Function · Regulatory & Quality
Regulatory Affairs & Quality recruiting across the life sciences lifecycle.
Regulatory affairs strategy, submissions, quality systems, QA, QMS, compliance. The discipline that holds the rest of the company accountable to the data.
- Regulatory Specialist through Chief Regulatory Officer
- QA, QMS, quality engineering, and compliance leadership
- Pharma (IND, NDA, BLA) and medical device (510(k), PMA, De Novo) submissions
- International regulatory (EMA, PMDA, NMPA) leadership
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Connected practice
How this work intersects the rest of the practice.
Frequently asked
Common questions, answered plainly.
- Can you find a Chief Regulatory Officer for biotech?
- Yes. CRO searches are a retained executive practice area — typical timeline 12–14 weeks with a confidential slate.
- Do you work medical device regulatory specifically?
- Yes. Device regulatory and pharma regulatory are distinct talent pools; we route accordingly. Pre-510(k) startups, PMA-pathway companies, and SaMD all served.
- Can you support quality systems / QMS overhauls?
- Yes — including post-warning-letter remediation hires, where the urgency and pattern recognition required are very specific.
Building out regulatory & quality?
We'll scope the role, benchmark comp, and surface a slate within two weeks.