Bio-Medical
Bio-Medical
Posted on :
21-08-2022
Employer Active
1 Vacancy
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Job Description
Req ID : 1451519
- Responsible for regulatory affairs activities to assist in regulatory submission, annual reports, registrations and listings. Assure compliance with applicable medical device regulations per jurisdiction, guidance and standards. Assist in creation and maintenance of regulatory files.
- Write, analyze, and edit technical documents to support countryspecific regulatory submissions and compile submissions in a format consistent with applicable guidance documents, including investigational device submissions in USA, Canada and Europe. Work with other departments and communicate the submission requirements when documents are needed for regulatory submission.
Employment Type
Full Time
Company Industry
Department / Functional Area
Key Skills
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