Chemistry Executive Job at Zentiva | Chemistry Graduates Apply Now
Are you a chemistry professional looking to grow your career in quality control? Zentiva is hiring an Executive – Quality Control at its Ankleshwar facility. This role provides hands-on exposure to advanced analytical instruments, GMP/GLP practices, and global quality systems, ensuring consistent delivery of high-standard products. If you have a strong background in organic or analytical chemistry, this position is an excellent opportunity to advance your career with a trusted global healthcare company.
- Job Role: Executive – Quality Control
- Location: Ankleshwar, Gujarat, India
About the Company
Zentiva is a leading European generics and specialty pharmaceutical company, committed to delivering high-quality and affordable medicines to patients worldwide. With a strong heritage in pharmaceuticals and operations in over 30 countries, Zentiva combines scientific expertise with innovation to strengthen healthcare access. In India, Zentiva’s facilities adhere to global quality and compliance standards, providing professionals with opportunities to work in world-class environments that shape the future of medicine and chemistry.
Job Overview
The Executive – Quality Control will implement QC activities at the Ankleshwar site, following regulatory directives, global quality standards, and HSE guidelines. The role ensures consistent, reliable testing and analysis to meet
both customer and regulatory requirements.Qualifications:Â
MSc (Organic/Analytical Chemistry)
Experience
- 2 – 6 years of experience as an analyst in the API industry
- Knowledge of GMP & GLP is essential
Key Responsibilities:
Analysis
- Perform timely sampling and analysis of raw materials, intermediates, bulk products, and finished goods.
- Analyze stability studies, process validation, and cleaning validation samples.
- Operate advanced instruments such as HPLC, GC, UV, IR spectrophotometer, dissolution tester, auto-titrator, and polarimeter.
Good Laboratory Practice
- Perform calibration and maintenance of lab equipment; support qualification activities.
- Prepare SOPs, analytical test records, and formats.
- Manage laboratory reagents, chemicals, reference, and working standards.
- Maintain records of control samples and support investigations into Out of Specification (OOS) results.
- Record and manage laboratory raw data related to testing activities.
Validation
- Perform analytical method validation and cleaning validation in accordance with the protocol.
Other
- Coordinate with production and warehouse teams for analytical activities.
- Ensure compliance with HSE requirements in the QC lab.
- Identify and correct unsafe conditions or behaviors.
- Carry out additional assignments as instructed by the department head.
Requirements:
- Strong analytical ability
- Knowledge of LIMS & QMS
- Good coordination and communication skills
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