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Executive, IPQA

Overview
Amneal Pharmaceuticalsamneal.comPosted 12 days ago
Ahmedabad, Gujarat, INOn-site
Quick apply
Seniority level
Executive
Employment type
Full time
Work experience
1 to 6 years
Specialization
Manufacturing & production

About the role

  • Responsible for line clearance activity before commencing the different operations like dispensing, manufacturing, filling, inspection, sealing, labelling, and packing.
  • Responsible for Process validation, cleaning validation/verification, hold time study, media fill & routine batch sampling as per protocol/SOP.
  • Responsible for review of executed BMRs and BPRs.
  • Responsible to perform the in-process test at different stages as per batch document/SOP.
  • Responsible to review the different type of planner and calibration certificates.
  • Responsible to monitor cGMP compliance at shop floor.
  • Responsible to review the different type of print outs i.e CIP, SIP, autoclave, filter integrity etc..
  • To maintain the Issuance/reconciliation record of items / media for Environment monitoring material e.g., plates, swabs, etc..
  • Responsible to participate in media fill simulation study.
  • Responsible to participate in perform qualification activities of manufacturing area.
  • Review of Media fill CD. Review of Visual inspector qualification record.

Requirements

  • In-Process Quality Controls (IPQC) & Sampling - Practitioner
  • Aseptic Process Simulation (Media Fill) Monitoring - Expert
  • Line Clearance & Batch Record Review - Practitioner
  • Good Documentation Practices (GDP) - Practitioner
  • Regulatory & Compliance Knowledge - Practitioner
  • Education: B.Sc./ M.Sc/ B.Pharma / M.Pharma
  • Total Experience - 1 - 6 Year inexperience in IPQA / Environmental Monitoring for sterile manufacturing plant
  • Note: Candidates who want to apply for internal jobs, must have completed atleast 2 years within existing role.