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.
About the Job
Experience : 4-8 years
Role
Required to perform routine and stability analysis of various formulations according to the laid regulatory guidelines
Able to prepare the standard operating and test procedures along with the justification and equivalency report As per the requirement
Able to transfer various analytical methods to quality control labs
Required to perform a handheld The calibration of various instruments like Karl Fischer Analytical balance, osmometer, liquid particulate counter, dissolution testing, HPLC, UPLC.
Required to prepare the working standard for the analytical support and need to have The knowledge on literature search for Various projects using online resources
Able to troubleshoot the existing analytical methods and upgrade the analytical methods fit for use
Able to perform the analytical method development for SA leader substances resolution methods for various formulations such as oral suspensions injectables for Europe US And other regulatory markets using UVHPLC&UPLC Within given timeline.
Preparation of equivalency reports for various methods and document handling required to have good knowledge on good laboratory and manufacturing practises
Able to handle various analytical techniques involved with Waters HPLC, Dissolution Type 4 apparatus, Zeta Sizer a liquid particulate sizer.