HH
$175,000 – $215,000
Listed on Hims and Hers’s own careers site. You apply with them directly — we never stand between you and the employer.
What this role is
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.
Our summary, not Hims and Hers’s wording. The full posting is on their site.
Skills this role names
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What they ask for
Required
- Bachelor's degree in Chemistry, Biochemistry, Chemical Engineering, Pharmaceutical Sciences, Microbiology, or related field
- 8+ years of Quality experience in pharmaceutical, biotech, API, sterile manufacturing, or GMP-regulated environments
- Strong working knowledge of cGMP requirements including 21 CFR 210/211 and ICH Q7
- Experience supporting qualification/validation, laboratory controls, investigations, and inspection readiness
- Ability to influence cross-functional teams and make sound quality decisions in ambiguous environments
Nice to have
- Prior experience building or scaling Quality systems in an early-stage, startup, or rapidly evolving site environment
- Experience with peptide API manufacturing, complex chemical synthesis, sterile manufacturing support, or product development quality oversight