Sampling of Raw Materials, Packing material, Intermediates and Finished Products.
Execution of Method validation / Method transfer activity.
Maintaining & monitoring of all the analytical method validation, cleaning validation and method transfer documents.
Preparation and standardization of volumetric solutions.
Calibration of all analytical instruments on need basis.
Raw Materials, In-Process, packing materials, Intermediates, Finished Products and stability samples analysis on need basis.
Performing Recertification of standards and impurities as required.
Upkeep of laboratory cleanliness, ensuring compliance to good laboratory and safety practices.
Coordination with other departments for smooth functioning of activities.
Documentation of all works as required as per relevant Standard Operation Procedure (SOP).
Qualification & Experience
Minimum M. Sc. in Chemistry
Knowledge, Skills and Abilities
Demonstrated ability to solve and trouble shoot problems based on the analysis, experience and judgement.
Excellent understanding of business and supporting technology related to the Pharmaceutical industry. Excellent Knowledge and Experience with regulatory Compliance.
Strong motivational skills allowing to function independently as well as a proven ability to motivate others.