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    Pharma Jobs in Amneal: Hiring a Manager – Packaging in Ahmedabad – Apply Now

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    Pharma Jobs in Amneal: Hiring a Manager – Packaging in Ahmedabad – Apply Now

    Looking for Pharma Jobs in Amneal? Here’s your opportunity!
    Amneal Pharmaceuticals is hiring a Manager – Packaging for its sterile manufacturing facility in Ahmedabad, Gujarat. This role offers an excellent opportunity for professionals with M.Sc., B.Pharm, or M.Pharm qualifications to lead packaging operations, ensure compliance with cGMP and global regulatory standards, and manage inspection readiness. The ideal candidate will play a key role in maintaining quality, documentation, and operational excellence within the sterile packaging department.

    About Amneal Pharmaceuticals

    Amneal Pharmaceuticals is a leading global pharmaceutical company dedicated to developing and delivering high-quality, affordable medicines across multiple therapeutic areas. Headquartered in the United States, with significant operations in India, Amneal combines scientific innovation, regulatory expertise, and operational excellence to serve patients worldwide. The company emphasizes diversity, equity, and inclusion, fostering a workplace where every employee can thrive. Amneal invests in research and development, state-of-the-art manufacturing, and quality systems to ensure compliance with global standards, including cGMP and regulatory guidelines. With a strong presence in formulation development, generic and specialty pharmaceuticals, Amneal continues to expand its portfolio and reach, providing medicines that improve health outcomes while maintaining affordability.

    Job Details:

    • Job Title: Manager – Packaging
    • Location: Ahmedabad City, Gujarat, India
    • Job Category: Manufacturing Process Operations
    • Job Schedule: Full Time
    • Apply Before: 10/30/2025

    Job Description:

    • Attend and ensure the training as per schedule and Training Need Identification (TNI).
    • Work according to Standard Operating Procedures (SOPs) in the sterile manufacturing department.
    • Prepare, review, revise, and control SOPs for the general area in sterile manufacturing.
    • Prepare Batch Production Records (BPR) and validate/calibrate all equipment and lines.
    • Record and check all logbooks related to general areas and equipment in packaging and inspection.
    • Train subordinates, technicians, and operators within the department.
    • Comply with cGMP, Good Documentation Practices, and departmental discipline.
    • Handle documentation related to packing and inspection.
    • Monitor all activities related to packing and inspection areas.

    Qualifications:

    M.Sc. / B.Pharm / M.Pharm

    Skills Required:

    • Experience in preparing for regulatory inspections (USFDA, WHO, EU, etc.)
    • Maintaining audit-ready documentation and compliant areas at all times.
    • Proficiency in handling quarantine, rejected, and returned goods.

    CLICK HERE TO APPLY

    Apply now

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