At a Glance
- Tasks: Develop quality assurance strategies and ensure compliance with ISO 13485.
- Company: Growing medical devices company in Cambridgeshire with a focus on innovation.
- Benefits: Competitive salary, pension scheme, and free lunches.
- Other info: Full-time office position with opportunities for professional growth.
- Why this job: Join a dynamic team and make a difference in the medical device industry.
- Qualifications: Background in engineering or biomedical engineering with 2-5 years of experience.
The predicted salary is between 35000 - 45000 £ per year.
Newton Colmore Consulting Ltd is looking for a Quality Assurance & Regulatory Affairs Specialist to join a growing medical devices company based in Cambridgeshire. The successful candidate will develop quality assurance strategies, ensure compliance with ISO 13485, and conduct internal audits.
This full-time office position offers a competitive salary package, company pension scheme, and additional benefits including free lunches.
Ideal candidates will have a background in engineering or biomedical engineering, with 2 to 5 years of experience in the medical device industry.
MedTech QA & Regulatory Specialist - ISO 13485 employer: Newton Colmore Consulting Ltd
Newton Colmore Consulting Ltd is an excellent employer, offering a dynamic work environment in the heart of Cambridgeshire's thriving medical devices sector. With a strong focus on employee development, competitive salary packages, and unique benefits like free lunches, we foster a culture of collaboration and innovation that empowers our team to excel in their roles and contribute meaningfully to the industry.
Contact Details:
Newton Colmore Consulting Ltd Recruitment Team
