Senior Medical Device Regulatory Affairs Specialist
Cambridge
Hologic, Inc. in Cambridge, UK, is seeking a Senior Regulatory Affairs Specialist to support submissions, audits, and documentation for medical…
Hologic, Inc. in Cambridge, UK, is seeking a Senior Regulatory Affairs Specialist to support submissions, audits, and documentation for medical devices. You will collaborate with R&D, Quality, Clinical, and international teams to ensure regulatory compliance for US, EU, and Canadian requirements.
The role emphasizes maintaining technical files, labeling reviews, and proactive risk-based assessments, with a focus on product lifecycle activities and inspections readiness.
#J-18808-Ljbffr
Full job description from WhatJobs. Apply for this role →
Cambridge
Hologic, Inc. in Cambridge, UK, is seeking a Senior Regulatory Affairs Specialist to support submissions, audits, and documentation for medical…
Cambridge
At Hologic, we are committed to enabling healthier lives everywhere, every day.
Cambridge
At Hologic, we are committed to enabling healthier lives everywhere, every day.
Cambridge
Hologic in Cambridge is seeking a Senior Regulatory Affairs Specialist to support regulatory submissions, audits, inspections, and lifecycle…
Cambridge
Hologic in Cambridge is seeking a Senior Regulatory Affairs Specialist to support regulatory submissions, audits, inspections, and lifecycle…
Woking
Building an AI‑first organisation is central to Clinisys’ purpose and the impact we deliver.
Explore: Clinical Research Associate jobs in the UK Specialist jobs in Cambridge
Worked with Verifera as a candidate or employer? Your honest review helps the next person trust verified hiring.