Production Manager - Oral (OSD)
loading..

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 careers@ashishlifescience.com mentioning your Current CTC, Expected CTC & Notice Period.

You Got This — Apply

You're almost there! It's just a few steps between you and job glory. For uploads, please use .pdf, .doc or .docx files. Employers recommend using .pdf.

By applying to this job, you agree to The Pharma Revolution Terms of Use and Privacy Policy.