9 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 ↗
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.
Associate Director, Sterility Assurance
Moderna
$142,500 – $256,500
This role leads contamination control and sterility assurance programs at a pharmaceutical manufacturing facility, overseeing compliance with regulatory standards, environmental monitoring, and aseptic practices. The position suits experienced quality and manufacturing professionals who can drive continuous improvement across complex sterile operations and work closely with cross-functional teams.
Listed on Moderna’s careers site · Apply there ↗
Data Reviewer, Quality Control Microbiology
Bristol Myers Squibb
Full-time · Indianapolis, IN · $31 – $38 / hour
This role reviews microbiological quality control data at a radiopharmaceutical manufacturing facility, ensuring compliance with cGMP and regulatory standards. It suits someone with laboratory microbiology experience who can work independently to validate testing results and support a manufacturing environment handling ionizing radiation.
Listed on Bristol Myers Squibb’s careers site · Apply there ↗
Director, IT SAP Product Lifecycle and Quality
Gilead Sciences
Full-time · United States - California - Foster City · $226,185 – $292,710
This director-level role leads Gilead's enterprise IT strategy and delivery for product lifecycle management and quality systems, overseeing SAP platforms and regulated manufacturing processes. It suits experienced IT leaders with deep SAP expertise and a track record of managing complex portfolios across life sciences organizations.
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.
Director, Clinical Sciences, Oncology
Moderna
Full-time · $183,800 – $330,300
This role leads clinical development strategy and execution for oncology studies at a biotechnology company, overseeing data quality, regulatory compliance, and study operations from early to late phases. It suits experienced clinical scientists with advanced degrees and deep oncology expertise who can drive complex programs across multiple internal and external stakeholders.
Listed on Moderna’s careers site · Apply there ↗
Scientist, Analytical Sciences and Technology
Moderna
$109,200 – $174,600
Moderna seeks a scientist to lead analytical method lifecycle management across pharmaceutical development and manufacturing, ensuring validation, transfer, and troubleshooting of testing processes in a highly regulated environment. This role suits someone with deep analytical chemistry expertise who can collaborate across quality, manufacturing, and regulatory functions to solve complex technical problems at scale.
Listed on Moderna’s careers site · Apply there ↗
Senior Manager, Study Management & Outsourcing (Canada)
Moderna
Full-time
Lead sponsor-side oversight of nonclinical studies at Moderna's Canadian operations, managing GLP and non-GLP research from protocol development through final reporting. This role suits experienced study managers and monitors in the biopharmaceutical sector who can manage complex outsourced research programs, work with CROs, and drive regulatory compliance across a matrixed organization.
Listed on Moderna’s careers site · Apply there ↗