapies and to improve success in drug development. Xaira is headquartered in the San Francisco Bay Area, Seattle, and London. Role Overview The Senior Director, Supply Chain and Strategic Sourcing will lead and integrate Xaira's supply chain, procurement, and contract governance functions, ensuring reliable access to the external partners, platforms, and services that support Research, Biomedical AI, Platform Engineering, and Corporate teams. This role is responsible for establishing disciplined sourcing strategy, strengthening vendor management, building contract governance infrastructure, and ensuring operational continuity across critical suppliers and service providers. The individual will provide strategic oversight while elevating two existing functions, procurement and contracts, into a cohesive, scalable supply chain capability. Operating at the intersection of research, technology infrastructure, and external partnerships, This role is responsible for bringing strategic focus to how Xaira engages its external partners, ensuring that sourcing, vendor, and contract decisions serve the company's mission, growth, and long-term goals Key Responsibilities Supply Chain Leadership - Develop and lead overall supply chain strategy - ### Pharmaceutical Sales Specialist Immunology - Alsace - Regeneron Pharmaceuticals - Location: Remote - France (remote) - Salary: Not disclosed - Posted: 2026-06-08 - 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://regeneron.wd1.myworkdayjobs.com/Careers/job/Remote---France/Pharmaceutical-Sales-Specialist-Immunology---Alsace_R47580 - Excerpt: Pharmaceutical Sales Specialist Immunology - Alsace Remote - France posted: Posted 4 Days Ago ### Associate Director, Computer Systems Assurance (Quality) - Nurix Therapeutics Inc - Location: Brisbane, CA (unspecified) - Salary: $190K-$216K - Posted: 2026-05-05 - 401(k) match: listed (not source-backed) - Apply: https://job-boards.greenhouse.io/nurix/jobs/8535914002 - Excerpt: Associate Director, Computer Systems Assurance (Quality) Brisbane, CA 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. Position The Senior Manager / Associate Director, Computer Systems Assurance (CSA) is an important technical and operational leader within the Nurix Quality Systems organization, responsible for owning and advancing Nurix's computer systems assurance program. As a virtual drug developer, Nurix operates through a lean internal infrastructure and relies on a curated ecosystem of Software-as-a-Service (SaaS) and cloud-hosted platforms to support GxP-regulated activities across clinical development, quality operations, manufacturing oversight, and regulatory submissions. This role will serve as the primary subject matter expert and program owner for all CSA and computerized system validation (CSV) activities at Nurix. Reporting to the Vice President / Senior Director, Quality Systems, this individual will establish and maintain Nurix's risk-based CSA framework aligned with current regulatory expectations, including the FDA's 2022 guidance on computer software assurance, GAMP 5 (2nd edition), and applicable 21 CFR Part 11 and Annex ### Senior Director, Channel Strategy and Patient Support - Apogee Therapeutics Inc - Location: Remote (remote) - Salary: $280K-$305K - Posted: 2026-05-13 - 401(k) match: listed (not source-backed) - Apply: https://job-boards.greenhouse.io/apogeetherapeutics/jobs/5137040007 - Excerpt: Senior Director, Channel Strategy and Patient Support 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 Channel Strategy - Conduct market research on distribution strategies and trends within ### 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 ### Vice President, Clinical Development - Septerna Inc - Location: South San Francisco, California, United States (unspecified) - Salary: $380K-$420K - Posted: 2026-04-12 - Apply: https://job-boards.greenhouse.io/septerna/jobs/5185908008 - Excerpt: Vice President, Clinical Development South San Francisco, California, United States Septerna is a biotechnology company based in South San Francisco, CA on a mission to develop life-changing medicines for patients with the vision to become the industry-leading G protein-coupled receptor (GPCR)-focused drug discovery company. The company's Native Complex Platform™ recapitulates GPCRs with their native structure, function, and dynamics outside of the cellular context. This approach enables novel access to modern structural and screening technologies used in industrial-scale drug discovery for the entire class of GPCRs. Septerna has an emerging pipeline of GPCR-targeted small molecule programs with potential for growth to target many GPCRs that have been undruggable and unexploited to date. We are excited to expand our multidisciplinary team of individuals focused on creating revolutionary medicines to address the unmet needs of patients. At Septerna we strive to embrace diversity of thought, expertise, and background through collaboration. To join our ambitious team, be prepared to bring your real self to work every day; grow and learn from a talented team of drug hunters, scientists, and business professionals; and contribute your passion, creativity, and energy to accomplish our mission. We share a fearless pursuit of ground-breaking innovations and cultivate an environment where our employees succeed by learning from each other and working as a team. We are committed to the development of meaningful therapeutics for patients with indications of high unmet need. This is a tremendous opportunity to work with talented individuals on the frontlines of therapeutic discovery and development. You ### 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 ### Lead Director, Pharmaceutical Contracting - CVS Health Corporation - Location: Work at Home, Illinois, United States (unspecified) - Salary: Not disclosed - Posted: 2026-06-10 - Non-birth-parent leave: 4 weeks (not source-backed) - 401(k) match: listed (not source-backed) - Apply: https://cvshealth.wd1.myworkdayjobs.com/CVS_Health_Careers/job/IL---Downers-Grove/Lead-Director--Pharmaceutical-Contracting_R0933942/apply - Excerpt: Lead Director, Pharmaceutical Contracting Work at Home, Illinois, United States Join us as Lead Director, Pharmaceutical Contracting and drive high-impact negotiations with major pharmaceutical manufacturers. Shape strategy, foster partnerships, and lead rebate initiatives in a dynamic healthcare environment. If you excel in complex contract negotiations and thrive in leadership roles, this is your opportunity to make a significant impact. ### Technician, Pharmaceutical - AbbVie Inc. - Location: Sligo, SO, Ireland (unspecified) - Salary: Not disclosed - Posted: 2026-06-12 - 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/3743990013577016-technician-pharmaceutical - Excerpt: Technician, Pharmaceutical Sligo, SO, Ireland 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: We are recruiting a Pharmaceutical Technician to join our team on site in Manorhamilton Road, Sligo on a 12 month fixed-term contract. This role is rotational shift work. In your role as Pharmaceutical Technician you will be responsible for producing drug product materials as per organizational needs in line with all relevant compliance requirements. This person will operate as a team member in a pharmaceutical processing facility in line with all regulatory and organizational requirements. A snapshot of your key responsibilities as a Pharmaceutical Technician would be: Pharmaceutical processing activities in our manufacturing building and support locations. Team co-ordination to maximise the effectiveness of the team members. Documentation of all activities in line with cGMP requirements. Cross training within the team and training of new team members. Participation in continuous improvement programs to implement improvements in the quality, safety, environmental and production systems. Execution of commissioning and validation protocols on an ongoing basis. Maintaining the overall cGMP of the pharmaceutical processing areas. Adheres ### Responsable Assurance Qualité - Pharmacien(ne) Délégué(e) - Eurofins Scientific - Location: Idron, Nouvelle-Aquitaine, France (unspecified) - Salary: Not disclosed - Posted: 2026-06-10 - 401(k) match: listed (not source-backed) - Apply: https://jobs.smartrecruiters.com/Eurofins/744000099507554-responsable-assurance-qualite-pharmacien-ne-delegue-e- - Excerpt: Responsable Assurance Qualité - Pharmacien(ne) Délégué(e) Idron, Nouvelle-Aquitaine, France Description de l'entreprise: Au sein de la branche biopharmaceutique du groupe, la division Eurofins CDMO, acteur majeur dans la sous-traitance pharmaceutique en Europe, compte 7 business units en France et en Belgique. Notre objectif est d'accompagner nos clients depuis les premières étapes de développement de leur substance médicamenteuse jusqu'à la production de lots cliniques ou commerciaux. Nous développons, formulons et fabriquons des produits biologiques et chimiques - stériles et non stériles -, nous assurons également le conditionnement et la distribution clinique GMP. Nous proposons par ailleurs des programmes complets de développement et de validation de méthodes analytiques, ainsi que l'évaluation de la stabilité des substances actives et des produits finis. Description du poste: Notre