Bioprocess Validation Specialist

Contrat à durée illimité

Bulle, Vaud

09 Mar 2026

    Company Presentation

    Akkodis is a global player in engineering and IT and a leader in smart industry. Present in 30 countries, our 50,000 experts combine technological expertise and sector knowledge to build a sustainable future, driven by a culture of inclusion and diversity.

    Akkodis is the technology brand of The Adecco Group.


    ℹ️ Job Information

    📍 Location: Bulle

    📄 Contract Type: Permanent

    🚩 Work Authorization: Valid Swiss work permit, Swiss nationality, or EU citizenship required


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    For one of our leading clients in the biotech industry, we are seeking a Bioprocess Validation Specialist to support the final phase of tech transfer and execute critical process validation activities for biologics downstream manufacturing.


    Mission (~80% validation execution / ~20% tech transfer support)


    • Write and prepare "Process Performance Qualification" protocols and reports
    • Execute and secure process validation phases for microbial biotechnological processes
    • Support tech transfer activities from development to commercial manufacturing
    • Coordinate sampling, analyses, and documentation in compliance with cGMP
    • Collaborate with development teams and QA stakeholders
    • Conduct risk assessments and ensure strict adherence to established processes
    • Support Health Authority inspections and regulatory documentation

    Votre profil

    • Master's or Engineering degree in Biotechnology, Life Sciences, or related field
    • Proven experience in biotech industry in a similar validation/tech transfer role (mandatory)
    • Experience with PPQ protocol writing and process validation (highly desirable)
    • Tech transfer experience is a strong asset


    • Strong understanding of biotechnological manufacturing processes (downstream)
    • Knowledge of cGMP requirements and quality standards
    • Hands-on experience with process validation and tech transfer activities
    • Ability to work with complex biotech manufacturing subjects


    • Bilingual French & English (written and verbal) – mandatory
    • Biotech industry exclusively (Pharma as second choice only)