24 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 ↗
Reagent Manufacturing Engineer
Beckman Coulter
Indianapolis, IN
This role involves overseeing the transition of reagent products from development to manufacturing and optimizing existing production processes at a life sciences company. It suits engineers with a regulated manufacturing background who want to bridge product development and operations in a diagnostics environment.
Listed on Beckman Coulter’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, Advanced Manufacturing Team
Medtronic
Full-time · Danvers, MA · $103,200 – $154,800
This Senior Process Engineer role focuses on developing and optimizing manufacturing processes for medical devices, with responsibility for driving automation, process validation, and cross-functional collaboration. The position suits experienced engineers with a background in regulated manufacturing who want to influence product scale-up and lead technical teams in a fast-paced healthcare environment.
Associate Director, Technical Operations - Small Molecule Drug Product
Merck
Full-time · Elkton, VA · $142,400 – $224,100
This role leads technical operations for a biopharmaceutical manufacturing site producing oral solid dose medications, overseeing process scale-up, technology transfer, and commercial production. It suits experienced pharmaceutical engineers and process specialists ready to manage manufacturing transitions from development to market while building team leadership capabilities.
Senior Engineer I, External MSAT
Moderna
Full-time · $109,200 – $174,600
This role oversees the transfer and optimization of Moderna's mRNA manufacturing processes to external contract manufacturers, ensuring quality and compliance across chemical and biologic production. It suits experienced pharmaceutical or biotech engineers with strong GMP expertise who thrive managing complex technical relationships and data-driven improvements across manufacturing networks.
Good Manufacturing Practice (GMP)Statistical AnalysisProcess ValidationData ManagementRisk Assessment
Listed on Moderna’s careers site · Apply there ↗
Lead Validation Engineer
Bristol Myers Squibb
Full-time · Indianapolis, IN · $124,449 – $150,803
This role leads validation and commissioning activities for a radiopharmaceutical manufacturing facility, ensuring GMP compliance as the operation transitions from construction to clinical and commercial production. It suits someone with deep manufacturing validation expertise who can independently manage complex programs while guiding a technical team through regulatory requirements and process improvements.
Good Manufacturing Practice (GMP)Root Cause AnalysisProcess ValidationTechnical WritingRisk Assessment
Listed on Bristol Myers Squibb’s careers site · Apply there ↗
Biologics Manufacturing Technical Expert III
Gilead Sciences
United States - California - Foster City · $126,820 – $164,120
A technical leadership role designing and operating a new biologics manufacturing facility from the ground up, combining strategic facility design with hands-on floor execution. Ideal for experienced manufacturing professionals who want to architect cutting-edge single-use systems while directly managing their startup and ongoing operations.
Listed on Gilead Sciences’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 ↗
Process Engineer II
Beckman Coulter
Full-time · West Sacramento, CA · $74,000 – $90,000
This is a manufacturing problem-solving role at a diagnostics company where you'd investigate production issues, lead corrective actions, and support pilot manufacturing for medical devices. It suits someone with a science degree and regulated manufacturing experience who can combine lab skills with quality troubleshooting.
Listed on Beckman Coulter’s careers site · Apply there ↗
Principal Manufacturing Engineer - Implantable Device Unit
Biogen
Full-time · Cambridge, MA · $159,000 – $219,000
This role leads manufacturing strategy and execution for implantable drug delivery systems, working across development and commercialization phases to establish scalable processes and best practices. It suits an experienced medical device engineer who can influence cross-functional decisions, manage external partnerships, and drive innovation within strict regulatory frameworks.
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 Supplier Quality Engineer
Medtronic
Full-time · 2 locations · $99,200 – $148,800
This role manages supplier quality and component qualification for new cardiac surgery devices at Medtronic, working across engineering, regulatory, and sourcing teams to ensure devices meet quality and regulatory standards. It suits someone with medical device manufacturing experience who can lead supplier audits, resolve quality issues, and coordinate development activities within tight program timelines.
