At a Glance
- Tasks: Support QA and regulatory compliance for medical devices across multiple regions.
- Company: Join a growing MedTech team at Newton Colmore Consulting Ltd.
- Benefits: Competitive salary and opportunities for professional growth.
- Other info: Dynamic work environment with a focus on innovation and compliance.
- Why this job: Make a difference in healthcare by ensuring safe and compliant medical devices.
- Qualifications: 2-5 years of experience and a degree in engineering or biomedical science.
The predicted salary is between 51750 - 63250 £ per year.
Newton Colmore Consulting Ltd in Cambridgeshire is seeking a Regulatory Affairs Specialist to join a growing Med Tech team.
You will support QA, regulatory compliance, and submissions across Europe, North America and APAC, helping ensure safe, compliant medical devices.
The ideal candidate has 2–5 years of experience, a bachelor’s degree in engineering or biomedical science, and strong knowledge of ISO 13485 and CE marking.
#J-18808-Ljbffr
MedTech Regulatory Affairs Specialist | ISO 13485 & CE employer: Newton Colmore Consulting Ltd
As a Mechanical Engineer in Robotics Design at this innovative start-up biotech company in London, you will be part of a dynamic team dedicated to developing cutting-edge biotechnology products. The company fosters a collaborative work culture that encourages creativity and growth, offering competitive salaries, equity options, and opportunities for professional development in a fast-paced environment. Joining this team means contributing to meaningful projects that have the potential to make a significant impact in the life sciences sector.
Contact Details:
Newton Colmore Consulting Ltd Recruitment Team
