Kochi Kerala Regulatory affairs manager Jobs – 2 Open Jobs Today

Manager Regulatory Affairs US and European Market
Silmed Scientific —Kochi, Kerala
- Medicine
- Doctoral degree
- Master's degree
Regulatory Affairs Manager (EU/US)
Silmed Scientific —Kochi, Kerala
- Doctoral degree
- Master's degree
- Communication skills

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Regulatory Affairs Manager (EU/US)
Silmed Scientific —Kochi, Kerala
Hands on experience to review and approve submission documents in accordance with the regulatory guidelines, evaluate changes in CMC documentation with respect…
Manager Regulatory Affairs US and European Market
Silmed Scientific —Kochi, Kerala
Author, review and edit regulatory documents and packages for submissions to national regulatory authorities (NRAs) and/or scientific or executive management…

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regulatory affairs manager jobs near kochi kerala

We are hiring dynamic regulatory affairs talents with capabilities in CMC and regulatory intelligence.

M.Pharma - Other Specialization/ MS/M.Sc(Science) - Bio-Chemistry/ Medical-MS/MD - Any Specialization/Ph.D/Doctorate - Any Specialization
Ph.D/Doctorate - Any Specialization
BVSC - Any Specialization/ BHM - Any Specialization/ BHMS - Any Specialization/ B.Pharma - Pharmacy/ BAMS - Any Specialization/ Other Graduate - Other Specialization
MS/M.Sc(Science) - Biotechnology/ Agriculture/ Bio-Chemistry/ Biology/ Botany/ Chemical Engineering & Materials Science/ Chemistry/ M.Pharma - Any Specialization/ M.Tech - Environmental/ Instrumentation/ Bio-Chemistry/Bio-Technology/ Biomedical/ Chemical
Author, review and edit regulatory documents and packages for submissions to national regulatory authorities (NRAs) and/or scientific or executive management meetings
Serve as the lead writer for high priority submissions such as Scientific advice meeting briefing materials/PIP/IMPD/IND submissions and amendments
Involvement in Training and development.
Experience in core regulatory function for US/EU/CANADA markets is preferred.
Detail oriented person, with strong capability to multi-task
Experience with developmental CMC of solids /sterile injectables/ eyedrops /respiratory products
Involve in training and development activities as and when required.
Participate in client discussions.