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Medical Device Regulatory Affairs: Lifecycle Specialist
Posted 6 days 5 hours ago by Perrigouk
Permanent
Full Time
Other
London, United Kingdom
Job Description
Perrigo is looking for an Associate Professional, Regulatory Affairs within our Medical Device Lifecycle Management team in London. The role supports regulatory activities across the product lifecycle to ensure conformity, documentation compliance, product availability and market access.
You will help with lifecycle management tasks including documentation updates, change assessments, regulatory notifications, registrations/listings and maintaining regulatory records, working with
Perrigouk
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