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Title:  Manager - 2

Date:  Nov 12, 2024
Location:  Dewas SGO - Operations Block P
Company:  Sun Pharmaceutical Industries Ltd

Job Description

Position: Packing + QMS In charge

Department: Production Block P

Designation: Manager II

Education Qualification: B. Pharma / M. Pharma

Total Years of experience: 10+ Years

Responsibilities:

  • End to end handling of QMS activities including OOT / OOS / Market complaint / Investigation / CAPA / deviation & change control.
  • To ensure implementation of CAPA on time.
  • To response external and internal inspection on time.
  • To prepare the SOP.
  • To review & approve for Master Batch Packing Record.
  • To perform in process checks & record in log books & PI / MI.
  • To manufacture and package the sterile dry powder injectable batches as per production plan.
  • To maintain Harmony relationship with peers, seniors at work place and ensure the win - win situation for resolution of issues.
  • To ensure contamination control are available and followed at site as per Contamination Control Strategy (CCS) and respective procedures.
  • To follow & implement the current Good Manufacturing Practices, EHS practices and SOP during work.
  • To plan the manufacturing & packing activities of the department as per weekly / monthly delivery schedule.
  • To meet the production schedule both in quantity & quality.
  • To ensure the effective control on usage of men, machine, & material in the packing department.
  • To organise & implement the on-job training activities in the department & ensure training of all team members of the packing department.
  • To ensure the hygiene & maintenance of packing department, system & equipment are in neat & tidy condition at all time.
  • To review & approve the SOPs, Validation protocols/reports, specifications, packing instruction relating to production & ensures their implementation.
  • To ensure the required initial & continuous training is being carrying out for all the employees in packing section.
  • To ensure timely completion of validation/qualification activities for aseptic process simulation (Media Fill), equipment’s & systems as per approved procedure.
  • To implement the recommendation of internal/external audits outcome.
  • Any other responsibility / Work activity that may be assigned from time to time.

 

 

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