I'm looking for a job. I exported this list from FewerJobs.com - a curated job board. Please: 1. Rank these jobs by fit for me, given my resume / skills. 2. Highlight the top 5 with a one-sentence rationale each. 3. Flag any concerns, including benefit values without source-backed evidence. 4. Suggest one or two filter changes I could make on FewerJobs to find more good matches. Filters I applied: - q: Myriad Genetics INC - quality_floor: default - match_401k_strict: true - parental_strict: true - non_birth_strict: true - pto_strict: true - include_older: false - verified_benefits_only: true - apply_url_verified: false - page: 1 - per_page: 100 - sort: relevance Jobs (100 total): --- TITLE: Commercial Strategic Planning and Forecasting Senior Manager EMPLOYER: Myriad Genetics INC LOCATION: United States (unspecified) SALARY: Not disclosed POSTED: 2026-04-13 PARENTAL_LEAVE_WEEKS: 2 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 2 (not source-backed) K401_MATCH: yes (not source-backed) APPLY_URL: https://ekgn.fa.us6.oraclecloud.com/hcmUI/CandidateExperience/en/sites/CX_2001/job/6043 EXCERPT: Commercial Strategic Planning and Forecasting Senior Manager United States About Myriad Genetics Myriad Genetics is a leader in molecular diagnostics, developing innovative genetic tests that determine disease risk, assess disease progression, and guide treatment decisions across Oncology, Women's Health, and Mental Health. We are committed to advancing personalized medicine through data-driven insights and scientific rigor. The Opportunity The Senior Manager, Commercial Strategic Planning and Forecasting will play a critical role in supporting enterprise commercial modeling and forecasting efforts across Myriad's portfolio. This is a hands-on, execution-focused position responsible for building and maintaining detailed volume and revenue models to support commercial and product strategy, growth initiatives, and long-range planning. The role partners cross-functionally with Product, Market Intelligence, Commercial Operations, PMO, and Finance to ensure forecasts are data-driven, structured, and aligned to business objectives. The ideal candidate is detail-oriented, analytically rigorous, comfortable working in Excel and large datasets, and energized by turning ambiguity into structured financial outputs. Key Responsibilities Commercial Model Ownership Build and maintain detailed bottom-up commercial models for new product launches, portfolio expansions, and growth initiatives Translate assumptions across epidemiology, eligibility, adoption, pricing, payer mix, and reimbursement into revenue projections Update models based on new data inputs and evolving business assumptions Ensure consistency and traceability of model logic across initiatives Forecast Execution & Iteration Support monthly, quarterly, and long-range planning cycles with updated volume and revenue projections Incorporate real-world performance data to refine assumptions and improve forecast accuracy Maintain scenario models (base / upside / downside) and sensitivity analyses Identify --- TITLE: Sales Incentive Compensation Sr Manager EMPLOYER: Myriad Genetics INC LOCATION: United States (unspecified) SALARY: Not disclosed POSTED: 2026-04-21 PARENTAL_LEAVE_WEEKS: 2 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 2 (not source-backed) K401_MATCH: yes (not source-backed) APPLY_URL: https://ekgn.fa.us6.oraclecloud.com/hcmUI/CandidateExperience/en/sites/CX_2001/job/6054 EXCERPT: Sales Incentive Compensation Sr Manager United States Myriad Genetics is a leader in molecular diagnostics, advancing personalized medicine across Oncology, Women's Health, and Mental Health. We are seeking a strategic and analytical Sales Incentive Compensation Senior Manager to lead the design, governance, and execution of commercial sales incentive programs that drive performance and fuel growth. This role partners closely with Commercial Leadership, Finance, HR, and Sales Operations to ensure compensation plans align with corporate objectives, motivate the field, and scale with business needs. This is a high-visibility role for a strategic leader who thrives at the intersection of analytics, finance, and commercial performance-and wants to shape how we reward and accelerate growth. Responsibilities Lead Incentive Strategy & Design Own enterprise-wide sales compensation strategy Design incentive compensation plans, pay curves, accelerators, SPIFs, and performance metrics Conduct financial modeling and scenario analysis to ensure ROI and cost alignment Drive plan design and refinements Ensure Governance & Operational Excellence Own accurate commission calculations and timely payouts Establish controls, documentation, and compliance standards Lead dispute resolution and maintain plan transparency Partner with Payroll, HR, and Finance on accruals and reporting Drive Analytics & Business Impact Deliver executive-ready reporting on attainment, pay-for-performance alignment, and plan effectiveness Forecast incentive compensation expense and analyze budget variance Identify trends, risks, and productivity opportunities Build scalable dashboards and reporting tools Optimize Systems & Processes Enhance incentive compensation systems and automation Partner cross-functionally to improve data integrity and reporting efficiency Lead process improvements that increase accuracy and reduce risk Lead --- TITLE: Manager Software Engineer EMPLOYER: Myriad Genetics INC LOCATION: United States (unspecified) SALARY: Not disclosed POSTED: 2026-04-21 PARENTAL_LEAVE_WEEKS: 2 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 2 (not source-backed) K401_MATCH: yes (not source-backed) APPLY_URL: https://ekgn.fa.us6.oraclecloud.com/hcmUI/CandidateExperience/en/sites/CX_2001/job/5494 EXCERPT: Manager Software Engineer United States We need a Software Engineering Manager to help Myriad Genetics, Inc. deliver innovative products that allow patients to make life-changing decisions. Our genetic screening and testing help to provide actionable insights to empower people to make critical and timely healthcare decisions by using molecular diagnostic tests for hereditary cancer, urological cancer, depression, and other diseases. We are excited about the future and remain committed to advancing the science of personalized medicine as we develop more products to address unmet medical needs. The software automation team is responsible for building software tools to support our highly automated production sequencing lab. We work closely with hardware engineers and molecular biology scientists to build automated workcells using the most advanced industrial automation and lab automation equipment available. Our software supports the simultaneous processing of thousands of samples across multiple workflows and our workcells run 24/7. For this position we have a strong preference for a Hybrid Office position in either our South San Francisco, CA or Salt Lake City, Utah locations. Your team and future hires will primarily be hybrid office in one of these locations. Our team is flexible on working from home, but we do need to go to the office to work with lab users and equipment for certain projects. WHAT YOU WILL DO Lead and Mentor : . Hire, manage, motivate, and mentor a small team of talented engineers. (4-6 direct reports estimated). Lead by example. Own Technical Direction : Architect and implement LIMS --- TITLE: Computational Scientist II EMPLOYER: Myriad Genetics INC LOCATION: United States (unspecified) SALARY: Not disclosed POSTED: 2026-04-13 PARENTAL_LEAVE_WEEKS: 2 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 2 (not source-backed) K401_MATCH: yes (not source-backed) APPLY_URL: https://ekgn.fa.us6.oraclecloud.com/hcmUI/CandidateExperience/en/sites/CX_2001/job/6080 EXCERPT: Computational Scientist II United States Overview The Computational Scientist II envisions, designs, builds, validates, and launches new genomic products and product features that directly improve patients' lives. Responsibility Author optimized and reliable analysis pipelines applied to samples. Rigorously analyze a variety of big datasets to gain actionable insights launched into the lab. Amplify the productivity of the entire R&D team by creating time-saving software tools and environments. Work on collaborative teams with experimental scientists, software engineers, automation engineers, and data scientists. Communicate results internally to key stakeholders and externally at conferences and in peer-reviewed literature. Qualifications PhD (or master's degree with relevant experience) in bioinformatics, computational biology, computer science, biophysics, physics, statistics, molecular biology, genetics, or related discipline required. Conversant in molecular biology and genetics. Exceptional software skills, preferably with fluency in Python. Impeccable integrity and palpable drive, with the competency to be self-sufficient and a strong desire to be part of a supportive team. Experience with Next Generation Sequencing preferred. Applicant must be a (i) U.S. citizen or national, (ii) U.S. lawful, permanent resident (aka green card holder) living full time in the USA We take geographic location into account when determining base salary to ensure equitable and competitive compensation. #LI-KO1 Computational Scientist II --- TITLE: Scientist III EMPLOYER: Myriad Genetics INC LOCATION: Salt Lake City, UT, United States (unspecified) SALARY: Not disclosed POSTED: 2026-03-02 PARENTAL_LEAVE_WEEKS: 2 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 2 (not source-backed) K401_MATCH: yes (not source-backed) APPLY_URL: https://ekgn.fa.us6.oraclecloud.com/hcmUI/CandidateExperience/en/sites/CX_2001/job/5829 EXCERPT: Scientist III Salt Lake City, UT, United States Overview Scientist III, Genomic Science - Salt Lake City UT Scientist III leads complex research projects, designs innovative assays, and provides strategic input to the R&D team. You will work collaboratively with cross-functional teams and contribute to the advancement of our genetic testing technologies. The Research and Development group at Myriad Genetics is responsible for creating and updating a portfolio of cancer tests. The role requires individuals who are aware of both the clinical and molecular aspects of the various genes, mutational mechanisms and diseases that we work with. This position will require both strong bench and analytical skills to design, execute and analyze experiment in cfDNA and NGS fields. Perform the experimental design, execution, data collection, and data analysis of molecular assays that utilize next generation sequencing (NGS) and other methodologies for analyzing cfDNA, DNA and RNA. Lead the design, development, and optimization of existing and new advanced, molecular assays. Manage and execute complex research projects from conception to completion. Analyze, interpret, and present high-level experimental data to stakeholders. Collaborate with cross-functional teams to integrate molecular biology with automated and data-driven systems. Ensure good documentation practices for assay development, validation, quality assurance, technical investigations, and operational support of molecular diagnostic tests in a highly regulated clinical laboratory environment. Maintain familiarity with the field's concepts, practices, and procedures. Qualifications An individual with a scientific background who works well in teams including large, diverse and cross-functional settings. The ideal candidate would be familiar --- TITLE: VP, Government Affairs & Public Policy (Enterprise) EMPLOYER: Myriad Genetics INC LOCATION: United States (unspecified) SALARY: Not disclosed POSTED: 2026-04-20 PARENTAL_LEAVE_WEEKS: 2 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 2 (not source-backed) K401_MATCH: yes (not source-backed) APPLY_URL: https://ekgn.fa.us6.oraclecloud.com/hcmUI/CandidateExperience/en/sites/CX_2001/job/6093 EXCERPT: VP, Government Affairs & Public Policy (Enterprise) United States Role Summary The VP, Government Affairs & Public Policy will lead Myriad's enterprise-wide policy, government affairs, and advocacy strategy, integrating federal, state, and regulatory engagement to advance patient access, reimbursement, and appropriate regulation of the company's product portfolio. This role operates at the intersection of policy, market access, regulatory strategy, and commercial growth, with direct accountability for helping shape the external environment to enable adoption and reimbursement of Myriad's products in oncology, women's health, and mental health. Reporting to the Chief Legal Officer, this leader will serve as a strategic advisor to the executive team, ensuring Myriad is positioned to anticipate, influence, and respond to an increasingly complex and dynamic policy landscape. Key Responsibilities Enterprise Policy Strategy Define and lead a government affairs and public policy strategy across federal, state, and regulatory domains Align policy priorities with enterprise growth objectives, including revenue expansion, reimbursement, and test adoption Serve as the single point of accountability for policy-related business impact Federal, State & Regulatory Leadership Lead coordinated engagement across: Congress, CMS, FDA, HHS, VA State legislatures and Medicaid programs Shape policy related to: HHS oversight of diagnostics (including LDTs and CDx) Medicare Clinical Lab Fee Schedule (CLFS) Coverage, coding, and reimbursement frameworks Prior authorization and utilization management Telehealth and digital diagnostics AI and algorithm governance in healthcare Reimbursement & Market Access Integration Partner with Market Access and Commercial leadership to: Influence coverage and payment policy Remove barriers to adoption across public and private --- TITLE: Medical Science Liaison (Germline Oncology - Dallas/Fort Worth, East TX, LA, AR, MS) EMPLOYER: Myriad Genetics INC LOCATION: Dallas, TX, United States (unspecified) SALARY: Not disclosed POSTED: 2026-04-17 PARENTAL_LEAVE_WEEKS: 2 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 2 (not source-backed) K401_MATCH: yes (not source-backed) APPLY_URL: https://ekgn.fa.us6.oraclecloud.com/hcmUI/CandidateExperience/en/sites/CX_2001/job/6087 EXCERPT: Medical Science Liaison (Germline Oncology - Dallas/Fort Worth, East TX, LA, AR, MS) Dallas, TX, United States Medical Science Liaison (MSL) - Oncology, Germline Geography: Texas East Territory (Dallas/Fort Worth, East TX, LA, AR, MS) Description : Myriad Genetics is seeking a Medical Science Liaison (MSL) to support our oncology portfolio with a primary focus on hereditary cancer (germline) testing across the cancer center settings, including medical oncology, gynecologic oncology, surgical oncology, and cancer genetics clinics. This is a field-based scientific and clinical expert role within Medical Affairs. The MSL serves as a trusted scientific partner to healthcare professionals and key opinion leaders (KOLs), facilitating high quality scientific exchange and bringing actionable insights back to the organization. The MSL will demonstrate strong clinical expertise, scientific acumen, and business awareness while collaborating cross-functionally with Medical Affairs, Commercial Sales and Marketing, Product, and Training teams. This role reports to the Germline Oncology MSL Manager within Medical Affairs. Key Responsibilities: Scientific and Clinical Expertise: Maintain deep expertise in Myriad's oncology germline testing portfolio and relevant areas of oncology, genetics, and genomics. Stay current on emerging data, guidelines, clinical practice trends, and the competitive landscape impacting hereditary cancer testing. Represent Myriad at scientific congresses, advisory boards, and educational forums to gather insights and support Medical Affairs objectives. Actively contribute to the Myriad Medical Affairs community through best practice sharing and collaboration. External Engagement and Education: Serve as a scientific and clinical resource to healthcare professionals by responding to medical inquiries, explaining test results, and --- TITLE: Computational Scientist III EMPLOYER: Myriad Genetics INC LOCATION: South San Francisco, CA, United States (unspecified) SALARY: Not disclosed POSTED: 2026-04-13 PARENTAL_LEAVE_WEEKS: 2 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 2 (not source-backed) K401_MATCH: yes (not source-backed) APPLY_URL: https://ekgn.fa.us6.oraclecloud.com/hcmUI/CandidateExperience/en/sites/CX_2001/job/6079 EXCERPT: Computational Scientist III South San Francisco, CA, United States The Computational Scientist III is member of the research team and contributes to design, development, maintenance, and validation of molecular assays and analytical pipelines working closely with molecular biologists, lab directors and software engineers. Responsibility Make critical contributions to wide range of products in a cutting-edge clinical genomics laboratory. Use rigorous data science and modern software best practices to create efficient, reliable, and optimized bioinformatics tools. Work closely with molecular biologists, clinical scientists, software engineers, automation engineers, and data scientists. Characterize data resulting from novel molecular assays and guide molecular protocol development from a statistical perspective. Mentor junior scientists and research associates, guiding the overall path and success of key projects. Author posters and publications demonstrating the scientific prowess of our products and algorithms that power the products. Work with legal staff to secure intellectual property rights for inventions pertaining to our products. Communicate results to stakeholders across the organization. Qualifications PhD in Computational Biology, Statistics, Molecular Biology, Genetics, Computer Science, Systems Biology, Biophysics, Physics, or a related discipline. 3+ years of experience developing methods to analyze large, noisy real-world data sets (in the context of molecular biology and/or human genetics, a plus). Experience developing custom analysis methods and algorithms and analysis pipelines. Experience working with CLIA-validated assays and authoring CLIA validation plans, Illumina Next Generation Sequencing (NGS), and other sequencing platforms. Strong computation skills, fluency in Python and a workflow definition language, and knowledge of software engineering best practices. Multiple --- TITLE: Area Sales Manager, MRD EMPLOYER: Myriad Genetics INC LOCATION: United States (unspecified) SALARY: Not disclosed POSTED: 2026-05-01 PARENTAL_LEAVE_WEEKS: 2 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 2 (not source-backed) K401_MATCH: yes (not source-backed) APPLY_URL: https://ekgn.fa.us6.oraclecloud.com/hcmUI/CandidateExperience/en/sites/CX_2001/job/6134 EXCERPT: Area Sales Manager, MRD United States Area Sales Manager, MRD Will be responsible for: The Area Sales Manager, MRD plays a critical role in advancing Myriad's oncology strategy by leading a high-performing sales team focused on MRD and Somatic testing. This leader will drive regional execution, build strong customer relationships, and develop talent to deliver sustained growth. In close partnership with the MRD National Sales Director, this role is responsible for recruiting, coaching, and leading a team of account executives while aligning day-to-day execution with broader business objectives. The ideal candidate brings both strategic perspective and a hands-on approach to driving results in a dynamic environment. This position supports a defined sales region and includes regular regional and occasional national travel. Business Planning Develop a deep understanding of the national business strategy and lead execution to achieve key objectives Execute national account targeting strategies in alignment with business priorities Partner with customers to assess needs and identify opportunities for growth Build and strengthen strategic customer relationships while setting clear development goals Monitor strategy effectiveness and adjust approach as needed to drive results Ensure performance expectations are consistently met Operations & Administration Review and approve expense reports in a timely manner Optimize resource allocation to support profitability and business goals Ensure timely and accurate completion of administrative requirements Champion consistent and effective use of CRM tools, including Salesforce People Leadership & Development Provide ongoing coaching and development through regular field engagement and feedback Align team goals with broader business priorities and --- TITLE: Regional Accounts Manager EMPLOYER: Myriad Genetics INC LOCATION: Salt Lake City, UT, United States (unspecified) SALARY: Not disclosed POSTED: 2026-04-21 PARENTAL_LEAVE_WEEKS: 2 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 2 (not source-backed) K401_MATCH: yes (not source-backed) APPLY_URL: https://ekgn.fa.us6.oraclecloud.com/hcmUI/CandidateExperience/en/sites/CX_2001/job/6086 EXCERPT: Regional Accounts Manager Salt Lake City, UT, United States Overview The Regional Accounts Manager, Payer Markets is a critical position responsible for shaping and advancing the company's relationships with regional and BCBS commercial insurers. They execute initiatives that establish and maintain favorable contract terms, influence payer policy, and ensure operational execution that supports sustained revenue growth and broad access to care. They collaborate closely with cross functional teams and leaders to resolve payer challenges, streamline processes, and align managed care strategies across the organization. They demonstrate Myriad's values of collaboration, integrity, and accountability while applying data driven insights, structured