Urgent Opening At Teva Pharma For Quality Control Department
QC also plays a crucial role in maintaining Good Manufacturing Practices (GMP) and ensuring that all manufacturing processes are carried out in compliance with regulatory requirements. They are responsible for reviewing and approving production and validation protocols, analytical methods and specifications, and manufacturing and testing records.
Other responsibilities include reviewing change controls, deviations, and non-conformances, investigating any quality-related incidents, and providing support during regulatory inspections. The QC department is an essential part of a pharmaceutical company’s quality system and helps provide assurance that products are safe, effective, and of high quality.
Teva pharmaceuticals is hiring for Quality Control Technician III
Department: Analytical Laboratory
Experience: 2 to 7 years
Location: Chennai, Taramani
Qualification: M.Sc/ B.Pharm
Job Responsibilities:
- Performing stability analysis & review of documents
- Calibration & Validation
- Preparation of Method transfer protocols
- Preparation of SOPs
- Handling LCMS software
Interested candidates can share CVs on
snehal.mokashi@teva.co.in
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