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    Job · 11959875

    Nitika Pharmaceutical Specialities logo

    IPQA Officer

    Nitika Pharmaceutical Specialities · Nagpur · onsite · Posted 61d ago

    Up to ₹1.5L PA0–3 yrsfulltimeSourced fromNaukri

    About a minute. You'll make an account on the way through.

    About this role

    Roles and Responsibilities :

    • Ensure compliance with GMP regulations and company policies in the IPQA department.
    • Conduct regular audits and inspections to identify areas for improvement and implement corrective actions.
    • Develop, review, and maintain SOPs (Standard Operating Procedures) related to documentation, testing, and release of pharmaceutical products.
    • Collaborate with cross-functional teams to resolve issues related to product quality, stability, and regulatory compliance.

    Job Requirements :

    • 0-3 years of experience in a similar role within the pharmaceutical industry.
    • Strong understanding of Good Manufacturing Practices (GMP) guidelines and regulations.
    • Ability to develop accurate documents such as protocols, reports, and records according to established standards.

    Sourced from naukri

    Skills

    SOPGMPDocumentation

    About Nitika Pharmaceutical Specialities

    Nitika Pharmaceutical Specialities logo

    Nitika Pharmaceutical Specialities

    Pharma

    375

    employees

    1991

    35 years old

    Nagpur, Maharashtra

    India

    Up to ₹1.5L PA

    This role

    About

    Nitika Pharmaceutical Specialities manufactures diverse products across various industries, adapting to technological advancements to remain competitive globally.

    Industries

    PharmaHealthcare / Pharma

    Employee ratings

    154 reviews

    3.5/ 5

    Culture

    3.4

    Career growth

    3.2

    Work-life

    3.3

    Employees rate it well for

    Salary17Work Life Balance11Work Culture8Learning8Senior Management7

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    IPQA Officer · waiting for your command