Remote Regulatory Affairs Specialist
Job Summary
To support a global healthcare technology leader, the Remote Regulatory Affairs Specialist will coordinate global submissions and ensure compliance with medical device regulations in the US and EU while working remotely on a contract basis.
Key responsibilities
- Support the execution of global regulatory project plans and maintain compliant regulatory files
- Compile and prepare draft responses to inquiries from external regulatory authorities
- Review, evaluate, edit, and proofread technical and scientific data, reports, and departmental SOPs
Required qualifications
- Bachelor's degree in a relevant scientific discipline
- Knowledge of basic scientific principles and regulatory concepts
- Strong technical system skills, including word processing and spreadsheets
- Proven administrative, task prioritization, and project management skills
- Rigorous proofreading and editing abilities
Complete Job Description
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