negotiation approaches, and disciplined project management to deliver measurable payer market outcomes. The role requires negotiation, industry knowledge, and the ability to influence decision makers across complex organizations. Responsibility Lead negotiations and maintain strategic relationships with regional and BCBS commercial payers to secure optimal reimbursement, coverage, and contract performance. Execute payer strategies that align to corporate strategies, while monitoring changes in reimbursement models, regulatory environments, and commercial insurance dynamics. Oversee and optimize existing payer contracts to ensure alignment with payer policies, operational requirements, and internal workflows. Serve as the primary point of contact with external stakeholders, monitoring updates to reimbursement methodologies, coverage criteria, and state‑specific policy changes and communicating impacts internally Build and strengthen multi‑level payer relationships across medical policy, contracting, network management, utilization management, government affairs, and legal teams to advance enterprise objectives. Collaborate with Sales, Billing, Authorization, Medical Policy, Government Affairs, Legal, and senior leadership to resolve payer specific --- TITLE: Medical Science Liaison (Germline Oncology - IL, IN, WI, IA, NE, SD, ND) EMPLOYER: Myriad Genetics INC LOCATION: Chicago, IL, United States (unspecified) SALARY: Not disclosed POSTED: 2026-04-14 PARENTAL_LEAVE_WEEKS: 2 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 2 (not source-backed) K401_MATCH: yes (not source-backed) APPLY_URL: https://ekgn.fa.us6.oraclecloud.com/hcmUI/CandidateExperience/en/sites/CX_2001/job/6078 EXCERPT: Medical Science Liaison (Germline Oncology - IL, IN, WI, IA, NE, SD, ND) Chicago, IL, United States Medical Science Liaison (MSL) - Oncology, Germline Geography: Position Based: Central US (IL, IN, WI, IA, NE, SD, ND) Description : Myriad Genetics is seeking a Medical Science Liaison (MSL) to support our oncology portfolio with a primary focus on hereditary cancer (germline) testing across the cancer center settings, including medical oncology, gynecologic oncology, surgical oncology, and cancer genetics clinics. This is a field-based scientific and clinical expert role within Medical Affairs. The MSL serves as a trusted scientific partner to healthcare professionals and key opinion leaders (KOLs), facilitating high quality scientific exchange and bringing actionable insights back to the organization. The MSL will demonstrate strong clinical expertise, scientific acumen, and business awareness while collaborating cross-functionally with Medical Affairs, Commercial Sales and Marketing, Product, and Training teams. This role reports to the Germline Oncology MSL Manager within Medical Affairs. Key Responsibilities: Scientific and Clinical Expertise: Maintain deep expertise in Myriad's oncology germline testing portfolio and relevant areas of oncology, genetics, and genomics. Stay current on emerging data, guidelines, clinical practice trends, and the competitive landscape impacting hereditary cancer testing. Represent Myriad at scientific congresses, advisory boards, and educational forums to gather insights and support Medical Affairs objectives. Actively contribute to the Myriad Medical Affairs community through best practice sharing and collaboration. External Engagement and Education: Serve as a scientific and clinical resource to healthcare professionals by responding to medical inquiries, explaining test results, --- TITLE: Product Mgr IV Technology EMPLOYER: Myriad Genetics INC LOCATION: United States (unspecified) SALARY: Not disclosed POSTED: 2026-05-05 PARENTAL_LEAVE_WEEKS: 2 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 2 (not source-backed) K401_MATCH: yes (not source-backed) APPLY_URL: https://ekgn.fa.us6.oraclecloud.com/hcmUI/CandidateExperience/en/sites/CX_2001/job/6092 EXCERPT: Product Mgr IV Technology United States The Product Mgr IV Technology role will help lead the expansion and adoption of our genetic tests. This role will drive innovative initiatives, and the ideal candidate will have a track record of building strong relationships with partners and customers, and who has demonstrated success influencing large cross-functional teams. Responsibility Drive prioritization efforts for their product area and champion product area throughout organization. Partner with PMO, clinical genomics, Lab Directors, clinical reporting, and business stakeholders to write crisp and clear product requirements that drive technical specifications and user experience and interface designs. Write crisp and clear product requirements that drive technical specifications and user experience and interface designs. Champion products throughout the organization and present updates to senior management. Define and analyze metrics that inform the success of products. Continually validate products with internal and external customer feedback and against business metrics. Qualifications Minimum of 5 years of Product Management experience with proven success shipping multiple technology products across releases. MS or Bachelor's degree with equivalent years of experience in a relevant field. Knowledge of Genomics, variant annotation and curation, and clinical reporting process. Experience or formal education in relevant Genomics field is preferred Knowledge of the healthcare space or genetics laboratory is preferred Strong leadership skills and proven ability to lead cross-functional teams. Track record of understanding stakeholder needs and delivering technology solutions to address those needs. Demonstrated ability to leverage AI tools and techniques to enhance day-to-day product management activities Proficient in --- TITLE: Medical Science Liaison (Somatic Oncology - TN, GA, SC, NC, AL, MS) EMPLOYER: Myriad Genetics INC LOCATION: Atlanta, GA, United States (unspecified) SALARY: Not disclosed POSTED: 2026-03-26 PARENTAL_LEAVE_WEEKS: 2 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 2 (not source-backed) K401_MATCH: yes (not source-backed) APPLY_URL: https://ekgn.fa.us6.oraclecloud.com/hcmUI/CandidateExperience/en/sites/CX_2001/job/5998 EXCERPT: Medical Science Liaison (Somatic Oncology - TN, GA, SC, NC, AL, MS) Atlanta, GA, United States Geography: TN, GA, SC, NC, AL, MS Myriad Genetics is seeking a Medical Science Liaison (MSL) to support the Somatic / Tumor Genomics portfolio within the Precision Oncology business unit. This field based, scientifically focused role supports liquid and tumor profiling across solid tumors, including NGS based assays, biomarker driven therapy selection, resistance mechanisms, and treatment monitoring. The MSL will engage with medical oncologists, gynecologic oncologists, surgeons, molecular pathologists, urologists, academic centers, and community oncology practices. This individual will serve as a conduit of clinical expertise, scientific exchange, and insights that inform medical strategy. This position reports to the Director of Medical Affairs, Somatic, and partners closely with Medical Affairs colleagues, R&D, clinical operations, marketing, commercial teams (if role design includes sales support), and cross-functional leadership. Responsibilities: Maintain MSL Expertise through: Demonstrating deep knowledge of Myriad's liquid and tumor profiling portfolio, including biomarkers, targeted therapies, immuno-oncology, therapy selection pathways, tumor biology, and NGS‑based testing. Staying current on emerging clinical data, guidelines (NCCN, ASCO, ESMO), competitive trends, and evolving precision oncology treatment standards. Attending and representing Myriad at national and regional medical conferences for scientific engagement and insight reporting. Building and maintaining relationships with regional and national KOLs in oncology, molecular pathology, and related specialties. Contributing to the Somatic Medical Affairs team through collaboration, best‑practice sharing, and training. Continually advances and grows with market issues, trends, monitors the competitive landscape, and product knowledge specific to --- TITLE: Medical Science Liaison (Somatic Oncology - PA, DC, MA, NY, NJ, VA) EMPLOYER: Myriad Genetics INC LOCATION: Philadelphia, PA, United States (unspecified) SALARY: Not disclosed POSTED: 2026-03-26 PARENTAL_LEAVE_WEEKS: 2 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 2 (not source-backed) K401_MATCH: yes (not source-backed) APPLY_URL: https://ekgn.fa.us6.oraclecloud.com/hcmUI/CandidateExperience/en/sites/CX_2001/job/6005 EXCERPT: Medical Science Liaison (Somatic Oncology - PA, DC, MA, NY, NJ, VA) Philadelphia, PA, United States Geography: MA, NY, NJ, PA, NJ, DC, VA Description: Myriad Genetics is seeking a Medical Science Liaison (MSL) to support the Somatic / Tumor Genomics portfolio within the Precision Oncology business unit. This field based , scientifically focused role supports liquid and tumor profiling across solid tumors, including NGS based assays, biomarker driven therapy selection, resistance mechanisms, and treatment monitoring. The MSL will engage with medical oncologists, gynecologic oncologists, surgeons, molecular pathologists, urologists, academic centers, and community oncology practices. This individual will serve as a conduit of clinical expertise, scientific exchange, and insights that inform medical strategy. This position reports to the Director of Medical Affairs, Somatic , and partners closely with Medical Affairs colleagues, R&D, clinical operations, marketing, commercial teams (if role design includes sales support), and cross - functional leadership. Responsibilities: Maintain MSL Expertise through: Demonstrating deep knowledge of Myriad's liquid and tumor profiling portfolio, including biomarkers, targeted therapies, immuno-oncology, therapy selection pathways, tumor biology, and NGS ‑ based testing. Staying current on emerging clinical data, guidelines (NCCN, ASCO, ESMO), competitive trends, and evolving precision oncology treatment standards. Attending and representing Myriad at national and regional medical conferences for scientific engagement and insight reporting. Building and maintaining relationships with regional and national KOLs in oncology, molecular pathology, and related specialties. Contributing to the Somatic Medical Affairs team through collaboration, best ‑ practice sharing, and training. Continually advances and grows with market issues, --- TITLE: Strategic Planning & Operations Sr Director EMPLOYER: Myriad Genetics INC LOCATION: Salt Lake City, UT, United States (unspecified) SALARY: Not disclosed POSTED: 2026-04-08 PARENTAL_LEAVE_WEEKS: 2 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 2 (not source-backed) K401_MATCH: yes (not source-backed) APPLY_URL: https://ekgn.fa.us6.oraclecloud.com/hcmUI/CandidateExperience/en/sites/CX_2001/job/6061 EXCERPT: Strategic Planning & Operations Sr Director Salt Lake City, UT, United States Overview The Strategic Planning & Operations Sr Director is responsible for defining, leading, and operationalizing Myriad's long‑range strategic planning processes, including multi‑year road mapping, cross‑functional strategic alignment, and enterprise‑level decision governance. This role oversees the design and execution of the “Futures Of” strategic planning framework, working across Myriad's business units to ensure inputs, milestones, deliverables, and communication mechanisms are in place to support long‑term company strategy. Responsibility Strategic Planning Frameworks & Long‑Range Road mapping: Establish and manage Myriad's 5‑year project roadmap planning process, including templates, contributors, and check‑in timepoints. Own ongoing governance and follow‑up of long‑range plans, including decision documentation and tracking. Future Visioning Program Leadership: Lead and manage company‑wide strategic assessment cycles for future visioning, ensuring execution rhythm, content readiness, and milestone achievement. Cross‑Functional Leadership & Alignment: Establish and drive process to align functional team priorities to enterprise strategy and goals. Facilitate decision‑making processes requiring negotiation and influence across stakeholder groups including R&D, Operations, Commercial, Business Development, Digital, and Project Management. Operational Excellence & Strategic Governance: Establish and maintain planning and evaluation templates, workflows, dashboards, and communication processes. Prepare executive‑level strategic materials including board updates. Supporting executive operations and executive leadership team alignment. Qualifications Bachelor's degree in business, Life Sciences, Engineering, Data Science, or related field. 12+ years of increasing responsibility in strategy, planning, project management or consulting roles. Demonstrated ability to lead complex cross‑functional initiatives at enterprise scale. Exceptional communication (written and verbal) and executive‑level synthesis --- TITLE: Specimen Processor I EMPLOYER: Myriad Genetics INC LOCATION: Salt Lake City, UT, United States (unspecified) SALARY: Not disclosed POSTED: 2026-04-29 PARENTAL_LEAVE_WEEKS: 2 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 2 (not source-backed) K401_MATCH: yes (not source-backed) APPLY_URL: https://ekgn.fa.us6.oraclecloud.com/hcmUI/CandidateExperience/en/sites/CX_2001/job/6116 EXCERPT: Specimen Processor I Salt Lake City, UT, United States Overview A Specimen Processor I prepares and handles specimens received for testing. Specimen Processors will work with management and quality team members to ensure laboratory activities are defined, documented, and completed to support inspection readiness. They will also ensure compliance is maintained through procedures, training, and documentation. Shift: Tuesday-Friday 8:00am-4:30pm and Saturday 8:30am-5:00pm Pay: Starting at $18/hr, plus $3/hr on Saturday Responsibility Works under the direct supervision of an employee or supervisor who is trained and competent in all relative procedures and processes pertaining to accessioning as well as other assigned processes. Prepares and handles specimens for testing: Assigns specimens an internal tracking number (accession ID). Compares and verifies identifiers on specimens match test order. Ensures specimens are labeled appropriately. Communicates important information pertaining to testing. Looks for and documents problems with specimens. Scans, files, and electronically saves paperwork received with specimens. Files and temporary stores specimens until test release. Transports specimens to testing labs. Packages specimens for return, or external/internal lab send out. Performs other duties as assigned. Complies with and maintains competency in all assigned laboratory policies and procedures. Observes all compliance and regulatory requirements, particularly those associated to data security and patient confidentiality. Actively participates in and maintains accepted laboratory standards for continuing education. Maintains ethical standards in the performance of testing and in interactions with co-workers and other staff. Plays an active role within the team and helps to create a positive work environment. This includes participating --- TITLE: Sales Operations Manager - Prenatal EMPLOYER: Myriad Genetics INC LOCATION: United States (unspecified) SALARY: Not disclosed POSTED: 2026-04-21 PARENTAL_LEAVE_WEEKS: 2 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 2 (not source-backed) K401_MATCH: yes (not source-backed) APPLY_URL: https://ekgn.fa.us6.oraclecloud.com/hcmUI/CandidateExperience/en/sites/CX_2001/job/6055 EXCERPT: Sales Operations Manager - Prenatal United States Role Overview The Sales Operations Manager will serve as the primary operations partner for the Prenatal team, leading analytics, reporting, and data-driven insights that support commercial growth. This role requires strong analytical expertise, exceptional attention to detail, and the ability to manage multiple priorities in a fast-paced environment. In this role, you will support Prenatal leadership with performance reporting, identify opportunities to enhance data quality and automation, and build dashboards and workflows that enable more effective decision-making. You will collaborate closely with Data & Analytics, Sales Enablement, and cross-functional partners to ensure the Prenatal organization has reliable, actionable insights. Our ideal candidate embodies our cultural pillars-collaborative, innovative, inclusive, caring, and committed-and brings curiosity, initiative, and the ability to work seamlessly across teams to advance our commercial strategy. Key Responsibilities Serve as the primary Sales Operations partner for Prenatal Leadership, providing data-driven insights and operational support. Attend Prenatal leadership meetings to deliver performance updates, trends, and strategic analysis. Identify opportunities to enhance data, reporting, and analytics capabilities across the Prenatal organization. Access, analyze, and integrate data from multiple sources to support operational recommendations. Build, automate, and maintain reporting tools and dashboards using Salesforce (SFDC), Looker, and other technologies. Conduct ad hoc analysis to investigate business challenges, uncover growth opportunities, and support leadership decision-making. Evaluate initiative and program performance (volume, revenue, and adoption) and communicate insights that drive commercial strategy. Partner with the Data & Analytics team to ensure data quality, accuracy, and consistency across --- TITLE: Somatic Medical Science Liaison III - West US EMPLOYER: Myriad Genetics INC LOCATION: United States (unspecified) SALARY: Not disclosed POSTED: 2026-04-24 PARENTAL_LEAVE_WEEKS: 2 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 2 (not source-backed) K401_MATCH: yes (not source-backed) APPLY_URL: https://ekgn.fa.us6.oraclecloud.com/hcmUI/CandidateExperience/en/sites/CX_2001/job/6119 EXCERPT: Somatic Medical Science Liaison III - West US United States Please submit a cover letter with your application for this position Geography: Multiple positions available across the U.S. Territory size and geography may vary and will be assigned based on evolving business needs and the location of the selected candidate Description: Myriad Genetics is seeking an experienced Medical Science Liaison (MSL) to support the Somatic / Tumor Genomics portfolio within Myriad Genetics. This field-based, scientifically focused role supports liquid and tumor profiling across solid tumors, including MRD testing, NGS based assays, biomarker driven therapy selection, resistance mechanisms, and treatment monitoring. The MSL will engage with medical oncologists, gynecologic oncologists, surgeons, molecular pathologists, and urologists across academic centers, and community oncology practices. This individual will serve as a conduit of clinical expertise, scientific exchange, and insights that inform medical strategy. This position reports to the Director of Medical Affairs, Somatic, and partners closely with Medical Affairs colleagues, product, R&D, clinical operations, marketing, commercial teams, and cross-functional leadership. Responsibilities: Maintain MSL Expertise through: Demonstrating deep knowledge of Myriad's liquid and tumor profiling portfolio, including biomarkers, targeted therapies, immuno-oncology, therapy selection pathways, tumor biology, and NGS ‑ based testing. Staying current on emerging clinical data, guidelines (NCCN, ASCO, ESMO), competitive trends, and evolving precision oncology treatment standards. Attending and representing Myriad at national and regional medical conferences for scientific engagement and insight reporting. Building and maintaining relationships with regional and national KOLs in oncology, molecular pathology, and related specialties. Contributing to the Somatic --- TITLE: Sales Executive - Urology - NJ EMPLOYER: Myriad Genetics INC LOCATION: Trenton, NJ, United States (unspecified) SALARY: $182K-$207K POSTED: 2026-04-16 PARENTAL_LEAVE_WEEKS: 12 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 2 (not source-backed) K401_MATCH: yes (not source-backed) FERTILITY_FAMILY_BUILDING_BENEFITS: yes (not source-backed) MENTAL_HEALTH_SUPPORT: yes (not source-backed) CHILDCARE_SUBSIDY: yes (not source-backed) APPLY_URL: https://ekgn.fa.us6.oraclecloud.com/hcmUI/CandidateExperience/en/sites/CX_2001/job/6088 EXCERPT: Sales Executive - Urology - NJ Trenton, NJ, United States In 2026, we're advancing this vision with innovations like the Prolaris Test enhanced by PATHOMIQ AI technology, delivering unprecedented accuracy in predicting disease recurrence and metastasis using digital pathology images. Support the launch of next-generation diagnostic solutions, including the AI-enhanced Prolaris Prostate Cancer Test, designed to improve prognostic accuracy and personalize treatment strategies. Collaborate with cross-functional teams to drive adoption of innovative technologies, such as digital pathology and AI-driven analytics, that redefine standards in prostate cancer care. Myriad Urology is looking for an Account Executive who is passionate about improving the lives of patients with prostate cancer risk and/or diagnosis. As an Account Executive for Myriad Urology, you will focus on developing business for Myriad Urology, promoting Prolaris ® , MyRisk , and Precise to hospital systems, large Urology Group practices and private practices focused on Urologists and Radiation Oncologists. Please use this link to learn more about the product portfolio; Genetic Testing for Prostate Cancer Treatment | Myriad Genetics . Job Responsibilities and Competencies: Achieve Sales Targets Drive growth for Prolaris , MyRisk , and Precise