futur(e) Pharmacien(ne) Délégué(e) - Responsable Assurance Qualité sera rattaché(e) à notre société EUROFINS AMATSIGROUP SAS , basée à Idron. Ce site d'une trentaine de collaborateurs est spécialisé dans la formulation et le remplissage aseptique de lots cliniques et précliniques, ainsi que de lots commerciaux. Ce site fournit également une large gamme de produits pharmaceutiques (flacons, liquides ou lyophilisés, seringues). Enfin, il est spécialisé dans les médicaments innovants, tel que les immunoglobulines, cytotoxiques, nanoparticules, anticancéreux, sérums, ou encore les vaccins. Directement rattaché au Responsable du site, notre futur Responsable Assurance Qualité aura principalement la charge de définir et coordonner la mise en œuvre de la politique d'Assurance Qualité (méthodes, organisation, process, audit), et manager l'équipe AQ (5 personnes) au quotidien. Il/elle reportera fonctionnellement au Pharmacien Responsable de l'entité, ### Alternant.e Technicien Contrôle Qualité (F/H/X) - AbbVie Inc. - Location: Martillac, Nouvelle-Aquitaine, France (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/3743990013529565-alternant-e-technicien-controle-qualite-f-h-x- - Excerpt: Alternant.e Technicien Contrôle Qualité (F/H/X) Martillac, Nouvelle-Aquitaine, France 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: Au sein des équipes de contrôle qualité, et sous la responsabilité d'un superviseur analytique contrôle qualité, vous intégrerez les laboratoires de Martillac selon les standards GMP (BPF). Vous interviendrez sur différentes analyses physico-chimiques et/ou biologiques en support des activités de production du site ou du réseau AbbVie, au sein d'un environnement à forte exigence qualité. 1. Réalisation des analyses physico-chimiques ou biologiques et des vérifications de méthodes Réaliser et vérifier les analyses suivantes (liste non exhaustive) : HPLC, ELISA, Compendiales, CE-SDS, cIEF, densité optique Transcrire des résultats analytiques sur la documentation ou le logiciel adapté. 2. Participation à la bonne gestion du laboratoire et des équipements Veiller au suivi et au bon fonctionnement des équipements nécessaires aux activités. Veiller à ce que les analyses soient effectuées sur des équipements qualifiés et calibrés. Participer au nettoyage et au bon maintien du laboratoire. 3. Suivi, documentation et qualité Traçabilité rigoureuse sur les documents analytiques et systèmes qualité. Ouvrir les évènements de non-conformité ### Senior Research Associate/Senior Scientist, Pharmaceutical Development - Ionis Pharmaceuticals - Location: 2280 Faraday-USA; 2830 Whiptail (unspecified) - Salary: Not disclosed - Posted: 2026-06-05 - 401(k) match: listed (not source-backed) - Apply: https://recruiting.ultipro.com/isi1000isis/JobBoard/14a66400-68fa-4847-8593-af776328cfd2/OpportunityDetail?opportunityId=ad2d13f5-0499-4011-b6d6-e4be422f0485 - Excerpt: Senior Research Associate/Senior Scientist, Pharmaceutical Development 2280 Faraday-USA; 2830 Whiptail Ionis Pharmaceuticals seeks an experienced pharmaceutical development scientist to support laboratory experiments, review development data, and author and standardize technical reports for injectable drug products in development. The ideal candidate will be an independent self-starter with experience in analytical, formulation and process support for early and late-stage development of oligonucleotide-based drug products including conjugated with small molecules, peptides and proteins. The successful candidate will be able to perform the following responsibilities with a high degree of independence and attention to detail. ### Senior Associate Scientist (Contract), Drug Product Analytics - Vaxcyte Inc - Location: San Carlos, California, United States (unspecified) - Salary: $56-$62/hr - Posted: 2026-03-23 - 401(k) match: listed (not source-backed) - Apply: https://boards.greenhouse.io/vaxcyte/jobs/5154315008?gh_jid=5154315008 - Excerpt: Senior Associate Scientist (Contract), Drug Product Analytics San Carlos, California, United States Join our Mission to Protect Humankind! Vaxcyte is a clinical-stage vaccine innovation company engineering high-fidelity vaccines to protect humankind from the consequences of bacterial diseases, which have serious and costly health consequences when left unchecked. Working to eradicate or treat bacterial infections such as invasive pneumococcal disease, Group A Strep, and Shigella is just the beginning. Our path to success is clear and well-defined, and Vaxcyte is set up to go the distance. WHAT we do is every bit as important as HOW we do it! Our work together is guided by four enduring core values: *RETHINK CONVENTION: We bring creative and intellectual diversity to every facet of the work we do in order to innovate and re-innovate the way vaccines are delivered. *AIM HIGH: We embody our collectively audacious goal to courageously make the most complex biologics ever attempted to protect humankind. *LEAD WITH HEART: Everyone leads at Vaxcyte with a kindness-first, inclusive approach to collaboration and vigorous debate that advances our business objectives. *MODEL EXCELLENCE: The magnitude of our challenge requires our shared commitment to demonstrating integrity, accountability, equality and clarity across communications and decision making. Summary: Vaxcyte is looking for an energetic and talented individual to join our Drug Product Development team. The candidate must have knowledge of and practical experience in analyzing and characterizing biomolecules (proteins, polysaccharide conjugates, vaccines) using a variety of methods, especially immunoassays and multiplexed immunoassay formats. Experience in analyzing vaccine ### Senior Legal Counsel - Pharmaceutical Contracting - CVS Health Corporation - Location: One CVS Drive, Woonsocket, Rhode Island,United States (unspecified) - Salary: Not disclosed - Posted: 2026-05-26 - Non-birth-parent leave: 4 weeks (not source-backed) - 401(k) match: listed (not source-backed) - Apply: https://cvshealth.wd1.myworkdayjobs.com/CVS_Health_Careers/job/RI---Woonsocket/Senior-Legal-Counsel---Pharmaceutical-Contracting_R0901888/apply - Excerpt: Senior Legal Counsel - Pharmaceutical Contracting One CVS Drive, Woonsocket, Rhode Island,United States Join our team as a Senior Legal Counsel - Pharmaceutical Contracting and play a pivotal role in shaping healthcare solutions. Advise on complex retail trade and pharmaceutical agreements, ensure regulatory compliance, and collaborate with cross-functional teams. Make a meaningful impact in a dynamic environment dedicated to innovation and patient care. ### Pharmaceutical Assistant - Pfizer - Location: United States - Kansas - McPherson (unspecified) - Salary: Not disclosed - Posted: 2026-06-12 - 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://pfizer.wd1.myworkdayjobs.com/PfizerCareers/job/United-States---Kansas---McPherson/Pharmaceutical-Assistant_4954329-1 - Excerpt: Pharmaceutical Assistant United States - Kansas - McPherson posted: Posted Today ### Staff Scientist, Pharmaceutical Development - Septerna Inc - Location: South San Francisco, California, United States (unspecified) - Salary: $160K-$180K - Posted: 2026-05-13 - Apply: https://job-boards.greenhouse.io/septerna/jobs/5218595008 - Excerpt: Staff Scientist, Pharmaceutical Development South San Francisco, California, United States Septerna is a biotechnology company based in South San Francisco, CA on a mission to develop life-changing medicines for patients with the vision to become the industry-leading G protein-coupled receptor (GPCR)-focused drug discovery company. The company's Native Complex Platform™ recapitulates GPCRs with their native structure, function, and dynamics outside of the cellular context. This approach enables novel access to modern structural and screening technologies used in industrial-scale drug discovery for the entire class of GPCRs. Septerna has an emerging pipeline of GPCR-targeted small molecule programs with potential for growth to target many GPCRs that have been undruggable and unexploited to date. We are excited to expand our multidisciplinary team of individuals focused on creating revolutionary medicines to address the unmet needs of patients. At Septerna we strive to embrace diversity of thought, expertise, and background through collaboration. To join our ambitious team, be prepared to bring your real self to work every day; grow and learn from a talented team of drug hunters, scientists, and business professionals; and contribute your passion, creativity, and energy to accomplish our mission. We share a fearless pursuit of ground-breaking innovations and cultivate an environment where our employees succeed by learning from each other and working as a team. We are committed to the development of meaningful therapeutics for patients with indications of high unmet need. This is a tremendous opportunity to work with talented individuals on the frontlines of therapeutic discovery and development. You ### Pharmaceutical Attendant - Pfizer - Location: United States - Kansas - McPherson (unspecified) - Salary: Not disclosed - Posted: 2026-06-11 - 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://pfizer.wd1.myworkdayjobs.com/PfizerCareers/job/United-States---Kansas---McPherson/Pharmaceutical-Attendant_4956657-1 - Excerpt: Pharmaceutical Attendant United States - Kansas - McPherson posted: Posted Yesterday ### Senior Scientist, Analytical Development and Quality Control (Drug Product) - Nurix Therapeutics Inc - Location: Brisbane, CA (unspecified) - Salary: Not disclosed - Posted: 2026-05-13 - 401(k) match: listed (not source-backed) - Apply: https://job-boards.greenhouse.io/nurix/jobs/8546901002 - Excerpt: Senior Scientist, Analytical Development and Quality Control (Drug Product) 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. Position Nurix Therapeutics seeks an experienced Senior Scientist to join the Analytical Development and Quality Control group. The Senior Scientist will be responsible for drug product (DP) analytical development, including method development, oversight of method validation at CDMOs, and lifecycle management in support of Nurix's oncology and inflammation & immunology (I&I) programs. This position provides technical oversight of analytical method development, validation, and testing conducted at external CDMO/CRO partners. The Senior Scientist will author analytical development reports and IND/IMPD/NDA sections and support late-phase tech transfer and validation activities. This role will also contribute to analytical development for new drug products and dosage forms. The Senior Scientist will work closely in cross-functional teams to ensure alignment and integration of analytical and QC strategies across development stages. The ideal candidate will have expertise in chromatographic and dissolution method development, stability ### Pharmaceutical Process Expert (PPE) - Ipsen - Location: Wrexham (unspecified) - Salary: Not disclosed - Posted: 2026-05-12 - 401(k) match: listed (not source-backed) - Apply: https://ipsen.wd103.myworkdayjobs.com/Ipsen_Careers/job/Wrexham/Pharmaceutical-Process-Expert--PPE-_R-21479 - Excerpt: Pharmaceutical Process Expert (PPE) Wrexham posted: Posted 30+ Days Ago ### Ausbildung 2027: Pharmakant:in, Standort Mannheim - Roche Holding AG - Location: Mannheim, Baden-Wurttemberg, Germany (unspecified) - Salary: Not disclosed - Posted: 2026-05-31 - Apply: https://roche.wd3.myworkdayjobs.com/roche-ext/job/Mannheim/Ausbildung-2027--Pharmakant-in--Standort-Mannheim_202605-111901/apply - Excerpt: Ausbildung 2027: Pharmakant:in, Standort Mannheim Mannheim, Baden-Wurttemberg, Germany This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Together, more than 100'000 employees across the globe are dedicat... ### Global Product Steward - Genetic Medicines - Eli Lilly and Company - Location: US, Indianapolis IN (unspecified) - Salary: Not disclosed - Posted: 2026-05-13 - 401(k) match: listed (not source-backed) - Apply: https://lilly.wd5.myworkdayjobs.com/LLY/job/US-Indianapolis-IN/Advisor-Parenteral-Global-Product-Steward---Genetic-Medicines_R-105669 - Excerpt: Global Product Steward - Genetic Medicines US, Indianapolis IN posted: Posted 30 Days Ago ### Account Manager - Pharmaceutical - Amcor - Location: 16 Locations (unspecified) - Salary: Not disclosed - Posted: 2026-05-12 - 401(k) match: listed (not source-backed) - Apply: https://amcor.wd5.myworkdayjobs.com/Amcor_External_Career_Site/job/AF-Deerfield-IL-Corporate/Account-Manager---Pharmaceutical_REQ_89081 - Excerpt: Account Manager - Pharmaceutical 16 Locations posted: Posted 30+ Days Ago ### Medical Director Pharmacovigilance - Apogee Therapeutics Inc - Location: Remote (remote) - Salary: $285K-$330K - Posted: 2026-06-01 - 401(k) match: listed (not source-backed) - Apply: https://job-boards.greenhouse.io/apogeetherapeutics/jobs/5151650007 - Excerpt: Medical Director Pharmacovigilance 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 Medical Director, Pharmacovigilance to join the Apogee Clinical Development team. In this ### M23 Pharmaceutical Attendant - Pfizer - Location: United States - Kansas - McPherson (unspecified) - Salary: Not disclosed - Posted: 2026-06-11 - 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://pfizer.wd1.myworkdayjobs.com/PfizerCareers/job/United-States---Kansas---McPherson/M23-Pharmaceutical-Attendant_4956770-2 - Excerpt: M23 Pharmaceutical Attendant United States - Kansas - McPherson posted: Posted Yesterday ### Associate Director, Global Drug Substance Commercialization, Critical Raw Materials - Vaxcyte Inc - Location: San Carlos, California, United States (unspecified) - Salary: $174K-$203K - Posted: 2025-11-07 - 401(k) match: listed (not source-backed) - Apply: https://boards.greenhouse.io/vaxcyte/jobs/4974572008?gh_jid=4974572008 - Excerpt: Associate Director, Global Drug Substance Commercialization, Critical Raw Materials San Carlos, California, United States Join our Mission to Protect Humankind! Vaxcyte is a clinical-stage vaccine innovation company engineering high-fidelity vaccines to protect humankind from the consequences of bacterial diseases, which have serious and costly health consequences when left unchecked. Working to eradicate or treat bacterial infections such as invasive pneumococcal disease, Group A Strep, and Shigella is just the beginning. Our path to success is clear and well-defined, and Vaxcyte is set up to go the distance. WHAT we do is every bit as important as HOW we do it! Our work together is guided by four enduring core values: *RETHINK CONVENTION: We bring creative and intellectual diversity to every facet of the work we do in order to innovate and re-innovate the way vaccines are delivered. *AIM HIGH: We embody our collectively audacious goal to courageously make the most complex biologics ever attempted to protect humankind. *LEAD WITH HEART: Everyone leads at Vaxcyte with a kindness-first, inclusive approach to collaboration and vigorous debate that advances our business objectives. *MODEL EXCELLENCE: The magnitude of our challenge requires our shared commitment to demonstrating integrity, accountability, equality and clarity across communications and decision making. Summary: The Associate Director for Drug Substance (DS) Commercialization has the accountability for launch readiness and commercial supply of associated raw materials for production of eCRM and associated components for glycoconjugate vaccines. This role focuses on technical launch planning and execution by bringing best-practices and coordinating cross-functional efforts ### Senior Analyst - Pharmaceutical Markets - IQVIA - Location: Madrid, Spain (unspecified) - Salary: Not disclosed - Posted: 2026-05-12 - 401(k) match: listed (not source-backed) - Apply: https://iqvia.wd1.myworkdayjobs.com/IQVIA/job/Madrid-Spain/Senior-Analyst---Pharmaceutical-Markets_R1537065 - Excerpt: Senior Analyst - Pharmaceutical Markets Madrid, Spain posted: Posted 30+ Days Ago ### Scientist II, Animal Model Development - Tonix Pharmaceuticals Holding Corp - Location: Frederick, MD (unspecified) - Salary: $70K-$120K - Posted: 2026-03-05 - 401(k) match: listed (not source-backed) - Apply: https://job-boards.greenhouse.io/tonixpharmaceuticals/jobs/4170744009 - Excerpt: Scientist II, Animal Model Development Frederick, MD Tonix Pharmaceuticals* is a fully integrated, commercial-stage biotechnology company focused on central nervous system (CNS) and immunology treatments in areas of high unmet medical need. TONMYA® (cyclobenzaprine HCl sublingual tablets 2.8 mg) is the first new treatment for fibromyalgia in adults in more than 15 years. Tonix's CNS commercial infrastructure supports its marketed products, including its acute migraine products, Zembrace® Symtouch® (sumatriptan injection 3 mg) and Tosymra® (sumatriptan nasal spray 10 mg). Tonix is investigating TONMYA® in Phase 2 clinical trials to evaluate its potential in major depressive disorder and acute stress disorder/acute stress reaction. Tonix is also advancing a pipeline of immunology programs, including TNX-4800, a Phase 2 ready long-acting human anti- Borrelia OspA monoclonal antibody (mAb) for the prevention of Lyme disease in the U.S., and TNX-1500, a Phase 2 ready third-generation CD40 ligand inhibitor for the prevention of kidney transplant rejection. In addition, the Company is progressing TNX-2900 (intranasal potentiated oxytocin), which is Phase 2 ready for the treatment of Prader-Willi syndrome, a rare disease. To learn more, visit www.tonixpharma.com and follow the Company on LinkedIn and X . *Tonix's product development candidates are investigational new drugs or biologics; their efficacy and safety have not been established and have not been approved for any indication. Zembrace SymTouch and Tosymra are registered trademarks of Tonix Medicines. TONMYA is a registered trademark of Tonix Pharma Limited. All other marks are property of their respective owners. Position Overview Tonix Research and Development Center ### Pharmaceutical Cleaner - AstraZeneca - Location: Australia – New South Wales (unspecified) - Salary: Not disclosed - Posted: 2026-06-03 - 401(k) match: listed (not source-backed) - Apply: https://astrazeneca.wd3.myworkdayjobs.com/Careers/job/Australia--New-South-Wales/Pharmaceutical-Cleaner_R-251307 - Excerpt: Pharmaceutical Cleaner Australia – New South Wales posted: Posted 9 Days Ago ### Pharmaceutical representative - The Procter & Gamble Company - Location: BUDAPEST GO - LIBERTY (unspecified) - Salary: Not disclosed - Posted: 2026-05-19 - Parental leave: 8 weeks (not source-backed) - Non-birth-parent leave: 8 weeks (not source-backed) - 401(k) match: listed (not