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
Experience : 2-4 years
Requirement : Need to have experience and knowledge in handling HPLC, GC, Dissolution tester and related instrument,
Required to have knowledge on WHO, ICH,EMEA guidelines
Able to develop analytical methods for analysis of routine analysis as well as stability samples
Able to able to finalise specifications test procedures and ensure timely delivery of the product to plants
Required to coordinate with cross functional team Add transfer analytical methods by demonstrating sound scientific rational and timely transfer of products
Able to maintain and handling the calibration of live instruments equipments to get help produce all analytical results for proper interpretation.
Require to maintain safety GMP&GLP environments in lab to minimise the accidents and incidents
Review the analytical data and calibration documents make recommended corruptions by coordinating with cross functional team And responsible for smooth operations