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Site Leader​/Operations Director - Peptide API

Remote / Online - Candidates ideally in
Menlo Park, San Mateo County, California, 94029, USA
Listing for: Femtech Insider Ltd.
Remote/Work from Home position
Listed on 2026-07-08
Job specializations:
  • Pharmaceutical
    Pharmaceutical Manufacturing, Regulatory Compliance Specialist
Salary/Wage Range or Industry Benchmark: 120000 - 160000 USD Yearly USD 120000.00 160000.00 YEAR
Job Description & How to Apply Below
Position: Site Leader/ Operations Director - Peptide API

Hims & Hers is the leading health and wellness platform, on a mission to help the world feel great through the power of better health. We are redefining healthcare by putting the customer first and delivering access to care that is affordable, accessible, and personal, from diagnosis to treatment to delivery. No two people are the same, so we provide access to personalized care designed for results.

By normalizing health & wellness challenges and innovating on their solutions, we’re making better health outcomes easier to achieve.

Hims & Hers is a public company, traded on the NYSE under the ticker symbol "HIMS." To learn more about the brand and offerings, you can visit  and  For information on the company’s outstanding benefits, culture, and its talent-first flexible/remote work approach, see below and visit

About the Role:

We are seeking a highly motivated, hands-on Operations Leader to help build and scale manufacturing operations for a peptide API facility. This role is responsible for establishing/enhancing production processes, implementing/modifying GMP systems, and leading day‑to‑day manufacturing activities. The ideal candidate thrives in fast‑paced, ambiguous environments and is equally comfortable setting strategy and executing on the floor.

You Will:
  • Build and scale peptide API manufacturing operations from early‑stage development through commercial readiness.
  • Develop and implement production workflows for peptide synthesis, including SPPS, purification, and lyophilization.
  • Drive facility readiness through equipment qualification (IQ/OQ/PQ), process validation, and manufacturing startup activities.
  • Provide hands‑on technical leadership by troubleshooting peptide synthesis, purification (HPLC), and downstream manufacturing processes.
  • Lead and develop a growing manufacturing team while remaining actively engaged in day‑to‑day operations as needed.
  • Establish production planning, scheduling, and operational systems to support scalable manufacturing.
  • Build and implement cGMP‑compliant quality systems, including batch records, SOPs, deviations, CAPAs, and change controls.
  • Partner closely with Quality to establish a strong culture of compliance and prepare the facility for regulatory inspections (FDA, EMA, etc.).
  • Collaborate with R&D to transfer peptide manufacturing processes into production and optimize processes for scalability, yield, and robustness.
  • Identify and implement process improvements that increase operational efficiency, product quality, and manufacturing reliability.
  • Establish and maintain environmental health and safety programs while proactively identifying and mitigating operational and compliance risks.
  • Partner cross‑functionally with Supply Chain, Engineering, Quality, and other stakeholders to ensure manufacturing readiness and continuous improvement.
  • Support hiring, onboarding, training, and development of a high‑performing manufacturing organization.
You Have:
  • Bachelor’s degree or higher in Chemistry, Chemical Engineering, Pharmaceutical Sciences, or a related scientific discipline.
  • 8+ years of experience in pharmaceutical or biotechnology manufacturing, preferably including early‑stage or startup environments.
  • Direct experience in peptide API manufacturing strongly preferred.
  • Proven experience building manufacturing processes, systems, and operational infrastructure from the ground up rather than inheriting mature operations.
  • Hands‑on technical expertise with solid‑phase peptide synthesis (SPPS), peptide purification (HPLC), and downstream processing, with the ability to troubleshoot complex manufacturing challenges.
  • Strong working knowledge of current Good Manufacturing Practices (cGMP), including experience implementing and maintaining quality systems in a regulated environment.
  • Demonstrated ability to lead and develop small, growing technical teams while remaining actively involved in day‑to‑day operations.
  • Ability to thrive in a fast‑paced, evolving environment with limited resources, balancing competing priorities and adapting to changing business needs.
  • A bias for action with strong decision‑making skills, capable of driving progress with incomplete information while…
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