Executive - Quality Control

Zentiva Poland; Ankleshwar; On-site; INR 600,000 - 800,000; Full time

Job summary

Zentiva Poland in Ankleshwar seeks an Executive Quality Control to drive testing and release of pharma materials in line with GMP/GLP and HSE guidelines.

You will plan sampling, analyze raw materials, intermediates, finished goods, and packaging samples, while maintaining records and calibration schedules. The role requires 2-4 years of lab experience and strong analytical and leadership skills.

Qualifications

• Post graduate in science with 2-4 years in chemical & instrumental testing lab.
• Experience with GMP and GLP in QC environment.
• Willingness to coordinate with production and warehouse teams and maintain documentation.

Responsibilities

• Testing and release of materials and products.
• Planning sampling and analysis of raw materials, intermediates, finished goods, and packaging materials.
• Maintaining SOPs, formats, and analytical test records.

Skills

Analytical ability

Troubleshooting

Coordination

Communication

Leadership

Education

Post Graduate in Science (Organic Chemistry)

Job description

JOB TITLEExecutive Quality Control, PharmaceuticalsJOB PURPOSEGenericImplement quality control activities for Pharmaceuticals at Ankleshwar adhering to regulatory / global quality guidelines 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 Ethics.REQUIREMENTSEducation / ExperiencePost Graduate in Science (Organic Chemistry )2-4 years in chemical & instrumental testing laboratory with exposure to GMP, GLP.Technical skills &Competencies / LanguageAnalytical abilityTrouble shootingsCo ordinationCommunicationLeadershipKEY ACCOUNTABILITIESTesting and releasePlanning of timely sampling and analysis and review of raw material, bulk product, intermediates, finished goods, packing material and other samples for Pharmaceuticals.Performing analysis of Raw Material Samples received from new vendors for Pharmaceuticals.Good Laboratory PracticePlanning for 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.Reviewing and observing Retention Samples and maintaining record.Investigating out of specification results, retesting and review the analysis records.Maintaining & reviewing laboratory raw data related to testing activity.Validation Preparing protocol for Analytical Method validation/Transfer, cleaning validation and performing the validation exercise as per the protocol.Management of laboratory ConsumablesIdentifying and planning requirement for laboratory consumables and monitoring the stock of chemical, glassware and printed material.Co ordinationCoordinating with production, and warehouse for analytical activities.OtherCompliance 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.