source-backed) - Apply: https://pg.wd5.myworkdayjobs.com/1000/job/BUDAPEST-GO---LIBERTY/Pharmaceutical-representative_R000151450 - Excerpt: Pharmaceutical representative BUDAPEST GO - LIBERTY posted: Posted 24 Days Ago ### Pharmareferent Cardiometabolic Health (m/w/d) Gebiet: Trier, Morbach, Idar-Oberstein, Kaiserslautern, Zweibrücken, Pirmasens, Landau, Wörth am Rhein - Eli Lilly and Company - Location: Germany, Bad Homburg (unspecified) - Salary: Not disclosed - Posted: 2026-05-12 - 401(k) match: listed (not source-backed) - Apply: https://lilly.wd5.myworkdayjobs.com/LLY/job/Germany-Bad-Homburg/Pharmareferent-Cardiometabolic-Health--m-w-d--Gebiet--Trier--Morbach--Idar-Oberstein--Kaiserslautern--Zweibrcken--Pirmasens--Landau--Wrth-am-Rhein_R-99044-5 - Excerpt: Pharmareferent Cardiometabolic Health (m/w/d) Gebiet: Trier, Morbach, Idar-Oberstein, Kaiserslautern, Zweibrücken, Pirmasens, Landau, Wörth am Rhein Germany, Bad Homburg posted: Posted 30+ Days Ago ### Vice President of Marketing - Nurix Therapeutics Inc - Location: Brisbane, CA (unspecified) - Salary: Not disclosed - Posted: 2026-06-04 - 401(k) match: listed (not source-backed) - Apply: https://job-boards.greenhouse.io/nurix/jobs/8579556002 - Excerpt: Vice President of Marketing 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. Position We are seeking a dynamic and experienced Vice President of Marketing with extensive experience launching new hematology / oncology products and incorporating commercial strategy into early development programs. The core objective is to build, lead and execute all aspects of Nurix Therapeutics marketing efforts. This individual will be responsible for developing all marketing strategies and tactical readiness for the commercialization of Nurix Therapeutics assets. In addition, this role will be accountable for driving commercial strategy in support of lifecycle management and our pipeline. Accountable for developing and executing all Global and US Marketing strategies that align with the overall company strategic imperatives. Ensure strategic alignment with cross-functional commercial partners in commercial insights and analytics, market access, and sales in order to produce high quality marketing efforts that achieve company performance objectives - Build and implement the marketing plan including, but not limited ### Graphic Designer – Pharmaceutical Marketing - Amgen - Location: India - Hyderabad (unspecified) - Salary: Not disclosed - Posted: 2026-05-12 - Parental leave: 6 weeks (not source-backed) - Non-birth-parent leave: 6 weeks (not source-backed) - 401(k) match: listed (not source-backed) - Apply: https://amgen.wd1.myworkdayjobs.com/Careers/job/India---Hyderabad/Graphic-Designer---Pharmaceutical-Marketing_R-240424 - Excerpt: Graphic Designer – Pharmaceutical Marketing India - Hyderabad posted: Posted 30+ Days Ago ### Senior Principal Research Scientist, Computational Drug Discovery HitGen/LeadGen Team Lead - AbbVie Inc. - Location: North Chicago, IL, United States (unspecified) - Salary: Not disclosed - Posted: 2026-06-12 - 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/3743990013568566-senior-principal-research-scientist-computational-drug-discovery-hitgen-leadgen-team-lead - Excerpt: Senior Principal Research Scientist, Computational Drug Discovery HitGen/LeadGen Team Lead 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 This position brings an opportunity to make innovative contributions that will define how AbbVie leverages AI-enabled drug discovery across our small molecule portfolio. Reports to Head of Computational Drug Discovery (CDD) and will lead the computational HitGen/LeadGen (HGLG) team. Will implement and enable close collaboration between members of the HGLG team and partners in the Target Enabling Technologies (TET) and Global Medicinal Chemistry (GMEC) teams. Must possess a strong expertise in modern medicinal chemistry, including a deep understanding of modern computational and experimental strategies, and property-based drug design. The ideal candidate will have a strong and established background from having worked on a broad range of diverse early-stage campaigns, and an established external footprint and network. Past experience will have included mentorship of early/mid-career scientists in matrixed and/or direct reporting relationships. Responsibilities Consult with project team to establish desirable project-relevant hit/lead criteria, and assigning an HGLG member to the project team that ### Pharmaceutical CIP/COP Technical Coordinator - Ecolab - Location: 3 Locations (unspecified) - Salary: Not disclosed - Posted: 2026-05-19 - Parental leave: 6 weeks (not source-backed) - Non-birth-parent leave: 6 weeks (not source-backed) - 401(k) match: listed (not source-backed) - Apply: https://ecolab.wd1.myworkdayjobs.com/Ecolab_External/job/DEU---Nordrhein-Westfalen---Monheim-am-Rhein/Pharmaceutical-CIP-COP-Technical-Coordinator_R00291546 - Excerpt: Pharmaceutical CIP/COP Technical Coordinator 3 Locations posted: Posted 24 Days Ago ### Senior Scientist II - Biologics Drug Product Development - AbbVie Inc. - Location: North Chicago, IL, United States (unspecified) - Salary: Not disclosed - Posted: 2026-06-12 - 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/3743990013581601-senior-scientist-ii-biologics-drug-product-development - Excerpt: Senior Scientist II - 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: 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, located in North Chicago, IL. We are seeking an accomplished scientist with a proven track record in biologics drug product formulation development, predictive stability, in-use, and quality risk management (QRM) . 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: Lead matrix drug product teams for one or more internal and external projects and represent Bio ### Pharmaceutical Strategic Account Manager - Becton Dickinson - Location: 2 Locations (unspecified) - Salary: Not disclosed - Posted: 2026-06-08 - 401(k) match: listed (not source-backed) - Apply: https://bdx.wd1.myworkdayjobs.com/EXTERNAL_CAREER_SITE_USA/job/USA---Massachusetts---Boston/Pharmaceutical-Strategic-Account-Manager_R-547506-1 - Excerpt: Pharmaceutical Strategic Account Manager 2 Locations posted: Posted 4 Days Ago ### Vice President, Pharmaceutical Development - Kymera Therapeutics Inc - Location: Watertown, MA (unspecified) - Salary: $315K-$395K - Posted: 2026-05-26 - 401(k) match: listed (not source-backed) - Apply: https://www.kymeratx.com/careers-culture/working-at-kymera/?gh_jid=7748334003#open-positions - Excerpt: Vice President, Pharmaceutical Development Watertown, MA Who we are: Kymera is a clinical-stage biotechnology company pioneering the field of targeted protein degradation (TPD) to develop medicines that address critical health problems and have the potential to dramatically improve patients' lives. Kymera is deploying TPD to address disease targets and pathways inaccessible with conventional therapeutics. Having advanced the first degrader into the clinic for immunological diseases, Kymera is focused on building an industry-leading pipeline of oral small molecule degraders to provide a new generation of convenient, highly effective therapies for patients with these conditions. Founded in 2016, Kymera has been recognized as one of Boston's top workplaces for the past several years. For more information about our science, pipeline and people, please visit www.kymeratx.com or follow us on X (formerly Twitter) or LinkedIn . How we work: - PIONEER : We are courageous, resilient and rigorous in our mission to improve patients' lives through our revolutionary degrader medicines. - COLLABORATE : We value trust + transparency from everyone. Our goals are shared, our decisions data-driven and our camaraderie genuine. - BELONG : We recognize our differences, inviting curiosity and inclusivity, so that our people are valued, seen, and heard. How you'll make an impact: - Define and lead the company's pharmaceutical development strategy across the portfolio, ensuring alignment with corporate priorities and development timelines - Provide strategic leadership for preformulation, biopharmaceutics, and formulation development activities supporting discovery, preclinical, and clinical-stage programs - Champion innovation in formulation sciences and enabling technologies to ### Pharmaceutical Production Lead - All Shifts - Medline Inc. - Location: Waukegan, Illinois (unspecified) - Salary: Not disclosed - Posted: 2026-05-14 - 401(k) match: listed (not source-backed) - Apply: https://medline.wd5.myworkdayjobs.com/Medline/job/Waukegan-Illinois/Pharmaceutical-Production-Lead---All-Shifts_R2605412 - Excerpt: Pharmaceutical Production Lead - All Shifts Waukegan, Illinois posted: Posted 29 Days Ago ### Director, Global Product Leader - Crinetics Pharmaceuticals INC - Location: Remote (remote) - Salary: $187K-$233K - Posted: 2026-05-23 - 401(k) match: listed (not source-backed) - Apply: https://crinetics.wd12.myworkdayjobs.com/CrineticsCareers/job/Remote/Director--Global-Product-Leader_JR000630 - Excerpt: Director, Global Product Leader Remote Crinetics is a pharmaceutical company based in San Diego, California, developing much-needed therapies for people with endocrine diseases and endocrine-related tumors. We were founded by a dedicated team of scientists