Helping you to win your compliance battles

Victory Compliance Group requires industry professionals to work throughout Asia, SE Asia and Austrialsia regions. If you have the right expeirence, dedication and eye for detail we would like to hear from you. Please apply to one of the job listings below or submit your CV at recruitmnet@victory-cg.org and we will be in touch.

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    Validation Consultant (Aseptic Manufacturing Equipment)

    To provide validation expertise for aseptic process / manufacturing equipment such as:
    • Filling machines (syringe/ vial / ampoule)
    • Depyrogenation Tunnels
    • Component and Parts Washers
    • Isolator technology
    • VHP Sterilisation processes
    • Cleanroom technology
    • Product visual inspection
    Provide Validation against client SOP’s and FDA / EMEA requirements.
    Accountable for writing, executing & reporting validation documentation (URS/ VP/ DQ / IQ / OQ / PQ / PPQ / pFMEA).
    Execution and documenting of risk assessment using tools such as FMEA.
    Performing validation functional testing as required.
    Track and resolve validation discrepancies identified during the qualification execution
    Work well in an unsupervised environment as well as in a team environment depending on project requirements.
    Have a good understanding of Data Integrity and Computer System Validati

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    Validation Consultant (Utilities)

    To provide validation expertise for Utility systems such as:
    • HVAC
    • BMS
    • Compressed Air
    • Compressed gases
    • Water for Injection (WFI)
    • Purified Water (PW)
    • Clean Steam
    Provide Validation against client SOP’s and FDA / EMEA requirements.
    Accountable for writing, executing & reporting validation documentation (URS/ VP/ DQ / IQ / OQ / PQ / PPQ / pFMEA).
    Execution and documenting of risk assessment using tools such as FMEA.
    Performing validation functional testing as required.
    Track and resolve validation discrepancies identified during the qualification execution
    Work well in an unsupervised environment as well as in a team environment depending on project requirements.
    Have a good understanding of Data Integrity and Computer System Validation.

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    Validation Consultant (Cleanrooms and Facilities)

    To provide validation expertise for:
    • Cleanrooms
    • Facilities
    Provide Validation against client SOP’s and FDA / EMEA requirements.
    Accountable for writing, executing & reporting validation documentation (URS/ VP/ DQ / IQ / OQ / PQ / PPQ / pFMEA).
    Execution and documenting of risk assessment using tools such as FMEA.
    Performing validation functional testing as required, including Cleanroom environmental testing such as; room pressure differentials, air change rate calculations, airflow visualisation studies, non-viable particulate monitoring to ISO14644.
    Track and resolve validation discrepancies identified during the qualification execution
    Work well in an unsupervised environment as well as in a team environment depending on project requirements.

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    Computerised Systems Validation Consultant

    To provide Computer System Validation expertise with experience in some of the following areas:
    • DCS Systems
    • PLC based manufacturing systems / equipment
    • SCADA systems
    • LIMS systems
    • Serialisation / Track & Trace
    • SAP Implementation and Qualification
    • IT Systems and IT Infrastructure
    Provide Validation against client SOP’s and FDA / EMEA requirements.
    Accountable for writing, executing & reporting validation documentation (URS/ VP/ DQ / IQ / OQ / PQ / PPQ / pFMEA).
    Provide CSV Assessments, ERES assessments, Disaster Recovery and Business Continuity Planning.
    Thorough understanding of the requirements of 21 CFR Part 11 Electronic Records, Electronic Signatures and the EU Annex 11 requirements.
    SME for Data Integrity with full demonstrable understanding of Data Integrity requirements (ALCOA)
    Execution and documenting of risk assessment using tools such as FMEA.
    Track and resolve validation discrepancies identified during the qualification execution
    Work well in an unsupervised environment as well as in a team environment depending on project requirements.