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    Freshers Job Alert | Senior Executive – QA Job at Piramal Pharma | Apply Now

    Senior Executive – QA Job at Piramal Pharma

    Piramal Pharma Solutions is hiring a Senior Executive – Quality Assurance for its Mahad, Maharashtra facility. This QA Job role is ideal for pharmacy professionals with strong exposure to GMP, in-process quality checks, documentation, audit compliance, and manufacturing oversight. Join a globally trusted CDMO and build a stable, long-term career in pharmaceutical quality assurance. Graduates seeking for B pharma jobs or M Pharma jobs can apply now.

    QA Job Details

    • Job Title: Senior Executive – Quality Assurance
    • Location: Mahad, Maharashtra, India

    About the Company

    Piramal Group, with over three decades of excellence, follows a strong strategy of organic and inorganic growth driven by ethical and value-based practices. Piramal Pharma Solutions (PPS) is a global Contract Development and Manufacturing Organization (CDMO) offering end-to-end solutions across the drug lifecycle. With facilities across North America, Europe, and Asia, PPS supports innovators and generic companies worldwide in APIs, finished dosage forms, biologics, and advanced drug delivery systems.

    Educational Requirements for QA Job Role

    • B. Pharm or M. Pharm

    Key Responsibilities

    • Area and line clearance for manufacturing, packing, and dispensing activities.
    • In-process quality checks in manufacturing and packing operations.
    • Inspection and verification of dispensing activities.
    • Daily verification of weighing balance calibration and environmental monitoring.
    • Review and verification of Batch Manufacturing Records (BMR).
    • Sampling of bulk stages and finished goods, including control samples is essential for this QA Job Role.
    • Monitoring and reporting daily non-conformances.
    • Online observation of process deviations and implementation of CAPA.
    • Ensuring data integrity compliance in production areas.
    • Execution of food and dietary supplement regulations for US export (21 CFR Part 111).
    • Training of shop floor personnel and new joiners.
    • Audit compliance, qualification, and validation activities.
    • Adherence to EHS norms and sanitation programs.

    Skills Required

    • Strong knowledge of GMP and in-process quality systems is essential for this QA Job Role.
    • Experience in line clearance and batch record review.
    • Understanding of data integrity, CAPA, and deviation management.
    • Exposure to tablet, liquid, HNH, and ANH manufacturing.
    • Familiarity with US FDA dietary supplement regulations.
    • Good documentation, communication, and training skills.

    Why This QA Job Role?

    • Opportunity to work with a globally reputed pharmaceutical CDMO.
    • Hands-on exposure to advanced quality systems and regulatory compliance.
    • Strong career growth in QA operations and audit management.
    • Experience across multiple dosage forms and global regulatory standards.
    • Stable, full-time role with a trusted industry leader.
    • Graduates seeking for B pharma jobs or M Pharma jobs can apply now.

    CLICK HERE TO APPLY ONLINE

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