Position:
- Has work experience of 3-6 years in the regulatory domain within the Medical Device industry
- Has expertise with drafting, reviewing and submission of Regulatory filings and Query responses in EU markets for obtaining CE marking in line with the latest EU Medical Device Regulation
- Regulatory knowledge of filing medical device applications in US and Canada will be an advantage
- Possesses good knowledge of ISO 13485 and ISO 14971
- Holds experience in ensuring compliant Regulatory lifecycle management of medical devices by coordination with internal stakeholders and regulatory agencies
- Assisting in the preparation of technical presentations/ meetings with Regulatory Consultants
An opportunity to work as a part of the Medical Affairs function for one of the fast growing organisations in the industry
Pratham Search is looking for Bachelor Of Science (b.sc) profile candidates.
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