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Quality Specialist, Peptide API & Development

Job in Menlo Park, San Mateo County, California, 94029, USA
Listing for: Hims, Inc.
Full Time position
Listed on 2026-07-11
Job specializations:
  • Quality Assurance - QA/QC
    Regulatory Compliance Specialist, QA Specialist - Analyst/Manager, Quality Control - QC Analysts/Managers, Data Analyst
Salary/Wage Range or Industry Benchmark: 110000 - 170000 USD Yearly USD 110000.00 170000.00 YEAR
Job Description & How to Apply Below

About the Role:

We are looking for a highly organized, detail-oriented Quality Specialist to support Quality operations at a peptide-focused API manufacturing and development site. This role will help execute and maintain core GMP quality systems needed to support peptide API manufacturing, laboratory activities, and an early-phase drug product development environment designed to feed future tech transfers into 503A and 503B operations.

The ideal candidate is comfortable working in a startup setting, can manage documentation and follow-through with a high level of discipline, and is eager to help build a practical, inspection-ready Quality foundation from the ground up.

Core Skills & Traits
  • Detail-Oriented:
    Maintains accuracy and consistency in GMP records and documentation.
  • Execution-Focused:
    Follows through on assignments and helps drive actions to closure.
  • Quality Mindset:
    Understands the importance of compliance, traceability, and controlled execution.
  • Collaborative:
    Works effectively across Quality, Operations, Engineering, and Technical teams.
  • Adaptable:
    Comfortable supporting a growing site where systems and responsibilities are evolving.
  • Proactive:
    Identifies gaps early, asks good questions, and brings solutions-oriented thinking.
You Will:
  • Support day-to-day execution of site Quality Systems, including document control, training, deviations, CAPA, change control, and record management.
  • Review GMP records for completeness, accuracy, and compliance with approved procedures and Good Documentation Practices.
  • Assist with issuance, tracking, reconciliation, and archival of controlled documents such as SOPs, forms, logbooks, protocols, and reports.
  • Support batch record review activities for peptide API manufacturing and related operations, escalating issues to Quality leadership as appropriate.
  • Assist in tracking and coordinating deviations, investigations, CAPAs, change controls, and associated action items to closure.
  • Support training administration, including assignment tracking, training matrix maintenance, and follow-up on overdue training.
  • Participate in routine walkthroughs of manufacturing, laboratory, warehouse, and support areas to reinforce compliance and identify improvement opportunities.
  • Support qualification, validation, and startup documentation activities, including protocol/report routing and document completeness checks.
  • Assist with supplier quality, material status controls, and documentation associated with incoming materials, specifications, and quality records.
  • Support inspection readiness activities, including preparation of records, document retrieval, and participation in internal and external audits.
  • Help maintain quality metrics, logs, and trackers to support trending, management review, and continuous improvement.
  • Partner with Operations, Engineering, and Technical teams to ensure quality expectations are understood and implemented consistently.
You Have:
  • Bachelor’s degree in Chemistry, Biology, Biochemistry, Pharmaceutical Sciences, or related field preferred.
  • 2–5+ years of experience in Quality, manufacturing, laboratory, or document control roles in pharmaceutical, biotech, or other GMP-regulated environments.
  • Experience with peptide API, sterile operations, laboratory controls, or startup/manufacturing support environments is a plus.
  • Working knowledge of cGMP principles, Good Documentation Practices, and basic quality systems concepts.
  • Strong organizational skills with the ability to manage multiple priorities and follow through on details.
  • Experience using electronic quality systems, document management systems, or training systems is preferred.
Working Environment
  • Startup environment with evolving processes and priorities.
  • Frequent interaction with manufacturing, laboratory, and development teams.
  • Regular onsite presence in GMP and support areas.
  • May require flexibility in working hours to support startup, validation, and operational needs.
Our Benefits (there are more but here are some highlights)
  • Competitive salary & equity compensation for full-time roles
  • Unlimited PTO, company holidays, and quarterly mental health days
  • Comprehensive health benefits including medical, dental & vision,…
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