HH
$140,000 – $160,000
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
A senior quality assurance engineer role supporting medical device design, development, and manufacturing at a digital health company. This suits experienced engineers in regulated industries who want to apply design controls, risk management, and validation expertise in a fast-paced environment.
Our summary, not Hims and Hers’s wording. The full posting is on their site.
Skills this role names
- Failure Mode and Effects Analysis (FMEA)
- ISO 13485
- Risk Management
- Statistical Analysis
- Technical Documentation
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What they ask for
Required
- Bachelor's degree in mechanical, biomedical, or related engineering discipline
- 5-8+ years in design assurance, new product development, or medical device/regulated industry experience
- Self-motivated problem-solver with bias for action
- Strong verbal and written communication
- Demonstrated use of quality tools and methodologies
- Ability to work in mixed onsite and remote environment
- Experience creating detailed technical documents
Nice to have
- Experience developing or manufacturing Class II medical devices
- Understanding of ISO 13485, ISO 14971, and Quality System Regulations with focus on Design Controls and Risk Analysis
- Experienced problem-solving and facilitation skills
- Adaptability and collaboration in team or self-directed settings
- Experience with design changes, complaint management, and corrective action