Job Purpose:
To perform, review and support in all day to day analytical activities and Product Release procedures in accordance to GLP compliance.
Key Responsibilities:Preparation and Review of SOP'sPreparation and review of specification and Method of analysisQualification and Maintenance of Equipment'sPreparation of Method of analysisEnsuring proper documentation inline with GLP/GDPPerform analysis of Raw materials and Finished products.Responsible for the delivering and promoting a culture of maintaining and improving the performance of SafetyUse gembas to identify abnormalities from the standard and to get them fixedQualifications:
Looking for candidates with Msc/BPharmacy with 2 to 7 years experience in Quality Control related to pharmaceutical oral dosage forms from a reputed pharma company.
Sound knowledge on pharmaceutical analytical requirements.
Knowledge on GLP, QMS, Regulatory & EHS regulations.
Education:UG -B.Sc - Any Specialization, B.Pharma - Pharmacy
PG - M.Sc - Any SpecializationApply here: https://www.naukri.com/job-listings-Quality-Control-Executive-Assistant-Manager-oral-Solid-Dosage-Forms-GlaxoSmithKline-Pharmaceuticals-Limited-Bengaluru-Bangalore-2-to-7-years-091116002291