Production Manager - Oral (OSD)

Production Manager - Oral (OSD)

Job description

  •   Should have handful of exposure in Tablet, liquid oral, oral power, bolus, paste. Ets
  • Should have worked at WHO GMP approved plant and have exposure to EU GMP audit also.
  • Executes the shift production schedule for deputed area and ensures strict compliance to the Standard Operating Procedures, cGMP norms and productivity standards to produce quality product as per plan.
  • Managing production activities in cost effective manner and Budget adherence
  • Sound knowledge on trouble shooting of products and should be able to support formulation and development.
  • Lead the team in achieving production target related to Quality, compliance, production and cost targets.
  • Co-ordination with planning and purchase department for availability
  • Material as per planning.
  • To ensure that the equipment's and machineries used in the plant are validated/revalidated in time by proper co-ordination with Engineering and QA departments.
  • Ensures reduction in wastages and maximises efficiencies (Avoiding reprocess of any batch).
  • Planning and its execution, Coordination with cross functional teams and utilisation of available resources
  • Effective implementation of production planning with CGMP norms.
  • Ensure online documentation on shop floor.
  • Co-ordinates with Engineering to promptly attend to breakdown / preventive maintenance during the shift.
  • Supervises the production/ packaging activity to ensure maximum productivity.
  • Implements & approve changes in operational procedures.
  • Prepares online documentation and generates shift reports; Prepares updated MIS reports and makes available to management as and when required.
  • Coordinates and supports Shift Lead during technology transfer and product commercialization and implements approved changes in operational procedures.
  • Ensures completion of process and equipment validation on a periodic basis.
  • Ensures safety, statutory and housekeeping standards are adhered to during each shift.
  • Identifies their training and development needs and ensures their fulfillment.
  • Ensures compliance with Company policies and values.
  • New ideas for optimizing efficiency & flow.        

Required Candidate profile

Technical -

  • Having knowledge of Tablets, liquid oral, sachet mfg. Process & skills. WHO GMP and EU GMP skills. 
  • Familiar with all pharma activity in production for WHO & EU GMP.                                                                                            

Note: Interested candidates please mail your updated resumes to mentioning your Current CTC, Expected CTC & Notice Period.

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