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Cipla Limited is an Indian multinational pharmaceutical and biotechnology company, headquartered in Mumbai, India. Cipla primarily develops medicines to treat respiratory, cardiovascular disease, arthritis, diabetes, weight control and depression; other medical conditions.
Job description
Purpose
To assist the RA Director to manage the Regulatory Processes related to all aspects of New Product Submissions, New Product Registrations and Life-Cycle management by ensuring high quality, timeous submissions and responses are submitted to all Health Authorities. To conduct and complete administration related to the Management of these processes for all products. This includes the RA management of processes for the Joint Venture with Teva/ Actavis and other 3rd party dossiers.
Education:
B Pharm or higher (post graduate) scientific degree
Experience:
5-10 years experience in a regulatory affairs covering specific Biological and Vaccines areas of the function.
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