by meeting or exceeding sales objectives. Develop and execute action plans to increase test orders and expand market share. Strategic Customer Engagement Focus efforts on urologists, urologic oncologists, pathologists, and radiation oncologists across community practices, large groups, and academic settings. Increase Access and Adoption Utilize an insightful selling model to educate providers, improve patient access to testing, and grow weekly order volumes. Promote --- TITLE: Part Time Specimen Processor I EMPLOYER: Myriad Genetics INC LOCATION: San Diego, CA, United States (unspecified) SALARY: Not disclosed POSTED: 2026-04-29 PARENTAL_LEAVE_WEEKS: 2 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 2 (not source-backed) K401_MATCH: yes (not source-backed) APPLY_URL: https://ekgn.fa.us6.oraclecloud.com/hcmUI/CandidateExperience/en/sites/CX_2001/job/6130 EXCERPT: Part Time Specimen Processor I San Diego, CA, United States Overview A Specimen Processor I prepares and handles specimens received for testing. Specimen Processors will work with management and quality team members to ensure laboratory activities are defined, documented, and completed to support inspection readiness. They will also ensure compliance is maintained through procedures, training, and documentation. Responsibility Works under the direct supervision of an employee or supervisor who is trained and competent in all relative procedures and processes pertaining to accessioning as well as other assigned processes. Prepares and handles specimens for testing: Assigns specimens an internal tracking number (accession ID). Compares and verifies identifiers on specimens match test order. Ensures specimens are labeled appropriately. Communicates important information pertaining to testing. Looks for and documents problems with specimens. Scans, files, and electronically saves paperwork received with specimens. Files and temporary stores specimens until test release. Transports specimens to testing labs. Packages specimens for return, or external/internal lab send out. Performs other duties as assigned. Complies with and maintains competency in all assigned laboratory policies and procedures. Observes all compliance and regulatory requirements, particularly those associated to data security and patient confidentiality. Actively participates in and maintains accepted laboratory standards for continuing education. Maintains ethical standards in the performance of testing and in interactions with co-workers and other staff. Plays an active role within the team and helps to create a positive work environment. This includes participating in team building events and communicating positively with others. Arrives to work on --- TITLE: Somatic Medical Science Liaison III - East US EMPLOYER: Myriad Genetics INC LOCATION: United States (unspecified) SALARY: Not disclosed POSTED: 2026-04-24 PARENTAL_LEAVE_WEEKS: 2 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 2 (not source-backed) K401_MATCH: yes (not source-backed) APPLY_URL: https://ekgn.fa.us6.oraclecloud.com/hcmUI/CandidateExperience/en/sites/CX_2001/job/6118 EXCERPT: Somatic Medical Science Liaison III - East US United States Please submit a cover letter with your application for this position Geography: Multiple positions available across the U.S. Territory size and geography may vary and will be assigned based on evolving business needs and the location of the selected candidate Description: Myriad Genetics is seeking an experienced Medical Science Liaison (MSL) to support the Somatic / Tumor Genomics portfolio within Myriad Genetics. This field-based, scientifically focused role supports liquid and tumor profiling across solid tumors, including MRD testing, NGS based assays, biomarker driven therapy selection, resistance mechanisms, and treatment monitoring. The MSL will engage with medical oncologists, gynecologic oncologists, surgeons, molecular pathologists, and urologists across academic centers, and community oncology practices. This individual will serve as a conduit of clinical expertise, scientific exchange, and insights that inform medical strategy. This position reports to the Director of Medical Affairs, Somatic, and partners closely with Medical Affairs colleagues, product, R&D, clinical operations, marketing, commercial teams, and cross-functional leadership. Responsibilities: Maintain MSL Expertise through: Demonstrating deep knowledge of Myriad's liquid and tumor profiling portfolio, including biomarkers, targeted therapies, immuno-oncology, therapy selection pathways, tumor biology, and NGS ‑ based testing. Staying current on emerging clinical data, guidelines (NCCN, ASCO, ESMO), competitive trends, and evolving precision oncology treatment standards. Attending and representing Myriad at national and regional medical conferences for scientific engagement and insight reporting. Building and maintaining relationships with regional and national KOLs in oncology, molecular pathology, and related specialties. Contributing to the Somatic --- TITLE: Lab Automation Engineer II EMPLOYER: Myriad Genetics INC LOCATION: Salt Lake City, UT, United States (unspecified) SALARY: Not disclosed POSTED: 2026-02-03 PARENTAL_LEAVE_WEEKS: 2 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 2 (not source-backed) K401_MATCH: yes (not source-backed) APPLY_URL: https://ekgn.fa.us6.oraclecloud.com/hcmUI/CandidateExperience/en/sites/CX_2001/job/5745 EXCERPT: Lab Automation Engineer II Salt Lake City, UT, United States Overview The Lab Automation Engineer II solves key workflow problems in large complex health systems. Supports a full technology stack of automated lab and software sequencing. Responsibility Design, implement, and test process automation using liquid handlers and other automated equipment. Utilize programming languages to integrate new or modifications to processes to the robotics software stack. Work cross-functionally with the science, lab, manufacturing, and maintenance teams. Design, deploy, and test liquid handler scripts and changes to custom automated work cells. Make impactful contributions to troubleshooting efforts, analyzing data and helping drive key process-related decisions. Develop automation related documentation for effective operation and maintenance of automated equipment. Travel to Myriad locations as needed during certain project phases. Qualifications Bachelor's degree in molecular biology, bioengineering, chemistry, or related field required. 2+ years of industry experience. Experience in programming in at least two of the major liquid handling systems (Tecan, Beckman, Hamilton). Experience with molecular biology lab processes. Software programming experience with Python, C#, or other languages is a plus. Applicant must be a (i) U.S. citizen or national, (ii) U.S. lawful, permanent resident (aka green card holder) Physical Requirements Lifting Requirements - light work or exerting up to 20 pounds of force frequently. Physical Requirements - stationary positioning, moving, operating, ascending/descending, communicating, observing, pushing or pulling, and reaching. Use of equipment and tools necessary to perform essential job functions. EEO We recognize that our people are our strength and the diverse talents they --- TITLE: Medical Science Liaison (Somatic Oncology - CA, OR, WA, MT) EMPLOYER: Myriad Genetics INC LOCATION: San Francisco, CA, United States (unspecified) SALARY: Not disclosed POSTED: 2026-03-26 PARENTAL_LEAVE_WEEKS: 2 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 2 (not source-backed) K401_MATCH: yes (not source-backed) APPLY_URL: https://ekgn.fa.us6.oraclecloud.com/hcmUI/CandidateExperience/en/sites/CX_2001/job/5991 EXCERPT: Medical Science Liaison (Somatic Oncology - CA, OR, WA, MT) San Francisco, CA, United States Geography: San Francisco, CA, Los Angeles, CA, San Diego, CA, Portland, OR, Seattle, WA, Boise, ID Description: Myriad Genetics is seeking a Medical Science Liaison (MSL) to support the Somatic / Tumor Genomics portfolio within the Precision Oncology business unit. This field based, scientifically focused role supports liquid and tumor profiling across solid tumors, including NGS based assays, biomarker driven therapy selection, resistance mechanisms, and treatment monitoring. The MSL will engage with medical oncologists, gynecologic oncologists, surgeons, molecular pathologists, urologists, academic centers, and community oncology practices. This individual will serve as a conduit of clinical expertise, scientific exchange, and insights that inform medical strategy. This position reports to the Director of Medical Affairs, Somatic , and partners closely with Medical Affairs colleagues, R&D, clinical operations, marketing, commercial teams (if role design includes sales support), and cross - functional leadership. Responsibilities: Maintain MSL Expertise through: Demonstrating deep knowledge of Myriad's liquid and tumor profiling portfolio, including biomarkers, targeted therapies, immuno-oncology, therapy selection pathways, tumor biology, and NGS‑based testing. Staying current on emerging clinical data, guidelines (NCCN, ASCO, ESMO), competitive trends, and evolving precision oncology treatment standards. Attending and representing Myriad at national and regional medical conferences for scientific engagement and insight reporting. Building and maintaining relationships with regional and national KOLs in oncology, molecular pathology, and related specialties. Contributing to the Somatic Medical Affairs team through collaboration, best‑practice sharing, and training. Continually advances and grows with --- TITLE: Medical Science Liaison (Somatic Oncology - TX) EMPLOYER: Myriad Genetics INC LOCATION: Dallas, TX, United States (unspecified) SALARY: Not disclosed POSTED: 2026-03-26 PARENTAL_LEAVE_WEEKS: 2 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 2 (not source-backed) K401_MATCH: yes (not source-backed) APPLY_URL: https://ekgn.fa.us6.oraclecloud.com/hcmUI/CandidateExperience/en/sites/CX_2001/job/5996 EXCERPT: Medical Science Liaison (Somatic Oncology - TX) Dallas, TX, United States Geography: TX, LA Description: Myriad Genetics is seeking a Medical Science Liaison (MSL) to support the Somatic / Tumor Genomics portfolio within the Precision Oncology business unit. This field based, scientifically focused role supports liquid and tumor profiling across solid tumors, including NGS based assays, biomarker driven therapy selection, resistance mechanisms, and treatment monitoring. The MSL will engage with medical oncologists, gynecologic oncologists, surgeons, molecular pathologists, urologists, academic centers, and community oncology practices. This individual will serve as a conduit of clinical expertise, scientific exchange, and insights that inform medical strategy. This position reports to the Director of Medical Affairs, Somatic , and partners closely with Medical Affairs colleagues, R&D, clinical operations, marketing, commercial teams (if role design includes sales support), and cross - functional leadership. Responsibilities: Maintain MSL Expertise through: Demonstrating deep knowledge of Myriad's liquid and tumor profiling portfolio, including biomarkers, targeted therapies, immuno-oncology, therapy selection pathways, tumor biology, and NGS‑based testing. Staying current on emerging clinical data, guidelines (NCCN, ASCO, ESMO), competitive trends, and evolving precision oncology treatment standards. Attending and representing Myriad at national and regional medical conferences for scientific engagement and insight reporting. Building and maintaining relationships with regional and national KOLs in oncology, molecular pathology, and related specialties. Contributing to the Somatic Medical Affairs team through collaboration, best‑practice sharing, and training. Continually advances and grows with market issues, trends, monitors the competitive landscape, and product knowledge specific to key therapeutic areas. Serves as --- TITLE: Sr Hardware Automation Engineer - South SF EMPLOYER: Myriad Genetics INC LOCATION: South San Francisco, CA, United States (onsite) SALARY: Not disclosed POSTED: 2026-02-25 PARENTAL_LEAVE_WEEKS: 2 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 2 (not source-backed) K401_MATCH: yes (not source-backed) APPLY_URL: https://ekgn.fa.us6.oraclecloud.com/hcmUI/CandidateExperience/en/sites/CX_2001/job/5839 EXCERPT: Sr Hardware Automation Engineer - South SF South San Francisco, CA, United States Overview The Sr Hardware Automation Engineer solves key workflow problems in large, complex health systems. Supports a full technology stack of automated lab and software sequencing. On-site South San Francisco Responsibility Applies principles, theories, and concepts from the broader industry to improve the Myriad platform. Own all aspects of the design process, prototyping, testing, and deployment for a fully automated robotic platform. Design layout, process, and custom components for a modular robotics platform by utilizing mechanical, electrical, and software expertise. Work with other development teams to integrate processes into custom robotic platform. Identify and drive process improvements to maximize the level of hands-free automation throughout the lab. Develop automation related documentation for effective operation and maintenance of automated equipment. Train and mentor junior Automation Engineers. Travel to Myriad locations as needed during certain project phases. Qualifications Bachelor's degree in mechanical, electrical, biomedical engineering, or related field required. 8+ years of experience with electro-mechanical design, assembly, wiring, and troubleshooting. 5+ years of experience integrating 3rd party devices (system integration). Experience with mechanical CAD software (SolidWorks, OnShape). Experience documenting designs (BOMs, drawings) and working with contract manufacturers. Proficiency with text-based PLC programming or Python and terminal usage. Demonstrated success in leading cross-functionally with multiple groups on projects. Physical Requirements Lifting Requirements - light work or exerting up to 20 pounds of force frequently. Physical Requirements - stationary positioning, moving, operating, ascending/descending, communicating, observing, pushing or pulling, and reaching. Use --- TITLE: Manager, Medical Science Liaison - Germline Oncology EMPLOYER: Myriad Genetics INC LOCATION: Salt Lake City, UT, United States (remote) SALARY: Not disclosed POSTED: 2026-05-01 PARENTAL_LEAVE_WEEKS: 2 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 2 (not source-backed) K401_MATCH: yes (not source-backed) APPLY_URL: https://ekgn.fa.us6.oraclecloud.com/hcmUI/CandidateExperience/en/sites/CX_2001/job/6132 EXCERPT: Manager, Medical Science Liaison - Germline Oncology Salt Lake City, UT, United States This is a US based remote position with some travel required Overview The Manager, Medical Science Liaisons (MSL) leads and develops a field-based Oncology Germline MSL team supporting Myriad's oncology portfolio with a focus on hereditary cancer testing. This role provides strategic and operational leadership within Medical Affairs to ensure effective execution of scientific priorities and alignment with organizational goals. The ideal candidate brings deep clinical and scientific expertise in oncology genetics, strong people leadership skills, and the ability to translate strategy into impactful field execution. Key Responsibilities People Leadership Lead, coach, and develop a high-performing team of Oncology Germline MSLs, including performance management, hiring, onboarding, and scientific training. Medical Affairs Strategy Execute Medical Affairs Oncology Germline strategy through effective field leadership and alignment with Medical Affairs leadership. Contribute to SOP development and performance metrics to drive consistency and impact. Scientific & Clinical Leadership Provide scientific, clinical, and business leadership in hereditary cancer genetic testing and oncology care, staying current on guidelines, literature, and market trends. Oversee development, review, and approval of medical content. Deliver and support high-quality scientific and clinical presentations to healthcare professionals. External Engagement Support identification and engagement of regional and national KOLs and represent Myriad at medical congresses and scientific meetings. Manage intake and coordination of research and evidence-generation requests through appropriate Medical Affairs channels. Compliance & Collaboration Ensure all field activities comply with corporate policies and healthcare regulations. Partner effectively with cross-functional --- TITLE: Medical Science Liaison (Somatic Oncology- FL) EMPLOYER: Myriad Genetics INC LOCATION: Jacksonville, FL, United States (unspecified) SALARY: Not disclosed POSTED: 2026-03-26 PARENTAL_LEAVE_WEEKS: 2 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 2 (not source-backed) K401_MATCH: yes (not source-backed) APPLY_URL: https://ekgn.fa.us6.oraclecloud.com/hcmUI/CandidateExperience/en/sites/CX_2001/job/5997 EXCERPT: Medical Science Liaison (Somatic Oncology- FL) Jacksonville, FL, United States Geography: FL Description: Myriad Genetics is seeking a Medical Science Liaison (MSL) to support the Somatic / Tumor Genomics portfolio within the Precision Oncology business unit. This field based , scientifically focused role supports liquid and tumor profiling across solid tumors, including NGS based assays, biomarker driven therapy selection, resistance mechanisms, and treatment monitoring. The MSL will engage with medical oncologists, gynecologic oncologists, surgeons, molecular pathologists, urologists, academic centers, and community oncology practices. This individual will serve as a conduit of clinical expertise, scientific exchange, and insights that inform medical strategy. This position reports to the Director of Medical Affairs, Somatic , and partners closely with Medical Affairs colleagues, R&D, clinical operations, marketing, commercial teams (if role design includes sales support), and cross - functional leadership. Responsibilities: Maintain MSL Expertise through: Demonstrating deep knowledge of Myriad's liquid and tumor profiling portfolio, including biomarkers, targeted therapies, immuno-oncology, therapy selection pathways, tumor biology, and NGS ‑ based testing. Staying current on emerging clinical data, guidelines (NCCN, ASCO, ESMO), competitive trends, and evolving precision oncology treatment standards. Attending and representing Myriad at national and regional medical conferences for scientific engagement and insight reporting. Building and maintaining relationships with regional and national KOLs in oncology, molecular pathology, and related specialties. Contributing to the Somatic Medical Affairs team through collaboration, best ‑ practice sharing, and training. Continually advances and grows with market issues, trends, monitors the competitive landscape, and product knowledge specific to key therapeutic --- TITLE: Medical Science Liaison (Family Health), Multiple US Territories EMPLOYER: Myriad Genetics INC LOCATION: United States (remote) SALARY: Not disclosed POSTED: 2026-05-05 PARENTAL_LEAVE_WEEKS: 2 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 2 (not source-backed) K401_MATCH: yes (not source-backed) APPLY_URL: https://ekgn.fa.us6.oraclecloud.com/hcmUI/CandidateExperience/en/sites/CX_2001/job/6149 EXCERPT: Medical Science Liaison (Family Health), Multiple US Territories United States Category: Medical/Health Location/City: Remote Base: We are hiring for three Medical Science Liaison's (MSL) position in the following territories: Northeast, Mid-Atlantic, and Southeast Open territories (may change depending on where employee is hired): Northeast: Pittsburgh, PA; Hartford, CT; Yonkers, NY Mid-Atlantic: Richmond/Virginia Beach/Arlington, VA; Washington, DC; Lexington/Louisville, KY Southeast: Chattanooga/Nashville/Knoxville, TN; Birmingham, AL; Savannah/Macon, GA Description Myriad Genetics is seeking 3 qualified individuals to fill the role of MSL within the Family Health (FH) Medical Affairs channel in three separate geographic areas. The commercial MSL position is a field- based scientific and clinical expert role. The commercial MSL is a critical partner to the Myriad Prenatal and Hereditary Cancer Screening Sales teams and supports and initiates strategic clinical education to clients. The ideal candidate will possess a unique blend of clinical expertise, strong business acumen, and market awareness. MSLs play a pivotal role in communicating Myriad's scientific advancements to healthcare professionals and key opinion leaders (KOLs) in alignment with the department-wide KOL strategy. MSLs collaborate with other functional groups, including Marketing, Product, Payer Markets, Training, and others. The successful candidate will join Myriad's Medical Affairs team and will report to an FH MSL Manager who reports to the FH Medical Affairs Director. This position will require regular travel (up to 40%) with a quarterly average of 2 days of travel per week within the aligned territory. Though most of the travel is within the assigned geography, there will be occasional --- TITLE: Sr Sales Executive - ONC -Ft Lauderdale, Fl EMPLOYER: Myriad Genetics INC LOCATION: Fort Lauderdale, FL, United States (unspecified) SALARY: $200K-$226K POSTED: 2026-04-27 PARENTAL_LEAVE_WEEKS: 12 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 2 (not source-backed) K401_MATCH: yes (not source-backed) FERTILITY_FAMILY_BUILDING_BENEFITS: yes (not source-backed) MENTAL_HEALTH_SUPPORT: yes (not source-backed) CHILDCARE_SUBSIDY: yes (not source-backed) APPLY_URL: https://ekgn.fa.us6.oraclecloud.com/hcmUI/CandidateExperience/en/sites/CX_2001/job/6114 