with the simple belief that better therapies developed from rigorous innovation can lead to better lives. Our work continues to make a real difference in the lives of patients. We have a prolific discovery engine and a robust preclinical and clinical development pipeline. We are driven by science with a patient-centric and team-oriented culture. Crinetics is known for its inclusive workplace culture. We are also a dog-friendly workplace. This is an exciting time to join Crinetics as we shape our organization into the world's premier fully-integrated endocrine company from discovery to patients. Join our team as we transform the lives of others. Position Summary: This position will lead several early or one late-stage development programs and contribute to portfolio strategy for other programs within a growing preclinical and clinical stage pipeline covering endocrinology and endocrine related tumors. The Director, Global Product Leader is responsible for the strategic leadership of a Global Product Team, overseeing strategic planning, decision making, and resource/budget management and prioritization across development, regulatory, CMC, operations, and business functions to ensure rapid, efficient, and successful progression of the program(s). This role will be responsible for the full lifecycle management of their product and ensure that strategic plans and goals are met. The Global Product Leader will ensure cross-functional and organizational readiness for regulatory ### Pharmaceutical Manufacturer Relations Executive - Humana Inc. - Location: Remote Nationwide (remote) - Salary: Not disclosed - Posted: 2026-06-10 - 401(k) match: listed (not source-backed) - Apply: https://humana.wd5.myworkdayjobs.com/CenterWell_External_Career_Site/job/Remote-Nationwide/Pharmaceutical-Manufacturer-Relations-Executive_R-419074 - Excerpt: Pharmaceutical Manufacturer Relations Executive Remote Nationwide posted: Posted 2 Days Ago ### Lead Director, Pharmaceutical Contracting - CVS Health Corporation - Location: 4 Locations (unspecified) - Salary: Not disclosed - Posted: 2026-06-10 - Parental leave: 4 weeks (not source-backed) - Non-birth-parent leave: 4 weeks (not source-backed) - 401(k) match: listed (not source-backed) - Apply: https://cvshealth.wd1.myworkdayjobs.com/CVS_Health_Careers/job/IL---Downers-Grove/Lead-Director--Pharmaceutical-Contracting_R0933942 - Excerpt: Lead Director, Pharmaceutical Contracting 4 Locations posted: Posted 2 Days Ago ### Vice President, Drug Safety & Pharmacovigilance - Braveheart - Location: San Francisco, CA or Remote or Hybrid (hybrid) - Salary: $330K-$400K - Posted: 2026-05-20 - Apply: https://job-boards.greenhouse.io/braveheartbio/jobs/4254374009 - Excerpt: Vice President, Drug Safety & Pharmacovigilance San Francisco, CA or Remote or Hybrid About us: Braveheart Bio is a Bay Area-based biopharmaceutical company pioneering best-in-class therapies for cardiovascular disease. Our lead program is a next-generation myosin inhibitor, licensed from Hengrui Pharma, being developed to transform the treatment of hypertrophic cardiomyopathy (HCM)-the most common inherited cardiac disease. Currently in Phase 3 clinical development in China for the more common obstructive form of HCM, our candidate has demonstrated a compelling clinical profile that may position it as a best-in-class therapy with meaningful differentiation. With a proven leadership team, a strong financial foundation, and a high-value late-stage asset, Braveheart Bio represents an outstanding opportunity for ambitious, mission-driven professionals to make a tangible impact in a high-profile and rapidly evolving therapeutic area. The role: The Vice President, Drug Safety and Pharmacovigilance will lead and scale the global drug safety and pharmacovigilance function at Braveheart Bio. Reporting into the Chief Medical Officer, the VP is accountable for the safety strategy and integrated benefit-risk profile across the portfolio, with immediate focus on supporting Phase 3 programs and preparing the organization for NDA submission and post-marketing readiness. The VP will partner with an established Senior Director of PV (a direct report) to design the PV operating model, select CRO/PV vendor partners, establish the safety governance framework, and represent Safety in cross-functional and regulatory interactions. This individual will be hands-on while setting strategic direction and has a track record of leveraging external partners to deliver inspection-ready DSPV at ### Pharmaceutical Internship - Pharmaziepraktikum* (f/m/d) - The Procter & Gamble Company - Location: Schwalbach Am Taunus (unspecified) - Salary: Not disclosed - Posted: 2026-05-18 - Parental leave: 8 weeks (not source-backed) - Non-birth-parent leave: 8 weeks (not source-backed) - 401(k) match: listed (not source-backed) - Apply: https://pg.wd5.myworkdayjobs.com/1000/job/Schwalbach-Am-Taunus/Pharmaceutical-Internship----Pharmaziepraktikum---f-m-d-_R000151566 - Excerpt: Pharmaceutical Internship - Pharmaziepraktikum* (f/m/d) Schwalbach Am Taunus posted: Posted 25 Days Ago ### Scientist, Drug Product Analytical - NewLimit - Location: South San Francisco (unspecified) - Salary: $130K-$170K - Posted: 2026-05-01 - 401(k) match: listed (not source-backed) - Apply: https://job-boards.greenhouse.io/newlimit/jobs/5986881004 - Excerpt: Scientist, Drug Product Analytical South San Francisco About NewLimit NewLimit is a biotechnology company working to radically extend human healthspan. We're developing medicines to treat age-related diseases by reprogramming the epigenome, a new therapeutic mechanism to restore regenerative potential in aged and diseased cells. We leverage functional genomics, pooled perturbation screening, and machine learning models to unravel the biology of epigenetic aging and disease using experiments of unprecedented scale. Position We are seeking a skilled and motivated Scientist to join our Delivery Sciences team. In this role, you will focus on building the analytical methods to characterize Lipid Nanoparticles (LNPs) to enable our nucleic acid delivery technologies and support the drug product development. Expertise in developing and implementing analytical methods to characterize RNA drug substances and LNP drug products, with experience managing method qualification, validation, and tech-transfer processes. What you'll do In your role as a Scientist, you will: - Design and execute analytical methods to assess the identity, integrity and purity of RNA drug substances and LNP drug products and LNP-conjugates - Perform deep-dive analysis into mRNA integrity, identity, lipid content and identity analysis to support drug product stability studies - Work closely with the cross-functional teams to support RNA and LNP analysis for drug development from early discovery to GLP/GMP stages. Act as a technical expert for our CRO/CDMO partners on drug substance and drug product analytical method development, validation phases and PK/PD assay developments - Interpret data from various analytical assays, reports and prepare data packages - ### Pharmaceutical Product Operator - All Shifts - Medline Inc. - Location: Waukegan, Illinois (unspecified) - Salary: Not disclosed - Posted: 2026-05-14 - 401(k) match: listed (not source-backed) - Apply: https://medline.wd5.myworkdayjobs.com/Medline/job/Waukegan-Illinois/Pharmaceutical-Product-Operator_R2605410 - Excerpt: Pharmaceutical Product Operator - All Shifts Waukegan, Illinois posted: Posted 29 Days Ago ### Vice President, Head of Alliance Management and Program Management ~ Onsite - Nurix Therapeutics Inc - Location: Brisbane, CA (onsite) - Salary: Not disclosed - Posted: 2026-05-07 - 401(k) match: listed (not source-backed) - Apply: https://job-boards.greenhouse.io/nurix/jobs/8540264002 - Excerpt: Vice President, Head of Alliance Management and Program Management ~ Onsite Brisbane, CA 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. Vice President, Head of Alliance Management and Program Management Nurix Therapeutics is seeking an accomplished and strategic Vice President, Head of Alliance Management and Program Management to lead both our external collaborations with pharmaceutical partners and the internal coordination of our late stage hematology/oncology program. In addition to leading a high-impact alliance, this role will drive internal program management discipline, ensuring organizational awareness of program priorities, clear accountability for key workstreams, aligned roadmaps across functions, and transparent communication of status and risks to senior leadership. The ideal candidate is a dynamic leader who thrives in complexity, bridges science and business, and delivers executional excellence across partnerships and programs. Key Responsibilities - Alliance Leadership and Strategy - Serve as the primary point of contact between Nurix Therapeutics and its pharmaceutical partners, fostering a transparent, collaborative, and goal-oriented relationship. ### Vice President, Drug Safety/Pharmacovigilance - Crinetics Pharmaceuticals INC - Location: Remote (remote) - Salary: $339K-$424K - Posted: 2026-05-12 - 401(k) match: listed (not source-backed) - Apply: https://crinetics.wd12.myworkdayjobs.com/CrineticsCareers/job/Remote/Vice-President--Drug-Safety-Pharmacovigilance_JR000557 - Excerpt: Vice President, Drug