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Amneal Pharmaceuticals IPQA Officer Jobs in India | B.Pharm M.Pharm QA Careers

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Amneal Pharmaceuticals IPQA Officer Jobs in India | B.Pharm M.Pharm QA Careers

Company: Amneal Pharmaceuticals

Position: Officer – IPQA

Department: IPQA / Quality Assurance

Qualification: B. Pharm / M. Pharm

Location: India

Key Skills & Job Description:

  • cGMP and compliance review in manufacturing areas
  • Machine and area clearance activities
  • Sampling of blend, intermediate stages, and finished products
  • In-process checks during batch manufacturing as per PSP, PVP, and BMR
  • Review of QA documents and records including:
    • Equipment logbooks
    • Dispensing logs
    • Housekeeping records
    • Environmental monitoring records
    • Calibration records
    • Batch Manufacturing Records (BMR)
  • Calibration of IPQA instruments

Why You Should Join Amneal Pharmaceuticals

  • Work with a globally recognized pharmaceutical company
  • Strong learning in IPQA, cGMP, and regulatory compliance
  • Career growth in quality assurance and manufacturing operations
  • Exposure to regulated pharma production standards

Who Can Apply

  • B. Pharm / M. Pharm qualified candidates
  • Freshers or experienced professionals interested in IPQA roles
  • Candidates seeking pharma quality assurance jobs in India

Interview Tips for Amneal IPQA Jobs

  • Prepare core cGMP and IPQA concepts
  • Understand BMR, PSP, and PVP documentation
  • Be clear on sampling, in-process checks, and compliance review
  • Revise environmental monitoring and calibration basics

How To Apply: Interested candidates Click Here For Apply

Frequently Asked Questions (FAQ)

  1. Which company is hiring for Officer IPQA? Amneal Pharmaceuticals is hiring for Officer – IPQA roles.
  2. What qualification is required? B. Pharm or M. Pharm.
  3. Is this a quality assurance role? Yes, this is an In-Process Quality Assurance (IPQA) position.
  4. Is experience required? Experience is not specified in the job details.
  5. What skills are important for IPQA roles? cGMP knowledge, documentation review, in-process checks, and QA compliance.

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