Remote Regulatory Affairs Specialist
Job Summary
Detail-oriented and driven, the part-time Remote Regulatory Affairs Specialist will coordinate global regulatory submissions and evaluate scientific data for medical devices while working remotely on a contract basis.
Key responsibilities
- Compile, edit, and proofread technical and scientific documents/packages for global regulatory submissions
- Support the execution of regulatory project plans and maintain compliant regulatory files
- Prepare responses to inquiries from external regulatory authorities under supervision
Required qualifications
- Bachelor's degree in a relevant scientific discipline or equivalent healthcare training
- Familiarity with US and EU medical device regulations
- Strong technical system skills, including word processing and spreadsheets
- Excellent interpersonal, multitasking, and organizational skills
Complete Job Description
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