Executive / Assistant Manager - Regulatory Affairs
SDP HR Solution
Vadodara, GujaratPosted about 2 months agoDiscoveredMatch locked
Full TimeHealthcare & Nursing Jobs
About the role
Job Description: Key Responsibilities: Prepare, compile, and review regulatory submissions (CTD/eCTD formats) for product registrations, renewals, and variations as per regional and international guidelines. Ensure timely submission and follow-up of applications with regulatory authorities. Maintain up-to-date knowledge of changes in drug regulatory environments and communicate impacts to relevant
Not included in the source posting: about the role, what you'll do, qualifications, benefits.
Skills
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Who can apply
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