Executive – Quality Control at Zentiva Ankleshwar – Apply Now!
Zentiva is hiring an experienced Executive – Quality Control to join its pharmaceutical operations in Ankleshwar, Gujarat. This full-time role offers hands-on responsibilities in analytical testing, instrument handling, method validation, and regulatory compliance. If you hold an M.Sc. or B. Pharm and have 2–6 years of experience in pharmaceutical or API QC, this is your opportunity to grow in a dynamic GMP/GLP-certified environment. Join Zentiva and contribute to delivering safe, high-quality products to global markets.
About Zentiva
Zentiva is a leading pharmaceutical company focused on delivering high-quality, affordable medicines to patients across Europe and emerging markets. With a strong heritage in innovation and manufacturing excellence, Zentiva empowers healthcare systems through trusted generic solutions. The company operates with a commitment to regulatory compliance, sustainability, and continuous improvement. Zentiva’s Ankleshwar site plays a vital role in producing active pharmaceutical ingredients (APIs) and finished dosage forms, supporting its global supply chain with integrity and efficiency.
Job Details:
Job Title: Executive – Quality Control
Location: Ankleshwar, Gujarat, India
Job Summary
Zentiva is seeking a skilled and motivated Executive—Quality Control for its pharmaceutical facility in Ankleshwar. This position is crucial in ensuring that products meet stringent quality standards through thorough analytical testing and compliance with regulatory guidelines.
Key Responsibilities:
- Analysis:
- Performing timely sampling and analysis of raw material, bulk product, intermediates, finished goods, and other samples.
- Performing analysis of Stability, process validation samples, and Cleaning Validation.
- Handling of sophisticated laboratory instruments viz., HPLC, GC, UV & IR spectrophotometer, Dissolution tester, auto-titrator, polarimeter, etc.
- Good Laboratory Practice
- Performing calibration & maintenance of the lab. Equipment and assistance for the qualification of laboratory equipment.
- Knowledge of the preparation of SOPs, formats, and Analytical Test records.
- Managing reference standards, working standards, laboratory reagents & chemicals.
- Arranging and observing Control Samples and maintaining the record.
- Participating in the Investigation of out-of-specification results.
- Maintaining laboratory raw data related to testing activity.
- Validation
- Performing Analytical Method validation and cleaning validation as per the protocol.
- Other
- Coordinating with production and the warehouse for analytical activities
- Compliance to HSE Requirements for QC laboratory.
Identifying and correcting unsafe conditions or behaviours, and promptly reporting other potentially hazardous situations.
Carrying out any other assignments or projects as per the instructions of the Department. Head to meet with the organizational objectives and priorities.
Requirements:
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Qualification: M.Sc. (Organic/Analytical Chemistry) or B. Pharm
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Experience: 2–6 years in pharmaceutical/API QC
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Knowledge of GMP, GLP, LIMS, QMS
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Strong analytical and coordination skills
This position offers excellent exposure to work in a GMP/GLP-regulated laboratory, providing a growth-oriented environment for quality-focused professionals.
Keywords: Zentiva, Executive Quality Control, Pharma, Job Posting, Ankleshwar, GMP, GLP, Analytical Chemistry, Quality Assurance and QC jobs
