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Manager Regulatory Affairs – CMC | MSD Pharmaceuticals | Mumbai, India | 5.00-12.00 L


Merck & Co., Inc., Kenilworth, New Jersey, USA is known as “Merck” in the United States, Canada & Puerto Rico. We are known as “MSD” in Europe, the Middle East, Africa, Latin America & Asia Pacific. We are a global biopharmaceutical leader with a diverse portfolio of prescription medicines, oncology, vaccines, and animal health products.

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In a world of rapid innovation, we seek brave Inventors who want to make an impact in all aspects of our business, enabling breakthroughs that will affect generations to come. We encourage you to bring your disruptive thinking, collaborative spirit, and diverse perspective to our organization. Together we will continue Inventing For Life, Impacting Lives while Inspiring Your Career Growth.

Designation: Manager CMC 

Location: Mumbai, Maharashtra

Job Description:

  • This Role is responsible for implementing CMC regulatory strategies for assigned pharmaceutical products in accordance with global regulations, guidance, and defined regulatory strategies. He would even be responsible for the preparation and review of the information required for the development of regulatory CMC dossiers for commercial products.

Primary responsibilities include, but are not limited to:

  •  Provide input to global product and project regulatory strategies by performing assessments of CMC changes, identifying global regulatory requirements, and critically evaluating supporting documentation to assess acceptability and identify potential risks.• Execute regulatory strategies by leading the development, authoring, and review of CMC submission components and documentation to support post-approval supplements/variations, annual reports, registration renewals, and responses to health authority questions per established business processes and systems.• Liaise with global CMC, Our Manufacturing Division, and external partners to support compliant execution of change management and conduct all activities with an unwavering focus on regulatory conformance.• Assess and communicate potential regulatory risks and propose mitigation strategies.• Deliver all regulatory milestones for assigned products across the product lifecycle• Identify and communicate potential regulatory issues to GRACS CMC management, as needed

Technical Skills:

• Experience in reviewing scientific information to assess technical merits and suitability of scientific rationale to ensure information is presented clearly and conclusions are adequately supported by data.

• Demonstrated oral and written communication skills and the ability to communicate issues in a succinct and logical manner. Strong listening skills.

• Demonstrated understanding of related fields (e.g., pharmaceutical manufacturing, analytical testing, and quality assurance).

• Proficient computer skills and previously demonstrated ability to operate in an electronic document based GMP systems

Leadership Skills:

• Demonstrated ability to generate innovative solutions to problems and effectively work with and communicate to key stakeholders.

• Demonstrated flexibility in responding to changing priorities or dealing with unexpected events.

• Capability to handle multiple priorities and balance work to achieve business goals.

• Demonstrated effective leadership, communication, and interpersonal skills

Qualification: Bachelor in Science/Pharma/Engineering/Bio/Micro/Viro/Biochem/ or Relevant

Experience: 5-7 Years in Pharma, out of which 4 years’ experience in managing CMC Regulatory submissions for small molecules/vaccines/biologics.

Note: The candidate may be required to travel to other MSD/ CMO sites on a need basis

Salary: 5,00,000 to 12,00,000 INR CTC/PA

Contact Details:

Sukirti Mishra


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