EXCERPT: Sr Sales Executive - ONC -Ft Lauderdale, Fl Fort Lauderdale, FL, United States Overview Myriad Genetics is seeking top-tier sales talent who are passionate about improving patients' lives through precision medicine. As an Oncology SR Sales Executive, you drive adoption of Myriad's full oncology portfolio, securing new oncology business while supporting existing accounts in a high-impact territory. This is more than just a sales role-it's an opportunity to be at the forefront of innovation in cancer diagnostics. You'll represent Myriad's industry-leading oncology portfolio, including hereditary cancer testing, tumor profiling, and companion diagnostics. You will practice a consultative approach, educating healthcare providers on the clinical utility of our germline and genomic tests, how to integrate them into patient care pathways, and leverage insights for better informed treatment decisions. At Myriad, our culture is defined by putting patients and people first-and we're looking for someone who shares that commitment. · Note: This is a field-based sales position. Candidates must reside within the territory and be able to travel locally daily to meet with healthcare providers and stakeholders. Regular in-person engagement is essential to the success of this role. Responsibilities · Sales Execution · Manage full lifecycle of the product sales process, including new business development and lead-generation via programs and other initiatives · Apply a consultative approach to identify customer needs, present solutions, and close business · Account Development · Build and maintain strong relationships with key oncology accounts, including community practices, academic centers, and integrated delivery networks · Identify, develop, and --- TITLE: Sales Executive - Hereditary Cancer Screening - Dayton, OH EMPLOYER: Myriad Genetics INC LOCATION: Dayton, OH, United States (unspecified) SALARY: $180K-$205K POSTED: 2026-03-31 PARENTAL_LEAVE_WEEKS: 12 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 2 (not source-backed) K401_MATCH: yes (not source-backed) FERTILITY_FAMILY_BUILDING_BENEFITS: yes (not source-backed) MENTAL_HEALTH_SUPPORT: yes (not source-backed) CHILDCARE_SUBSIDY: yes (not source-backed) APPLY_URL: https://ekgn.fa.us6.oraclecloud.com/hcmUI/CandidateExperience/en/sites/CX_2001/job/6022 EXCERPT: Sales Executive - Hereditary Cancer Screening - Dayton, OH Dayton, OH, United States Myriad Genetics is seeking top-tier sales talent who are passionate about improving patients' lives through genetic and genomic testing and precision medicine. As a Hereditary Cancer Screening Sales Executive , you will drive adoption of MyRisk, securing new MyRisk business while supporting existing accounts in a high-impact territory. This is more than just a sales role-it's an opportunity to be at the forefront of innovation in hereditary cancer screening and drive previvorship. You will practice a consultative approach, educating healthcare providers on the clinical utility of our hereditary cancer screen and insights, how to integrate them into patient care pathways, and leverage insights for better informed healthcare decisions. At Myriad, our culture is defined by putting patients and people first-and we're looking for someone who shares that commitment. Note: This is a field-based sales position. Candidates must reside within the territory and be able to travel locally daily to meet with healthcare providers and stakeholders. Regular in-person engagement is essential to the success of this role. Responsibilities Sales Execution Manage full lifecycle of the product sales process, including new business development and lead-generation via programs and other initiatives Apply a consultative approach to identify customer needs, present solutions, and close business Account Development Build and maintain strong relationships with key OB/GYN, Primary Care, Internal Medicine and other clinicians, including community practices, academic centers, and integrated delivery networks Identify, develop, and manage commercial relationships with key opinion leaders --- TITLE: Meeting Coordinator EMPLOYER: Myriad Genetics INC LOCATION: Salt Lake City, UT, United States (unspecified) SALARY: Not disclosed POSTED: 2026-04-01 PARENTAL_LEAVE_WEEKS: 2 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 2 (not source-backed) K401_MATCH: yes (not source-backed) MENTAL_HEALTH_SUPPORT: yes (not source-backed) APPLY_URL: https://ekgn.fa.us6.oraclecloud.com/hcmUI/CandidateExperience/en/sites/CX_2001/job/5966 EXCERPT: Meeting Coordinator Salt Lake City, UT, United States Overview The Event Planner will be part of the Enterprise Marketing Team, reporting to the Senior Events Manager. The role is based out of the Salt Lake City Myriad offices this role plays a critical administrative and operational support function for the Events team, with a primary focus on internal meetings and behind-the-scenes execution that enables internal meetings, conferences and trade shows to run seamlessly. This position is ideal for a highly organized, detail-oriented professional who excels at managing paperwork, logistics, and coordination, and who takes pride in delivering white-glove support to senior leaders and internal partners. While this is a support-oriented role, it offers meaningful exposure to enterprise-level events and the opportunity to grow within a best-in-class corporate events function. Responsibilities Provide core administrative and operational support for internal onsite meetings, conferences and trade shows, including managing documentation, contracts, approvals, and internal coordination with vendors, venues, and partners to keep events on track and compliant. Deliver white-glove support that elevates the execution of internal meetings and events, anticipating needs and ensuring a polished, professional experience for attendees and stakeholders. Coordinate all logistical aspects of internal meetings, including communications, speaker coordination, registration, hotel and transportation arrangements, meals and menus, giveaways, and gifts. Support the full event lifecycle for internal meetings-from pre-planning and resource coordination to onsite execution and post-event follow-up-ensuring timelines, details, and deliverables are met. Manage the tabletop program and inventory for regional and local meetings, including scheduling, shipping, receiving, storage, --- TITLE: Patient Advocate - Hereditary Cancer (Remote) **Call Center Experience Preferred** EMPLOYER: Myriad Genetics INC LOCATION: Salt Lake City, UT, United States (remote) SALARY: Not disclosed POSTED: 2026-04-28 PARENTAL_LEAVE_WEEKS: 2 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 2 (not source-backed) K401_MATCH: yes (not source-backed) HIRE_STATES: UT APPLY_URL: https://ekgn.fa.us6.oraclecloud.com/hcmUI/CandidateExperience/en/sites/CX_2001/job/6126 EXCERPT: Patient Advocate - Hereditary Cancer (Remote) **Call Center Experience Preferred** Salt Lake City, UT, United States Overview The Patient Advocate will be on the front lines and will act as the face of the organization for our customers including clinics, physicians, medical staff, and patients. The Patient Advocate will handle a variety of complex inbound and outbound inquiries to assist and empathize with our customers. Responsibility Responsible for coordinating testing services for patients by: Reviewing test request forms and additional documentation submitted with a patient specimen to ensure accurate and timely testing. Working with healthcare providers to complete the required documentation and sample submission. Confirming insurance eligibility and benefit levels. Communicating with patients to explain insurance coverage benefits and test information including process and turnaround time. Employee will be on the phone approximately 60-80% of the time. Independently manage assigned work and meet production and quality metrics. Be the hub across all departments: work with the technology, revenue cycle, field sales, and lab teams on prompt handling of orders and billing processes. Identify issues and trends and collaborate with your team and leadership to develop best practices to ensure we are providing the best service and experience to all customers. Participate in the Quality Assurance plan. Comply with applicable CLIA and HIPAA regulations. Qualifications High School diploma or equivalent required with at least 1 year of relevant experience, or associate or bachelor's degree. Fluent in Spanish is preferred/encouraged. Excellent interpersonal and communication skills. Preference given to higher net typing speed --- TITLE: Part Time Patient Advocate - Hereditary Cancer (Remote) **Call Center Experience Preferred** EMPLOYER: Myriad Genetics INC LOCATION: Salt Lake City, UT, United States (remote) SALARY: Not disclosed POSTED: 2026-05-05 PARENTAL_LEAVE_WEEKS: 2 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 2 (not source-backed) K401_MATCH: yes (not source-backed) HIRE_STATES: UT APPLY_URL: https://ekgn.fa.us6.oraclecloud.com/hcmUI/CandidateExperience/en/sites/CX_2001/job/6153 EXCERPT: Part Time Patient Advocate - Hereditary Cancer (Remote) **Call Center Experience Preferred** Salt Lake City, UT, United States Overview The Patient Advocate will be on the front lines and will act as the face of the organization for our customers including clinics, physicians, medical staff, and patients. The Patient Advocate will handle a variety of complex inbound and outbound inquiries to assist and empathize with our customers. Responsibility Responsible for coordinating testing services for patients by: Reviewing test request forms and additional documentation submitted with a patient specimen to ensure accurate and timely testing. Working with healthcare providers to complete the required documentation and sample submission. Confirming insurance eligibility and benefit levels. Communicating with patients to explain insurance coverage benefits and test information including process and turnaround time. Employee will be on the phone approximately 60-80% of the time. Independently manage assigned work and meet production and quality metrics. Be the hub across all departments: work with the technology, revenue cycle, field sales, and lab teams on prompt handling of orders and billing processes. Identify issues and trends and collaborate with your team and leadership to develop best practices to ensure we are providing the best service and experience to all customers. Participate in the Quality Assurance plan. Comply with applicable CLIA and HIPAA regulations. Qualifications High School diploma or equivalent required with at least 1 year of relevant experience, or associate or bachelor's degree. Fluent in Spanish is preferred/encouraged. Excellent interpersonal and communication skills. Preference given to higher net --- TITLE: Mgr Sales - Prenatal Testing - Central US EMPLOYER: Myriad Genetics INC LOCATION: Chicago, IL, United States (unspecified) SALARY: Not disclosed POSTED: 2026-03-17 PARENTAL_LEAVE_WEEKS: 2 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 2 (not source-backed) K401_MATCH: yes (not source-backed) APPLY_URL: https://ekgn.fa.us6.oraclecloud.com/hcmUI/CandidateExperience/en/sites/CX_2001/job/5938 EXCERPT: Mgr Sales - Prenatal Testing - Central US Chicago, IL, United States The Area Sales Manager will be responsible for generating sales strategy and implementation of tactics to achieve financial targets. This individual must have a strategic mind with solid tactical execution. The Area Sales Manager will be responsible for: Business Planning Work to develop a full understanding of the content and then execute the area business plan to achieve the fulfillment of plan objectives/requirements. Execute area level account targeting strategy to fulfill targeting strategy requirements. Manage customer needs assessment. Manage critical relationships and set account relationship development objectives staff. Monitor area strategy effectiveness. Ensure performance requirements are met. Administration Review and audit expense reports in a timely manner. Evaluate appropriate use of resources to ensure attainment of profitability goals. Ensure timely and accurate submission of administrative requirements. Monitor and reinforce the use of the Customer Relationship Management (“CRM”) and Salesforce.com. People Development / Management Ensure that all reporting personnel have Field Rides and Coaching Reports (completed within 72hrs) a minimum of 2x per Quarter. Align reporting personnel's annual goals and measurements to be consistent with the priorities of the business. Execute a cadence of interim reviews to ensure reporting personnel's work is focused on key priorities and create accountability for results and the measurement process. Ensure that development and training plans are in place for all reporting personnel to enable the achievement of personal and professional goals to assume increased levels of responsibility. Requirements: At least 10 years of --- TITLE: Lab Technologist I (Day Shift) EMPLOYER: Myriad Genetics INC LOCATION: Mason, OH, United States (unspecified) SALARY: Not disclosed POSTED: 2026-04-22 PARENTAL_LEAVE_WEEKS: 2 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 2 (not source-backed) K401_MATCH: yes (not source-backed) APPLY_URL: https://ekgn.fa.us6.oraclecloud.com/hcmUI/CandidateExperience/en/sites/CX_2001/job/6090 EXCERPT: Lab Technologist I (Day Shift) Mason, OH, United States Overview The Lab Technologist I is responsible for conducting laboratory processes that support specimen processing and testing. This position works with department management and quality team members to ensure that laboratory activities are defined, documented, and completed to support inspection readiness and that compliance is maintained through procedures, training, and documentation. Shift: Monday-Friday 8:30am-5:00pm Pay: Starting at $22/hr Responsibility Each employee's specific job responsibilities are uniquely defined by their individual training plan and assigned duties, but are generally defined as follows: Complying with the laboratory's technical, administrative and safety policies, and procedures. Operating high complexity testing. Participating in the laboratory's quality assurance plan, adhering to quality control and preventive maintenance policies, and appropriately documenting these activities. Working as part of a team to produce repeatable quality results. Maintaining a clean and organized laboratory space. Participating in proficiency testing in the same manner as routine samples. Participating in continuing education according to accepted laboratory standards. Actively participating in successful and timely completion of training and competency assessment as outlined in the laboratory and departmental training programs. Qualifications Doctoral, bachelor's, or master's degree in medical technology or a chemical, physical, biological, or clinical laboratory science. California only: CLS trainee license or a CLS or CGMBS license issued by California. Ability to adapt to changes in a fast-paced and evolving work environment. Some schedule flexibility- occasional overtime hours may be required. Basic proficiency with computers (Excel, other Office tools) and statistics. Strong verbal and --- TITLE: Lab Technologist II - MRD (Day Shift) EMPLOYER: Myriad Genetics INC LOCATION: Salt Lake City, UT, United States (unspecified) SALARY: Not disclosed POSTED: 2026-04-30 PARENTAL_LEAVE_WEEKS: 2 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 2 (not source-backed) K401_MATCH: yes (not source-backed) APPLY_URL: https://ekgn.fa.us6.oraclecloud.com/hcmUI/CandidateExperience/en/sites/CX_2001/job/5898 EXCERPT: Lab Technologist II - MRD (Day Shift) Salt Lake City, UT, United States Overview The Lab Technologist II is responsible for conducting laboratory processes that support specimen processing and testing. This position works with department management and quality team members to ensure that laboratory activities are defined, documented, and completed to support inspection readiness and that compliance is maintained through procedures, training, documentation, and continuous improvement projects. Shift: Thursday-Sunday 8:00am-6:00pm Responsibility Each employee's specific job responsibilities are uniquely defined by their individual training plan and assigned duties, but are generally defined as follows: Complying with the laboratory's technical, administrative, and safety policies and procedures. Operating high complexity testing. Participating in the laboratory's quality assurance plan, adhering to quality control and preventive maintenance policies, and appropriately documenting these activities. Working as part of a team to produce repeatable quality results. Maintaining a clean and organized laboratory space. Participating in proficiency testing in the same manner as routine samples. Participating in continuing education according to accepted laboratory standards. Actively participating in successful and timely completion of training and competency assessment as outlined in the laboratory and departmental training programs. Following the laboratory's policies and procedures whenever test systems are not within acceptable limits and documenting the problem and any corrective action. Troubleshooting and identifying problems that may adversely affect test performance and/or reporting of test results by initiating corrective action and using the defined electronic system to make the required management notification. Participates within the departmental team to resolve problems or implement --- TITLE: Sr Commercial Sales Enablement and Training Manager EMPLOYER: Myriad Genetics INC LOCATION: United States (unspecified) SALARY: Not disclosed POSTED: 2026-04-08 PARENTAL_LEAVE_WEEKS: 2 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 2 (not source-backed) K401_MATCH: yes (not source-backed) APPLY_URL: https://ekgn.fa.us6.oraclecloud.com/hcmUI/CandidateExperience/en/sites/CX_2001/job/6042 EXCERPT: Sr Commercial Sales Enablement and Training Manager United States Role Overview The Sr. Commercial Sales Enablement Manager serves as the primary enablement and training partner for the Strategic Accounts team. This role supports digital product integrations-including EHR connections, screening protocols, and strategic partnerships-by building operational workflows, defining CRM (Salesforce) processes, and delivering targeted training for new hires and field teams. You will collaborate closely with Product, Technology, and Commercial teams to launch digital health solutions, manage deployment timelines, and create training content that drives adoption of digital tools and workflows. Success in this role requires strategic thinking, strong leadership, and the ability to execute effectively across functions. Our ideal candidate embodies our cultural pillars-collaborative, innovative, inclusive, caring, and committed-and brings curiosity, proactivity, and a passion for shaping the future of our digital health offerings. Key Responsibilities Serve as the primary sales enablement partner for the Strategic Accounts team, leading new-hire training and ensuring alignment of digital tools, processes, and resources. Deliver commercial team training focused on digital solutions, partnership workflows, and cross‑functional operational processes. Define, document, and maintain Salesforce (SFDC) workflows that support digital integrations, partnership programs, and account-level execution. Build and implement operational processes that enable scalable adoption of digital partnerships and integration initiatives across commercial teams. Collaborate with Training and Commercial Enablement to develop training strategies and content related to Myriad's digital health solutions for field sales teams. Create cross‑functional resources-such as FAQs, user guides, and quick‑reference materials-to support Strategic Accounts and broader sales teams. Qualifications Bachelor's degree --- TITLE: Sr. Director, Digital Clinical Experience EMPLOYER: Myriad Genetics INC LOCATION: United States (unspecified) SALARY: Not disclosed POSTED: 2026-04-02 PARENTAL_LEAVE_WEEKS: 2 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 2 (not source-backed) K401_MATCH: yes (not source-backed) APPLY_URL: https://ekgn.fa.us6.oraclecloud.com/hcmUI/CandidateExperience/en/sites/CX_2001/job/6038 EXCERPT: Sr. Director, Digital Clinical Experience United States Sr. Director, Digital Clinical Experience The Sr. Director, Product Customer Experience leads and advances the organization's platforms that support the full care journey across medical clinics, physician practices, and hospital systems. This role oversees patient and provider portal ecosystems, clinical system integrations (including EMR/EHR), and guides a cross‑functional UX team. They are responsible for ensuring that digital tools deliver seamless, intuitive, and highly impactful experiences for clinicians, staff, and patients in real-world care settings. This leader partners closely with Clinical Operations, IT, Product, Compliance, and Physician Leadership to translate clinical workflows and user needs into digital solutions that improve efficiency, access, and patient outcomes at scale. Responsibilities Digital Strategy & Leadership Develop and evolve the digital vision, roadmap, and execution plan for patient and provider experiences across clinics, practices, and hospital departments. Ensure digital initiatives support care delivery goals, regulatory requirements, and clinical usability standards. Serve as a champion for user-centered clinical design, accessibility, and workflow optimization. Align customer experience strategy with organizational goals