Reliance Life Sciences hiring for Regulatory affairs department

Reliance Life Sciences is Hiring: Regulatory Affairs Specialist-Biosimilars

Are you ready to take your career in regulatory affairs to the next level? We are looking for a dedicated and experienced professional to join our Biosimilar business team. If you have a passion for regulatory submissions and a keen eye for detail, this could be the perfect opportunity for you!

Job Purpose: Support regulatory submissions in developed and emerging markets for our Biosimilar business.

Accountabilities:

Reviewing and preparing regulatory filing packages/ dossiers for product registrations in the US, EU, and emerging markets.

Coordinating with concerned groups on regulatory deliverables.

Educational Qualifications:

Necessary: M. Pharm / M.Sc. in Biotechnology or Life Science.

Desirable: Diploma in Regulatory Affairs.

Relevant Experience:

Necessary: 6 to 9 years of regulatory experience, with at least 5 years in handling biological products or biosimilars. Additionally, at least 2 years should be focused on regulatory filings in developed markets, with expertise in technical review and scientific writing of CMC sections.

Desirable: Experience participating in Scientific advice/ BPD/IND meetings with agencies, and prior experience in QA or Process Development functions in Biopharma.

If you are ready to contribute to a dynamic team and make a significant impact in the field of biosimilars, apply now and take the next step in your professional journey with us!

To apply, please send your resume to [email protected]