Head of Quality — Peptide API & Development

hims-and-hers

Edison (CA)

On-site

USD 150,000 - 210,000

Full time

14 days+
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Benefits offered by this job

Competitive salary & equity
Unlimited PTO
Comprehensive health benefits
ESPP
401k benefits with employer matching
Offsite team retreats

Job summary

Hims & Hers seeks a hands-on Quality Manager to build and scale the Quality function for a peptide API manufacturing site with early-phase development capabilities. You will establish an inspection-ready quality system that supports peptide API manufacturing, laboratory controls, and a small GMP development space for formulation and sterile finished product work intended for transfer.

The ideal leader brings strong GMP judgment, cross-functional collaboration, and a bias for execution in a

Qualifications

  • Bachelor’s degree or higher in a relevant science or engineering field.
  • 8+ years of Quality experience in GMP-regulated environments.
  • Experience building or scaling Quality systems in startup or fast-changing settings.

Responsibilities

  • Lead development, implementation, and ongoing oversight of the site Quality Management System for peptide API manufacturing.
  • Establish and maintain core quality systems: document control, training, deviations, investigations, CAPA, change control, batch record review, management review.
  • Provide Quality oversight for peptide API manufacturing operations, including raw material control, in-process controls, lab results review, disposition support, and batch release/rejection decisions.

Skills

Builder Mindset
Quality Leadership
Hands-On Execution
Regulatory Judgment
Cross-Functional Collaboration
Adaptability

Education

Bachelor’s degree or higher in Chemistry, Biochemistry, Chemical Engineering, Pharmaceutical Sciences, Microbiology, or related field

Job description

Hims & Hers seeks a hands-on Quality Manager to build and scale the Quality function for a peptide API manufacturing site with early-phase development capabilities. You will establish an inspection-ready quality system that supports peptide API manufacturing, laboratory controls, and a small GMP development space for formulation and sterile finished product work intended for transfer.

The ideal leader brings strong GMP judgment, cross-functional collaboration, and a bias for execution in a

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