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Quality & Regulatory Affairs Lead – Digital Health
BeamQuality & Regulatory Affairs Lead managing clinical compliance and regulation for healthcare products at Beam. Driving Class IIa medical device certification while collaborating with cross-functional teams.
About the role
Key responsibilities & impact- Owning clinical compliance and the regulatory roadmap
- Driving certification through to completion
- Shaping the healthcare product roadmap
- Being the subject-matter expert
- Driving operational excellence
- Keeping everyone aligned
Requirements
What you’ll need- A Compliance Manager with experience owning clinical compliance and regulation roadmap (Medical Device Classifications; DCB docs)
- Expert in working with PMs on healthcare-required product roadmaps (e.g. ongoing clinical evaluations; integrations with NHS EPR systems; etc.)
- Skilled project manager in complex, multi-functional environments related to compliance
- Detail-Oriented Operator
- Reliable Independent Worker
- Technically Curious
- Clear Communicator
- Commercially Minded
Benefits
Comp & perks- Top-tier coaching and personal development budgets
- Competitive salaries
- Hybrid working approach
ATS Keywords
✓ Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
Medical Device ClassificationsDCB DocumentationOngoing Clinical EvaluationsNHS EPR System IntegrationOperational Excellence
Soft Skills
Detail-OrientedReliable Independent WorkerTechnically CuriousClear CommunicatorCommercially Minded