At a Glance
- Tasks: Lead quality assurance and regulatory affairs for medical devices across global standards.
- Company: Dynamic medical devices company based in Cambridge.
- Benefits: Tailored salary package, bonuses, and extensive training opportunities.
- Why this job: Significant career advancement in a vital industry with global impact.
- Qualifications: Experience in regulatory affairs and quality assurance in medical devices.
The predicted salary is between 60000 - 80000 £ per year.
Newton Colmore is seeking a Regulatory Affairs Specialist for a medical devices company in Cambridge. In this role, you will lead quality assurance and regulatory affairs initiatives while working to meet European, American, and Asian standards.
This opportunity promises a tailored salary package, bonuses, and extensive training, making it a significant career advancement for professionals in the industry.
Global Regulatory Affairs Lead - Medical Devices & QA in Cambridge employer: Newton Colmore
Newton Colmore is an exceptional employer, offering a dynamic work culture that prioritises professional growth and development in the medical devices sector. Located in the innovative hub of Cambridge, employees benefit from a competitive salary package, performance bonuses, and comprehensive training programmes, ensuring a rewarding career path in regulatory affairs and quality assurance.
