14 open listings
Roles posted by organizations here, alongside roles we found on employers’ own careers sites. Crawled roles say so on the card and send you to the employer to apply. Only show organizations on Career App
HH
Quality Manager, Peptide API & Development
Hims and Hers
Full-time · Menlo Park, CA · $130,000 – $155,000
This role leads the establishment and scaling of quality systems for a newly built peptide API manufacturing site with early-phase development capabilities. The ideal candidate is a hands-on quality leader who thrives in startup environments, can build practical GMP-compliant systems from the ground up, and works closely with operations and technical teams to ensure inspection readready manufacturing and development operations.
Data IntegrityProcess ValidationDocument ControlCorrective And Preventive Action (CAPA)Change Control
Listed on Hims and Hers’s careers site · Apply there ↗
Quality Assurance Specialist II
Beckman Coulter
Full-time · 3 locations
This Quality Assurance role supports manufacturing operations in regulated life sciences, handling complaint investigations, nonconformance assessments, and continuous improvement at a Cytiva filtration and diagnostics facility. It suits someone with 5-10 years of pharma or medical device quality experience who wants hands-on involvement in investigations and process improvement in a compliant manufacturing environment.
Root Cause AnalysisData AnalysisRisk AssessmentCorrective And Preventive Action (CAPA)Change Control
Listed on Beckman Coulter’s careers site · Apply there ↗
Choose a location to apply
Sr Engineer I, Automation (Syncade MES)
Biogen
Research Triangle Park, NC · $93,000 – $121,000
This role manages Syncade manufacturing execution systems at a biopharmaceutical facility, handling configuration, troubleshooting, and compliance in a heavily regulated GMP environment. It suits experienced automation engineers who have worked with MES platforms and want to own a critical system supporting drug manufacturing operations.
Listed on Biogen’s careers site · Apply there ↗
Senior Process Engineer, Technical Operations - Small Molecule Drug Substance
Merck
Full-time · Elkton, VA · $117,000 – $184,200
A senior technical role leading small molecule drug substance manufacturing at a new U.S. facility, responsible for process ownership from design through commercial production. Suits experienced process engineers ready to drive technical excellence and guide technology transfers in a fast-paced biopharmaceutical setting.
Senior Manager of CMC - Quality Assurance
Bristol Myers Squibb
Full-time · Indianapolis, IN · $141,515 – $171,483
This role oversees quality assurance strategies for radiopharmaceutical manufacturing and analytics across the development lifecycle, from preclinical through post-approval. It suits experienced quality professionals in biologics or sterile drug manufacturing who want to drive CMC strategy and regulatory submissions at a biotech focused on oncology.
Listed on Bristol Myers Squibb’s careers site · Apply there ↗
Principal Specialist QA Tech Ops
Moderna
A senior quality assurance role leading pharmaceutical manufacturing oversight at Moderna's Melbourne facility, focused on validation, process compliance, and regulatory readiness for mRNA drug production. Suits experienced pharma quality professionals who thrive in complex, regulated environments and want to drive operational excellence while supporting rapid innovation.
Good Manufacturing Practice (GMP)Process ValidationCorrective And Preventive Action (CAPA)Change Control
Listed on Moderna’s careers site · Apply there ↗
RS
Customer Program Manager
Relativity Space
Long Beach, CA · $104,000 – $156,000
This role leads complex aerospace and advanced manufacturing programs from conception through delivery, partnering with engineering, operations, and customers to meet cost, schedule, and technical targets. It suits experienced program managers who can translate customer needs into executable plans, influence cross-functional teams, and own both technical execution and commercial success in a regulated environment.
Budget ManagementConfiguration ManagementRisk ManagementTechnical WritingProject ManagementChange Control
Listed on Relativity Space’s careers site · Apply there ↗
HH
Sr. Process & Operations Engineer
Hims and Hers
Full-time · Minnetonka, MN · $130,000 – $150,000
This role oversees contract manufacturing operations for FDA-regulated medical devices, serving as the technical liaison between internal teams and external manufacturers. It suits experienced process engineers with deep medical device manufacturing expertise who can manage complex regulatory compliance and drive operational excellence across suppliers.
Listed on Hims and Hers’s careers site · Apply there ↗
Director, Risk Intelligence and Analytics
Biogen
Full-time · Cambridge, MA · $188,000 – $259,000
This director-level role leads a team building data systems and intelligence to monitor risks across Biogen's manufacturing and supply network, translating complex operational data into executive guidance for strategic decisions. The position suits experienced analytics leaders with deep pharmaceutical manufacturing knowledge who can combine technical rigor with clear stakeholder communication.
Senior Process Engineer, Technical Operations – Small Molecule Drug Product (Oral Solid Dose)
Merck
Full-time · Elkton, VA · $117,000 – $184,200
This role leads the technical operations for oral solid dose tablet manufacturing at a biopharmaceutical facility, supporting everything from equipment design and commissioning through commercial production. It suits experienced process engineers in pharmaceutical manufacturing who want to own tablet and coating processes at scale and drive operational improvements in a fast-moving manufacturing environment.
Senior Manager - QA Operations
Bristol Myers Squibb
Full-time · Indianapolis, IN · $141,515 – $171,483
This senior operations quality assurance role oversees compliance and quality activities across manufacturing and supply chain functions at a radiopharmaceutical manufacturing site, managing up to 8 staff members. The position suits experienced quality professionals with deep FDA/EMA regulatory knowledge and hands-on shop-floor expertise who can lead teams through complex manufacturing challenges in a fast-paced biotech environment.
Listed on Bristol Myers Squibb’s careers site · Apply there ↗
Sr. Associate III, Compliance - QRM Lead
Biogen
Full-time · Research Triangle Park, NC · $111,000 – $149,000
This role leads quality risk management and compliance operations at a pharmaceutical manufacturing site, ensuring regulatory readiness and driving continuous improvement across quality systems. It suits experienced quality assurance professionals with pharmaceutical expertise who want to take on operational leadership in a regulated manufacturing environment.
Listed on Biogen’s careers site · Apply there ↗
Senior Specialist, Associate Aseptic Process Validation Engineer
Bristol Myers Squibb
Full-time · Devens, MA · $87,660 – $106,224
This role supports aseptic process validation and sterilization testing for a cell therapy manufacturing facility, authoring protocols and leading cross-functional teams through the qualification lifecycle. It suits someone with a science degree and biopharmaceutical operations experience who wants to ensure safe, compliant drug manufacturing.
Listed on Bristol Myers Squibb’s careers site · Apply there ↗
HH
VP, Engineering & Facilities
Hims and Hers
Full-time · US Remote · $290,000 – $310,000
This VP role leads engineering strategy and execution for Hims' pharmaceutical manufacturing and pharmacy fulfillment network, overseeing facility design, cleanroom systems, automation, and capital investments of $100M+. The position suits experienced engineering leaders with deep expertise in regulated manufacturing environments who can translate compliance requirements into scalable operations while building and leading multi-disciplinary technical teams.
Listed on Hims and Hers’s careers site · Apply there ↗