USV Pvt Ltd Hiring CMC Regulatory Expert

USV Pvt Ltd jobs - recruitment
  • Full Time
  • Anywhere

USV Pvt Ltd Jobs: CMC Regulatory Expert Opportunity


USV Pvt. Ltd currently looking for a skilled CMC regulatory expert to contribute to our Biosimilar dossier submissions and Life cycle management initiatives in regulated markets (EU/US).


USV Pvt Ltd Hiring CMC Regulatory Expert: Make Your Mark in Pharma Regulation


Key Responsibilities: As a CMC regulatory expert at USV Pvt. Ltd., your role will involve:

  1. Leading Biosimilar dossier submissions and ensuring compliance with regulatory standards.
  2. Managing the Life cycle of pharmaceutical products in regulated markets such as EU/US.
  3. Providing expertise in Small molecule sterile drugs (injectables) for the US market.
  4. Collaborating with cross-functional teams to drive regulatory strategies and submissions.
  5. Contributing to the development of regulatory processes and best practices.

Qualifications and Experience: To excel in this role, you should have:

  • Minimum 5 years of experience in CMC regulatory affairs.
  • Strong expertise in Biosimilar dossier submissions and Life cycle management.
  • Experience with Small molecule sterile drugs (injectables) for the US market is advantageous.
  • Knowledge of regulatory requirements in EU and US markets.
  • Excellent communication and collaboration skills.
USV Pvt Ltd  jobs - recruitment
USV Pvt Ltd jobs – recruitment

Company Overview: USV Pvt. Ltd. is a leading pharmaceutical company known for its commitment to innovation and quality. With a focus on research and development, we strive to bring life-saving medicines to patients worldwide.


How to Apply: To apply for the position of CMC regulatory expert at USV Pvt. Ltd., please send your CV to pankajs.chaudhari@usv.in. Join us in making a difference in the healthcare industry!

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