About the Company
Cipla is an Indian MNC with pharma and biotechnological products having the head quarters in Mumbai started in the year 1935. This has market capitalization of $7 billion. Company has footprints in India, South Africa, North America, Europe, and Australia. The company having primary focus areas in diabetes, arthritis, weight control, depression, cardiovascular and respiratory with 7 brands in top 100.
The firm also have numerous FDA approved bulk facilities. It acquired south African company in 2013 and named as Cipla-Medpro. It has more than 10,000 colleagues and 7 million chemists. Cipla believes that it not only produces medicines but makes difference in patients’ lives. Received Thomson Reuters India innovation award in 2012.
The formulation pipeline has equipped with more than 250+ complex products and with state of art facility for the development of innovative technological products. Developing the products with upcoming technologies like QBD (Quality by design) principles enabling robust and reproducible products in the market. Cipla biotech, stempeutics (in the area of osteoarthritis) and CIPTEC discovery engine are the new ventures of the company.
About the Job
Education Qualification
B.Pharm/ M.Pharm
Relevant Work Experience
5-7 years of experience in formulation development and /or manufacturing, having knowledge of regulatory market
Job roles and Responsibility
Able to Participate in execution of placebo, feasibility, assessment, regulatory and amendment batches within defined timeframe
Needed to Gather and collate batch, process, in-process, physical, analytical and stability data for dossier compilation.
Required to Identify and list requirements and prerequisites (RM, PM, tooling, accessories, machines, etc.) for execution of batches as per monthly rolling plan.
Able to Assist in evaluation and extrapolation of acquired batch data during the transfer process, to define control strategy for commercial launch.
Able to Conduct effective transfer of knowledge about the product and process to formulations manufacturing unit with required documentation for successful implementation of new product technology
Required to Extend technical support to implement CIP, AVD and site transfer activities to drive product life cycle management for sustained growth
Needed to Participate in Tech Transfer activities at CMO for new products