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    Job · 12103419

    PUNE · FULLTIME

    Associate Scientist DQA

    Lupin logo

    Lupin

    Pune · onsite · Posted 65d ago

    Sourced fromNaukri
    Undisclosed6–10 yrsfulltimePune

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

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    Section · 01

    About this role

    Role & responsibilities


    1. Experience in handling of payload linker and ADC molecules and Support to establish the ADC lab and ensure the Qualification of ADC lab including equipment qualification, calibration and AMC to meet the GMP requirements.

    2. Implement the SOP procedures and guidelines as per the requirement.

    3. Experience in handling of Peptides &HPAPI/Oncology molecules and ensure to meet the GMP requirements .

    4. Ensure Quality and compliance, audit readiness to meet the GMP & Regulatory requirements.

    5. Drive product and service quality by collaborating with clients, vendors and industry experts to adopt the best practices and new technologies.

    6. To review and approval of the process related documents .

    7. To review and approval of analytical related documents such as raw material, in-process, intermediate, drug substance specification and Standard Test Procedures. To review and approval of stability study protocol/ hold time stability protocol etc.,

    8. To prepare and update product review checklist for drug substance.

    9. Review and approval of Analytical Method Transfer Protocols and waivers.

    10. To ensure pharmacopeial updation of drug substances for specification limits and method of analysis against current official monograph.

    11. To review and management of Change control, Deviation and CAPA to avoid any delay in technology transfer and regulatory filing.

    12. To review and compliance of different online records and analytical data without any deviation and provide inputs as applicable.

    13. Review and approval of protocols and reports of Analytical Method Validations of drug substance, Starting Materials and intermediates.

    14. Review and approval of protocols and reports of Analytical Method Equivalence of drug substance and other query related data etc.

    15. To review and approval of instrument and equipment hardware qualification.

    16. To review and approval of SOP and guideline of Analytical Research & Development department.

    17. Performing Lab rounds and sharing observations to cross functional team and follow up for their closure



    Sourced from naukri

    Section · 02

    Skills

    ADC Lab Setup & QualificationDrug Substance DevelopmentHPAPI HandlingOncology MoleculesPayload LinkersPeptides DevelopmentAnalytical Method DevelopmentAnalytical Research Development

    Section · Company

    About Lupin

    Lupin logo

    Lupin

    Pharma

    20.9k+

    employees

    1968

    58 years old

    Mumbai, Maharashtra

    India

    About

    Global pharmaceutical leader, reporting over ₹20,000 crore in FY24 revenue and a leading global manufacturer of generic medicines with a product footprint in more than 100 countries.

    Industries

    PharmaBiotech & Life sciencesManufacturing

    Employee ratings

    7,366 reviews

    4.1/ 5

    Culture

    3.9

    Career growth

    3.4

    Work-life

    3.8

    Employees rate it well for

    Work Culture998Salary451Senior Management426Work Environment389Learning384

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