Quality Control Scientist

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 hims.com/about and hims.com/how-it-works . For information on the company’s outstanding benefits, culture, and its talent-first flexible/remote work approach, see below and visit www.hims.com/careers-professionals.

About the Role:

We are seeking a hands-on, startup-minded Quality Control (QC) Scientist to own analytical Quality oversight for a peptide-focused API manufacturing site with early-phase drug product development capabilities. This role supports two parallel programs for GMP peptide API manufacturing and sterile peptide formulation and development. This role also fills the dedicated analytical/QC function that ensures batches and data are generated, tested, and dispositioned to a compliant, inspection-ready standard.

The ideal candidate brings strong analytical fundamentals, practical GMP judgment, and the ability to operate in a build-as-you-go setting. This individual is comfortable qualifying methods, writing specifications, leading laboratory investigations, and managing outsourced testing, while partnering closely with Quality, Operations, and Technical teams to keep tech transfer and batch disposition timelines on track.

You Will:

• Own QC analytical oversight across both the peptide API manufacturing and sterile formulation development programs, including in-process, release, and stability-related testing as applicable.

• Develop, review, and maintain specifications, analytical test methods, and in-process control strategies for API synthesis and sterile drug product development.

• Plan, execute, and oversee analytical method qualification and validation activities in accordance with ICH and compendial (USP) expectations.

• Lead and document OOS/OOT and other laboratory investigations, identifying root cause and driving appropriate corrective and preventive actions.