MSc Chemistry Job at Zentiva | Quality Control Executive Role
Are you looking for a Quality Control Executive role, a Zentiva career, or an opportunity to build a strong chemical science career in the pharmaceutical industry? Zentiva is hiring for the position of Executive – Quality Control in Ankleshwar. This is a great opportunity for MSc Chemistry candidates seeking pharma jobs, QC jobs, and hands-on experience in laboratory testing and regulatory compliance.
About Zentiva
Zentiva is a leading pharmaceutical company known for delivering high-quality and affordable medicines across global markets. It offers excellent opportunities through Zentiva career paths, including roles like Quality Control Executive, helping professionals build strong chemical science careers. The company focuses on innovation, compliance, and quality assurance, providing employees with exposure to advanced pharmaceutical processes. With a strong emphasis on ethics and teamwork, Zentiva creates a supportive work environment for growth. It is an ideal organization for candidates seeking stable pharma jobs and long-term career development in quality control and research.
- Job Title: Executive Quality Control, Pharmaceuticals
- Site / Unit: Pharmaceuticals Ankleshwar
- Department: Quality Control
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 customers’ requirements, Living Group’s Values and Code of Ethics.Key Accountabilities
Testing
Performing timely analysis of raw material, bulk product, intermediates, finished goods, and other samples for Pharmaceuticals. Performing analysis of market complaints, Stability, process validation samples, and cleaning validation of Pharmaceuticals.
Good Laboratory Practice
Performing calibration & maintenance of the lab. Equipment and assistance for the qualification of laboratory equipment. Reviewing pharmacopeias for specification preparation. Preparing SOPs, formats, and analytical test records. Managing reference standards, working standards, laboratory reagents & chemicals. Arranging and observing Control Samples and maintaining records. Participating in the investigation of out-of-specification results, retesting, and reviewing the analysis records. Maintaining & reviewing laboratory raw data related to testing activity.
Validation
Preparing protocol for Analytical Method validation, cleaning validation, and performing the validation exercise as per the protocol.
Management of Laboratory Consumables
Identifying and planning requirements for laboratory consumables and monitoring the stock of chemicals, spares, glassware, and printed material.
Coordination
Coordinating with production and the warehouse for analytical activities.
Other
Compliance with HSE Requirements for QC Laboratory. Identifying and correcting unsafe conditions or behaviors, and promptly reporting other potentially hazardous situations. Carrying out any other assignments or projects as per the instructions of the Dept. Head to meet with the organizational objectives and priorities.
Requirements
- Education: Master’s in Chemistry
- Experience:1-5 years in a Pharmaceutical Company.
- Technical skills & Competencies : Analytical ability, Troubleshooting, Coordination, Communication
- Behavioural Competencies: Accountability, Authenticity, Collaboration, Courage, and Trust.
