Senior Medical Device Regulatory Affairs Specialist
Listed on 2026-10-16
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Healthcare
Healthcare Compliance, Medical Science Liaison, Medical Device Industry
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.
As a Senior Medical Device Regulatory Affairs Specialist, you will play an important part at Hologic, Inc. in Cambridge, England, United Kingdom.
This is a strong role to take on the Senior Medical Device Regulatory Affairs Specialist role at Hologic, Inc.
We invite applications for the Senior Medical Device Regulatory Affairs Specialist position located in Cambridge, England, United Kingdom.
The following opportunity is for a Senior Medical Device Regulatory Affairs Specialist with Hologic, Inc.
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