around patient engagement, clinician efficiency, operational performance, and quality-of-care outcomes. Product & Platform Ownership Lead the development and enhancement of paper and digital portals for patients, clinicians, and administrative staff-ensuring secure, intuitive, and role‑appropriate access to clinical information, results, scheduling, and communication tools. Drive EMR/EHR integration strategy to support frictionless workflows, order management, result routing, interoperability, and clinical documentation needs. Collaborate with product, engineering, and clinical IT teams to ensure platform scalability, reliability, and regulatory compliance. Ensure all ordering --- TITLE: Scientist II - R&D - SLC Utah EMPLOYER: Myriad Genetics INC LOCATION: Salt Lake City, UT, United States (unspecified) SALARY: Not disclosed POSTED: 2026-03-05 PARENTAL_LEAVE_WEEKS: 2 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 2 (not source-backed) K401_MATCH: yes (not source-backed) APPLY_URL: https://ekgn.fa.us6.oraclecloud.com/hcmUI/CandidateExperience/en/sites/CX_2001/job/5901 EXCERPT: Scientist II - R&D - SLC Utah Salt Lake City, UT, United States Overview Research and Development Scientist II - SLC Scientist II independently designs and optimizes molecular assays, contributes to research projects, and mentors research associates. They collaborate with cross-functional teams to integrate molecular biology workflows with automated systems. Responsibility Perform the experimental design, execution, data collection and data analysis of molecular assays that utilize next generation sequencing (NGS) and other methodologies for analyzing DNA and RNA. Conduct experimental research to validate and improve existing methodologies and protocols. Analyze and interpret complex experimental data, presenting findings to internal teams. Collaborate with operations, bioinformatics, robotics, and software teams on project integration. Mentor and provide technical guidance to research associates. Ensure good documentation practices for assay development, validation, quality assurance, technical investigations and operational support of molecular diagnostic tests in a highly regulated clinical laboratory environment. Qualifications Must meet one of the following education and experience requirements: B.S. with 8+ years of industry experience in chemical, physical, biological, or clinical laboratory science. M.S. with 6+ years of industry experience in chemical, physical, biological, or clinical laboratory science. Ph.D. with 2+ years of industry experience in chemical, physical, biological, or clinical laboratory science. Proficiency in molecular biology techniques that include DNA and RNA extraction, Next Generation Sequencing laboratory workflows, and informatics analysis. Strong problem-solving and troubleshooting abilities. Excellent communication and interpersonal skills. Detail oriented with strong organizational skills. Experience with lab automation preferred. Physical Requirements Lifting Requirements - light work or exerting --- TITLE: Mental Health Customer Service Representative (Remote) EMPLOYER: Myriad Genetics INC LOCATION: Mason, OH, United States (remote) SALARY: Not disclosed POSTED: 2026-05-01 PARENTAL_LEAVE_WEEKS: 2 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 2 (not source-backed) K401_MATCH: yes (not source-backed) HIRE_STATES: OH APPLY_URL: https://ekgn.fa.us6.oraclecloud.com/hcmUI/CandidateExperience/en/sites/CX_2001/job/6060 EXCERPT: Mental Health Customer Service Representative (Remote) Mason, OH, United States Overview The Patient Advocate will be on the front lines and will act as the face of the organization for our customers including clinics, physicians, medical staff, and patients. The Patient Advocate will handle a variety of complex inbound and outbound inquiries to assist and empathize with our customers. Responsibility Responsible for coordinating testing services for patients by: Reviewing test request forms and additional documentation submitted with a patient specimen to ensure accurate and timely testing. Working with healthcare providers to complete the required documentation and sample submission. Confirming insurance eligibility and benefit levels. Communicating with patients to explain insurance coverage benefits and test information including process and turnaround time. Employee will be on the phone approximately 60-80% of the time. Independently manage assigned work and meet production and quality metrics. Be the hub across all departments: work with the technology, revenue cycle, field sales, and lab teams on prompt handling of orders and billing processes. Identify issues and trends and collaborate with your team and leadership to develop best practices to ensure we are providing the best service and experience to all customers. Participate in the Quality Assurance plan. Comply with applicable CLIA and HIPAA regulations. Qualifications High School diploma or equivalent required with at least 1 year of relevant experience, or associate or bachelor's degree. Fluent in Spanish is preferred/encouraged. Excellent interpersonal and communication skills. Preference given to higher net typing speed applicants . Excellent listening, transcribing, and --- TITLE: Hardware Automation Engineer III- Onsite South SF EMPLOYER: Myriad Genetics INC LOCATION: South San Francisco, CA, United States (onsite) SALARY: $125K-$153K POSTED: 2026-04-15 PARENTAL_LEAVE_WEEKS: 2 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 2 (not source-backed) K401_MATCH: yes (not source-backed) APPLY_URL: https://ekgn.fa.us6.oraclecloud.com/hcmUI/CandidateExperience/en/sites/CX_2001/job/6070 EXCERPT: Hardware Automation Engineer III- Onsite South SF South San Francisco, CA, United States Overview The Hardware Automation Engineer III solves key workflow problems in large complex health systems. Supports a full technology stack of automated lab and software sequencing. Responsibility Own all aspects of the design process, prototyping, testing, and deployment for fully automated robotic platform. Design layout, process, and custom components for a modular robotics platform by utilizing mechanical, electrical, and software expertise. Work with other development teams to integrate processes into custom robotic platform. Drive process improvements to maximize the level of hands-free automation throughout the lab. Develop automation related documentation for effective operation and maintenance of automated equipment. Train and mentor junior Automation Engineers. Travel to Myriad locations as needed during certain project phases. Qualifications Bachelor's degree in mechanical, electrical, biomedical engineering, or related field required. 5+ years of experience with electro-mechanical design, assembly, wiring, and troubleshooting. 2+ years of experience integrating 3rd party devices (system integration). Experience with mechanical CAD software (SolidWorks, OnShape). Experience documenting designs (BOMs, drawings) and working with contract manufacturers. Experience with text-based PLC programming or Python and terminal usage. Experience working cross-functionally with multiple groups on projects. For Bay Area candidates, compensation starts at $125,000 with a market-aligned midpoint of $153,000, plus RSUs and a generous performance-based bonus plan. Physical Requirements Lifting Requirements - light work or exerting up to 20 pounds of force frequently. Physical Requirements - stationary positioning, moving, operating, ascending/descending, communicating, observing, pushing or pulling, and reaching. Use of --- TITLE: Lab Technologist I - Clean Lab (Day Shift) EMPLOYER: Myriad Genetics INC LOCATION: Salt Lake City, UT, United States (unspecified) SALARY: Not disclosed POSTED: 2026-04-13 PARENTAL_LEAVE_WEEKS: 2 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 2 (not source-backed) K401_MATCH: yes (not source-backed) APPLY_URL: https://ekgn.fa.us6.oraclecloud.com/hcmUI/CandidateExperience/en/sites/CX_2001/job/6071 EXCERPT: Lab Technologist I - Clean Lab (Day Shift) Salt Lake City, UT, United States Overview The Lab Technologist I is responsible for conducting laboratory processes that support specimen processing and testing. This position works with department management and quality team members to ensure that laboratory activities are defined, documented, and completed to support inspection readiness and that compliance is maintained through procedures, training, and documentation. Shift: Thursday, Friday, Saturday 6:00am-6:30pm Pay: $22/hr, plus $3/hr on Saturday Responsibility Each employee's specific job responsibilities are uniquely defined by their individual training plan and assigned duties, but are generally defined as follows: Complying with the laboratory's technical, administrative and safety policies, and procedures. Operating high complexity testing. Participating in the laboratory's quality assurance plan, adhering to quality control and preventive maintenance policies, and appropriately documenting these activities. Working as part of a team to produce repeatable quality results. Maintaining a clean and organized laboratory space. Participating in proficiency testing in the same manner as routine samples. Participating in continuing education according to accepted laboratory standards. Actively participating in successful and timely completion of training and competency assessment as outlined in the laboratory and departmental training programs. Qualifications Doctoral, bachelor's, or master's degree in medical technology or a chemical, physical, biological, or clinical laboratory science. California only: CLS trainee license or a CLS or CGMBS license issued by California. Ability to adapt to changes in a fast-paced and evolving work environment. Some schedule flexibility- occasional overtime hours may be required. Basic proficiency with computers --- TITLE: Supv Histopathology EMPLOYER: Myriad Genetics INC LOCATION: Salt Lake City, UT, United States (unspecified) SALARY: Not disclosed POSTED: 2026-04-28 PARENTAL_LEAVE_WEEKS: 2 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 2 (not source-backed) K401_MATCH: yes (not source-backed) APPLY_URL: https://ekgn.fa.us6.oraclecloud.com/hcmUI/CandidateExperience/en/sites/CX_2001/job/6123 EXCERPT: Supv Histopathology Salt Lake City, UT, United States Overview The Supv Histopathology is responsible for the day-to-day supervision of the histopathology laboratory. The lab performs various techniques involved in the preparation of tissue specimens for examination by the pathologist and subsequent molecular genetic testing. Responsibilities may include sample accessioning, re-embedding, microtomy, hematoxylin and eosin (H&E) staining, immunohistochemical (IHC) staining, macrodissection of tumor tissue and digital pathology. In addition, they will be involved with training as part of the Histotechnology OTJ training program, quality control, and maintenance of laboratory equipment. The Supervisor will be under the general direction of the Laboratory Manager and/or Director of Laboratory Operations. The Supervisor shall be on the laboratory premises during all hours in which laboratory procedures are performed or be available by telephone or electronic means. Responsibility Ensuring laboratory compliance with all laboratory procedures including administrative, and safety policies. Development and implementation of departmental procedures in accordance with the laboratory's policies and procedures. Ensuring participation of all department personnel in the laboratory's quality assurance plan, adhering to quality control and preventive maintenance policies, and appropriately documenting these activities. Being available to laboratory personnel at all times while sample processing is being performed to provide on-site, telephone, or electronic consultation to resolve problems in accordance with the laboratory's policies and procedures. Whenever the supervisor is not available, a qualified designee must be available to the staff. Monitoring testing systems to ensure that acceptable levels of performance are maintained and ensuring appropriate corrective action is taken whenever --- TITLE: Director Commercial Enablement EMPLOYER: Myriad Genetics INC LOCATION: United States (unspecified) SALARY: Not disclosed POSTED: 2026-04-08 PARENTAL_LEAVE_WEEKS: 2 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 2 (not source-backed) K401_MATCH: yes (not source-backed) APPLY_URL: https://ekgn.fa.us6.oraclecloud.com/hcmUI/CandidateExperience/en/sites/CX_2001/job/6040 EXCERPT: Director Commercial Enablement United States Role Overview The Director of Commercial Enablement leads the strategy, implementation, and optimization of the commercial technology ecosystem, with Salesforce (SFDC) as the core platform. This role owns the CRM roadmap, drives system adoption and usability, and ensures that processes, workflows, content, and training support an effective end‑to‑end go‑to‑market (GTM) motion. The director partners across Sales Leadership, Commercial Operations, Marketing, Product, and Technology to align strategy and execution. Key Responsibilities CRM Strategy & Ownership Serve as the commercial business owner of Salesforce and lead CRM relaunch and enhancements. Translate sales and leadership needs into clear functional and technical requirements. Improve usability, data integrity, workflow automation, reporting, and adoption. Monitor system usage, identify gaps, and manage the enhancement backlog and sprint planning. Enablement & Workflow Optimization Develop and execute enablement strategies aligned to GTM priorities and business objectives. Map current‑state vs. future‑state workflows to streamline processes and eliminate friction. Design scalable sales workflows that improve productivity and consistency across teams. Training, Support & Adoption Provide training and support for Salesforce and adjacent tools. Drive adoption through structured feedback collection, process improvements, and user education. Translate field insights into enhancements that improve seller and leader effectiveness. Cross‑Functional Partnership Partner across Sales, Operations, Marketing, and Technology to align CRM and enablement needs. Ensure processes support core commercial priorities such as forecasting, territory planning, and pipeline management. Qualifications Bachelor's degree required; business or related field preferred. 15+ years in sales enablement, sales operations, commercial technology, or similar roles. 5+ --- TITLE: Sales Operations Manager - Urology EMPLOYER: Myriad Genetics INC LOCATION: United States (unspecified) SALARY: Not disclosed POSTED: 2026-04-24 PARENTAL_LEAVE_WEEKS: 2 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 2 (not source-backed) K401_MATCH: yes (not source-backed) APPLY_URL: https://ekgn.fa.us6.oraclecloud.com/hcmUI/CandidateExperience/en/sites/CX_2001/job/6081 EXCERPT: Sales Operations Manager - Urology United States Role Overview The Sales Operations Manager will serve as the primary operations partner for the Urology sales team, leading analytics, reporting, and data-driven insights that support commercial growth. This role requires strong analytical expertise, exceptional attention to detail, and the ability to manage multiple priorities in a fast-paced environment. In this role, you will support Urology commercial and sales leadership with performance reporting, identify opportunities to enhance data quality and automation, and build dashboards and workflows that enable more effective decision-making. You will collaborate closely with Data & Analytics, Sales Enablement, and cross-functional partners to ensure the Urology sales organization has reliable, actionable insights. Our ideal candidate embodies our cultural pillars-collaborative, innovative, inclusive, caring, and committed-and brings curiosity, initiative, and the ability to work seamlessly across teams to advance our commercial strategy. Key Responsibilities Serve as the primary Sales Operations partner for Urology commercial and sales leadership, providing data-driven insights and operational support. Attend Urology leadership meetings to deliver performance updates, trends, and strategic analysis. Identify opportunities to enhance data, reporting, and analytics capabilities across the Prenatal organization. Access, analyze, and integrate data from multiple sources to support operational recommendations. Build, automate, and maintain reporting tools and dashboards using Salesforce (SFDC), Looker, and other technologies. Conduct ad hoc analysis to investigate business challenges, uncover growth opportunities, and support leadership decision-making. Evaluate initiative and program performance (volume, revenue, and adoption) and communicate insights that drive commercial strategy. Partner with the Data & Analytics team --- TITLE: Service Engineer II (3rd Shift) EMPLOYER: Myriad Genetics INC LOCATION: South San Francisco, CA, United States (unspecified) SALARY: Not disclosed POSTED: 2026-03-27 PARENTAL_LEAVE_WEEKS: 2 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 2 (not source-backed) K401_MATCH: yes (not source-backed) APPLY_URL: https://ekgn.fa.us6.oraclecloud.com/hcmUI/CandidateExperience/en/sites/CX_2001/job/5976 EXCERPT: Service Engineer II (3rd Shift) South San Francisco, CA, United States Shift: Wednesday-Saturday 9:00pm-7:30am Pay: Starting at $42/hr, plus an additional $2.50/hr on Wednesday and Thursday night and an additional $4.50/hr on Friday and Saturday night Responsibilities Taking responsibility for uptime on a multi-million dollar pipeline through equipment maintenance, instrument qualification, and rapid response to issues Interfacing with CLIA laboratory personnel to troubleshoot problems and schedule work on instrumentation Performing regular maintenance to keep robotics and instrumentation running in top shape Working closely with automation engineers to define critical feature requests and potential improvements Maintaining the most advanced laboratory technology in molecular diagnostics Developing, optimizing, and troubleshooting liquid-handling processes on multiple instrument platforms Specifying and supporting the implementation of custom hardware and software solutions to continuously improve the MWH laboratory platform (e.g., robots, gantries, PLCs, scheduling, tracking, safety) Applying cutting-edge technology to literally save lives Qualifications Have a BS in electrical engineering, biomedical engineering, or their equivalent, and/or independent experience servicing complex laboratory instrumentation and/or robotic hardware, as displayed by prior employment or projects Have seven or more years of experience repairing and/or maintaining laboratory instrumentation or instruments of similar complexity (Tecan is desirable) Have the attentiveness and vigilance to maintain a complex suite of instrumentation and robotic equipment Know when the solution to a problem is hardware, software, or chemistry Recognize quickly when he or she sees a superior solution and be unafraid to recommend changes Be punctual and able to work a steady schedule and help cover other --- TITLE: Director Statistical Genetics (Oncology) EMPLOYER: Regeneron Pharmaceuticals LOCATION: TARRYTOWN (unspecified) SALARY: Not disclosed POSTED: 2026-06-08 PARENTAL_LEAVE_WEEKS: 12 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 12 (not source-backed) K401_MATCH: yes (not source-backed) APPLY_URL: https://regeneron.wd1.myworkdayjobs.com/Careers/job/TARRYTOWN/Director-Statistical-Genetics--Oncology-_R46218 EXCERPT: Director Statistical Genetics (Oncology) TARRYTOWN posted: Posted 4 Days Ago --- TITLE: Associate Director Neuroscience & Ophthalmology Genetics EMPLOYER: Regeneron Pharmaceuticals LOCATION: TARRYTOWN (unspecified) SALARY: Not disclosed POSTED: 2026-06-08 PARENTAL_LEAVE_WEEKS: 12 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 12 (not source-backed) K401_MATCH: yes (not source-backed) APPLY_URL: https://regeneron.wd1.myworkdayjobs.com/Careers/job/TARRYTOWN/Associate-Director-Neuroscience---Ophthalmology-Genetics_R46973 EXCERPT: Associate Director Neuroscience & Ophthalmology Genetics TARRYTOWN posted: Posted 4 Days Ago --- TITLE: Senior Scientist I - Bioinformatics, Biotherapeutics and Genetic Medicine EMPLOYER: AbbVie Inc. LOCATION: Worcester, MA, United States (unspecified) SALARY: Not disclosed POSTED: 2026-06-10 PARENTAL_LEAVE_WEEKS: 12 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 12 (not source-backed) K401_MATCH: yes (not source-backed) APPLY_URL: https://jobs.smartrecruiters.com/AbbVie/3743990012920057-senior-scientist-i-bioinformatics-biotherapeutics-and-genetic-medicine EXCERPT: Senior Scientist I - Bioinformatics, Biotherapeutics and Genetic Medicine Worcester, MA, 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: Biotherapeutics and Genetic Medicine (BGM), a part of Discovery Research within AbbVie's R&D, is a global organization dedicated to the discovery and optimization of innovative drug candidate molecules for biotherapeutic modalities (monoclonal antibodies, multispecifics, proteins, conjugates, etc.) and genetic medicines (AAV, LNPs, siRNA, etc.) across all therapeutic areas. We are seeking a highly driven and innovative scientist with expertise in bioinformatics to design, develop, and optimize data capture workflows and dynamic visualization dashboards for biologics discovery. Responsibilities: Independently design digital workflows or tools to streamline biologics discovery and evaluate improvements in operational efficiency Identify, champion and test software solutions and that map to the needs of BGM Proactively identify scientist needs that further our digital transformation strategy and propose solutions to meet them