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  • Posted: Nov 14, 2025
    Deadline: Dec 3, 2025
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    Biovac was founded in 2003 to revive and restore South Africas vaccine manufacturing capabilities. We are an African based manufacturer contributing towards filling the gap that exists in the lack of African vaccine manufacturing capability. We recognise that well only achieve this if we match scientific innovation through local biotechnology skills with ...
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    3X- Validation Technician

    • BIOVAC is one of the leading sterile vaccine manufacturers rooted in Africa, with our core purpose being to "protect life". We are looking to hire a dynamic, passionate, confident, proactive and meticulous 3X- Validation Technician to join a goal-oriented team.

    QUALIFICATIONS NEEDED:

    • Completed qualification within any field of Natural/Health Sciences/ Engineering.

    NECESSARY EXPERIENCE & INDUSTRY KNOWLEDGE:

    • Experienced in writing of technical documents.
    • Basic experience in testing and troubleshooting practices.
    • At least 6 months in a qualification / validation role within the pharmaceutical industry.

    KEY DUTIES & RESPONSIBILITIES OF THE ROLE:

    Core Technical Delivery:

    • Liaising with service providers.
    • Participate in Process Development activities.
    • Execution of validation processes: PD, PV, CV, CSV, Mapping, Cold Chain, Facility Decontamination, Periodic Reviews and Periodic Revalidations as per defined timelines and according to cGMP
    • Assist equipment owners with identifying maintenance and calibration requirements.
    • Participates in troubleshooting a wide range of problems which require creative thinking. Exercises significant technical discretion in design, execution, and interpretation, and pursues new validation/qualifications studies as a result of experimental outcomes.
    • Communication status and any delays/ issues/ changes experienced during validation.
    • Communicate with departments regarding validation planning and time needed on validation activities.
    • Provide guidance to staff from other departments regarding the required content of procedures.
    • Manage internal customer relations and communication.
    • Ensure relevant OOS and OOT investigation non-conformances/ deviations, change controls and CAPAs are initiated and completed to the correct standard.
    • Identify quality risks in the section and initiate risk management where required, e.g. to support investigation or choices.

    Application Deadline: 21 November 2025

    Check how your CV aligns with this job

    Method of Application

    Interested and qualified? Go to Biovac on www.careers-page.com to apply

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