HH
$130,000 – $155,000
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 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.
Our summary, not Hims and Hers’s wording. The full posting is on their site.
Skills this role names
- Change Control
- Corrective And Preventive Action (CAPA)
- Data Integrity
- Document Control
- Process Validation
Log in to see which of these are already on your profile.
What they ask for
Required
- Bachelor's degree in Chemistry, Biochemistry, Chemical Engineering, Pharmaceutical Sciences, Microbiology, or related field
- 6–10+ years of Quality experience in pharmaceutical, biotech, API, sterile manufacturing, or related 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
- Data integrity expertise