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Remote Quality Assurance Engineer
Remote / Online - Candidates ideally in
Wigan, Greater Manchester, WN1, England, UK
Listed on 2026-06-17
Wigan, Greater Manchester, WN1, England, UK
Listing for:
Owen Daniels
Full Time, Contract, Remote/Work from Home
position Listed on 2026-06-17
Job specializations:
-
Engineering
Quality Engineering -
Quality Assurance - QA/QC
Quality Engineering
Job Description & How to Apply Below
Role:
Quality Assurance Engineer – Medical Devices
Type: 6 Month Contract
Pay: £40 per hour – Inside IR35
Hours: 09:00 – 17:00 Mon-Fri
Location:
Fully Remote with occasional visits to Birmingham site
Are you a Quality Assurance Engineer contractor looking for your next contract? I’m currently representing my Medical Devices client based in Birmingham who are looking for a Quality Engineer to join them on a contract basis.
Quality Engineer - Job Description
- Supplier & Purchasing Oversight:
Ensure supplier and purchasing processes comply with regulations; develop supporting documents, supplier controls, and quality agreements. - Labelling Compliance:
Review and create procedures for product and software labelling to meet all regulatory requirements. - Regulatory Registration Support:
Prepare documentation packs for global device registrations; maintain a master list of active registrations and develop related procedures. - Technical Documentation & Risk Management:
Maintain regulatory files, support risk management activities, and document process risks per ISO 14971. - Quality Data & Trend Analysis:
Develop systems for collecting and analysing quality data to identify trends and drive improvements. - Training Development:
Create training materials on applicable regulations and standards and implement a refresher training process for key quality procedures.
- Proven experience in quality assurance and regulatory affairs within the medical device sector, including creating procedures and technical documentation.
- Strong analytical, problem-solving, and detail-oriented skills with the ability to manage multiple projects and priorities.
- In-depth knowledge of international medical device regulations and standards (e.g., MDSAP, EU MDR 2017/745, ISO 13485, ISO 9001, ISO 14971).
- Excellent regulatory writing, communication, and interpersonal collaboration skills.
- Proficient in using QMS tools and electronic document management systems; experienced with MS Office, SharePoint, and MS Teams.
- Highly organized, professional, and collaborative; effective in team environments and capable of independently planning and managing tasks.
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