Executive Job in Pharma: Zentiva is Hiring an Executive – Quality Control in Pharma at Ankleshwar – Apply Now
Looking for an Executive Job in Pharma to achieve a promising career in the pharmaceutical industry? Zentiva is Hiring an Executive – Quality Control in Pharma at Ankleshwar, India, is an excellent opportunity for candidates with a background in B.Pharm with 2–6 years of experience. This role offers hands-on exposure to GMP/GLP practices, advanced analytical instruments, and quality control operations, ensuring growth in a regulated pharma environment.
About the Company
Zentiva is a major pharmaceutical company headquartered in Prague, Czech Republic, with deep roots tracing back over 500 years to the historic Black Eagle Pharmacy. The company develops, produces, and delivers high-quality, affordable medicines, including generics, OTC, branded generics, value-added medicines, and specialty products. Zentiva operates four wholly owned manufacturing sites located in Prague (Czech Republic), Bucharest (Romania) (two sites), and Ankleshwar (India). Over 70% of its product supply comes from these own sites, supported by a network of external manufacturing partners. The company has two R&D centres (in Prague and Ankleshwar) which drive innovation in drug product formulation, bioequivalent and value-added medicines, and focus on regulatory submissions and lifecycle management of active pharmaceutical ingredients. Zentiva is committed to sustainability: its European sites already use 100% renewable electricity, and all sites (including in India) are working on energy efficiency, reducing environmental footprint, and aligning with ambitious goals like carbon neutrality for Scope 1 & 2 emissions by 2030. Zentiva is actively contributing by creating more Quality Control Jobs in Pharma industry.
Job Details:
- Job Title: Executive – Quality Control
- Job Location: Ankleshwar, India
Qualification and Experience:
B.Pharm with 2–6 years of experience as an analyst in the Pharmaceuticals / API industry. Candidates must possess strong knowledge of GMP & GLP guidelines.
Key Responsibilities:
Analysis:
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Conduct timely sampling and analysis of raw materials, intermediates, bulk products, and finished goods.
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Perform stability testing, process validation, and cleaning validation.
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Operate sophisticated laboratory instruments such as HPLC, GC, UV & IR spectrophotometer, Dissolution tester, auto-titrator, and polarimeter.
Good Laboratory Practices:
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Perform calibration and maintenance of laboratory equipment.
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Assist in equipment qualification and ensure GLP compliance.
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Prepare SOPs, formats, and analytical test records.
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Manage reference standards, reagents, chemicals, and control samples.
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Investigate out-of-specification (OOS) results and maintain laboratory raw data.
Validation:
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Conduct analytical method validation and cleaning validation as per protocols.
Other Responsibilities:
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Coordinate with production and warehouse teams for analytical support.
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Ensure compliance with HSE requirements for QC laboratories.
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Identify, correct, and report unsafe conditions or hazards promptly.
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Carry out additional assignments or projects as directed by the Department Head to align with organizational priorities.
Requirements:
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Strong knowledge of GMP & GLP.
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Good coordination and communication skills.
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Analytical ability and knowledge of LIMS & QMS.
