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Nashik
In-Process Monitoring: Conduct regular inspections and quality checks on the production line. This includes verifying raw materials, components, and the final product to ensure they meet specified standards.
Documentation and Record-Keeping: Maintain meticulous records of all quality checks, test results, and production data. Ensure all batch records and logbooks are accurately filled out and signed.
Deviation Handling: Identify and report any deviations or non-conformances from the standard operating procedures (SOPs). Investigate the root cause of these deviations and collaborate with the production team to implement corrective actions.
Compliance: Ensure strict adherence to Good Manufacturing Practices (GMP), regulatory guidelines, and company quality policies.
Sampling and Testing: Collect samples of products at various stages for laboratory testing. Perform basic in-process tests (e.g., tablet hardness, capsule weight variation, liquid volume).
Training: Provide guidance and training to production staff on quality procedures and GMP requirements to foster a culture of quality.
| Experience | 1 - 3 Years |
| Salary | 1 Lac 50 Thousand To 2 Lac 50 Thousand P.A. |
| Industry | Manufacturing / Production / Quality |
| Qualification | B.Pharma, M.Pharma |
| Key Skills | Technical & Procedural Skills Knowledge Of Good Manufacturing Practices In-Process Testing and Inspection |
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