Pilot new software and AI tools to evaluate utility for BGM and train others on how to use them Design and implement standard analyses and visualizations that balance customization and increased efficiency --- TITLE: Commercial Operations and Enablement Project Manager EMPLOYER: Myriad Genetics INC LOCATION: United States (unspecified) SALARY: Not disclosed POSTED: 2026-04-08 PARENTAL_LEAVE_WEEKS: 2 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 2 (not source-backed) K401_MATCH: yes (not source-backed) APPLY_URL: https://ekgn.fa.us6.oraclecloud.com/hcmUI/CandidateExperience/en/sites/CX_2001/job/6041 EXCERPT: Commercial Operations and Enablement Project Manager United States Role Overview We are seeking an experienced Operations Project Manager to design, build, and operationalize a scalable project management framework that enables and accelerates our commercial initiatives across sales, marketing, and revenue operations. The Sr. Operations Project Manager, Commercial plays a critical role in driving execution and operational excellence across the Commercial organization. The individual in this role will manage complex cross‑functional projects, and establishes the operational infrastructure needed to proactively prioritize, plan, and deliver high‑impact work. This systems and process-oriented project leader will bring structure to complex, fast-moving, and cross-functional environments. You will be embedded in the Commercial Operations team, managing, supporting and driving technology and process optimization projects and develop the foundation for how commercial enablement work is prioritized, resourced, governed, and delivered. Our ideal candidate: Will have experience supporting commercial sales and operations project management that specifically supports and drives commercial optimization in the form of tools and processes that will help sales, sales training, sales ops analysts, marketing and other commercial professionals win business Will embody our cultural pillars-collaborative, innovative, inclusive, caring, and committed-and brings curiosity, strategic thinking, and a passion for building operational systems that move the commercial sales organization from reactive work to structured, high‑value execution. Responsibilities Commercial Project Leadership Lead end‑to‑end planning, coordination, and delivery of cross‑functional commercial initiatives, ensuring alignment to strategic objectives and on‑time execution. Partner with stakeholders to scope project requirements, estimate resource needs, and develop actionable project timelines. Commercial Operations & --- TITLE: Principal Research Scientist I, siRNA Synthesis & Analytical Development EMPLOYER: AbbVie Inc. LOCATION: Worcester, MA, United States (unspecified) SALARY: Not disclosed POSTED: 2026-06-10 PARENTAL_LEAVE_WEEKS: 12 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 12 (not source-backed) K401_MATCH: yes (not source-backed) APPLY_URL: https://jobs.smartrecruiters.com/AbbVie/3743990013503219-principal-research-scientist-i-sirna-synthesis-analytical-development EXCERPT: Principal Research Scientist I, siRNA Synthesis & Analytical Development Worcester, MA, United States Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: The Biotherapeutics and Genetic Medicine (BGM) department at AbbVie is seeking a motivated Principal Research Scientist to join the growing siRNA team. In this role, you will work with the genetic medicine teams to establish siRNA synthesis, purification, and analytical capabilities. You will serve as a subject matter expert in oligonucleotide chemistry and siRNA production, with responsibility for generating high-quality siRNA materials to advance genetic medicine studies. Responsibilities: Lead the siRNA synthesis platform to support various stages of siRNA studies. Oversee solid-phase oligonucleotide synthesis, deprotection, purification, desalting, and analytical characterization of siRNA. Troubleshoot synthesis, purification, and analytical challenges to improve yield, purity, and scalability. Partner with cross-functional teams, including the siRNA screening team, the antibody conjugation group, and CMC, to support platform and project objectives. Ensure rigorous documentation, data integrity, and compliance with internal quality standards. Track and evaluate emerging technologies and best practices in oligonucleotide and RNA-based therapeutics. Manage and develop a team of --- TITLE: Physician Scientist – Obesity and Liver Disease Human Genetics EMPLOYER: Regeneron Pharmaceuticals LOCATION: TARRYTOWN (unspecified) SALARY: Not disclosed POSTED: 2026-06-08 PARENTAL_LEAVE_WEEKS: 12 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 12 (not source-backed) K401_MATCH: yes (not source-backed) APPLY_URL: https://regeneron.wd1.myworkdayjobs.com/Careers/job/TARRYTOWN/Associate-Director-Integrative-Translational-Genetics_R39319 EXCERPT: Physician Scientist – Obesity and Liver Disease Human Genetics TARRYTOWN posted: Posted 4 Days Ago --- TITLE: Associate Director, Strategy & Operations, Genetic Medicines EMPLOYER: Regeneron Pharmaceuticals LOCATION: TARRYTOWN (unspecified) SALARY: Not disclosed POSTED: 2026-06-09 PARENTAL_LEAVE_WEEKS: 12 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 12 (not source-backed) K401_MATCH: yes (not source-backed) APPLY_URL: https://regeneron.wd1.myworkdayjobs.com/Careers/job/TARRYTOWN/Associate-Director--Strategy---Operations--Genetic-Medicines_R48279 EXCERPT: Associate Director, Strategy & Operations, Genetic Medicines TARRYTOWN posted: Posted 3 Days Ago --- TITLE: Principal Research Scientist I, siRNA Platform Automation EMPLOYER: AbbVie Inc. LOCATION: Worcester, MA, United States (unspecified) SALARY: Not disclosed POSTED: 2026-06-10 PARENTAL_LEAVE_WEEKS: 12 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 12 (not source-backed) K401_MATCH: yes (not source-backed) APPLY_URL: https://jobs.smartrecruiters.com/AbbVie/3743990013502644-principal-research-scientist-i-sirna-platform-automation EXCERPT: Principal Research Scientist I, siRNA Platform Automation Worcester, MA, United States Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: AbbVie's Biotherapeutics and Genetic Medicine (BGM) department is seeking a highly motivated Principal Research Scientist to join our expanding siRNA team. In this role, you will partner with genetic medicine teams to establish a high-throughput siRNA screening platform that advances pipeline innovation through next-generation delivery modalities and supports the discovery of therapeutic leads across multiple disease areas. Responsibilities: Establish and implement a high-throughput siRNA screening platform using automated liquid-handling systems. Serve as a subject matter expert in siRNA screening experimental design, execution, and data interpretation. Lead research efforts and mentor scientists to advance siRNA optimization, including sequence design and novel chemical modifications, across multiple programs. Generate new scientific hypotheses and proposals, improve existing screening workflows, and evaluate emerging technologies in the siRNA field. Communicate clearly and effectively with internal siRNA teams and cross-functional collaborators to identify needs and support platform enhancement and program advancement. Manage and develop a team of at least 2-3 scientists, providing technical guidance, --- TITLE: Associate Scientist - Genetic Medicines, In Vivo EMPLOYER: Regeneron Pharmaceuticals LOCATION: TARRYTOWN (unspecified) SALARY: Not disclosed POSTED: 2026-06-08 PARENTAL_LEAVE_WEEKS: 12 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 12 (not source-backed) K401_MATCH: yes (not source-backed) APPLY_URL: https://regeneron.wd1.myworkdayjobs.com/Careers/job/TARRYTOWN/Associate-Scientist---Genetic-Medicines--In-Vivo_R47944 EXCERPT: Associate Scientist - Genetic Medicines, In Vivo TARRYTOWN posted: Posted 4 Days Ago --- TITLE: Associate Director Therapeutic Area Genetics (Immunology) EMPLOYER: Regeneron Pharmaceuticals LOCATION: TARRYTOWN (unspecified) SALARY: Not disclosed POSTED: 2026-06-08 PARENTAL_LEAVE_WEEKS: 12 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 12 (not source-backed) K401_MATCH: yes (not source-backed) APPLY_URL: https://regeneron.wd1.myworkdayjobs.com/Careers/job/TARRYTOWN/Associate-Director-Therapeutic-Area-Genetics--Immunology-_R46254 EXCERPT: Associate Director Therapeutic Area Genetics (Immunology) TARRYTOWN posted: Posted 4 Days Ago --- TITLE: Medical Director – Medical Genetics & Genomics – EviCore EMPLOYER: The Cigna Group LOCATION: United States Work at Home (unspecified) SALARY: Not disclosed POSTED: 2026-05-28 PARENTAL_LEAVE_WEEKS: 8 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 8 (not source-backed) K401_MATCH: yes (not source-backed) APPLY_URL: https://cigna.wd5.myworkdayjobs.com/cignacareers/job/United-States-Work-at-Home/Medical-Director---Medical-Genetics---Genomics---EviCore_26005721 EXCERPT: Medical Director – Medical Genetics & Genomics – EviCore United States Work at Home posted: Posted 15 Days Ago --- TITLE: Senior Scientist I, siRNA Pipeline Development & SAR Optimization EMPLOYER: AbbVie Inc. LOCATION: Cambridge, MA, United States (unspecified) SALARY: Not disclosed POSTED: 2026-06-10 PARENTAL_LEAVE_WEEKS: 12 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 12 (not source-backed) K401_MATCH: yes (not source-backed) APPLY_URL: https://jobs.smartrecruiters.com/AbbVie/3743990013524454-senior-scientist-i-sirna-pipeline-development-sar-optimization EXCERPT: Senior Scientist I, siRNA Pipeline Development & SAR Optimization Cambridge, MA, United States Company Description: 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 - immunology, oncology, neuroscience, and eye care - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on X , Facebook , Instagram , YouTube , LinkedIn and Tik Tok . Job Description: At AbbVie, we are dedicated to solving some of the world's most complex and serious diseases. Our mission is to develop and deliver advanced therapeutics that change lives. We are looking for talented, passionate, and driven individuals to join our Biotherapeutics and Genetic Medicine (BGM) team. As a Senior Scientist in our siRNA group, you will be part of an innovative team focused on advancing RNA-based therapies that have the potential to revolutionize patient care. AbbVie is looking for a Senior Scientist I to join our siRNA group within the Biotherapeutics and Genetic Medicine (BGM) department. This role will involve designing and executing innovative experimental approaches to address key scientific challenges related to oligonucleotide therapeutics. The successful candidate will drive scientific innovation, identify new methods and techniques, and collaborate across functions to support the development of novel RNA-based therapies. Responsibilities Lead research efforts within a cross-functional team to advance new --- TITLE: Senior Scientist I, siRNA Pipeline Development & Targeted Delivery EMPLOYER: AbbVie Inc. LOCATION: Cambridge, MA, United States (unspecified) SALARY: Not disclosed POSTED: 2026-06-10 PARENTAL_LEAVE_WEEKS: 12 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 12 (not source-backed) K401_MATCH: yes (not source-backed) APPLY_URL: https://jobs.smartrecruiters.com/AbbVie/3743990013513327-senior-scientist-i-sirna-pipeline-development-targeted-delivery EXCERPT: Senior Scientist I, siRNA Pipeline Development & Targeted Delivery Cambridge, MA, United States Company Description: 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 - immunology, oncology, neuroscience, and eye care - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on X , Facebook , Instagram , YouTube , LinkedIn and Tik Tok . Job Description: At AbbVie, we are dedicated to solving some of the world's most complex and serious diseases. Our mission is to develop and deliver advanced therapeutics that change lives. We are looking for talented, passionate, and driven individuals to join our Biotherapeutics and Genetic Medicine (BGM) team. As a Senior Scientist in our siRNA group, you will be part of an innovative team focused on advancing RNA-based therapies that have the potential to revolutionize patient care. AbbVie is looking for a Senior Scientist I to join our siRNA group within the Biotherapeutics and Genetic Medicine (BGM) department. This role will involve designing and executing innovative experimental approaches to address key scientific challenges related to oligonucleotide therapeutics. The successful candidate will drive scientific innovation, identify new methods and techniques, and collaborate across functions to support the development of novel RNA-based therapies. Responsibilities Lead research efforts within a cross-functional team to advance new --- TITLE: Principal Research Scientist I, Biologics Screening - Discovery Biotherapeutics EMPLOYER: AbbVie Inc. LOCATION: San Francisco, CA, United States (unspecified) SALARY: Not disclosed POSTED: 2026-06-10 PARENTAL_LEAVE_WEEKS: 12 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 12 (not source-backed) K401_MATCH: yes (not source-backed) APPLY_URL: https://jobs.smartrecruiters.com/AbbVie/3743990012912319-principal-research-scientist-i-biologics-screening-discovery-biotherapeutics EXCERPT: Principal Research Scientist I, Biologics Screening - Discovery Biotherapeutics San Francisco, CA, United States Company Description: 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 - immunology, oncology, neuroscience, and eye care - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on X , Facebook , Instagram , YouTube , LinkedIn and Tik Tok . Job Description: Discovery Biotherapeutics and Genetic Medicine (BGM) at AbbVie is seeking a highly motivated Principal Scientist to join the Biotherapeutics group at the AbbVie Bay Area (ABA) site based in South San Francisco, CA. This role seeks a skilled and experienced individual to contribute to and lead therapeutic programs, focusing on biophysical screening to advance biotherapeutics from early exploration through lead identification and optimization. Close partnerships with Oncology will be required to drive transformative ideas to the clinic. The ideal candidate must possess expertise in high-throughput biologics screening and characterization methods (e.g. ELISA, FACS, BLI, SPR, etc.) and have a solid foundation in protein sciences and antibody discovery with a proven ability to work effectively on cross-functional teams. Responsibilities Lead from the lab to advance large molecule biologics projects from exploratory to optimization stages and drive Go / No Go decisions. Effectively partner with functional and therapeutic areas to achieve --- TITLE: Senior Scientist II / Principal Scientist I, Biologics Drug Product Development EMPLOYER: AbbVie Inc. LOCATION: North Chicago, IL, United States (unspecified) SALARY: Not disclosed POSTED: 2026-06-10 PARENTAL_LEAVE_WEEKS: 12 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 12 (not source-backed) K401_MATCH: yes (not source-backed) APPLY_URL: https://jobs.smartrecruiters.com/AbbVie/3743990013490176-senior-scientist-ii-principal-scientist-i-biologics-drug-product-development EXCERPT: Senior Scientist II / Principal Scientist I, Biologics Drug Product Development North Chicago, IL, United States Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: Description: Biologics Drug Product Development (Bio DPD), a part of Development Sciences within AbbVie's R&D, is a global organization that is responsible for drug product formulation and process development, and definition of the product presentation for biologics (proteins, conjugates, peptides, neurotoxins etc.) and genetic medicine (AAV, LNPs, Cell Therapy). AbbVie is seeking a highly motivated candidate for the position of Senior Scientist II / Principal Scientist I, located in North Chicago, IL. We are seeking an accomplished scientist with a proven track record in biologics drug product formulation and process development, scale-up and tech transfer. This position will be an integral part of the product development and CMC teams and will have strong collaborations with several stakeholders, including discovery research, analytical research and development, bioprocess development, combination products development, product development science and technology, pilot plants and third-party manufacturers. Key Responsibilities: Represent Bio DPD in the cross-functional Product Presentation and Device Strategy --- TITLE: Sr Buyer EMPLOYER: Myriad Genetics INC LOCATION: Salt Lake City, UT, United States (unspecified) SALARY: Not disclosed POSTED: 2026-04-29 PARENTAL_LEAVE_WEEKS: 2 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 2 (not source-backed) K401_MATCH: yes (not source-backed) APPLY_URL: https://ekgn.fa.us6.oraclecloud.com/hcmUI/CandidateExperience/en/sites/CX_2001/job/6109 EXCERPT: Sr Buyer Salt Lake City, UT, United States Overview The Senior Buyer is responsible for managing complex purchasing activities, supplier relationships, and operational procurement execution to ensure continuity of supply, cost management, and policy compliance. This role operates with increased autonomy and serves as a subject matter resource to internal stakeholders and junior buyers. The Senior Buyer manages higher risk or higher value purchases, supports sourcing initiatives, and plays a key role in supplier performance management and issue resolution. Responsibility Manage end‑to‑end purchasing of assigned categories, suppliers, or business units Create and maintain accurate purchase orders and ensure on‑time delivery Ensure continuity of supply through issue resolution, expediting, and demand changes Own day‑to‑day supplier relationships and manage performance (delivery, quality, service) Lead supplier issue resolution and support performance reviews Negotiate pricing, lead times, and commercial terms within authority Identify cost savings, cost avoidance, and efficiency opportunities Ensure compliance with contracts, procurement policies, and approval thresholds Act as a trusted procurement advisor to internal stakeholders Support sourcing initiatives, process improvements, and mentoring of buyers Qualifications Bachelor's degree in Business, Supply Chain, Finance, or a related field, or equivalent professional experience 5 years of experience in procurement, purchasing, or supply chain roles Strong understanding of procurement best practices, contracts, and commercial terms Proven negotiation, supplier management, and issue‑resolution skills Experience working in ERP and/or e‑procurement systems, with proficiency in Excel and reporting or analytics tools Ability to manage multiple priorities independently with sound judgment Strong analytical, problem‑solving, and decision‑making capabilities Effective written --- TITLE: Director Precision Medicine EMPLOYER: Regeneron Pharmaceuticals LOCATION: 2 Locations (unspecified) SALARY: Not disclosed POSTED: 2026-06-08 PARENTAL_LEAVE_WEEKS: 12 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 12 (not source-backed) K401_MATCH: yes (not source-backed) APPLY_URL: https://regeneron.wd1.myworkdayjobs.com/Careers/job/Armonk/Director-Precision-Medicine_R44954 EXCERPT: Director Precision Medicine 2 Locations posted: Posted 4 Days Ago --- TITLE: Director, Computational Biology, Precision Medicine EMPLOYER: Amgen LOCATION: India - Hyderabad (unspecified) SALARY: Not disclosed POSTED: 2026-06-11 PARENTAL_LEAVE_WEEKS: 6 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 6 (not source-backed) K401_MATCH: yes (not source-backed) APPLY_URL: https://amgen.wd1.myworkdayjobs.com/Careers/job/India---Hyderabad/Associate-Director--Computational-Biology--Precision-Medicine_R-238154 EXCERPT: Director, Computational Biology, Precision Medicine India - Hyderabad posted: Posted Yesterday --- TITLE: Principal Research Scientist I, tLNP Process Development EMPLOYER: AbbVie Inc. LOCATION: North Chicago, IL, United States (unspecified) SALARY: Not disclosed POSTED: 2026-06-10 PARENTAL_LEAVE_WEEKS: 12 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 12 (not source-backed) K401_MATCH: yes (not source-backed) APPLY_URL: https://jobs.smartrecruiters.com/AbbVie/3743990013481726-principal-research-scientist-i-tlnp-process-development EXCERPT: Principal Research Scientist I, tLNP Process 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: Overview Targeted lipid nanoparticles (tLNPs) represent a key new modality to enable the effective delivery of mRNA. The tLNP chemistry, manufacturing, and control (CMC) team (TCT) is a newly formed group under Biologics CMC, Development Sciences, R&D. The tLNP CMC team focuses on process development for tLNPs, including mRNA process development, tLNP process development, and formulation development. The targeted lipid nanoparticle (tLNP) process development team is seeking a highly motivated, talented, and innovative scientist. This position will play a key role in advancing tLNP programs by serving as a technical expert in targeting moiety conjugation technologies, including monoclonal antibodies (mAbs), Fabs, and related ligand formats. The successful candidate will partner with mRNA and LNP process development team members to design and implement robust strategies for commercial process development and process characterization. In addition, this individual will work cross-functionally with internal stakeholders and external partners to ensure right-first-time technology transfer of mRNA, LNP, and conjugation processes into --- TITLE: Principal Research Scientist I - Bio CMC Developability Modeling EMPLOYER: AbbVie Inc. LOCATION: North Chicago, IL, United States (unspecified) SALARY: Not disclosed POSTED: 2026-06-12 PARENTAL_LEAVE_WEEKS: 12 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 12 (not