Regulatory Affairs

1 day ago

Mumbai, India Win in Life Academy Full time

Position: Sr. Executive/Asst. Manager/Deputy Manager-Regulatory Affairs (Domestic).

Location: Andheri, Mumbai.

Qualification: M. Pharm. (Experienced preferred).

Experience- 1-5 Years

JOB DESCRIPTION – Regulatory Affairs (Domestic)

The role will involve expertise in D & C Act and Rules as well as FSSAI regulations with

experience in FDA related activities. This profile will ensure timely and robust functional/cross-functional coordination (R&D, QC, Marketing, Legal, Production, etc.), transparent execution

and implementation of regulatory affairs and safety processes.

Local Regulatory Function (Licensing):

· Prepare registration dossier for procuring certificates/license from local FDA, DCGI and

· FSSAI. This would entail thorough familiarity with FDA, Sugam & FSSAI online portal, Drugs

· & Cosmetics Act and its various Schedules e.g. Sch Y, M, etc.

· Confirm product formula and label acceptability, as well as the receipt of necessary licenses,

· prior to the release of product.

· Co-ordinate with QC and R&D departments for technical documents (manufacturing

· documents like batch records, specifications, analytical methods, validation reports, and

· stability data) required to be incorporated in the registration dossiers.

· Ensure timely renewal of drug and food licenses maintained by head office and also branch

· offices based at various states in the country.

· Online application for obtaining test license for import purpose.

· Maintain archival of all regulatory permissions.

· Keep abreast of the updates pertaining to regulatory requirements and accordingly

· implement them.

· Prepare responses to the legal & technical queries raised by the Regulatory authorities.

Compliance of Packaging Modules:

· Formulate and implement statutory requirements pertaining to the artworks of the

· products (label, carton, package insert, patient information leaflet, etc.).

· Review the artwork of all packaging material.

· Prepare package insert as per New Drugs and Clinical Trials Rules 2019.

· Pharmacovigilance

· Provide high quality medical writing from planning and coordination of literature research.

· Draft and review PSURs with focus on medical aspects of the products and safety sections.

· Review of Risk Management Plans as per Regulatory requirement.

· Good knowledge in assessing the risk-benefit of a product and identify any gaps in the

· aggregate documents.

· Perform scientific review of aggregate reports / ICSRs produced by PV Associates.

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