Scientific Medical Information Specialist jobs
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- BMS Performance LtdNorth West London
- 3+ years' medical device regulatory experience.
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- The Christie NHS Foundation TrustManchester M20 4BX
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- Leeds Teaching Hospitals NHS TrustLeeds LS9 7TF
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- Work with clinicians and other scientists in the healthcare environment providing specialist physical sciences bioinformatics services to patient care.
- Beckman Coulter DiagnosticsLondon SE1
- Annual leave
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- Beckman Coulter DiagnosticsLondon SE1
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- Quotient SciencesAlnwick NE66
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- Zenopa RecruitmentSouth West Region
- Annual leave
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- UK Health Security AgencyColindale
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- Scottish GovernmentGlasgow
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- UK Health Security AgencyDidcot
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- Produce scientific reports and peer reviewed publications.
- Extensive experience in publishing scientific reports and peer-reviewed papers.
- Animal and Plant Health AgencyNew Haw KT15
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Job Post Details
Regulatory Medical Affairs - Office Based - job post
4.54.5 out of 5 stars
North West London
£50,000 - £56,000 a year - Permanent, Full-time
Job details
Pay
- £50,000 - £56,000 a year
Job type
- Permanent
- Full-time
Location
North West London
Full job description
Join a leading SME where your regulatory expertise will directly impact advanced wound care products that improve patient outcomes.
Senior Regulatory Affairs Specialist | Advanced Wound Care & Infection Prevention
NW London (office based 5 days per week)
£56K + Bonus + Excellent Benefits
Strong knowledge of EU MDR 2017/745 & ISO 13485 required
Looking for a regulatory role where your work directly supports products that improve patient outcomes?
Learning and development supported - clear progression!
The company is a well-regarded SME and a leading force in advanced wound care and infection prevention, with a product portfolio backed by strong clinical evidence.
Why This Role?
- Senior RA position with real ownership and influence
- Innovative medical device SME with a strong reputation
- Key role supporting EU MDR compliance and product growth
- Diverse, clinically meaningful wound care portfolio
- Clear progression and ongoing development opportunities
What You'll Do:
- Lead and maintain EU MDR technical documentation
- Support Class I to Class II product transitions
- Collaborate with Clinical, R&D, Marketing and Operations teams
- Manage regulatory submissions and compliance activities
- Engage with Notified Bodies and Competent Authorities
- Help shape global regulatory strategy
Requirements:
- 3+ years' medical device regulatory experience
- Strong knowledge of EU MDR 2017/745 & ISO 13485
- Experienced with technical documentation
- Detail-focused, proactive and commercially aware
- Excellent stakeholder management skills
Benefits:
- £52-56K basic
- 5% annual bonus
- 25 days holiday + bank holidays
Ready to take ownership of a high-impact regulatory portfolio? Apply now.
Reference for internal use only: [FE14B0]
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