Quality Specialist, Peptide API & Development
Hims & Hers · Menlo Park, California · US
Posted 60+ days ago
Quality Improvement
On-site
Not yet analysed
Demand75
Career growth70
Healthcare fit70
Remote potential20
5-year outlook
Competitive for pharma quality roles, with potential for advancement to senior quality management positions as experience and expertise grow.
Clinical license
Not required
Applicant reach
moderate
Seniority
entry
Employment type
full-time
Date found
2026-08-26
Intelligence details
Why this is worth applying to
This is a strong entry point for clinicians interested in pharmaceutical quality and non-clinical careers. It offers hands-on experience in building quality systems from the ground up, which is valuable for future roles in quality assurance, regulatory affairs, or operations.
Who should apply
Pharmacists, allied health professionals, or healthcare graduates with strong attention to detail, documentation skills, and an interest in GMP and pharmaceutical manufacturing quality.
CV angle
Highlight clinical experience with documentation, adherence to protocols, attention to detail, and understanding of patient safety. Emphasize any experience with quality improvement, audits, or regulatory compliance, and frame clinical workflow knowledge as relevant to GMP documentation and process control.
Skills to highlight
- Documentation
- GMP knowledge
- Attention to detail
- Deviation management
- CAPA
- Change control
- Training administration
- Compliance
Role summary
A Quality Specialist role supporting GMP quality systems for peptide API manufacturing and development at Hims & Hers, focusing on document control, deviations, CAPA, and inspection readiness.
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