At a Glance
- Tasks: Support the RA/QA Manager in device development and regulatory submissions.
- Company: Join a leading medical devices company in vibrant Cambridge.
- Benefits: Gain valuable experience in a growing industry with potential for career advancement.
- Other info: Dynamic team environment with opportunities to learn and grow.
- Why this job: Make a difference in healthcare by ensuring quality and compliance in innovative medical devices.
- Qualifications: Knowledge of ISO 13485 and FDA 510k; engineering or sciences degree preferred.
The predicted salary is between 27000 - 33000 £ per year.
Newton Colmore Consulting seeks a Regulatory Affairs and Quality Assurance Assistant for a medical devices company in Cambridge.
You will support the RA/QA Manager and be involved with R&D to advise on device development and regulatory submissions.
Applicants should have ISO 13485 and FDA 510k knowledge, with QA experience; a 1st or 2:1 degree in engineering or sciences is desirable, and exposure to QMS is advantageous.
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Regulatory & QA Associate – Medical Devices (Cambridge) employer: Newton Colmore Consulting
Join a dynamic mechanical engineering services company that prioritises employee growth and development, offering clear progression pathways and a supportive work culture. With a focus on building long-term relationships and delivering exceptional service, you'll thrive in an environment that values your expertise and encourages innovation. Located centrally in Hampshire, this role provides the unique advantage of engaging with diverse industrial sectors across the South Coast, ensuring your contributions have a meaningful impact on the business's success.
