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    Job · 14133621

    Nitika Pharmaceutical Specialities logo

    Sr. Executive QA

    Nitika Pharmaceutical Specialities · Nagpur · onsite · Posted 55d ago

    Undisclosed3–8 yrsfulltimeSourced fromNaukri

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

    About this role

    Roles and Responsibilities :

    • Conduct CAPA investigations to identify root causes of deviations, non-conformities, and out-of-specification results.
    • Develop and implement corrective actions to prevent recurrence of issues in accordance with cGMP regulations.
    • Collaborate with cross-functional teams to resolve quality-related issues and ensure compliance with QMS requirements.
    • Review and approve CAPAs before implementation to ensure they meet regulatory requirements.

    Job Requirements :

    • 3-8 years of experience in a pharmaceutical or life sciences industry in a similar role.
    • Strong understanding of GMP/cGMP regulations and their application in a manufacturing environment.
    • Experience with investigation techniques such as FMEA, Fishbones, etc.

    Sourced from naukri

    Skills

    Audit HandelingCGMPCAPAInvestigationQMSGMP

    About Nitika Pharmaceutical Specialities

    Nitika Pharmaceutical Specialities logo

    Nitika Pharmaceutical Specialities

    Pharma

    375

    employees

    1991

    35 years old

    Nagpur, Maharashtra

    India

    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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