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Assistant Manager - Regulatory Affairs API @ Hetero

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 Assistant Manager - Regulatory Affairs API

Job Description

    Key Responsibilities: Prepare and compile Drug Master Files (DMFs) for China in compliance with regulatory guidelines. Conduct thorough reviews of technical and regulatory documentation to ensure accuracy and compliance. Prepare and submit responses to deficiency letters (DL) from regulatory authorities. Manage the entire regulatory life cycle of API products, including updates, renewals, and variations. Work closely with internal teams (R&D, Quality, Manufacturing) and external regulatory agencies to ensure smooth approvals and compliance. Maintain up-to-date knowledge of global regulatory requirements and ensure adherence to the latest guidelines. Skills Strong understanding of global regulatory guidelines, especially China requirements. Ability to analyse and interpret regulatory requirements with precision. Excellent written and verbal communication to effectively interact with regulatory authorities and internal stakeholders. Proactive approach to identifying regulatory challenges and developing solutions. Educational Qualification: M.Pharm / B.Pharm / M.Sc. in Chemistry or a related scientific discipline. Experience: 5-10 years of experience in Regulatory Affairs (API) with hands-on expertise in China DMF compilation, review, and submission.,

Employement Category:

Employement Type: Full time
Industry: Medical / Healthcare
Role Category: Not Specified
Functional Area: Not Specified
Role/Responsibilies: Assistant Manager - Regulatory Affairs API

Contact Details:

Company: Hetero
Location(s): Hyderabad

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Keyskills:   verbal communication

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Hetero

Company ProfileHetero Drugs LimitedM/s. Hetero Drugs Ltd is one of the Largest Pharmaceutical Company in India.