Posted:2 days ago|
Platform:
Work from Office
Full Time
Role & responsibilities Responsible for compliance as per 9001:2015, ISO 14001:2015, ISO 45001:2018. Responsible for validation/ verification of Analytical Methods on ICP-MS, AAS, HPLC and instruments as per ICH Q2 (R2). Responsible for development of Cost-effective, rugged and robust analytical methods on ICP-MS, AAS, HPLC, and wet lab instruments as per ICH Q14 and Analytical QbD. To maintain GLP compliance as per OECD or other regulatory/ general guidelines in ARD lab. Responsible for performing technology transfer of analytical method in QC(Plant). Any other responsibility assign by ARD head, time to time on need basis. Preferred candidate profile Post graduate (M.Pharma/M.Sc) Must be from Pharmaceuticals (preferably API) background.
Akums
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