Job Opening: Regulatory Affairs Executive
Company: Asence Pharma Pvt. Ltd.
Location: Ranoli, Vadodara, Gujarat
Qualification : M.Pharma / B.Pharma / M.Sc. in Pharmaceutical Regulatory Affairs, Organic Chemistry, or a relevant discipline.
Experience : 3β5 years of relevant experience in API manufacturing units.
Candidates with a Quality Control (QC) background will be preferred.
Key Responsibilities :
Support the preparation of regulatory documents, including DMF sections, CoPP, GMP and CEP documentation.
Collect and review technical and quality data from Ramp;D, QC, QA and Production departments.
Assist in regulatory submissions across international markets and track approval status.
Maintain regulatory databases, filing records and regulatory documentation.
Coordinate deficiency responses and post-approval changes.
Interested candidates may share their updated CV at:π§ Email: hr@asence.com
β Asence Pharma Pvt Ltd
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