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  • 1) Production schedule, co-ordination for Raw material arrangements and executer of planned quantities. 2) Ensure the changes to vendor / processes / equipment / procedures. 3) Ensure the investigation of deviation s, complaints based on QA Communi

  • 1) Production schedule, co-ordination for Raw material arrangements and executer of planned quantities. 2) Ensure the changes to vendor / processes / equipment / procedures. 3) Ensure the investigation of deviation s, complaints based on QA Communi

  • 1) Production schedule, co-ordination for Raw material arrangements and executer of planned quantities. 2) Ensure the changes to vendor / processes / equipment / procedures. 3) Ensure the investigation of deviation s, complaints based on QA Communi

  • 1) Production schedule, co-ordination for Raw material arrangements and executer of planned quantities. 2) Ensure the changes to vendor / processes / equipment / procedures. 3) Ensure the investigation of deviation s, complaints based on QA Communi

  • 1) Production schedule, co-ordination for Raw material arrangements and executer of planned quantities. 2) Ensure the changes to vendor / processes / equipment / procedures. 3) Ensure the investigation of deviation s, complaints based on QA Communi

  • World Safety Culture & pay main role to implement in Production • Qualifying all equipment’s before production as per c GMP, Selection of equipment’s for execution of new product & process, planning & organize modification in plant as per HAZOP requirement. • Effective resource planning **Urgent Req. of Pharma "Production Manager' (B/M.Pharma) from API Background for kolkata Factory** factory location: kolkata ...

  • Validation and method transfer team as and when required. - Take Care of OOS, OOT justification reports, deviations and its assessments by roots cause investigation and CAPA. - Set up , manage and maintain the analytical laboratory by ensuring proper care/use of instruments, updating SOPs, risk assessment

  • Validation and method transfer team as and when required. - Take Care of OOS, OOT justification reports, deviations and its assessments by roots cause investigation and CAPA. - Set up , manage and maintain the analytical laboratory by ensuring proper care/use of instruments, updating SOPs, risk assessment

  • Validation and method transfer team as and when required. - Take Care of OOS, OOT justification reports, deviations and its assessments by roots cause investigation and CAPA. - Set up , manage and maintain the analytical laboratory by ensuring proper care/use of instruments, updating SOPs, risk assessment

  • Validation and method transfer team as and when required. - Take Care of OOS, OOT justification reports, deviations and its assessments by roots cause investigation and CAPA. - Set up , manage and maintain the analytical laboratory by ensuring proper care/use of instruments, updating SOPs, risk assessment

  • Validation and method transfer team as and when required. - Take Care of OOS, OOT justification reports, deviations and its assessments by roots cause investigation and CAPA. - Set up , manage and maintain the analytical laboratory by ensuring proper care/use of instruments, updating SOPs, risk assessment

  • Validation and method transfer team as and when required. - Take Care of OOS, OOT justification reports, deviations and its assessments by roots cause investigation and CAPA. - Set up , manage and maintain the analytical laboratory by ensuring proper care/use of instruments, updating SOPs, risk assessment

  • M.Sc / BE / B.Tech Chemical / MPharma with experience in Manufacturing / Production of STERILE API in US FDA approved plant ...

  • M.Sc / BE / B.Tech Chemical / MPharma with experience in Manufacturing / Production of STERILE API in US FDA approved plant ...

  • M.Sc / BE / B.Tech Chemical / MPharma with experience in Manufacturing / Production of STERILE API in US FDA approved plant ...

  • M.Sc / BE / B.Tech Chemical / MPharma with experience in Manufacturing / Production of STERILE API in US FDA approved plant ...

  • M.Sc / BE / B.Tech Chemical / MPharma with experience in Manufacturing / Production of STERILE API in US FDA approved plant ...

  • M.Sc / BE / B.Tech Chemical / MPharma with experience in Manufacturing / Production of STERILE API in US FDA approved plant ...

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