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Location
In office (Ankleshwar)
Seniority
Senior · 5+ years exp
Employment
Full-Time

Confirmed on the employer's own hiring board on Nov 4, 2026. First seen by Alion on Nov 2, 2026. Zentiva scores B on the Alion truth index.

Overview
Company
Impact
Profile match
Zentiva is a prominent European pharmaceutical enterprise specializing in the production and supply of high-quality generic medicines and consumer healthcare products. Headquartered in Prague, Czech Republic, the company operates across dozens of international markets, delivering accessible treatments to millions of patients. Managing the complete lifecycle from laboratory research and manufacturing to global distribution, it focuses on expanding access to affordable, essential medications.

Position Title:Executive - Quality Control

Qualification and Experience:

M. Sc (Organic / Analytical Chemistry) / B. Pharm with 5 - 8 years of Experience as an analyst in the Pharmaceuticals / API industry. GMP & GLP knowledge

Job overview:

  • Implement quality control activities 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 customers’ requirements.

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 on the preparation of SOPs and 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, 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

  • GMP & GLP knowledge
  • Good coordination & communication skills.
  • Analytical ability
  • Knowledge on LIMS & QMS

What makes this position unique?

  • This position will provide good exposure to work in GMP/ GLP environment.

Location information: Ankleshwar, Gujarat, India

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