Listed on Medtronic’s careers site · Apply there ↗
Choose a location to apply
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 ↗
Senior Validation Engineer
Bristol Myers Squibb
Full-time · Indianapolis, IN · $107,904 – $130,754
This role leads validation and commissioning efforts for a new radiopharmaceutical manufacturing facility, supporting the transition from construction through clinical and commercial operations. It suits experienced validation engineers who can independently manage complex GMP projects while mentoring others in a specialized biotech environment.
Listed on Bristol Myers Squibb’s careers site · Apply there ↗
Senior Biologics Manufacturing Technical Expert
Gilead Sciences
Full-time · United States - California - Foster City · $146,540 – $189,640
This role involves designing, building, and operating a new biopharmaceutical manufacturing facility from the ground up, combining strategic facility planning with hands-on floor execution. It suits experienced biologics manufacturing experts who want to own a greenfield project and translate technical vision directly into operations.
Listed on Gilead Sciences’s careers site · Apply there ↗
Associate Director, Technical Operations - Small Molecule Drug Substance
Merck
Full-time · Elkton, VA · $142,400 – $224,100
Lead technical operations for small molecule drug manufacturing at a newly built U.S. site, overseeing process scale-up, technology transfer, and commercial production of active pharmaceutical ingredients. Suited to experienced pharmaceutical process engineers seeking to drive operational excellence and build manufacturing capability from startup through commercialization.
HH
Project Manager, Peptide API Operations
Hims and Hers
Full-time · Menlo Park, CA · $110,000 – $130,000
This role leads the setup and technology transfer of peptide manufacturing facilities, coordinating across operations, quality, and engineering teams to move production processes from development into commercial GMP compliance. It suits experienced project managers in pharma or biotech who have managed complex manufacturing startups and can navigate regulated environments with multiple stakeholders.
Listed on Hims and Hers’s careers site · Apply there ↗
Senior Process Engineer, Technical Operations – Small Molecule Drug Product (Spray Drying)
Merck
Full-time · Elkton, VA · $117,000 – $184,200
A senior technical role leading spray drying and drug product intermediate manufacturing at a biopharmaceutical facility, suitable for experienced process engineers ready to own particle engineering and scale-up from technology transfer through commercial production.
Listed on Merck’s careers site · Apply there ↗
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.
Director, Technical Operations (Small Molecule Drug Substance)
Merck
Full-time · Elkton, VA · $173,200 – $272,600
A director-level role leading technical operations for small molecule drug manufacturing at a U.S. biopharmaceutical facility. The position combines hands-on expertise in process engineering, scale-up, and manufacturing with people leadership to drive operational excellence, regulatory compliance, and continuous improvement across a growing site.
Listed on Merck’s careers site · Apply there ↗
Director, Technical Operations (Small Molecule Drug Product)
Merck
Full-time · Elkton, VA · $173,200 – $272,600
A director-level technical operations role leading small molecule drug manufacturing at a biopharmaceutical facility, responsible for process excellence, technology transfer, regulatory compliance, and building high-performing teams. This position suits experienced manufacturing leaders who combine deep process expertise with the ability to drive organizational transformation across a regulated environment.
Associate Process Engineer, Technical Operations - Small Molecule Drug Substance
Merck
Full-time · Elkton, VA · $71,900 – $113,200
This role supports the design, commissioning, and commercial operation of a small-molecule drug manufacturing facility, with early focus on capital projects and technology transfer before moving into routine production support. It suits engineers with some pharmaceutical manufacturing experience who want to grow expertise in API processes while contributing to operational improvements at a U.S.-based site.
Listed on Merck’s careers site · Apply there ↗
Associate Director, Biologics New Product Commercialization
Merck
Full-time · $142,400 – $224,100
This role leads the transfer of new monoclonal antibody products from research into commercial manufacturing, coordinating between internal labs, manufacturing sites, and external partners. It suits experienced biotech leaders who excel at managing complex cross-functional projects in regulated environments and can translate technical challenges into practical execution plans.
Listed on Merck’s careers site · Apply there ↗