Ph.D. in analytical chemistry having about 19 years of hands on experience in method development and validation by HPLC, LCMS, GC, GCMS, XRD, ICPAES/MS and particle size analyzer, preparation of lab development report, specification finalization and Leachable and extractable study for container closer system of all types of drug product.
Oversee the daily activities in the laboratory to ensure compliance to cGMP, GCP, ISO 17025, WHO, contractual obligations and customer requirements.
Ensure operational efficiency, quality, service and cost-effective management of resources.
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