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Manager - Medical & Regulatory Affairs

Piramal Pharma
Piramal Pharma
5-8 years
Not Disclosed
10 Jan. 9, 2026
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Manager – Medical & Regulatory Affairs

Location: Mumbai, Maharashtra, India
Business Unit: Piramal Consumer Healthcare
Category: Regulatory Affairs / Pharmacovigilance
Job Type: Full-Time
Travel: Low


About Piramal Consumer Healthcare

Piramal Consumer Products Division (CPD) is a leading consumer healthcare business under Piramal Pharma Limited, serving over 7 crore consumers across India. With a legacy of Knowledge, Action, Care, and Impact, CPD delivers a wide range of products including Skin Care, Digestives, Women’s Intimate Care, Kids Wellbeing & Baby Care, Pain Management, Oral Care, Gut Health, Respiratory Solutions, Multivitamins, and Food Supplements.

With an extensive distribution network covering 1500+ towns, 2.8 lakh+ outlets, 12,000+ organized retail outlets, e-commerce channels, and a 1,200+ strong field force, Piramal CPD is one of the fastest-growing consumer healthcare divisions in India.


Role Overview

The Manager – Medical & Regulatory Affairs will provide scientific, regulatory, and compliance leadership to ensure safe, effective, and compliant consumer healthcare products. You will work closely with internal teams (Marketing, Supply Chain, QA, R&D, Business Development, Analytical, Packaging, Consumer Insights) and external stakeholders (KOLs, Corporate Legal, Third-Party Manufacturing Partners, Consultants) to drive regulatory excellence.


Key Responsibilities

  • Provide scientific input for new product development and validate product claims.

  • Conduct claim substantiation studies and review medico-marketing materials.

  • Plan and deliver scientific training for marketing and sales teams.

  • Coordinate with third-party manufacturers for timely licensing, licence archival, and regulatory compliance.

  • Respond to medical and regulatory queries from internal and external stakeholders.

  • Provide scientific support for consumer queries and monitor adverse events.

  • Ensure quality and integrity of information shared with stakeholders.

  • Collaborate with cross-functional teams to support business objectives and regulatory compliance.


Qualifications & Experience

  • Master’s degree in Pharmacy (M.Pharm) or M.Sc. in Pharmaceutical Sciences.

  • 5–8 years of relevant experience, preferably in OTC drug regulatory affairs.

  • Strong understanding of pharmacovigilance and materiovigilance operations.

  • Knowledge of regulatory frameworks, including D&C Act, DMR Act, UCPMP, and ASCI codes.

  • Strong analytical, communication, and presentation skills.

  • Ability to critically review documents for scientific and regulatory compliance.


Reporting Structure

  • Reports to Chief Manager – Regulatory Affairs.


Why Join Piramal Consumer Healthcare

  • Work in a dynamic, fast-growing consumer healthcare division.

  • Contribute to a business that touches millions of lives in India.

  • Collaborate with diverse internal and external stakeholders.

  • Be part of a values-driven organization that emphasizes career growth, learning, and innovation.

  • Opportunity to work on a wide portfolio of OTC products across multiple therapeutic areas.


Apply Now: Ensure your application is submitted by 29th January 2026.

Location: Piramal Agastya, PRL Agastya Pvt Ltd., LBS Marg, Kamani Junction, Mumbai, Maharashtra, 400070, India