About the Company :
The firm is one of the integrated Company having relations with top MNC's delivering them high class medicine and pesticides. The company is equipped with around 8000 employees with 2400 in North America and ~1100 in R&D. It is having its footprints in USA, India, Europe, North America and China. while connected to the top MNC's this is delivering the products with quality and competitive prices. The company have sales in about 100 countries.
The Portfolios of the firm include Solid Dosage Formulations, APIs, Radio pharmaceuticals, Advance Intermediates, Fine Ingredients, Allergy Therapy Products, Life Science Chemicals, Crop Science Ingredients and Nutritional Products.
Jubilant is having a strong expertise in chemistry and in bio-sciences, and is continuously improving its values and strategies to deliver the ultimate outputs. The efforts of this are reported from 2003. The company having the strengths of Strong R&D team and facilities, non infringement process for product development. The company having the title of "Partner of Choice" for the TOP MNC's.
Training and Experience:
Location: Roorkee Plant
Experience: B. Pharma with 1-5 years in sampling and in-process checks
Key duties:
Responsible for monitoring and ensuring on line review of batch manufacturing documents, batch packing documents.
Responsible for review of batch manufacturing Packaging and Analytical records, equipment logs etc. before batch release
Responsible for carrying out In Process control tests, line clearances activities, sampling during process validations, cleaning validation, batch manufacturing, packing
Responsible for monitoring adherence to various cGMP activities and laid down procedures in receipt, storage, testing, processing and dispatch of products