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Zentiva in Ankleshwar, Gujarat, India invites a postgraduate in Organic or Analytical Chemistry for the Executive Quality Control, Pharmaceuticals role. The candidate will implement quality control activities for Pharmaceuticals, ensuring compliance with regulatory and global quality directives while optimizing resource use to meet customer requirements.
The role involves testing raw materials, bulk products, intermediates, and finished goods; performing investigations on out-of-spec results;
Post Graduate in Science (Organic or Analytical Chemistry )
Post Graduate in Science (Organic or Analytical Chemistry )
1-4 years in a Pharmaceutical Company.
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 Code of Ethics.
Performing timely 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.
Performing calibration & maintenance of lab. Equipment and assisting for the qualification of laboratory equipment.
Reviewing pharmacopeias for specification preparation.
Preparing SOPs and Formats and Analytical Test Record.
Managing reference standards, working standards, laboratory reagents & chemicals.
Arranging and observing Control Samples and maintaining record.
Participating in Investigation of out of specification results, retesting and review the analysis records.
Maintaining & reviewing laboratory raw data related to testing activity.
Preparing protocol for Analytical Method validation, cleaning validation and performing the validation exercise as per the protocol.
Identifying and planning requirement for laboratory consumables and monitoring the stock of chemical, spares, glassware and printed material.
Coordinating with production, and warehouse for analytical activities.
Compliance to HSE Requirements for QC Laboratory
Identifying and correcting unsafe conditions or behaviors and promptly reporting other potentially hazardous situations.
Carrying out any other assignments or projects as per the instruction of the Dept. Head to meet with the organizational objectives and priorities.