Zentiva

Generic Implement quality control activities for Pharmaceuticals at Ankleshwar adhering to regulatory / global quality Directives and HSE guidelines with optimum utilization of resources to ensure consistent good quality of products to meet with customers’ requirements, living Group’s Values and…

KEY ACCOUNTABILITIES Testing Performing timely sampling and analysis of raw material, bulk product, intermediates, finished goods and other samples for Pharmaceuticals. Performing analysis of market complaints, Stability, process validation samples, Cleaning Validation of Pharmaceuticals. Good Laboratory Practice Performing calibration &…

Quality Management/Continuous Improvement Investigation of Deviations Implementation of Zentiva corporate policies, Management and Control of Documents, such as SOPs, Master Documents, etc. Review the Annual Product Quality Review Batch Reworking/Reprocessing/Reincorporation (Coordination from QA point of view) Review of Master Batch…

Education & Experience: M.Sc. or Higher Qualification in Analytical/Organic Chemistry / Pharmaceutical Chemistry. Min. 8 10 years Experience in a Quality Control/Analysis laboratory in a cGMP/ISO environment, with exposure to method development and validation activities. Technical skills & Competencies /…