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| DESIGNATION | MANAGER (QUALITY CONTROL) | | Experience | 10-15 years in Pharmaceutical industry | | Education | B.Pharm/M.Sc (Organic/Analytical Chemistry) | | Location | Nagpur | | Remuneration | Best in Industry | | Job Responsibilities | Preferably working with Parenteral /Solid dosage manufacturing plant, responsible for monitoring the working of QC functions and taking corrective actions, responsible for conducting audits in plant, to implement cGLP system, to train QC personnels, to ensure that pharmaceutical products manufactured by the company meets the quality standards, Responsible for preparation, approval and compliances of following documents and records… 1) Standard Operating Procedures. 2) Protocols (Process Validation, Equipment Validation and stability). 3) Analytical validation. 4) Vendor Approval (RM and PM) | | Forward your Resume to
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| | DESIGNATION | QUALITY CONTROL CHEMIST | | Experience | Min. 1 year, fresher may also apply. | | Education | D. Pharm / B. Pharm / B.Sc. | | Location | Nagpur | | Remuneration | Best in Industry | | Job Responsibilities | - Quality Control Chemist to apply knowledge of quality standards and procedures to review instructions, specifications, and production schedules. Also responsible for determining methods of conducting inspection and tests, sequence of operations and work assignments.
- Preparation of Specifications & STP of Packing Materials.
- Maintain inspection and test records.
- Prepare CoA reports for products when required by customer.
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| | DESIGNATION | MICROBIOLOGIST | | Experience | Min. 1 year, fresher may also apply. | | Education | B.Sc. (Micro.) / M. Sc. (Micro.) | | Location | Nagpur | | Remuneration | Best in Industry | | Job Responsibilities | - To conduct Microbiological Analysis of Purified Water & finished product and maintaining relevant records for all such group products.
- Carrying out Environmental Monitoring of Different Areas.
- Carrying out Microbiological validations for disinfectants & calibrations of Instruments in micro.
- Effecting utilizations of Lab inputs including Glassware and Chemicals, timely analysis and reporting support for such activities to maintains ZERO Pending reports on a day to day basis, maintain documents as required under Drugs and Cosmetics Act, train and get trained by peers and sub ordinates in areas of expertise.
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