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    Job · 20640952

    HYDERABAD · FULLTIME

    Immediate Opening For QC Position

    Vimta Labs

    Vimta Labs

    Hyderabad · onsite · Posted 12d ago

    Sourced fromNaukri
    Undisclosed7–12 yrsfulltimeHyderabad

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    Section · 01

    About this role

    Dear All,


    Greeting From Vimta Labs.


    Company Name: Vimta Labs

    Location: Shamirpet, Hyderabad

    Experience: 8 to 12 Years

    Education: M.Sc. / B.Pharmacy / M.Pharmacy


    Key Responsibilities Core QMS & Investigations

    • Investigate quality issues: Lead and participate in QMS investigations concerning Incidents, Out of Specification/Expectation (OOS/OOE/OOX), Occurrences, and Deviations.
    • Review documentation requests: Serve as a designee for authorizing procedural document issuance.
    • Monitor environmental conditions: Record and witness temperature monitoring protocols within the biopharma department.

    Documentation & Compliance Review

    • Author and review SOPs: Prepare and review Standard Operating Procedures, instrument qualification protocols, raw data, and final reports.
    • Audit logbooks: Perform periodic reviews of instrument usage and maintenance logbooks across the department.
    • Manage standards: Review the usage, maintenance, and tracking of reference standards.

    Equipment Qualification & Data Integrity

    • Ensure instrument compliance: Review analytical instrument software user roles, privileges, project-related protocols, and raw data to ensure data integrity.
    • Oversee maintenance schedules: Review equipment lists, calibration schedules, and preventive maintenance (PM) timelines.
    • Verify equipment safety: Review periodic calibrations, PM, and electrical safety protocols for all biopharma equipment.

    Training & People Management

    • Deliver training: Provide technical training on system-related procedures and quality management systems to the team.
    • Authorize training records: Act as a designee for the review and authorization of Training Documentation Forms (TDF) and Training Assessment Forms (TAF).

    Required Technical Skills & Competencies

    • Deep understanding of regulatory compliance (GxP, FDA, MHRA) in a biopharma or analytical testing environment.
    • Strong expertise in Data Integrity principles and software user-privilege management for analytical instruments.
    • Proven track record in handling complex root cause analysis (RCA) for OOS and deviations.

    Interested Candidates Please share Profiles to [email removed]

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    Section · 02

    Skills

    Sop PreparationQMSreview

    Section · Company

    About Vimta Labs

    Vimta Labs

    Vimta Labs

    Clinical Research

    1.3k+

    employees

    1984

    42 years old

    Hyderabad/Secunderabad, Telangana

    India

    About

    VIMTA Labs is one of the leading CRO in India, providing clinical research & development services to global pharmaceutical & biotechnology companies.

    Industries

    Clinical ResearchAnalytics & KPO

    Employee ratings

    544 reviews

    3.4/ 5

    Culture

    3.2

    Career growth

    2.8

    Work-life

    3.3

    Employees rate it well for

    Work Culture57Senior Management46Learning44Salary42Job Security26

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