Responsibilities: * Ensure quality control measures are enforced * Collaborate with cross-functional teams on projects * Oversee daily production planning & execution * Manage manpower resources effectively
Compilation and submission of eCTD dossier for new product application & post approval submission Query response, PAS,CBE and annual report, drug listing Review of artwork and submission of labelling section Maintain product life cycle.
Compilation and submission of eCTD dossier for new product (Finished) application & post approval submission Query response, PAS,CBE and annual report, drug listing Review of artwork and submission of labelling section Maintain product life cycle.
experience of analysis of Raw Material & Finished Product by HPLC/GCTechniques in pharma industry.knowledge of calibration of analytical instruments.having knowledge of analytical method validation & worked for regulated market will be preferred Annual bonus Provident fund