2.0 - 7.0 years

2 - 7 Lacs

vadodara, gujarat, india

On-site

Conduct analysis of various pharmaceutical materials, including: In-process samples Intermediates Raw materials Packing materials Finished products Stability study samples Hold time study samples Process validation samples Cleaning samples Vendor development samples Any other analysis allocated by the team leader. Release analytical results with thorough and accurate documentation. Ensure all analyses are performed in compliance with Good Laboratory Practices (GLP). Ensure all raw analytical data is documented electronically and in real-time. Initiate, complete, and file daily analysis reports meticulously. Immediately report any abnormal results, incidents, deviations, or discrepancies to t...

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