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    Amneal Pharmaceuticals is hiring for Quality Control Professionals | Pharma Quality Control Job Opportunity | Apply Now

    Quality Control Job Opportunity for B Pharm & M Pharm Pharm Graduates | Amneal Pharmaceuticals is hiring | Apply Now

    Looking for a Quality Control Job in a reputed Pharma Job company? Amneal Pharmaceuticals is hiring for an Officer – Quality Control role in Dahej, Gujarat. This opportunity offers hands-on experience in QC laboratory operations, cGMP compliance, and analytical testing, making it an excellent Quality Control Job for candidates seeking growth in a leading Pharma Job environment.

    • Job Title: Officer, Quality Control
    • Location: Dahej SIR, Gujarat, India
    • Job Identification: 7456

    About the Company

    Amneal Pharmaceuticals is a global pharmaceutical company known for developing, manufacturing, and distributing high-quality generic and specialty medicines. The company focuses on innovation, regulatory compliance, and delivering affordable healthcare solutions worldwide, making it a preferred destination for professionals seeking a Quality Control Job and long-term growth in a Pharma Job.

    Job Description

    • Perform routine QC lab activities, including analysis and documentation
    • Ensure compliance with cGMP and GLP requirements
    • Handle testing of raw materials, in-process, and finished products
    • Support stability studies and sample testing
    • Maintain and ensure compliance of QC instruments
    • Assist in deviation and OOS investigations
    • Follow SOPs and support data integrity practices
    • Contribute to continuous improvement in QC operations

    Key Responsibilities

    • Perform preventive maintenance, calibration, and verification of QC instruments
    • Analyze and support the release of raw materials, intermediates, and packing material
    • Ensure compliance with GLP, safety, and housekeeping standards
    • Handle stability sample testing and documentation
    • Support deviation, OOS, OOAL investigations and CAPA implementation
    • Prepare and follow SOPs, test methods, and specifications
    • Ensure data integrity through audit trail checks
    • Maintain and verify analytical data in LIMS
    • Participate in training and team knowledge sharing
    • Manage analytical columns, reference standards, and lab consumables

    Qualifications

    • M.Sc / M.Pharm / B.Pharm – Chemistry or related discipline preferred.

    Experience

    • 1-6 years of hands-on experience in QC operations within an API manufacturing facility.

    CLICK HERE TO APPLY ONLINE

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