At a Glance
- Tasks: Ensure compliance and regulatory standards for innovative medical technologies.
- Company: Growing medical devices company in Cambridge with a focus on innovation.
- Benefits: Performance bonuses, pension, and a strong benefits package.
- Other info: Join a dynamic team with opportunities for professional growth.
- Why this job: Play a key role in shaping the future of medical technology.
- Qualifications: 2-5 years of experience in QA and regulatory affairs, knowledge of ISO 13485.
The predicted salary is between 40000 - 50000 £ per year.
Newton Colmore Consulting is seeking a Quality Assurance & Regulatory Affairs Specialist in Cambridge to join their growing medical devices company. This role is pivotal in ensuring compliance and regulatory standards are met throughout the lifecycle of innovative medical technologies.
Applicants should have 2-5 years of experience in the field, in-depth knowledge of ISO 13485 and CE Marking, and ideally a bachelor's degree in engineering or biomedical engineering.
The company offers a strong package, including performance bonuses, pension, and other benefits.
MedTech QA & Regulatory Affairs Specialist (EU/NA) in Cambridge employer: Newton Colmore Consulting
Newton Colmore Consulting is an exceptional employer, offering a dynamic work environment in the heart of Cambridge, where innovation meets compliance in the medical devices sector. With a strong focus on employee development, competitive performance bonuses, and a comprehensive benefits package, the company fosters a culture of collaboration and growth, making it an ideal place for professionals looking to make a meaningful impact in healthcare technology.
