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    Manager, Packaging Job at Amneal Pharmaceuticals | Apply Now for Sterile Manufacturing Career Opportunity

    Manager, Packaging Job at Amneal Pharmaceuticals | Apply Now for Sterile Manufacturing Career Opportunity

    Are you searching for Pharma Jobs with a reputed global pharmaceutical company? Explore exciting opportunities through Amneal Careers with this Manager, Packaging position in Ahmedabad, Gujarat. This role offers hands-on experience in sterile manufacturing, regulatory compliance, and packaging operations, making it an excellent opportunity for professionals seeking growth in Pharma Jobs at Amneal Careers.

    • Job Title: Manager, Packaging
    • Location: Ahmedabad City, Gujarat, India
    • Job Identification: 5755

    About the Company

    Amneal Pharmaceuticals is a global pharmaceutical company committed to developing, manufacturing, and distributing high-quality medicines worldwide. Through Amneal Careers, professionals can build strong pharmaceutical careers in manufacturing, quality, regulatory compliance, and packaging operations. The organization follows international regulatory standards, including USFDA, WHO, and EU guidelines, ensuring excellence in sterile manufacturing environments.

    Job Description

    • Attend and ensure the training as per the training schedule and TNI
    • Work according to standard operating procedures in the sterile manufacturing department
    • Prepare, review, revise, and control the Standard Operating Procedures of the General Area in the Sterile Manufacturing Department
    • Prepare BPR
    • Validate and calibrate all equipment and lines
    • Record and check all the logbooks related to the general area and equipment of the packaging and inspection area
    • Train all the subordinates, technicians, and operators of the department
    • Comply with cGMP, Good Document Practice, and departmental discipline
    • Handle the document of Packing and Inspection
    • Monitor all the activities related to packing and inspection

    Key Responsibilities

    • Ensuring adherence to sterile manufacturing SOPs
    • Preparing and controlling Standard Operating Procedures
    • Handling Batch Production Records (BPR)
    • Equipment validation and calibration
    • Maintaining audit-ready documentation
    • Supervising packaging and inspection activities
    • Training technicians and operators
    • Ensuring compliance with cGMP and Good Document Practice
    • Preparing for regulatory inspections (USFDA, WHO, EU, etc.)
    • Keeping documents and areas audit-ready at all times
    • Handling quarantine, rejected, and returned goods

    Qualifications

    • M.Sc. / B. Pharm / M.Pharm

    Skills

    • Preparing for regulatory inspections (USFDA, WHO, EU, etc.).
    • Keeping documents and areas audit-ready at all times.
    • Familiarity with quarantine, rejected, and returned goods handling

    CLICK HERE TO APPLY ONLINE

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