Safety/Pharmacovigilance Remote Crinetics is a pharmaceutical company based in San Diego, California, developing much-needed therapies for people with endocrine diseases and endocrine-related tumors. We were founded by a dedicated team of scientists with the simple belief that better therapies developed from rigorous innovation can lead to better lives. Our work continues to make a real difference in the lives of patients. We have a prolific discovery engine and a robust preclinical and clinical development pipeline. We are driven by science with a patient-centric and team-oriented culture. Crinetics is known for its inclusive workplace culture. We are also a dog-friendly workplace. This is an exciting time to join Crinetics as we shape our organization into the world's premier fully-integrated endocrine company from discovery to patients. Join our team as we transform the lives of others. Position Summary: The Vice President of Drug Safety/Pharmacovigilance will be instrumental in supporting the growth of the organization as it continues to build the value of its current products and develop new products. The incumbent will design and develop the Global Crinetics Drug Safety and Pharmacovigilance system, ensuring adequate resourcing, efficient and compliant safety reporting, designing implementation of Safety Surveillance Programs, oversight of the safety profiles of Crinetics products and playing a leading role in safety risk management activities. Essential Job Functions and Responsibilities: These may include but are not limited to: Safety reporting processes. Ensure the accurate receipt and processing of safety assessment reports. Ensure that medical and causality assessments of all ### Apprentice Chemical and Pharmaceutical Technologist 2026 - Biogen - Location: Solothurn, Switzerland (unspecified) - Salary: Not disclosed - Posted: 2026-05-12 - 401(k) match: listed (not source-backed) - Apply: https://biibhr.wd3.myworkdayjobs.com/external/job/Solothurn-Switzerland/Apprentice-Chemical-and-Pharmaceutical-Technologist-2026_REQ21851 - Excerpt: Apprentice Chemical and Pharmaceutical Technologist 2026 Solothurn, Switzerland posted: Posted 30+ Days Ago ### Scientist I (Contract), Drug Product Analytics - Vaxcyte Inc - Location: San Carlos, California, United States (unspecified) - Salary: $62-$68/hr - Posted: 2026-05-21 - 401(k) match: listed (not source-backed) - Apply: https://boards.greenhouse.io/vaxcyte/jobs/5224535008?gh_jid=5224535008 - Excerpt: Scientist I (Contract), Drug Product Analytics San Carlos, California, United States Join our Mission to Protect Humankind! Vaxcyte is a clinical-stage vaccine innovation company engineering high-fidelity vaccines to protect humankind from the consequences of bacterial diseases, which have serious and costly health consequences when left unchecked. Working to eradicate or treat bacterial infections such as invasive pneumococcal disease, Group A Strep, and Shigella is just the beginning. Our path to success is clear and well-defined, and Vaxcyte is set up to go the distance. WHAT we do is every bit as important as HOW we do it! Our work together is guided by four enduring core values: *RETHINK CONVENTION: We bring creative and intellectual diversity to every facet of the work we do in order to innovate and re-innovate the way vaccines are delivered. *AIM HIGH: We embody our collectively audacious goal to courageously make the most complex biologics ever attempted to protect humankind. *LEAD WITH HEART: Everyone leads at Vaxcyte with a kindness-first, inclusive approach to collaboration and vigorous debate that advances our business objectives. *MODEL EXCELLENCE: The magnitude of our challenge requires our shared commitment to demonstrating integrity, accountability, equality and clarity across communications and decision making. Summary: Vaxcyte is looking for an energetic and talented individual to join our Drug Product Development team. The candidate must have knowledge of and practical experience in analyzing and characterizing biomolecules (proteins, polysaccharide conjugates, vaccines) using a variety of methods, especially immunoassays and multiplexed immunoassay formats. Experience in analyzing vaccine and ### Pharmaceutical Production Technician - All Shifts - Medline Inc. - Location: Waukegan, Illinois (unspecified) - Salary: Not disclosed - Posted: 2026-05-14 - 401(k) match: listed (not source-backed) - Apply: https://medline.wd5.myworkdayjobs.com/Medline/job/Waukegan-Illinois/Pharmaceutical-Production-Technician---All-Shifts_R2605411 - Excerpt: Pharmaceutical Production Technician - All Shifts Waukegan, Illinois posted: Posted 29 Days Ago ### Associate Scientist II (Contract), Drug Product Analytics - Vaxcyte Inc - Location: San Carlos, California, United States (unspecified) - Salary: $51-$56/hr - Posted: 2026-05-21 - 401(k) match: listed (not source-backed) - Apply: https://boards.greenhouse.io/vaxcyte/jobs/5224522008?gh_jid=5224522008 - Excerpt: Associate Scientist II (Contract), Drug Product Analytics San Carlos, California, United States Join our Mission to Protect Humankind! Vaxcyte is a clinical-stage vaccine innovation company engineering high-fidelity vaccines to protect humankind from the consequences of bacterial diseases, which have serious and costly health consequences when left unchecked. Working to eradicate or treat bacterial infections such as invasive pneumococcal disease, Group A Strep, and Shigella is just the beginning. Our path to success is clear and well-defined, and Vaxcyte is set up to go the distance. WHAT we do is every bit as important as HOW we do it! Our work together is guided by four enduring core values: *RETHINK CONVENTION: We bring creative and intellectual diversity to every facet of the work we do in order to innovate and re-innovate the way vaccines are delivered. *AIM HIGH: We embody our collectively audacious goal to courageously make the most complex biologics ever attempted to protect humankind. *LEAD WITH HEART: Everyone leads at Vaxcyte with a kindness-first, inclusive approach to collaboration and vigorous debate that advances our business objectives. *MODEL EXCELLENCE: The magnitude of our challenge requires our shared commitment to demonstrating integrity, accountability, equality and clarity across communications and decision making. Summary: Vaxcyte is looking for an energetic and talented individual to join our Drug Product Development team. The candidate must have knowledge of and practical experience in analyzing and characterizing biomolecules (proteins, polysaccharide conjugates, vaccines) using a variety of methods, including immunoassays, chromatography, spectrophotometric techniques, light scattering, and particle sizing. ### Pharmaceutical Representative (Dnipro) - Abbott Laboratories - Location: Ukraine > Kyiv: Senator Business Center (unspecified) - Salary: Not disclosed - Posted: 2026-06-11 - Parental leave: 8 weeks (not source-backed) - Non-birth-parent leave: 8 weeks (not source-backed) - 401(k) match: listed (not source-backed) - Apply: https://abbott.wd5.myworkdayjobs.com/abbottcareers/job/Ukraine--Kyiv-Senator-Business-Center/Pharmaceutical-Representative--Dnipro-_31153247 - Excerpt: Pharmaceutical Representative (Dnipro) Ukraine > Kyiv: Senator Business Center posted: Posted Yesterday ### Manager, Analytical Development and Quality Control (Brisbane, CA) - Nurix Therapeutics Inc - Location: Brisbane, CA (unspecified) - Salary: $147K-$171K - Posted: 2026-05-20 - 401(k) match: listed (not source-backed) - Apply: https://job-boards.greenhouse.io/nurix/jobs/8553686002 - Excerpt: Manager, Analytical Development and Quality Control (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. Position The Manager, Analytical Development and Quality Control provides strategic and technical leadership for analytical CMC activities across multiple programs, with a strong emphasis on technology transfer and knowledge management. This role ensures successful transfer of analytical methods and associated knowledge to internal teams and external stakeholders, enabling consistent execution across development and manufacturing sites. The position requires deep expertise in analytical method development, validation, transfer, and lifecycle management in alignment with ICH guidelines, along with the ability to interpret data from a range of analytical techniques to support sound technical decision-making. In addition, this role is responsible for establishing and clearly communicating analytical control strategies across cross-functional teams, ensuring alignment and scientific rigor. The Manager drives robust knowledge management practices through high-quality technical writing, documentation, and data governance, including authoring and reviewing validation, transfer, and investigation reports. Strong ### Demand Planner - Novartis - Location: Bogota (Pharmaceuticals / GDD / NTO / CTS) (unspecified) - Salary: Not disclosed - Posted: 2026-05-18 - 401(k) match: listed (not source-backed) - Apply: https://novartis.wd3.myworkdayjobs.com/Internal_Careers_for_Acquired_Entities/job/Bogota-Pharmaceuticals--GDD--NTO--CTS/Demand-Planner_REQ-10078093 - Excerpt: Demand Planner Bogota (Pharmaceuticals / GDD / NTO / CTS) posted: Posted 25 Days Ago ### Chemielaborant/Pharmakant/Chemikant/PTA/CTA/BTA für die Herstellung