Executive, Quality Control, Pharmaceuticals

Zentiva; Ankleshwar; On-site; INR 400,000 - 600,000; Full time

Job summary

Zentiva in Ankleshwar is seeking an Executive/Sr. Executive for Quality Control in Pharmaceuticals. The role involves implementing quality control activities, conducting timely analyses, and ensuring compliance with global quality directives.

The ideal candidate should have a Post Graduate degree in Science and 2-5 years of experience in the pharmaceutical sector. Key skills include analytical ability, troubleshooting, and coordination.

Qualifications

• 2–5 years of experience in a Pharmaceutical Company.
• Understanding of Good Laboratory Practices and validation.

Responsibilities

• Implement quality control activities adhering to quality directives.
• Perform timely analysis of raw materials and finished goods.
• Coordinate with production and warehouse for analytical activities.

Skills

Analytical ability

Troubleshooting

Coordination

Communication

Education

Post Graduate in Science (Organic or Analytical Chemistry)

Job description

Executive/Sr. Executive, Quality Control, Pharmaceuticals

Job Purpose

Implement quality control activities for Pharmaceuticals 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 customer requirements, living Group’s Values and Code of Ethics.

Key Accountabilities

Testing

Perform timely analysis of raw material, bulk product, intermediates, finished goods and other samples for Pharmaceuticals. Perform analysis of market complaints, stability, process validation samples, cleaning validation of Pharmaceuticals. Test on nitrosamine and related impurities.

Good Laboratory Practice

Perform calibration & maintenance of lab equipment and assist with qualification of laboratory equipment. Review pharmacopeias for specification preparation. Prepare SOPs, formats and Analytical Test Record. Manage reference standards, working standards, laboratory reagents & chemicals. Arrange and observe control samples and maintain records. Participate in investigation of out‑of‑specification results, retesting and review of analysis records. Maintain & review laboratory raw data related to testing activity.

Validation

Prepare protocol for analytical method validation/verification & transfer, cleaning validation and perform the validation exercise as per protocol for the material and drug products. Perform analytical method validation/verification & transfer for nitrosamine and NDSRIs using LCMS/MS. Conduct analytical method development and related troubleshooting samples on LCMS/MS.

Management of Laboratory Consumables

Identify and plan requirement for laboratory consumables and monitor stock of chemical spares, glassware and printed material.

Coordination

Coordinate with production and warehouse for analytical activities.

Other

Compliance to HSE Requirements for QC Laboratory. Identify and correct unsafe conditions or behaviors and promptly report other potentially hazardous situations. Carry out any other assignments or projects as per the instruction of the Dept. Head to meet organizational objectives and priorities.

Qualifications

Post Graduate in Science (Organic or Analytical Chemistry). 2‑5 years in a Pharmaceutical Company.

Technical Skills & Competencies / Language

• Analytical ability
• Troubleshooting
• Coordination
• Communication