Overview
Role: Medical Device Quality Inspector at a fast-growing, innovation-driven medical device manufacturer based in Oxford. This is a hands-on, precision-focused position focused on production quality assurance and ensuring devices meet internal procedures and global regulatory expectations.
Location: On-Site, Oxford, United Kingdom
Employment Type: FTC - 6 months, Full Time
Responsibilities
* Perform in-process, final release, and incoming goods inspections in accordance with ISO 13485 and company SOPs
* Review DHRs and batch documentation for completeness and compliance
* Use precision measuring equipment to verify critical dimensions and tolerances
* Document and escalate any NCRs, support root cause investigations and CAPA
* Liaise with production and QA teams to support continuous improvement in inspection protocols and process efficiency
* Maintain accurate inspection records in accordance with GMP and data integrity expectations
* Contribute to internal audits and support regulatory inspections when required
Qualifications
* Minimum 2+ years’ experience in a Quality Inspector or QA Technician role within the medical device or life sciences sector
* Strong working knowledge of ISO 13485, 21 CFR Part 820, and GMP
* Competent in the use of mechanical inspection tools and visual inspection techniques
* Familiarity with documentation review and batch release processes
* Attention to detail with a methodical, risk-based approach to quality
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