Quality Assurance Officer - Medical Devices (m/f)
CRITICAL CATALYST · Portugal
Regulatory Affairs
Remote
Not yet analysed
Demand72
Career growth65
Healthcare fit58
Remote potential55
5-year outlook
Medical device regulatory and QA skills remain steady in demand, especially with EU/UK/US compliance exposure. Salary growth will depend on gaining specific MDR/FDA/ISO 13485 experience and progressing into senior regulatory or quality roles.
Clinical license
Not required
Applicant reach
moderate
Seniority
unclear
Employment type
full-time
Date found
2026-10-25
Intelligence details
Flexible work details
- Engagement type
- Permanent
- Hours
- Full-time
- Eligible countries
- United States, United Kingdom
- Rate period
- Annual
Listing via Himalayas.
Eligibility, licensing, and location restrictions can change. Always confirm details on the source posting before applying.
Why this is worth applying to
Worth considering if you have quality, audit, regulatory, or medical device exposure and want a non-clinical compliance pathway. Because the posting is thin, clarify responsibilities, required regulatory knowledge, location, and salary before investing heavily.
Who should apply
Clinicians with quality improvement, audit, SOP, governance, or regulatory exposure who want to move into medical device QA/regulatory affairs; pharmacists, nurses, allied health professionals, and healthcare graduates with life-sciences compliance interest.
CV angle
Reframe clinical governance, audit, SOP development, risk management, incident review, documentation, and compliance work as transferable QA/regulatory experience. Highlight any exposure to medical devices, clinical trials, regulatory submissions, quality systems, or cross-functional project work without overstating it.
Skills to highlight
- Quality Assurance
- Regulatory Compliance
- Medical Devices
- Audit and Documentation
- Risk Management
- SOP Development
- Project Management
- Cross-functional Collaboration
Role summary
A consultancy-based QA/regulatory affairs officer role supporting medical device clients with compliance, regulations, and market access across the EU, UK, and US.
We publish our own intelligence summary, never the full job description. Always confirm details with the employer when you apply.