Zentiva is inviting applications for the role of Executive – Quality Control at its Ankleshwar location in India. This opportunity is suitable for candidates with a postgraduate background in Organic Chemistry and experience in chemical and instrumental testing laboratories within a pharmaceutical quality control environment.
Job Details
| Company | Zentiva |
| Position | Executive – Quality Control |
| Department | Quality Control |
| Location | India / Ankleshwar; Ankleshwar |
| Industry | Pharmaceuticals |
Job Description
The Executive Quality Control role involves implementing quality control activities for pharmaceuticals at Ankleshwar while adhering to regulatory, global quality and HSE guidelines. The position focuses on optimum utilization of resources to ensure consistent product quality and to meet customer requirements while following Group Values and Code Ethics.
Key Responsibilities
Testing and Release
- Plan timely sampling, analysis and review of raw material, bulk product, intermediates, finished goods, packing material and other pharmaceutical samples.
- Perform analysis of raw material samples received from new vendors for pharmaceuticals.
Good Laboratory Practice
- Plan calibration and maintenance of laboratory equipment and assist in qualification of laboratory equipment.
- Review pharmacopeias for specification preparation.
- Prepare SOPs, formats and Analytical Test Record.
- Manage reference standards, working standards, laboratory reagents and chemicals.
- Review and observe retention samples and maintain records.
- Investigate out of specification results, conduct retesting and review analysis records.
- Maintain and review laboratory raw data related to testing activity.
Validation
- Prepare protocols for Analytical Method validation/Transfer and cleaning validation.
- Perform validation exercises as per the protocol.
Management of Laboratory Consumables
- Identify and plan requirements for laboratory consumables.
- Monitor stock of chemicals, glassware and printed material.
Coordination and HSE Compliance
- Coordinate with production and warehouse teams for analytical activities.
- Ensure compliance with HSE requirements for the QC laboratory.
- Identify and correct unsafe conditions or behaviors and promptly report other potentially hazardous situations.
- Carry out any other assignments or projects as instructed by the Department Head to meet organizational objectives and priorities.
Qualification
- Post Graduate in Science (Organic Chemistry ).
- Exposure to GMP and GLP in a chemical and instrumental testing laboratory.
- Analytical ability.
- Trouble shootings.
- Co ordination.
- Communication.
- Leadership.
Experience
2-4 years in chemical & instrumental testing laboratory with exposure to GMP, GLP.
How to Apply
Interested candidates can apply online through the official Zentiva application link given below.