Job Location : Dholka, Near to Ahmedabad, Gujarat
About the Company :
Company : Cadila Pharmaceutical Ltd.
About Us : Cadila Pharmaceuticals Ltd, is one of the Largest Privately- held Pharmaceuticals companies in India. Over the past seven decades, We have been developing and manufacturing affordable medicines for the 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 strong track record in research and development have produced medical miracles that have changed lives and made a profound impact on real life.
Being a care-focused, research-driven company, we are committed to complying with the highest ethical standards in the clinical research and medical practice. We lead our industry in demonstrating the application of cutting edge research to ethical business practices in producing the alchemy of optimum health outcomes for all.
About the Role :
To leverage my expertise in formulation development and regulatory compliance to develop stable and bioequivalent solid oral dosage forms for global markets, ensure successful technology transfer to manufacturing facilities, support regulatory submissions, address agency queries, and provide technical support for commercial production, contributing to the overall growth and compliance of the organization.
Responsibilities :
Qualifications : Ph / D
Required Skills :
Preferred Skills :
Hands-on Experience with Formulation and Development
Pay range and compensation package :
8 LPA to 12 LPA
Research Assistant • Ahmedabad, Gujarat, India