USV Pvt Ltd Hiring CMC Regulatory Expert

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.

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 [email protected]. Join us in making a difference in the healthcare industry!