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Regulatory Affairs Job at Cadila Pharmaceuticals Ltd | M.Pharm, MSc

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Regulatory Affairs Job at Cadila Pharmaceuticals Ltd

Cadila Pharmaceuticals Ltd. is one of the largest privately-held pharmaceutical companies in India. Over the past six decades, we have been developing and manufacturing affordable medicines for patients around the world.  Our innovation-led drug discovery processes ensure the health and well-being of people around the world. Our enhanced investment in innovation and a strong track record in research and development have produced medical miracles that have changed lives and made a profound impact on real life.

Post : Executive, Sr. Executive, Assistant Manager, Dy. Manager, Manager

Skills Required :
1) Analytical method validation exposure along with RA experience (USBU )
2) Topical ANDA submission exposure, Life cycle management/Post approval submission(USBU)
3) Thorough knowledge of drug development and approval process Prior regulatory experience with EU/Australia/New Zealand/WHO filings is a must Experience in preparing requests and briefing documents for scientific advice/pre-submission
meetings is preferable Excellent verbal and written communication skills

Education Qualification : M.Pharm /MSc (Regulatory Affairs)


Experience : 2 - 12 Years experience with RA

Job Location : Cadila Pharmaceuticals Limited, Dholka, Ahmedabad (Gujarat)


Candidate can share updated resume at apeksha.langhanoja@cplbio.com

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