source-backed) K401_MATCH: yes (not source-backed) APPLY_URL: https://jobs.smartrecruiters.com/AbbVie/3743990013561446-principal-research-scientist-i-bio-cmc-developability-modeling EXCERPT: Principal Research Scientist I - Bio CMC Developability Modeling 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: Overview The Development Sciences Biologics Drug Product Development organization within AbbVie develops and characterizes drug product formulations and manufacturing processes to provide clinical dosage forms to enable the development of AbbVie's pipeline. AbbVie is seeking a highly motivated person to join the Biologics CMC Developability Team. Our team utilizes start-of-the-art biophysical and analytical instrumentation to assess candidates coming out of the Discovery pipeline. We collaboratively influence protein design paradigms to yield biologic candidates that will be successful drug products. Key to our success is developing models of protein structure and function to augment decision making in protein design and development. We utilize high throughput instrumentation and digital data systems to capture ML-ready data on industry leading datasets of therapeutic proteins. To drive maximum benefit from this data, we are seeking an experienced scientist to lead modeling efforts within our team. The successful candidate will bring deep experience of modeling protein stability or related properties --- TITLE: Associate Director, Biostatistics - Genetic Medicine EMPLOYER: Regeneron Pharmaceuticals LOCATION: 3 Locations (unspecified) SALARY: Not disclosed POSTED: 2026-06-08 PARENTAL_LEAVE_WEEKS: 12 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 12 (not source-backed) K401_MATCH: yes (not source-backed) APPLY_URL: https://regeneron.wd1.myworkdayjobs.com/Careers/job/TARRYTOWN/Associate-Director--Biostatistics---Genetic-Medicine_R46282 EXCERPT: Associate Director, Biostatistics - Genetic Medicine 3 Locations posted: Posted 4 Days Ago --- TITLE: Principal Scientist – Computational Biology & Translational AI (Oncology Precision Medicine) EMPLOYER: Amgen LOCATION: 2 Locations (unspecified) SALARY: Not disclosed POSTED: 2026-05-12 PARENTAL_LEAVE_WEEKS: 6 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 6 (not source-backed) K401_MATCH: yes (not source-backed) APPLY_URL: https://amgen.wd1.myworkdayjobs.com/Careers/job/US---California---South-San-Francisco/Principal-Scientist---Computational-Biology---Translational-AI--Oncology-Precision-Medicine-_R-237397 EXCERPT: Principal Scientist – Computational Biology & Translational AI (Oncology Precision Medicine) 2 Locations posted: Posted 30+ Days Ago --- TITLE: Senior Manager, Clinical Scientist, Genetics Medicine EMPLOYER: Regeneron Pharmaceuticals LOCATION: TARRYTOWN (unspecified) SALARY: Not disclosed POSTED: 2026-06-08 PARENTAL_LEAVE_WEEKS: 12 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 12 (not source-backed) K401_MATCH: yes (not source-backed) APPLY_URL: https://regeneron.wd1.myworkdayjobs.com/Careers/job/TARRYTOWN/Senior-Manager--Clinical-Scientist--Genetics-Medicine_R47576 EXCERPT: Senior Manager, Clinical Scientist, Genetics Medicine TARRYTOWN posted: Posted 4 Days Ago --- TITLE: Manager Precision Medicine EMPLOYER: Regeneron Pharmaceuticals LOCATION: 2 Locations (unspecified) SALARY: Not disclosed POSTED: 2026-06-08 PARENTAL_LEAVE_WEEKS: 12 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 12 (not source-backed) K401_MATCH: yes (not source-backed) APPLY_URL: https://regeneron.wd1.myworkdayjobs.com/Careers/job/Armonk/Manager-Precision-Medicine_R47135 EXCERPT: Manager Precision Medicine 2 Locations posted: Posted 4 Days Ago --- TITLE: Enterprise GenAI and DevOps Technical Lead EMPLOYER: AbbVie Inc. LOCATION: Florham Park, NJ, United States (unspecified) SALARY: Not disclosed POSTED: 2026-06-10 PARENTAL_LEAVE_WEEKS: 12 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 12 (not source-backed) K401_MATCH: yes (not source-backed) APPLY_URL: https://jobs.smartrecruiters.com/AbbVie/3743990013336392-enterprise-genai-and-devops-technical-lead EXCERPT: Enterprise GenAI and DevOps Technical Lead Florham Park, NJ, United States Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: We are seeking an experienced and highly skilled Technical Leader to join our GenAI and DevOps team. The ideal candidate will have over 8 years of hands-on DevOps and AI, GenAI, Python experience with a strong technical leadership background. This position will play a pivotal role in driving the development and implementation of our GenAI and DevOps deliveries, ensuring seamless integration of AI technologies into our software development and operational support. Responsibilities : Provide technical leadership and guidance to the GenAI and DevOps teams. Develop and deliver a container based approach to hosting apps. Develop and execute the overall GenAI and DevOps process from a delivery and operational perspective. Drive innovation in GenAI and DevOps processes and technologies to enhance efficiency and productivity across our business. Ensure Python development and DevOps are working efficiently across the business groups Oversee the design, implementation, and maintenance of the CI/CD pipelines for GenAI. Define and deliver API access to GenAI --- TITLE: Medical Director, Clinical Development, MASH/Metabolism (Regeneron Genetics Medicine) EMPLOYER: Regeneron Pharmaceuticals LOCATION: TARRYTOWN (unspecified) SALARY: Not disclosed POSTED: 2026-06-08 PARENTAL_LEAVE_WEEKS: 12 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 12 (not source-backed) K401_MATCH: yes (not source-backed) APPLY_URL: https://regeneron.wd1.myworkdayjobs.com/Careers/job/TARRYTOWN/Medical-Director--Clinical-Development--MASH-Metabolism--Regeneron-Genetics-Medicine-_R47478 EXCERPT: Medical Director, Clinical Development, MASH/Metabolism (Regeneron Genetics Medicine) TARRYTOWN posted: Posted 4 Days Ago --- TITLE: Genetic Counselor Clinical Reviewer - EviCore - Remote EMPLOYER: The Cigna Group LOCATION: United States Work at Home (remote) SALARY: Not disclosed POSTED: 2026-05-29 PARENTAL_LEAVE_WEEKS: 8 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 8 (not source-backed) K401_MATCH: yes (not source-backed) APPLY_URL: https://cigna.wd5.myworkdayjobs.com/cignacareers/job/United-States-Work-at-Home/Genetic-Counselor-Clinical-Reviewer---EviCore---Remote_26006701 EXCERPT: Genetic Counselor Clinical Reviewer - EviCore - Remote United States Work at Home posted: Posted 14 Days Ago --- TITLE: Process Development Senior Scientist - Synthetic Peptides, Oligonucleotides, ADCs EMPLOYER: Amgen LOCATION: US - California - Thousand Oaks (unspecified) SALARY: Not disclosed POSTED: 2026-05-29 PARENTAL_LEAVE_WEEKS: 6 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 6 (not source-backed) K401_MATCH: yes (not source-backed) APPLY_URL: https://amgen.wd1.myworkdayjobs.com/Careers/job/US---California---Thousand-Oaks/Process-Development-Senior-Scientist---Synthetic-Peptides--Oligonucleotides--ADCs_R-246322 EXCERPT: Process Development Senior Scientist - Synthetic Peptides, Oligonucleotides, ADCs US - California - Thousand Oaks posted: Posted 14 Days Ago --- TITLE: Director, Data Governance and Contract Compliance, Regeneron Genetics Center (RGC) EMPLOYER: Regeneron Pharmaceuticals LOCATION: TARRYTOWN (unspecified) SALARY: Not disclosed POSTED: 2026-06-08 PARENTAL_LEAVE_WEEKS: 12 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 12 (not source-backed) K401_MATCH: yes (not source-backed) APPLY_URL: https://regeneron.wd1.myworkdayjobs.com/Careers/job/TARRYTOWN/Director--Data-Governance-and-Contract-Compliance--Regeneron-Genetics-Center--RGC-_R47043 EXCERPT: Director, Data Governance and Contract Compliance, Regeneron Genetics Center (RGC) TARRYTOWN posted: Posted 4 Days Ago --- TITLE: Scientist I, Biologics Drug Substance Development, Cell Culture Development EMPLOYER: AbbVie Inc. LOCATION: San Francisco, CA, United States (unspecified) SALARY: Not disclosed POSTED: 2026-06-10 PARENTAL_LEAVE_WEEKS: 12 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 12 (not source-backed) K401_MATCH: yes (not source-backed) APPLY_URL: https://jobs.smartrecruiters.com/AbbVie/3743990013479536-scientist-i-biologics-drug-substance-development-cell-culture-development EXCERPT: Scientist I, Biologics Drug Substance Development, Cell Culture Development San Francisco, CA, United States Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: The Cell Culture Development Group in South San Francisco, CA is seeking a Scientist I to join a talented and collaborative team to develop cell culture processes for GMP applications. In this position, you will perform cell culture process development, scale-up, and technology transfer activities in a well-supported and dynamic environment to help advance novel biotherapeutics into human clinical studies. KEY RESPONSIBILITIES: Perform inoculum expansion and cell bank generation Execute cell culture experiments using Ambr250 and 2L bioreactors Perform pilot scale material generation using 50L, 200L and 500L single use bioreactors Execute small scale and pilot scale depth filtration and centrifugation primary recovery processes Perform tech transfer of Master cell bank generation, cell culture and primary recovery processes to the GMP manufacturing facilities Provide person-in-plant support at the GMP manufacturing facility Perform cell culture experiments to optimize N-1 perfusion processes as well as intensified fed-batch processes Represent the cell culture development group for pipeline --- TITLE: Senior Principal Research Scientist, Computational Drug Discovery HitGen/LeadGen Team Lead EMPLOYER: AbbVie Inc. LOCATION: North Chicago, IL, United States (unspecified) SALARY: Not disclosed POSTED: 2026-06-12 PARENTAL_LEAVE_WEEKS: 12 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 12 (not source-backed) K401_MATCH: yes (not source-backed) APPLY_URL: 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 --- TITLE: Sr. Principal Scientist, Bioinformatics, Computational Biology, Precision Medicine EMPLOYER: Amgen LOCATION: India - Hyderabad (unspecified) SALARY: Not disclosed POSTED: 2026-05-12 PARENTAL_LEAVE_WEEKS: 6 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 6 (not source-backed) K401_MATCH: yes (not source-backed) APPLY_URL: https://amgen.wd1.myworkdayjobs.com/Careers/job/India---Hyderabad/Sr-Principal-Scientist--Bioinformatics--Computational-Biology--Precision-Medicine_R-238155 EXCERPT: Sr. Principal Scientist, Bioinformatics, Computational Biology, Precision Medicine India - Hyderabad posted: Posted 30+ Days Ago --- TITLE: Senior Scientific Director, Medical Affairs - Precision Medicine EMPLOYER: AbbVie Inc. LOCATION: Mettawa, IL, United States (unspecified) SALARY: Not disclosed POSTED: 2026-06-10 PARENTAL_LEAVE_WEEKS: 12 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 12 (not source-backed) K401_MATCH: yes (not source-backed) APPLY_URL: https://jobs.smartrecruiters.com/AbbVie/3743990013134636-senior-scientific-director-medical-affairs-precision-medicine EXCERPT: Senior Scientific Director, Medical Affairs - Precision Medicine Mettawa, IL, United States Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: Oncology remains a core therapeutic area at AbbVie, featuring a robust portfolio of marketed products and a promising oncology pipeline. AbbVie is currently seeking a dynamic Executive Medial Director/Sr. Scientific Director for Medical Affairs, Precision Medicine, to lead US CDx strategy in oncology. This role requires a strong background in cancer diagnostics, pathology, biomarkers, and cancer therapeutics, as well as a demonstrated commitment to precision medicine. Key Responsibilities: Lead and deliver a comprehensive, US focused medical strategy for upcoming CDx launches, overseeing execution of key deliverables. Develop and implement the medical affairs strategy for upcoming CDx launches. Build and maintain key external relationships with diagnostic partners, academic and community labs, and reference labs. Cultivate relationships with expert pathologists and key opinion leaders. Forge strong partnerships with leading pathology societies and develop EQA/PT programs. Represent Medical Affairs in cross-functional Oncology Precision Medicine teams across the organization. Act as the medical affairs lead on the integrated brand team --- TITLE: Senior Scientist I, siRNA in vitro Biology EMPLOYER: AbbVie Inc. LOCATION: Cambridge, MA, United States (unspecified) SALARY: Not disclosed POSTED: 2026-06-10 PARENTAL_LEAVE_WEEKS: 12 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 12 (not source-backed) K401_MATCH: yes (not source-backed) APPLY_URL: https://jobs.smartrecruiters.com/AbbVie/3743990012913220-senior-scientist-i-sirna-in-vitro-biology EXCERPT: Senior Scientist I, siRNA in vitro Biology Cambridge, MA, United States Company Description: 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 - immunology, oncology, neuroscience, and eye care - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on X , Facebook , Instagram , YouTube , LinkedIn and Tik Tok . Job Description: At AbbVie, we are dedicated to solving some of the world's most complex and serious diseases. Within AbbVie's Biotherapeutics and Genetic Medicine (BGM) organization, our siRNA team is advancing therapeutic programs from early discovery through development, applying rigorous biology and data-driven decision making to build differentiated RNA medicines. AbbVie is seeking a Senior Scientist I with deep, hands-on expertise in siRNA therapeutic discovery to join the siRNA group within Biotherapeutics and Genetic Medicine (BGM). This role will involve designing and executing innovative experimental approaches to address key scientific challenges related to oligonucleotide therapeutics. The successful candidate will drive scientific innovation, identify new methods and techniques, and collaborate across functions to support the development of novel RNA-based therapies. This role is best suited for candidates with direct, hands-on experience in therapeutic siRNA discovery, where siRNA biology directly informed experimental and program-level decisions. Responsibilities Independently lead in vitro siRNA discovery biology, including experimental strategy, --- TITLE: Senior Scientist I, Analytical Development - Mass Spectrometry tLNP CMC EMPLOYER: AbbVie Inc. LOCATION: North Chicago, IL, United States (unspecified) SALARY: Not disclosed POSTED: 2026-06-10 PARENTAL_LEAVE_WEEKS: 12 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 12 (not source-backed) K401_MATCH: yes (not source-backed) APPLY_URL: https://jobs.smartrecruiters.com/AbbVie/3743990013517326-senior-scientist-i-analytical-development-mass-spectrometry-tlnp-cmc- EXCERPT: Senior Scientist I, Analytical Development - Mass Spectrometry tLNP CMC 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: The Analytical Development group within the Targeted LNP (tLNP) CMC Development Team at AbbVie is dedicated to advancing state-of-the-art analytical capabilities for tLNP therapeutics development. Our team provides critical support to tLNP drug substance, drug product, and formulation development. We leverage advanced biophysical, separation, and mass spectrometry techniques to deeply characterize antibodies, mRNA, lipids, and intact LNP particles. We are building a strong team of scientists who will be instrumental in developing and deploying the analytical toolbox needed to deliver high-quality, innovative tLNP medicines to patients. Position Overview: As the mass spectrometry SME within the Analytical Development group of tLNP CMC Development team, you will work in an innovative analytical research and development lab and develop LC-MS method for characterizing biotherapeutic products to support tLNP development, with an emphasis on mRNA and oligonucleotide analysis. The successful candidate will have hands-on analytical method development experience of LC-MS analysis. Additionally, the candidate must foster productive --- TITLE: Systems Support Engineer EMPLOYER: Accendra Health INC LOCATION: 3610 Accendra India (unspecified) SALARY: Not disclosed POSTED: 2026-05-12 PARENTAL_LEAVE_WEEKS: 3 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 3 (not source-backed) APPLY_URL: https://owensminor.wd1.myworkdayjobs.com/OMCareers/job/3610-Accendra-India/Systems-Support-Engineer_REQ_24_19937 EXCERPT: Systems Support Engineer 3610 Accendra India At Owens & Minor, we are a critical part of the healthcare process. As a Fortune 500 company with 350+ facilities across the US and 22,000 teammates in over 90 countries, we provide integrated technologies, products and services across the full continuum of care. Customers-and their patients-are at the heart of what we do. Our mission is to empower our customers to advance healthcare, and our success starts with our teammates. If you feel this opportunity could be the next step in your career, we encourage you to apply. This position will accept applications on an ongoing basis. Owens & Minor is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, national origin, sex, sexual orientation, genetic information, religion, disability, age, status as a veteran , or any other status prohibited by applicable national, federal, state or local law. --- TITLE: Enterprise DBA III EMPLOYER: Accendra Health INC LOCATION: 3610 Accendra India (unspecified) SALARY: Not disclosed POSTED: 2026-05-12 PARENTAL_LEAVE_WEEKS: 3 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 3 (not source-backed) APPLY_URL: https://owensminor.wd1.myworkdayjobs.com/OMCareers/job/3610-Accendra-India/Enterprise-DBA-III_REQ_24_19851 EXCERPT: Enterprise DBA III 3610 Accendra India At Owens & Minor, we are a critical part of the healthcare process. As a Fortune 500 company with 350+ facilities across the US and 22,000 teammates in over 90 countries, we provide integrated technologies, products and services across the full continuum of care. Customers-and their patients-are at the heart of what we do. Our mission is to empower our customers to advance healthcare, and our success starts with our teammates. If you feel this opportunity could be the next step in your career, we encourage you to apply. This position will accept applications on an ongoing basis. Owens & Minor is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, national origin, sex, sexual orientation, genetic information, religion, disability, age, status as a veteran , or any other status prohibited by applicable national, federal, state or local law. --- TITLE: Director, Precision Medicine (Cell Medicine) EMPLOYER: Regeneron Pharmaceuticals LOCATION: 2 Locations (unspecified) SALARY: Not disclosed POSTED: 2026-06-08 PARENTAL_LEAVE_WEEKS: 12 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 12 (not source-backed) K401_MATCH: yes (not source-backed) APPLY_URL: https://regeneron.wd1.myworkdayjobs.com/Careers/job/Cambridge/Director--Precision-Medicine_R46672-1 EXCERPT: Director, Precision Medicine (Cell Medicine) 2 Locations posted: Posted 4 Days Ago --- TITLE: Expert Scrum Master EMPLOYER: Accendra Health INC LOCATION: 3610 Accendra India (unspecified) SALARY: Not disclosed POSTED: 2026-05-12 PARENTAL_LEAVE_WEEKS: 3 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 3 (not source-backed) APPLY_URL: https://owensminor.wd1.myworkdayjobs.com/OMCareers/job/3610-Accendra-India/Expert-Scrum-Master_REQ_24_22442 EXCERPT: Expert Scrum Master 3610 Accendra India At Owens & Minor, we are a critical part of the healthcare process. As a Fortune 500 company with 350+ facilities across the US and 22,000 teammates in over 90 countries, we provide integrated technologies, products and services across the full continuum of care. Customers-and their patients-are at the heart of what we do. Our mission is to empower our customers to advance healthcare, and our success starts with our teammates. If you feel this opportunity could be the next step in your career, we encourage you to apply. This position will accept applications on an ongoing basis. Owens & Minor is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, national origin, sex, sexual orientation, genetic information, religion, disability, age, status as a veteran , or any other status prohibited by applicable national, federal, state or local law. --- TITLE: Scientist I - Early Analytical Development, Synthetic Molecules EMPLOYER: AbbVie Inc. LOCATION: North Chicago, IL, United States (unspecified) SALARY: Not disclosed POSTED: 2026-06-10 PARENTAL_LEAVE_WEEKS: 12 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 12 (not source-backed) K401_MATCH: yes (not source-backed) APPLY_URL: https://jobs.smartrecruiters.com/AbbVie/3743990013491756-scientist-i-early-analytical-development-synthetic-molecules EXCERPT: Scientist I - Early Analytical Development, Synthetic Molecules 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: For the Scientist I position, we are seeking a highly motivated candidate who can efficiently develop and optimize new methods and techniques to generate reliable and reproducible data in a timely manner and demonstrate broad versatile technical expertise. They will support early phase development of New Synthetic Molecules particularly newly emerging modalities such as peptides, siRNA, conjugatable payloads for Antibody Drug Conjugates, and small molecules , in both the preclinical- and clinical-development space and collaborate within the global Analytical R&D organization and with R&D cross-functional partners such as Pre-Clinical Safety (PCS), Process Chemistry, Process Engineering, Drug Product Development (DPD), Quality Assurance (QA), and CMC-Regulatory Affairs. This position will focus primarily on transitioning NCEs from Discovery into Development Sciences and the individual will independently