QA-Assistant Manager/Dy.Manager Sterile/Injectable

10 - 18 years

12 - 17 Lacs

Posted:None| Platform: Naukri logo

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Work from Office

Job Type

Full Time

Job Description

  1. Quality Management System:

    • Oversight/Handling of Handling of Change Control, Incident / Deviation and CAPA.
    • Following and tracking of Change Control, Incident /Deviation and CAPA.
    • Involved in the investigation activity whenever required.
    • Ensure that products are manufactured in compliance to Regulatory requirements and as per Good Manufacturing Practices.
    • Ensure that production and manufacturing activities are undertaken in compliance to SOPs, systems, procedure and GMP/GLP requirements.
    • Maintain GMP compliance in various departments to manage the production in line with the current GMP requirement.
    • Handling of Change Control, Deviation, risk assessment and CAPA as per company procedure
    • Verification & Follow-up of CAPA implementation as per provided target completion date.
    • Involved in the handling of Market Complaints

Vendor Qualification Activity:

    • Oversight of Vendor Qualification related documentation.
    • Planning and execution of the vendor Qualification activity with co-ordination with user department.
    • Preparation and review of document related to Vendor Qualification.
    • Execution of schedule / planned Vendor/Supplier Qualification as per the Protocol.
    • Qualification/ Validation - Data compilation and Report preparation.
    • Review and compilation of data generated in validation and qualification of vendors.
    • Coordination with external agency for Qualification, validation, calibration and outside services related to Vendor Qualification.
    • Qualification of External agency for Qualification, Validation and Calibration agency as per the SOP.
    • Planning of the vendor audit as per requirement.

Note : Must have sterile/Injectable experience.

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MJ Biopharm

Biopharmaceuticals

Boston

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