HH
$130,000 – $150,000
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 contract manufacturing operations for FDA-regulated medical devices, serving as the technical liaison between internal teams and external manufacturers. It suits experienced process engineers with deep medical device manufacturing expertise who can manage complex regulatory compliance and drive operational excellence across suppliers.
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
- Bachelor's degree in Engineering (Mechanical, Biomedical, Industrial, Manufacturing, or related field)
- 8+ years in process engineering, operations engineering, or manufacturing engineering in medical device or diagnostics industry
- Experience supporting Class II FDA-regulated medical devices in GMP manufacturing environment
- Direct experience managing or working with Contract Manufacturing Organizations (CMOs)
- Strong understanding of design controls, process validation, FDA regulations, ISO 13485, CAPA and change control systems
- Ability to collaborate with Quality, Regulatory, and R&D teams in regulated environments
- Medical clearance to wear respiratory protection
- Ability to work with hazardous drugs and wear required PPE
- Physical capability to walk up to 50%, stand up to 100%, squat and bend up to 20%, and lift up to 50 lbs for up to 12-hour shifts