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5 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
Hims and Hers
Full-time · Menlo Park, CA · $175,000 – $215,000
This role leads quality operations for a new peptide API manufacturing and development facility, building GMP systems from the ground up while overseeing manufacturing compliance, lab controls, and early-stage drug product development. It suits experienced quality professionals comfortable working hands-on in startup environments who can balance regulatory rigor with practical problem-solving.
Listed on Hims and Hers’s careers site · Apply there ↗
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 ↗
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.
Impulse Space
Redondo Beach
This is a hands-on materials testing role in a space company's lab, where you'll run mechanical tests on metals, polymers, composites, and ceramics according to strict standards. It suits someone with laboratory experience and attention to detail who wants to contribute directly to spacecraft and propulsion system development.
Listed on Impulse Space’s careers site · Apply there ↗
Moderna
Full-time
A quality assurance specialist providing real-time oversight of mRNA drug manufacturing and quality control operations at Moderna's Melbourne facility, ensuring compliance with cGMP standards and supporting continuous improvement. Ideal for someone with pharmaceutical manufacturing experience who enjoys hands-on quality work, cross-functional collaboration, and making direct patient impact in a high-growth biotech environment.
Listed on Moderna’s careers site · Apply there ↗
Listed on Gilead Sciences’s careers site · Apply there ↗