Listed on Hims and Hers’s own careers site. You apply with them directly — we never stand between you and the employer.
What this role is
This role oversees quality control and compliance in a pharmaceutical manufacturing setting, inspecting products throughout production and managing documentation to meet regulatory standards. It suits someone with quality assurance or process engineering experience who can work independently on a night shift and handle both hands-on testing and administrative compliance work.
Our summary, not Hims and Hers’s wording. The full posting is on their site.
Skills this role names
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What they ask for
Required
- 2+ years quality assurance, quality control, process engineering, or product formulation experience
- Working knowledge of USP <795>, <797>, <800> standards
- Knowledge of cGMP and regulated pharmaceutical environment
- Ability to perform in-process and post-production quality checks and testing
- Experience with batch record review and documentation
Nice to have
- B.S. in chemistry, biology, quality management, or related discipline
- Experience in 503b outsourcing facility
- Aseptic processing experience
- Knowledge of ISO 14644
- Experience with FDA 21 CFR 210 and 211
- Knowledge of technical writing and auditing
- Experience with MRP systems