Our motto “Growth is Life” aptly captures the ever-evolving spirit of Reliance. Our activities span hydrocarbon exploration and production, petroleum refining and marketing, petrochemicals, retail, and telecommunications. In each of these areas, we are committed to innovation-led, exponential growth. Our vision has pushed us to achieve global leadership in many of our businesses – including our position as the largest polyester yarn and fiber producer in the world. Reliance Industries Limited is a Fortune 500 company and the largest private sector corporation in India.
- Vacancy details:
- Department: Regulatory Affairs Specialist – Biosimilars
- Qualification: M. Pharm / M.Sc/Diploma
- Experienced:6 to 9
- Salary:₹Not Disclosed
Job Description: Greeting from Reliance Life Sciences Ltd. .!!!!!
- Important Details :
- Location:India
- Post of date :18/07/2024
- Selection Process: The selection will be on the basis of Interview.
- Mode of Interview: Face to face
- Interview Rounds of Interview: HR
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 Ashwini.Pachpute@relbio.com
