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:
- Leading Biosimilar dossier submissions and ensuring compliance with regulatory standards.
- Managing the Life cycle of pharmaceutical products in regulated markets such as EU/US.
- Providing expertise in Small molecule sterile drugs (injectables) for the US market.
- Collaborating with cross-functional teams to drive regulatory strategies and submissions.
- 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.
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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! https://pharmastuff.org.in/job/usv-pvt-ltd-cmc-regulatory-expert?feed_id=9357
