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| Job Location | Vishakhapatnam |
| Education | Not Mentioned |
| Salary | Not Disclosed |
| Industry | Recruitment Services |
| Functional Area | Quality (QA-QC) |
| EmploymentType | Full-time |
To Lead the Analytical team, Ensuring release of the raw materials, in-process, bulk, packaging materials and finished products as per the timelines based on production plan. And maintain the compliance level in the Laboratory.- Ensuring release of the raw materials, in-process, bulk, packaging materials and finished products as per the timelines based on production plan.- Review of Stability samples and its timely analysis.- Review of analytical documents.- To participate in investigation of complaint handling.- To participate in investigation of complaint handling , to investigate /review deviations, incidents, OOS and CAPA results if any and to take remedial measures.- To maintain the compliance of the laboratory by implementing online GLP reviews in the laboratory. - Approval/Rejection COA of raw materials, Packing materials, In-process materials and stability batches.BenefitsBrand reputationClient IntroductionManufacturer of Pharmaceuticals API and formulations, R&D (API Generics) skillsAnalytical, QC, API, Formulation qualificationMinimum 10-15 Years of Exposure to l analytical equipment like HPLC,UPLC ,GC (GC with auto sampler and Head space) (waters/shimadzu/Agilent)UV spectrophotometer, IR, polarimeter, analytical balance water purification system ,particle size analyzer,Toc,NIR,Dissolution apparatus, Glassware washing machine etc.,
Keyskills :
misaccountancy particle sizeraw materials finished productscomplaint handling water purificationanalytical equipment