Quality Inspector

ZipRecruiter; Oxford; On-site; GBP 30,000 - 40,000; Full time

Job summary

A leading medical device manufacturer is seeking a Quality Inspector in Oxford to perform inspections ensuring compliance with ISO 13485 and GMP. Ideal candidates will have 2+ years of experience, strong attention to detail, and the ability to work in a fast-paced, regulated environment. You'll be instrumental in maintaining product integrity and patient safety, ensuring every device meets rigorous quality standards.

Qualifications

• Minimum 2+ years’ experience in a Quality Inspector or QA Technician role.
• Strong knowledge of ISO 13485, 21 CFR Part 820, and GMP.
• Competent in using mechanical inspection tools.

Responsibilities

• Perform in-process, final release, and incoming goods inspections.
• Review DHRs and batch documentation for completeness.
• Use precision measuring equipment to verify dimensions.

Skills

ISO 13485

GMP

Mechanical inspection tools

Attention to detail

Job description

Job Description

Job Title: Medical Device Quality Inspector

Location: On-Site, Oxford, United Kingdom

Employment Type: FTC - 6 months, Full Time

Role:

A fast-growing and innovation-driven medical device manufacturer based in Oxford is hiring for a Quality Inspector.

This company has seen consistent growth in regulated markets and is now seeking a Quality Inspector with a strong grounding in ISO 13485 and GMP principles to support its production quality assurance operations. This is a key hire in the Quality function. This role is ideal for someone who thrives in a hands-on, precision-focused environment and takes pride in being the last line of defence before a device reaches the patient, as well as being highly detail-oriented.

The Opportunity:

This role will place you right at the heart of the quality operations, working alongside engineering, manufacturing, and quality teams to ensure every device released is fully compliant with internal procedures and global regulatory expectations. You’ll be conducting in-process and final inspections on Class II devices, contributing directly to patient safety and product integrity.

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 of 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

Requirements

• 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