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    Job · 20634905

    FULLTIME

    Manager - IPQA

    Acme Generics LLP

    Acme Generics LLP

    Not specified · onsite · Posted 12d ago

    Sourced fromNaukri
    Undisclosed10–16 yrsfulltimeNot specified

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    Section · 01

    About this role

    Job Responsibilities:

    1. Responsible for review and Approval of Standard Operating Procedure& BMR/BPR through EDCS.

    2. Responsible for review and Approval of Master formula Record.

    3. Responsible for Approval of Annual Product Quality review (APQR) and Interim Product Quality Review (IPQR).

    4. Responsible for implementation and compliance of all Standard Operating Procedure on shop floor.

    5. Responsible to ensure the compliance of Quality Management System as per the requirement.

    6. Responsible for shop floor management w.r.t IPQA activities (Line clearance/ In process control/In process sampling).

    7. Responsible for effective execution of Process Validation, Cleaning Validation and Hold Time activities.

    8. Responsible for approval of Bill of material through ERP software.

    9. Responsible for coordination with cross functional department / sites for submission of required documents to different clients in timely manner.

    10. Responsible to imparting training on departmental SOPs, Good Manufacturing Practices (GMP) and Good Document Practices (GDP)

    11. Responsible for review and approval of QMS documents through EQMS.

    12. Responsible to ensure stage wise release of batches through LIMS and ERP software.

    13. Responsible to ensure the release of batches at QA level within required time for GB block

    14. Responsible to ensure on line review of executed log books, records and BMR /BPR.

    15. Responsible to assist the cross functional department to complete the investigation related to shop floor.

    16. Responsible for Self-Inspection or Internal Audit and its compliance.

    17. Responsible to ensure that products are manufactured as per approved Procedure.

    18. Responsible for review, implementation and verification of Corrective Action and Preventive Action (CAPA).

    19. Responsible to Ensure work discipline in the department.

    20. To coordinate perform the risk assessment of various areas as per the risk matrix.

    21. Responsible for handling (Investigation and implementation of CAPA) of incident and market complaint.

    22. Responsible for online review of e-log entries on daily basis

    23. Responsible for Handling Incident/Deviation change control and CAPA

    24. Ensure that the entry & exit procedures, gowning (Primary & Secondary, color code) procedures and Personnel Hygiene procedures are followed strictly.



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    Section · 02

    Skills

    process validationdeviationChange ControlIPQAIn Process Quality Assurance

    Section · Company

    About Acme Generics LLP

    Acme Generics LLP

    Acme Generics LLP

    Pharma

    2.5k+

    employees

    2005

    21 years old

    Baddi, Himachal Pradesh

    India

    ₹3.9L PA avg

    Avg at Acme Generics LLP

    About

    Pharma Manufacturing

    Industries

    Pharma

    Employee ratings

    10 reviews

    3.7/ 5

    Culture

    2.3

    Career growth

    2.6

    Work-life

    2.7

    Employees rate it well for

    Compensation & Benefits37Skill Development37

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