At a Glance
- Tasks: Provide strategic input on regulatory requirements and ensure compliance with ISO and FDA guidelines.
- Company: Join Analog Devices, a leader in digital healthcare innovation.
- Benefits: Competitive salary, health benefits, and opportunities for professional growth.
- Other info: Be part of a dedicated team focused on improving healthcare outcomes.
- Why this job: Make a real difference in patient care while navigating exciting regulatory challenges.
- Qualifications: MS in Regulatory Affairs and experience with ISO 13485 and FDA regulations.
The predicted salary is between 50000 - 70000 £ per year.
Analog Devices, Inc. is seeking a Principal Regulatory Affairs Specialist in Cambridge, United Kingdom. This role involves providing strategic input and technical guidance on regulatory requirements for new technologies, participating in regulatory submissions, and maintaining compliance with ISO and FDA guidelines.
The ideal candidate will have an MS in Regulatory Affairs and experience with ISO 13485 and FDA regulations. Join a team focused on improving patient care while navigating complex regulatory landscapes.
Regulatory Affairs Specialist, Digital Healthcare in Cambridge employer: Analog Devices, Inc.
At Analog Devices, Inc., we pride ourselves on being an exceptional employer that fosters a collaborative and innovative work culture in the heart of Cambridge. Our commitment to employee growth is evident through continuous training opportunities and a focus on meaningful contributions to patient care, making this role not just a job, but a rewarding career path in the dynamic field of digital healthcare.
