
Regulatory Affairs Consultant
Full Time Permanent @Medical Device Client posted 2 months ago in Medical Devices Shortlist Email JobJob Detail
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Job ID 490
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Experience 5 Years
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Industry Medical Device
Job Description
Regulatory Affairs Consultant
Location: Remote
To provide expert UK/EU/US Medical Device Regulatory advice to Clients and prospective Clients. Update or create technical files /regulatory documentation for a medical device or In vitro medical device. Visit clients to conduct regulatory/ quality meetings, audits, or other relevant regulatory requirement.
CER writing experience.