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A talent solutions company in the United Kingdom is seeking a Quality Assurance and Regulatory Affairs Specialist. You will be responsible for ensuring compliance with regulations and improving the Quality Management System. The ideal candidate has experience in the medical device industry and strong analytical skills. This role offers a negotiable salary up to £37,000 and various benefits including a pension scheme.
Job Title : Quality Assurance and Regulatory Affairs Specialist
Location : Corsham, Wiltshire
Hours of Work : Monday to Friday, 8.30am to 5pm
Salary : Negotiable : circa £37,000 depending in experience
Holiday & Benefits : 25 days plus bank holidays, company pension scheme.
Are you passionate about quality, compliance, and making a real impact in the medical device industry? We're looking for a Quality Assurance and Regulatory Affairs Specialist to join our team and help ensure that our products meet the highest standards of safety and performance.
This is an exciting opportunity to work in a dynamic environment where innovation and quality are at the heart of everything we do. You'll play a key role in ensuring compliance and driving improvements that make a difference worldwide.
In this role, you'll support the Quality and Regulatory team in maintaining compliance with medical device and IVD standards and regulations. You'll monitor and advise on the performance of the Quality Management System (QMS), produce reports on key indicators, and drive continuous improvement initiatives across the organisation.
Implement, maintain, and improve the Quality Management System in line with applicable standards and regulations.
Monitor and report on quality performance, including tracking key performance indicators (KPIs).
Contribute to regulatory submission…