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    Job · 14996128

    HYDERABAD · FULLTIME

    Executive

    Sssv Solutions Visakhapatnam logo

    Sssv Solutions Visakhapatnam

    Hyderabad · onsite · Posted 50d ago

    Sourced fromNaukri
    Undisclosed3–7 yrsfulltimeHyderabad

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    Section · 01

    About this role

    Executive QA (IPQA & AQA) | API Pharma | Hyderabad

    Position: Executive QA (IPQA & AQA)
    Experience: 37 Years
    Industry: API Pharma – Mandatory
    Location: Hyderabad

    Role & Responsibilities

    • Perform IPQA activities on the shop floor in API manufacturing areas.
    • Conduct line clearance, in-process checks, area clearance, and batch documentation review.
    • Ensure compliance with cGMP, GDP, SOPs, and quality standards throughout manufacturing operations.
    • Review and verify Batch Manufacturing Records (BMR), Batch Packaging Records (BPR), and other GMP documents.
    • Handle and support deviation, CAPA, change control, and investigation activities.
    • Prepare, review, and maintain quality-related documentation in compliance with regulatory requirements.
    • Coordinate with Production, QA, QC, and other cross-functional teams during manufacturing and quality activities.
    • Support preparation and review of Annual Product Quality Review (APQR/PQR).
    • Perform SOP review, document control, and periodic review of quality documents.
    • Ensure timely closure and effective implementation of deviations, CAPAs, change controls, and investigations.
    • Support internal, customer, and regulatory audits and ensure compliance with audit requirements.
    • Monitor adherence to GMP and regulatory requirements across manufacturing and quality processes.
    • Identify quality and compliance gaps and coordinate with relevant departments for appropriate corrective and preventive actions.
    • Maintain accurate and complete QA records and documentation as per approved procedures.

    Key Skills:


    API Pharma | QA | IPQA | AQA | In-Process Quality Assurance | APQR | PQR | cGMP | GDP | SOP | Batch Records | BMR | BPR | Line Clearance | Deviation | CAPA | Change Control | Investigation | Document Control | Audit Compliance | Regulatory Compliance

    Candidate Profile

    • 3–7 years of relevant experience in Quality Assurance within the API Pharma industry.
    • Hands-on experience in IPQA/shop floor activities and QA documentation.
    • Good knowledge of cGMP, GDP, SOPs, deviations, CAPA, change control, investigations, and audits.
    • Candidates with exposure to both IPQA and AQA/Quality Systems activities will be preferred.
    • Good documentation, communication, coordination, and analytical skills.

    INTRESTED CANDIDATES CAN CONTACT:-[phone removed]

    Sourced from naukri

    Section · 02

    Skills

    QualityAPQRAPI ManufacturingCGMPBulk DrugsPQRIPQAAQAQMSQuality AssuranceAPI

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