Jobs

    CQV Engineer - Singapore - NO DEVIATION PTE. LTD.

    NO DEVIATION PTE. LTD.
    NO DEVIATION PTE. LTD. Singapore

    Found in: Talent SG 2A C2 - 5 days ago

    Default job background
    Description
    Roles & Responsibilities

    No Deviation is a provider of patient-centric solutions for the pharmaceutical industry, and we are currently seeking individuals who are passionate about joining our team. Our areas of expertise include engineering consultancy, Commissioning Qualification Validation (CQV), as well as Quality, Compliance, and Regulatory services.

    We strongly uphold our core values of Empathy, Integrity, and Transparency, and we strive to create a collaborative, innovative, and inclusive work environment that fosters personal growth and development.

    By joining our team, you will have the opportunity to make a meaningful impact in the pharmaceutical industry while advancing your career.

    Scope and Responsibilities

    • Perform Commissioning and Qualification/Validation for Project in compliance with GMP regulations, specification requirements.
    • Protocol generation or review for the assigned areas and summary reports for initial and subsequent re qualification programs related to E/F/U systems.
    • Review vendor or construction turnover document
    • Participate/lead system walkdowns to assure compliance with design.
    • Support or direct execution of full Commissioning and Qualifying project lifecycle, including URS, Design Verification, FAT, SAT, DQ, IQ, OQ and PQ etc.
    • Trouble shooting equipment with cross functional teams.
    • Support or lead summary report writing
    • Support the review and revision of design document
    • Support the handover of assigned system
    • Support the management of project schedule.
    • Compliant to quality and safety requirements.

    Qualifications:

    • Bachelor of Science, Engineering or related scientific degree
    • Experience in Pharma Industry is preferred
    • Min. 3 years of experience in Commissioning and Qualifying project is required
    • Knowledge of cGMP regulations and industry standards such as ISPE GAMP, and FDA guidance documents
    • Ability to work in a fast-paced environment.
    • Time management skill and attention to detail
    • Strong interpersonal and communication skills

    At No deviation, we strive to deliver our best every day. We apply our core values of empathy, integrity, and transparency to every activity, including engagement with our candidates. We are an equal opportunity employer, value diversity, and promote inclusivity at our company. We do not discriminate based on race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.

    EA Licence: 19C9587

    Tell employers what skills you have

    Pharmaceutical Industry
    Report Writing
    FDA
    Construction
    GMP
    GAMP
    Transparency
    Protocol
    Compliance
    Attention to Detail
    Time Management
    Communication Skills
    Turnover
    Commissioning
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