Medical Device Regulatory Affairs
Location
Bangalore | India
Job description
Medical Device Regulatory Affairs Job duties of a Regulatory Affairs Specialist include:
- Developing and implementing regulatory strategies for new and existing products
- Preparing and submitting regulatory documentation to regulatory authorities
- Liaising with regulatory authorities to answer questions and resolve issues
- Ensuring that all products meet relevant government regulations.
- Keeping up to date with changes in regulatory legislation and guidelines
- Providing advice and support to other departments on regulatory matters
- Managing regulatory audits and inspections.
Interested to apply can share Cv or call/whatsapp to
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Job tags
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