parenteraler klinischer Prüfpräparate (all genders) (Vollzeit, unbefristet) - AbbVie Inc. - Location: Ludwigshafen, RP, Germany (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/3743990012977056-chemielaborant-pharmakant-chemikant-pta-cta-bta-fur-die-herstellung-parenteraler-klinischer-prufpraparate-all-genders-vollzeit-unbefristet- - Excerpt: Chemielaborant/Pharmakant/Chemikant/PTA/CTA/BTA für die Herstellung parenteraler klinischer Prüfpräparate (all genders) (Vollzeit, unbefristet) Ludwigshafen, RP, Germany Unternehmensbeschreibung: 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. Stellenbeschreibung: Herzlich willkommen bei Abbvie! Als Teil eines internationalen Unternehmens mit über 48.000 Mitarbeitern weltweit und rund 3.000 Mitarbeitern in Deutschland hast Du die Möglichkeit, eng mit uns zusammenzuarbeiten, um die gesundheitlichen Herausforderungen von morgen zu meistern. Du hast eine Leidenschaft für die Verbesserung der Gesundheitsversorgung auf der ganzen Welt? Du möchtest Dein Fachwissen einsetzen, um die Lebensqualität von Patienten zu verbessern? In einem herausfordernden Arbeitsumfeld, das Dir die Möglichkeit bietet, Deine eigenen Fähigkeiten zu erweitern und zu entwickeln? Dann bist Du bei uns richtig! Gemeinsam großes bewegen - als Chemielaborant/Pharmakant/Chemikant/PTA/CTA/BTA für die Herstellung parenteraler klinischer Prüfpräparate (all genders) Für unser motiviertes und engagiertes Team in der Entwicklung und Herstellung von parenteralen Arzneiformen suchen wir tatkräftige Unterstützung. Routine ist uns fremd, da unsere Abteilung an innovativen Prozessen und Produkten für klinische Studien arbeitet und einen reibungslosen Transfer aus der Entwicklung in die Herstellung klinischer Prüfpräparate gewährleistet. Unsere Aufgaben und Chargengrößen passen sich den jeweiligen Forschungs- und Entwicklungsprojekten ### Commercial Excellence Manager (Pharmaceutical / Lifesciences) - IQVIA - Location: Leiden, Netherlands (unspecified) - Salary: Not disclosed - Posted: 2026-06-04 - 401(k) match: listed (not source-backed) - Apply: https://iqvia.wd1.myworkdayjobs.com/IQVIA/job/Leiden-Netherlands/Commercial-Excellence-Manager--Pharmaceutical---Lifesciences-_R1549255 - Excerpt: Commercial Excellence Manager (Pharmaceutical / Lifesciences) Leiden, Netherlands posted: Posted 8 Days Ago ### Senior Vice President, Sales - Amylyx Pharmaceuticals Inc - Location: Flexible/ U.S. Based (unspecified) - Salary: $353K-$397K - Posted: 2026-05-13 - 401(k) match: listed (not source-backed) - Apply: https://job-boards.greenhouse.io/amylyx/jobs/5994725004 - Excerpt: Senior Vice President, Sales Flexible/ U.S. Based Amylyx has an audacious mission to usher in a new era for treating diseases with high unmet needs. Where others see challenges, we see opportunities that we pursue with urgency, rigorous science, and unwavering commitment to the communities we serve. We are a clinical-stage company currently focused on post-bariatric hypoglycemia (PBH), Wolfram syndrome, and amyotrophic lateral sclerosis (ALS). Our mission is powered by our people. Our core values - be audacious, be curious, be authentic, be engaged, and be accountable - creating a culture of caring. Amylyx has assembled an experienced team ready to take action because the communities we serve have no time to wait. If you share our passion and are determined to tackle some of medicine's toughest problems, we encourage you to read the opportunity below and apply. The Opportunity The SVP of Sales will play a critical leadership role in building and executing the commercial strategy for a pre‑commercial biotechnology company preparing for its first product launch. This individual will be responsible for designing and implementing the Go‑To‑Market (GTM) strategy, recruiting and developing a high‑performing sales organization, establishing strong relationships with Key Opinion Leaders (KOLs), ensuring full sales force readiness ahead of launch and driving performance. We anticipate hiring the Senior Vice President, Sales in September 2026. The ideal candidate combines strategic vision with hands‑on execution experience in specialty pharma or biotech launches and thrives in a fast‑paced, build‑from‑scratch environment. Responsibilities Enterprise Commercial Leadership - Shape overall U.S. commercial ### Manager, Pharmaceutical Sales Training - Asahi Kasei Corp. - Location: Cary, NC (unspecified) - Salary: Not disclosed - Posted: 2026-05-12 - 401(k) match: listed (not source-backed) - Apply: https://akamerica.wd501.myworkdayjobs.com/aka/job/Cary-NC/Manager--Pharmaceutical-Sales-Training_R5468-1 - Excerpt: Manager, Pharmaceutical Sales Training Cary, NC posted: Posted 30+ Days Ago ### Senior Manager, Regulatory Affairs - Apogee Therapeutics Inc - Location: Remote (remote) - Salary: $155K-$175K - Posted: 2026-04-24 - 401(k) match: listed (not source-backed) - Apply: https://job-boards.greenhouse.io/apogeetherapeutics/jobs/5120442007 - Excerpt: Senior Manager, Regulatory Affairs 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 Senior Manager, Regulatory Affairs. This newly created role offers an opportunity ### Pharmaceutical QC Technical Services Manager - Smithfield Foods - Location: Cincinnati, OH (unspecified) - Salary: Not disclosed - Posted: 2026-05-22 - 401(k) match: listed (not source-backed) - Apply: https://smithfieldfoods.wd1.myworkdayjobs.com/Careers/job/Cincinnati-OH/Pharmaceutical-QC-Technical-Services-Manager_R-2026-6094 - Excerpt: Pharmaceutical QC Technical Services Manager Cincinnati, OH posted: Posted 21 Days Ago ### Research Associate II/III– Bioanalytical/In Vitro ADME/DMPK - Nurix Therapeutics Inc - Location: Brisbane, CA (unspecified) - Salary: $93K-$107K - Posted: 2026-06-08 - 401(k) match: listed (not source-backed) - Apply: https://job-boards.greenhouse.io/nurix/jobs/8582171002 - Excerpt: Research Associate II/III– Bioanalytical/In Vitro ADME/DMPK 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. Position Nurix Therapeutics is searching for a motivated Research Associate to join our Bioanalytical-In Vitro DMPK team. The successful candidate will contribute to the bioanalytical efforts to support Nurix drug discovery programs involving in vivo and in vitro studies. We are seeking a highly motivated research associate to characterize the in vitro and in vivo ADME properties of drug candidates. The primary responsibilities will be to conduct bioanalysis for in vivo samples and to conduct in vitro experiments. The scope of the daily responsibilities for this position includes, but is not limited to, developing bioanalytical methods, quantitating drug candidates and their metabolites, endogenous biomarkers in biological matrices (e.g. blood, plasma, tissue, tumor, CSF, etc.), reporting bioanalytical results and managing projects outsourced in CROs to support all in vitro and in vivo studies. The successful candidate will have extensive experience in bioanalytical ### Pharmaceutical Information Specialist - Merck & Co., Inc. - Location: CHN - Shanghai - Shanghai (Tower A) (unspecified) - Salary: Not disclosed - Posted: 2026-06-05 - 401(k) match: listed (not source-backed) - Apply: https://msd.wd5.myworkdayjobs.com/SearchJobs/job/CHN---Shanghai---Shanghai-Tower-A/Pharmaceutical-Information-Specialist_R401276-1 - Excerpt: Pharmaceutical Information Specialist CHN - Shanghai - Shanghai (Tower A) posted: Posted 7 Days Ago ### Pharmareferent Cardiometabolic Health (m/w/d) Gebiet: Mettlach, Sankt Wendel, Homburg, Blieskastel, Mandelbachtal, Saarbrücken, Neunkirchen, Überherrn, Rehlingen-Siersburg - Eli Lilly and Company - Location: Germany, Remote (remote) - Salary: Not disclosed - Posted: 2026-05-12 - 401(k) match: listed (not source-backed) - Apply: https://lilly.wd5.myworkdayjobs.com/LLY/job/Germany-Remote/Pharmareferent-Cardiometabolic-Health--m-w-d--Gebiet--Mettlach--Sankt-Wendel--Homburg--Blieskastel--Mandelbachtal--Saarbrcken--Neunkirchen--berherrn--Rehlingen-Siersburg_R-99046-2 - Excerpt: Pharmareferent Cardiometabolic Health (m/w/d) Gebiet: Mettlach, Sankt Wendel, Homburg, Blieskastel, Mandelbachtal, Saarbrücken, Neunkirchen, Überherrn, Rehlingen-Siersburg Germany, Remote posted: Posted 30+ Days Ago ### Pharmaceutical Operator - Ashland Global - Location: US-OH-COLUMBUS (ATLAS) (unspecified) - Salary: Not disclosed - Posted: 2026-05-27 - Apply: https://ashland.wd12.myworkdayjobs.com/AshlandCareers1/job/US-OH-COLUMBUS-ATLAS/Pharmaceutical-Operator_2026-0250 - Excerpt: Pharmaceutical Operator US-OH-COLUMBUS (ATLAS) posted: Posted 16 Days Ago ### Pharmaceutical Information Manager - Merck & Co., Inc. - Location: CHN - Shanghai - Shanghai (Trading) (unspecified) - Salary: Not disclosed - Posted: 2026-06-04 - 401(k) match: listed (not source-backed) - Apply: https://msd.wd5.myworkdayjobs.com/SearchJobs/job/CHN---Shanghai---Shanghai-Trading/Pharmaceutical-Information-Manager_R401755-2 - Excerpt: Pharmaceutical Information Manager CHN - Shanghai - Shanghai (Trading) posted: Posted 8 Days Ago ### AI Scientist - Biomedical Multimodal Modeling - Xaira - Location: South San Francisco, California, United States (unspecified) - Salary: $170K-$240K - Posted: 2026-05-04 - Apply: https://job-boards.greenhouse.io/xairatherapeutics/jobs/5036777007 - Excerpt: AI Scientist - Biomedical Multimodal Modeling South San Francisco, California, United States