Jobs
My ads
My job alerts
Sign in
Find a job Career Tips Companies
Find

Quality assurance and regulatory affairs specialist

Corsham
Permanent
Hawk 3 Talent Solutions
Regulatory affairs specialist
€37,000 a year
Posted: 24 November
Offer description

Job Title: Quality Assurance and Regulatory Affairs Specialist

Location: Corsham, Wiltshire

Hours of Work: Monday to Friday, 8.30am to 5pm

Salary: Negotiable: circa A GBP 37,000 depending in 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? Were 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. Youll play a key role in ensuring compliance and driving improvements that make a difference worldwide.

About the Role

In this role, youll support the Quality and Regulatory team in maintaining compliance with medical device and IVD standards and regulations. Youll 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.

What Were Looking For

* Bachelors 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.

Closing date is 20.12.2025 Please note this could change subject to suitable applications.

If you would like for the role of Project Manager then please to or call Craig on

Hawk 3 Talent Solutions are acting as an employment agency on behalf of its client.

By applying for the above position and providing your personal data to us you understand that your data will be processed in line with our Privacy Policy. To view our full Privacy Policy our website.

Hawk 3 Talent Solutions are committed to the selection, recruitment and development of the best people, basing judgements solely on suitability for the job. Whilst we endeavour to respond to all applications individually, due to high volumes, this is not always possible. Thank you for your interest in this role and we look forward to working with you in the future

Apply
Create E-mail Alert
Job alert activated
Saved
Save
See more jobs
Similar jobs
Science jobs in Corsham
jobs Corsham
jobs Wiltshire
jobs England
Home > Jobs > Science jobs > Regulatory affairs specialist jobs > Regulatory affairs specialist jobs in Corsham > Quality Assurance and Regulatory Affairs Specialist

About Jobijoba

  • Career Advice
  • Company Reviews

Search for jobs

  • Jobs by Job Title
  • Jobs by Industry
  • Jobs by Company
  • Jobs by Location
  • Jobs by Keywords

Contact / Partnership

  • Contact
  • Publish your job offers on Jobijoba

Legal notice - Terms of Service - Privacy Policy - Manage my cookies - Accessibility: Not compliant

© 2025 Jobijoba - All Rights Reserved

Apply
Create E-mail Alert
Job alert activated
Saved
Save