serve as an Analytical Research and Development analyst to support a highly cross-functional team, which includes Discovery, Process Chemistry, Quantitative and Translational ADME Sciences (QTAS), Safety Pharmacology, Pre-Clinical Safety (PCS), and Molecular --- TITLE: Senior Pega Developer EMPLOYER: Accendra Health INC LOCATION: 3610 Accendra India (unspecified) SALARY: Not disclosed POSTED: 2026-05-12 PARENTAL_LEAVE_WEEKS: 3 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 3 (not source-backed) APPLY_URL: https://owensminor.wd1.myworkdayjobs.com/OMCareers/job/3610-Accendra-India/Senior-Pega-Developer_REQ_25_24203 EXCERPT: Senior Pega Developer 3610 Accendra India At Owens & Minor, we are a critical part of the healthcare process. As a Fortune 500 company with 350+ facilities across the US and 22,000 teammates in over 90 countries, we provide integrated technologies, products and services across the full continuum of care. Customers-and their patients-are at the heart of what we do. Our mission is to empower our customers to advance healthcare, and our success starts with our teammates. If you feel this opportunity could be the next step in your career, we encourage you to apply. This position will accept applications on an ongoing basis. Owens & Minor is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, national origin, sex, sexual orientation, genetic information, religion, disability, age, status as a veteran , or any other status prohibited by applicable national, federal, state or local law. --- TITLE: WMS Developer III EMPLOYER: Accendra Health INC LOCATION: 3610 Accendra India (unspecified) SALARY: Not disclosed POSTED: 2026-05-12 PARENTAL_LEAVE_WEEKS: 3 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 3 (not source-backed) APPLY_URL: https://owensminor.wd1.myworkdayjobs.com/OMCareers/job/3610-Accendra-India/WMS-Developer-III_REQ_24_19734 EXCERPT: WMS Developer III 3610 Accendra India At Owens & Minor, we are a critical part of the healthcare process. As a Fortune 500 company with 50+ facilities across the US and 18,000 teammates in over 90 countries, we provide integrated technologies, products and services across the full continuum of care. Customers-and their patients-are at the heart of what we do. Our mission is to empower our customers to advance healthcare, and our success starts with our teammates. If you feel this opportunity could be the next step in your career, we encourage you to apply. This position will accept applications on an ongoing basis. Owens & Minor is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, national origin, sex, sexual orientation, genetic information, religion, disability, age, status as a veteran , or any other status prohibited by applicable national, federal, state or local law. --- TITLE: Global Safety Medical Director, Rare Disease EMPLOYER: Amgen LOCATION: United States - Remote (remote) SALARY: Not disclosed POSTED: 2026-05-12 PARENTAL_LEAVE_WEEKS: 6 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 6 (not source-backed) K401_MATCH: yes (not source-backed) APPLY_URL: https://amgen.wd1.myworkdayjobs.com/Careers/job/United-States---Remote/Global-Safety-Medical-Director--Rare-Disease_R-240778 EXCERPT: Global Safety Medical Director, Rare Disease United States - Remote posted: Posted 30+ Days Ago --- TITLE: Applied Scientist EMPLOYER: Amazon LOCATION: Seattle, Washington, USA (unspecified) SALARY: $143K-$193K POSTED: 2026-03-20 PARENTAL_LEAVE_WEEKS: 6 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 6 (not source-backed) K401_MATCH: yes (not source-backed) FERTILITY_FAMILY_BUILDING_BENEFITS: yes (not source-backed) ADOPTION_ASSISTANCE_OFFERED: yes (not source-backed) MENTAL_HEALTH_SUPPORT: yes (not source-backed) CHILDCARE_SUBSIDY: yes (not source-backed) APPLY_URL: https://www.amazon.jobs/en/jobs/10372619/applied-scientist EXCERPT: Applied Scientist Seattle, Washington, USA At Amazon Selection and Catalog Systems (ASCS), our mission is to power the online buying experience for customers worldwide so they can find, discover, and buy any product they want. We innovate on behalf of our customers to ensure uniqueness and consistency of product identity and to infer relationships between products in Amazon Catalog to drive the selection gateway for the search and browse experiences on the website. We're solving a fundamental AI challenge: establishing product identity and relationships at unprecedented scale. Using Generative AI, Visual Language Models (VLMs), and multimodal reasoning, we determine what makes each product unique and how products relate to one another across Amazon's catalog. The scale is staggering: billions of products, petabytes of multimodal data, millions of sellers, dozens of languages, and infinite product diversity-from electronics to groceries to digital content. The research challenges are immense. GenAI and VLMs hold transformative promise for catalog understanding, but we operate where traditional methods fail: ambiguous problem spaces, incomplete and noisy data, inherent uncertainty, reasoning across both images and textual data, and explaining decisions at scale. Establishing product identities and groupings requires sophisticated models that reason across text, images, and structured data-while maintaining accuracy and trust for high-stakes business decisions affecting millions of customers daily. Amazon's Item and Relationship Platform group is looking for an innovative and customer-focused applied scientist to help us make the world's best product catalog even better. In this role, you will partner with technology and business leaders to --- TITLE: Principal Analyst - Workday EMPLOYER: Accendra Health INC LOCATION: 3610 Accendra India (unspecified) SALARY: Not disclosed POSTED: 2026-05-12 PARENTAL_LEAVE_WEEKS: 3 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 3 (not source-backed) APPLY_URL: https://owensminor.wd1.myworkdayjobs.com/OMCareers/job/3610-Accendra-India/Principal-Analyst---Workday_REQ_24_21123 EXCERPT: Principal Analyst - Workday 3610 Accendra India At Owens & Minor, we are a critical part of the healthcare process. As a Fortune 500 company with 350+ facilities across the US and 22,000 teammates in over 90 countries, we provide integrated technologies, products and services across the full continuum of care. Customers-and their patients-are at the heart of what we do. Our mission is to empower our customers to advance healthcare, and our success starts with our teammates. If you feel this opportunity could be the next step in your career, we encourage you to apply. This position will accept applications on an ongoing basis. Owens & Minor is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, national origin, sex, sexual orientation, genetic information, religion, disability, age, status as a veteran , or any other status prohibited by applicable national, federal, state or local law. --- TITLE: Workday Integration Developer EMPLOYER: Accendra Health INC LOCATION: 3610 Accendra India (unspecified) SALARY: Not disclosed POSTED: 2026-05-12 PARENTAL_LEAVE_WEEKS: 3 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 3 (not source-backed) APPLY_URL: https://owensminor.wd1.myworkdayjobs.com/OMCareers/job/3610-Accendra-India/Workday-Integration-Developer_REQ_25_24557 EXCERPT: Workday Integration Developer 3610 Accendra India At Owens & Minor, we are a critical part of the healthcare process. As a Fortune 500 company with 350+ facilities across the US and 22,000 teammates in over 90 countries, we provide integrated technologies, products and services across the full continuum of care. Customers-and their patients-are at the heart of what we do. Our mission is to empower our customers to advance healthcare, and our success starts with our teammates. If you feel this opportunity could be the next step in your career, we encourage you to apply. This position will accept applications on an ongoing basis. Owens & Minor is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, national origin, sex, sexual orientation, genetic information, religion, disability, age, status as a veteran , or any other status prohibited by applicable national, federal, state or local law. --- TITLE: Principal Consultant - Workday EMPLOYER: Accendra Health INC LOCATION: 3610 Accendra India (unspecified) SALARY: Not disclosed POSTED: 2026-05-12 PARENTAL_LEAVE_WEEKS: 3 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 3 (not source-backed) APPLY_URL: https://owensminor.wd1.myworkdayjobs.com/OMCareers/job/3610-Accendra-India/Principal-Consultant---Workday_REQ_25_24567 EXCERPT: Principal Consultant - Workday 3610 Accendra India At Owens & Minor, we are a critical part of the healthcare process. As a Fortune 500 company with 350+ facilities across the US and 22,000 teammates in over 90 countries, we provide integrated technologies, products and services across the full continuum of care. Customers-and their patients-are at the heart of what we do. Our mission is to empower our customers to advance healthcare, and our success starts with our teammates. If you feel this opportunity could be the next step in your career, we encourage you to apply. This position will accept applications on an ongoing basis. Owens & Minor is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, national origin, sex, sexual orientation, genetic information, religion, disability, age, status as a veteran , or any other status prohibited by applicable national, federal, state or local law. --- TITLE: Data Scientist II - AMZ9774210 EMPLOYER: Amazon LOCATION: New York, New York, USA (unspecified) SALARY: $170K-$208K POSTED: 2026-04-06 PARENTAL_LEAVE_WEEKS: 6 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 6 (not source-backed) K401_MATCH: yes (not source-backed) FERTILITY_FAMILY_BUILDING_BENEFITS: yes (not source-backed) ADOPTION_ASSISTANCE_OFFERED: yes (not source-backed) MENTAL_HEALTH_SUPPORT: yes (not source-backed) CHILDCARE_SUBSIDY: yes (not source-backed) APPLY_URL: https://www.amazon.jobs/en/jobs/10384056/data-scientist-ii-amz9774210 EXCERPT: Data Scientist II - AMZ9774210 New York, New York, USA MULTIPLE POSITIONS AVAILABLE Employer: AMAZON DEVELOPMENT CENTER U.S., INC. Offered Position: Data Scientist II Job Location: New York, New York Job Number: AMZ9774210 Position Responsibilities: Design and implement scalable and reliable approaches to support or automate decision making throughout the business. Apply a range of data science techniques and tools combined with subject matter expertise to solve difficult business problems and cases in which the solution approach is unclear. Acquire data by building the necessary SQL / ETL queries. Import processes through various company specific interfaces for accessing Oracle, RedShift, and Spark storage systems. Build relationships with stakeholders and counterparts. Analyze data for trends and input validity by inspecting univariate distributions, exploring bivariate relationships, constructing appropriate transformations, and tracking down the source and meaning of anomalies. Build models using statistical modeling, mathematical modeling, econometric modeling, network modeling, social network modeling, natural language processing, machine learning algorithms, genetic algorithms, and neural networks. Validate models against alternative approaches, expected and observed outcome, and other business defined key performance indicators. Implement models that comply with evaluations of the computational demands, accuracy, and reliability of the relevant ETL processes at various stages of production. Position Requirements: Master's degree or foreign equivalent degree in Statistics, Applied Mathematics, Economics, Engineering, Computer Science, or a related field and one year of experience in the job offered or a related occupation. Employer will accept a Bachelor's degree or foreign equivalent degree in Statistics, Applied Mathematics, Economics, Engineering, Computer --- TITLE: Scientist I, Cell and Molecular Biologist EMPLOYER: AbbVie Inc. LOCATION: North Chicago, IL, United States (unspecified) SALARY: Not disclosed POSTED: 2026-06-12 PARENTAL_LEAVE_WEEKS: 12 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 12 (not source-backed) K401_MATCH: yes (not source-backed) APPLY_URL: https://jobs.smartrecruiters.com/AbbVie/3743990013580676-scientist-i-cell-and-molecular-biologist EXCERPT: Scientist I, Cell and Molecular Biologist North Chicago, IL, United States Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: Description: AbbVie Oncology Discovery is seeking a highly motivated and experienced cancer cell biologist to support drug discovery projects in our in vitro cancer biology team with a focus on antibody-drug conjugates. The candidate will work closely with a team of experienced scientists to develop and optimize key pharmacological, biochemical and cell-based assays to support multiple programs. Key Responsibilities: Design and execute in vitro studies to assess novel antibody-drug conjugates Analyze and interpret experiments and present data to the broader project team and group meetings. Propose relevant follow-up experiments as needed. Troubleshoot and/or optimize experimental procedures as needed to further the program goals. Contribute to the preparation of data packages for scientific publications, regulatory documents, and patent applications Work independently in a fast paced, multi-tasking environment as part of a diverse research team. Collaborate with cross-functional teams to advance programs from early discovery to preclinical development Qualifications: Qualifications Required: Bachelor's Degree with 5 years of experience, or --- TITLE: Data Scientist II - AMZ24268.1 EMPLOYER: Amazon LOCATION: New York, New York, USA (unspecified) SALARY: $170K-$208K POSTED: 2026-05-01 PARENTAL_LEAVE_WEEKS: 6 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 6 (not source-backed) K401_MATCH: yes (not source-backed) FERTILITY_FAMILY_BUILDING_BENEFITS: yes (not source-backed) ADOPTION_ASSISTANCE_OFFERED: yes (not source-backed) MENTAL_HEALTH_SUPPORT: yes (not source-backed) CHILDCARE_SUBSIDY: yes (not source-backed) APPLY_URL: https://www.amazon.jobs/en/jobs/10408859/data-scientist-ii-amz24268-1 EXCERPT: Data Scientist II - AMZ24268.1 New York, New York, USA Employer: Metro-Goldwyn-Mayer Studios Inc. Position: Data Scientist II Location: New York, NY Multiple Positions Available: Design and implement scalable and reliable approaches to support or automate decision making throughout the business. Apply a range of data science techniques and tools combined with subject matter expertise to solve difficult business problems and cases in which the solution approach is unclear. Acquire data by building the necessary SQL / ETL queries. Import processes through various company specific interfaces for accessing Oracle, RedShift, and Spark storage systems. Build relationships with stakeholders and counterparts. Analyze data for trends and input validity by inspecting univariate distributions, exploring bivariate relationships, constructing appropriate transformations, and tracking down the source and meaning of anomalies. Build models using statistical modeling, mathematical modeling, econometric modeling, network modeling, social network modeling, natural language processing, machine learning algorithms, genetic algorithms, and neural networks. Validate models against alternative approaches, expected and observed outcome, and other business defined key performance indicators. Implement models that comply with evaluations of the computational demands, accuracy, and reliability of the relevant ETL processes at various stages of production. (40 hours / week, 8:00am-5:00pm, Salary Range $169541 - $207500) Amazon.com is an Equal Opportunity - Affirmative Action Employer - Minority / Female / Disability / Veteran / Gender Identity / Sexual Orientation Basic Qualifications: Master's degree or foreign equivalent degree in Statistics, Applied Mathematics, Economics, Engineering, Computer Science, or a related field and one year of experience in the --- TITLE: Postdoctoral Fellow - Cardiometabolic Disorders (Discovery) EMPLOYER: Amgen LOCATION: US - California - Thousand Oaks (unspecified) SALARY: Not disclosed POSTED: 2026-05-12 PARENTAL_LEAVE_WEEKS: 6 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 6 (not source-backed) K401_MATCH: yes (not source-backed) APPLY_URL: https://amgen.wd1.myworkdayjobs.com/Careers/job/US---California---Thousand-Oaks/Postdoctoral-Fellow---Cardiometabolic-Disorders--Discovery-_R-244268 EXCERPT: Postdoctoral Fellow - Cardiometabolic Disorders (Discovery) US - California - Thousand Oaks posted: Posted 30+ Days Ago --- TITLE: Equipment Operator EMPLOYER: Accendra Health INC LOCATION: Kennesaw, GA (unspecified) SALARY: Not disclosed POSTED: 2026-05-12 PARENTAL_LEAVE_WEEKS: 3 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 3 (not source-backed) LEARNING_BUDGET_OFFERED: yes (not source-backed) APPLY_URL: https://owensminor.wd1.myworkdayjobs.com/OMCareers/job/Kennesaw-GA/Equipment-Operator_REQ_25_27174 EXCERPT: Equipment Operator Kennesaw, GA At Owens & Minor, we are a critical part of the healthcare process. As a Fortune 500 company with 350+ facilities across the US and 22,000 teammates in over 90 countries, we provide integrated technologies, products and services across the full continuum of care. Customers-and their patients-are at the heart of what we do. Our mission is to empower our customers to advance healthcare, and our success starts with our teammates. Owens & Minor teammate benefits include: Medical, dental, and vision insurance, available on first working day 401(k), eligibility after one year of service Employee stock purchase plan Tuition reimbursement If you feel this opportunity could be the next step in your career, we encourage you to apply. This position will accept applications on an ongoing basis. Owens & Minor is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, national origin, sex, sexual orientation, genetic information, religion, disability, age, status as a veteran , or any other status prohibited by applicable national, federal, state or local law. --- TITLE: Director, PDS&T Analytical CMC Development EMPLOYER: AbbVie Inc. LOCATION: Worcester, MA, United States (unspecified) SALARY: Not disclosed POSTED: 2026-06-12 PARENTAL_LEAVE_WEEKS: 12 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 12 (not source-backed) K401_MATCH: yes (not source-backed) APPLY_URL: https://jobs.smartrecruiters.com/AbbVie/3743990013572636-director-pds-t-analytical-cmc-development EXCERPT: Director, PDS&T Analytical CMC Development Worcester, MA, United States Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: Abbvie Product Development Science and Technology (PDS&T) Biologics Analytical-CMC Strategy is responsible for driving the analytical CMC control strategy for late-stage development of biologics. The Analytical CMC Strategy team is responsible for ensuring late phase to commercial method development, optimization, validation, advanced characterization, process development support, regulatory authoring, and control strategy for biologics. The team works cross-functionally with process development, regulatory, and quality within the Abbvie network. This role requires a strategic thinker with a strong technical analytical background in gene therapy and tLNP technologies, manage complex projects, and effectively communicate cross-functionally. Responsibilities: Drives overall analytical control strategy, including justifying appropriate specifications, determining critical quality attributes, assessing product shelf-life, and risk-based comparability strategies for the biologics pipeline. Establish collaborations across the organization to ensure delivery of critical analytical BLA enabling activities. Setting team strategies, managing resources and defining risk mitigation strategies. Communicate project strategy, key issues, and risks to relevant teams and escalate risks and facilitate resolution within/across functional --- TITLE: Corporate Recruiter, India EMPLOYER: Accendra Health INC LOCATION: 3610 Accendra India (unspecified) SALARY: Not disclosed POSTED: 2026-05-12 PARENTAL_LEAVE_WEEKS: 3 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 3 (not source-backed) APPLY_URL: https://owensminor.wd1.myworkdayjobs.com/OMCareers/job/3610-Accendra-India/Corporate-Recruiter--India_REQ_26_30255 EXCERPT: Corporate Recruiter, India 3610 Accendra India At Accendra Health, we understand that healthcare is complex, and we're here to make it easier. We help deliver care beyond traditional settings, making essential products and services more accessible through every stage of life. As part of the care team, our teammates play a critical role in delivering personalized, long-term care for the patients we serve. With deep expertise promoting health outside the hospital and a presence in communities nationwide through our Apria and Byram Healthcare brands, Accendra Health does more than just deliver the essentials. If you're interested in meaningful work with impact, explore our career opportunities and join us in our purpose of Bringing Care To Life™. If you feel this opportunity could be the next step in your career, we encourage you to apply. Accendra is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, national origin, sex, sexual orientation, genetic information, religion, disability, age, status as a veteran, or any other status prohibited by applicable national, federal, state or local law. Note: Accendra is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at our Company via email, the Internet, or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of our Company. No fee will be paid in the event --- [PASTE YOUR RESUME OR SKILLS HERE]