At a Glance
- Tasks: Develop and implement regulatory strategies for medical devices across multiple regions.
- Company: Join a leading consulting firm in the MedTech industry based in Cambridge.
- Benefits: Enjoy a competitive salary, performance bonuses, and more perks.
- Other info: Be part of a dynamic team with opportunities for professional growth.
- Why this job: Make a difference in healthcare by ensuring compliance with vital regulations.
- Qualifications: 2-5 years of experience in medical devices and a degree in engineering or biomedical engineering.
The predicted salary is between 40000 - 50000 £ per year.
Newton Colmore Consulting is seeking an experienced Quality Assurance & Regulatory Affairs Specialist to join our team in Cambridge. This role involves developing and implementing regulatory strategies for medical devices across Europe, North America, and APAC, ensuring compliance with ISO 13485 and CE Marking.
The ideal candidate will have 2 to 5 years of relevant experience in the medical device industry and a degree in engineering or biomedical engineering.
Benefits include a competitive salary package, performance bonuses, and more.
MedTech QA & Regulatory Specialist - ISO 13485 in Cambridge employer: Newton Colmore Consulting
Newton Colmore Consulting is an excellent employer, offering a dynamic work culture that fosters innovation and collaboration in the heart of Cambridge. Employees benefit from competitive salaries, performance bonuses, and ample opportunities for professional growth within the thriving medical device sector, making it an ideal place for those seeking meaningful and rewarding careers.
