Quality Assurance and Regulatory Affairs Specialist
1 day ago
Quality Assurance and Regulatory Affairs Specialist 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 on experience Holiday and 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. About The Role 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. Key Responsibilities 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 submissions, technical documentation, and product registrations. Provide guidance on compliance with EU MDR, IVDR, and other international regulations. Support internal and external audits and ensure timely resolution of findings. Drive problem‑solving and continuous improvement initiatives across departments. Qualifications Bachelor’s degree in a relevant discipline (e.g., Biomedical Engineering, Life Sciences, Regulatory Affairs). Minimum of 4 years experience in Quality Assurance or Regulatory Affairs within the medical device industry. Strong knowledge of domestic and international medical device standards and regulations, including EU MDR and IVDR. Excellent written and verbal communication skills. Strong analytical, problem‑solving, and critical‑thinking abilities. High attention to detail and organisational skills. Ability to collaborate effectively within cross‑functional teams. Seniority Level Mid‑Senior level Employment Type Full‑time Job Function Quality Assurance Industry Advertising Services Closing Date 20.12.2025 By applying for this position, you understand that your personal data will be processed in line with our Privacy Policy. To view our full Privacy Policy, visit our website. #J-18808-Ljbffr
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