4 - 8 years
3 - 6 Lacs
Posted:2 days ago|
Platform:
Work from Office
Full Time
To ensure the implementation of Good Laboratory Practice and Good Documentation Practice in Quality Control. Analysis of In-process, finished products, stability samples of various formulation products: oral solids, Topical, cosmetics. Responsible for investigation and initiation of change control, Laboratory incidents, CAPA, OOS, OOT. To Co-ordinate with Quality control Manager to prepared the Analytical Method Validation protocol and Report. To perform the analytical method validation as per requirmnet. To ensure the implementation of Good Laboratory Practice and Good Documentation Practice in Quality Control Also having sound knowledge about data integrity, ALCOA principals and respective regulatory guidelines.
KLM Laboratories
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