About Xaira Therapeutics Xaira is an innovative biotech startup focused on leveraging AI to transform drug discovery and development. The company is leading the development of generative AI models to design protein and antibody therapeutics, enabling the creation of medicines against historically hard-to-drug molecular targets. It is also developing foundation models for biology and disease to enable better target elucidation and patient stratification. Collectively, these technologies aim to continually enable the identification of novel therapies and to improve success in drug development. Xaira is headquartered in the San Francisco Bay Area, Seattle, and London. About the Role We are building foundation models for biological systems, focusing on learning from complex, multimodal data. Our approach combines representation learning and generative modeling to capture structure, variation, and latent organization in high-dimensional settings. We work with both image-based data and high-dimensional molecular (omics) measurements, treating them as complementary views of the same underlying system. Our goal is to develop models that can both encode rich representations and generate or infer missing aspects from partial observations. What You'll Do - Develop multimodal foundation models spanning image and molecular data - Design approaches that unify representation learning and generative modeling - Train large-scale models on structured, high-dimensional datasets - Explore cross-modal alignment, prediction, and generation - Build scalable systems for data processing, training, and evaluation - Work in a research-driven environment with evolving problem definitions What We're Looking For Strong background in deep ### Senior Specialist, Supply Chain Management - Apogee Therapeutics Inc - Location: Remote (remote) - Salary: $115K-$130K - Posted: 2026-06-08 - 401(k) match: listed (not source-backed) - Apply: https://job-boards.greenhouse.io/apogeetherapeutics/jobs/5158901007 - Excerpt: Senior Specialist, Supply Chain Management 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 - Review clinical trial synopsis and/or protocols to understand IMP supply and demand requirements. ### Pharmaceutical Sales Representative- Glendale,CA - GSK plc - Location: 4 Locations (unspecified) - Salary: Not disclosed - Posted: 2026-06-02 - 401(k) match: listed (not source-backed) - Apply: https://gsk.wd5.myworkdayjobs.com/GSKCareers/job/USA---California---Los-Angeles/Pharmaceutical-Sales-Representative--Glendale-CA_441304 - Excerpt: Pharmaceutical Sales Representative- Glendale,CA 4 Locations posted: Posted 10 Days Ago ### Associate Director, Device Development - Apogee Therapeutics Inc - Location: Remote (remote) - Salary: $180K-$200K - Posted: 2026-05-22 - 401(k) match: listed (not source-backed) - Apply: https://job-boards.greenhouse.io/apogeetherapeutics/jobs/5145512007 - Excerpt: Associate Director, Device Development 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 Associate Director, Device Development to join the Technical Operations team ### Pharmaceutical Laboratory Analyst - Ashland Global - Location: US-OH-COLUMBUS (ATLAS) (unspecified) - Salary: Not disclosed - Posted: 2026-05-20 - Apply: https://ashland.wd12.myworkdayjobs.com/AshlandCareers1/job/US-OH-COLUMBUS-ATLAS/Pharmaceutical-Laboratory-Analyst_2026-0235 - Excerpt: Pharmaceutical Laboratory Analyst US-OH-COLUMBUS (ATLAS) posted: Posted 23 Days Ago ### MR-RIN-长沙 - AstraZeneca - Location: China (unspecified) - Salary: Not disclosed - Posted: 2026-06-03 - 401(k) match: listed (not source-backed) - Apply: https://astrazeneca.wd3.myworkdayjobs.com/Careers/job/China/MR-RIN-_R-249611 - Excerpt: MR-RIN-长沙 China posted: Posted 9 Days Ago ### Business Development Associate - Pharmaceutical - Ecolab - Location: USA - North Carolina - Raleigh (unspecified) - Salary: Not disclosed - Posted: 2026-05-12 - Parental leave: 6 weeks (not source-backed) - Non-birth-parent leave: 6 weeks (not source-backed) - 401(k) match: listed (not source-backed) - Apply: https://ecolab.wd1.myworkdayjobs.com/Ecolab_External/job/USA---North-Carolina---Raleigh/Business-Development-Associate---Pharmaceutical_R00293604 - Excerpt: Business Development Associate - Pharmaceutical USA - North Carolina - Raleigh posted: Posted 30+ Days Ago ### Associate Director, Regulatory Strategy - Syndax Pharmaceuticals Inc - Location: New York, NY (unspecified) - Salary: $200K-$225K - Posted: 2026-03-09 - 401(k) match: listed (not source-backed) - Apply: https://syndax.com/join-us/careers/?gh_jid=5819781004 - Excerpt: Associate Director, Regulatory Strategy New York, NY Syndax Pharmaceuticals is looking for an Associate Director, Regulatory Strategy At Syndax, we are determined to realize a future in which people with cancer live longer and better than ever before. Syndax Pharmaceuticals is a commercial stage biopharmaceutical company developing an innovative pipeline of cancer therapies. The Role: The Associate Director, Regulatory Strategy will be responsible for developing and implementing regulatory strategies to secure global investigational and marketing applications for assigned product(s) in the assigned therapeutic area. Leads the Product Regulatory Sub team. Ensures strategic messaging and content of global regulatory dossiers. May serve as the primary regulatory interface with the Asset Strategy Team and sub teams. Proactively anticipates and mitigates regulatory risks. Ensures compliance with global regulatory requirements. Manages assets through all phases of development from pre-FIH through active life cycle management activities. Demonstrates an understanding of drug development and exhibits leadership behaviors consistent with level. Has direct experience with regulatory acceleration strategies, developing regulatory strategy, analyzing regulatory precedence and operational excellence in execution of regulatory strategy. This role may lead a team of regulatory professionals. Key Responsibilities: - Ensure the development and flawless execution of regulatory strategies for the assigned products/projects. - Strategic partner for internal cross functional stakeholders both within and external to the regulatory organization.. - Represents Syndax to regulatory health authorities, e.g. FDA, for all products and businesses. - Lead the preparation of submissions, which may include INDs, Briefing Documents, Orphan Drug Applications, and Marketing Applications, etc. Work ### Pharmaceutical Sales Representative - Raleigh-Durham NC - IQVIA - Location: 2 Locations (unspecified) - Salary: Not disclosed - Posted: 2026-06-11 - 401(k) match: listed (not source-backed) - Apply: https://iqvia.wd1.myworkdayjobs.com/IQVIA/job/Raleigh-NC/Pharmaceutical-Sales-Representative---Raleigh-Durham-NC_R1550762 - Excerpt: Pharmaceutical Sales Representative - Raleigh-Durham NC 2 Locations posted: Posted Yesterday ### Gerente de Produto Sr. Neurociências - AbbVie Inc. - Location: São Paulo, SP, Brazil (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/3743990013063706-gerente-de-produto-sr-neurociencias - Excerpt: Gerente de Produto Sr. Neurociências São Paulo, SP, Brazil 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: Seu papel será: Responsável por liderar a estratégia de marketing de produtos do portfólio farmacêutico, garantindo crescimento sustentável, fortalecimento de marca, excelência na execução comercial e alinhamento crossfuncional. Atua como líder estratégico na construção do posicionamento da marca, geração de demanda e desenvolvimento de iniciativas orientadas ao mercado, stakeholders e pacientes. Você será responsável por: Gerenciar lançamento dos novos produtos/indicações, desenvolver o plano estratégico em conjunto com o Brand Team, acompanhar implementação das ações para garantir que todas as ações sejam conduzidas de acordo com o planejado; Liderar análises de mercado, concorrência, tendências e comportamento dos stakeholders para identificação de oportunidades, bem como monitorar performance de mercado e propor planos de ação, conforme necessidade. Construir e acompanhar forecast, budget e KPIs da marca, em conjunto com Brand Team (time de marca) e garantir alinhamento com os objetivos da companhia Elaborar/adaptar estratégias de posicionamento juntamente com o Brand Team, segmentação e targeting. Trabalhar de forma integrada com áreas multifuncionais, incluindo: ### Pharmaceutical Sales Representative - Washington DC - IQVIA - Location: Washington DC, DC (unspecified) - Salary: Not disclosed - Posted: 2026-05-28 - 401(k) match: listed (not source-backed) - Apply: https://iqvia.wd1.myworkdayjobs.com/IQVIA/job/Washington-DC-DC/Pharmaceutical-Sales-Representative---Washington-DC_R1547672 - Excerpt: Pharmaceutical Sales Representative - Washington DC Washington DC, DC posted: Posted 15 Days Ago ### Senior Manager, Medical Writing - Apogee Therapeutics Inc - Location: Remote (remote) - Salary: $160K-$180K - Posted: 2026-05-08 - 401(k) match: listed (not source-backed) - Apply: https://job-boards.greenhouse.io/apogeetherapeutics/jobs/5132727007 - Excerpt: Senior Manager, Medical Writing 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 and motivated medical writer who is responsible for providing clinical --- Source-backed benefit claims include source links; other benefit values are labeled separately.