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Job details

Summary

  • Corsier-sur-Vevey, Vaud
  • Temporary

Posted 3. june 2026

Reference number
176180-644
get in touch

we are here to help you with your questions.

C

Clelia Liberatore

next steps

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randstad operational

randstad operational

We find, nurture, and connect uniquely skilled talent with employers when they need it, building successful teams that scale as their business grows while positioning individuals for rewarding careers and businesses for operational success.

Job details

This role supports
GLP/GMP microbiology analyses within a flagship biotech development program,
leveraging advanced analytical technologies in a flexible, agile, and
collaborative lab environment.

Reporting to the Lab
Manager, Global Analytical Development, this position contributes to the ...

microbiology laboratory by executing GLP and GMP analyses. It interfaces with
QA, GAD (all functions), and manufacturing colleagues to enable smooth analysis
execution, documentation management, and problem solving, while supporting
growth, simplification, and change initiatives to deliver the biotech pipeline
to patients.

Key responsibilities

  • Execute tests (Bioburden,
    Bacterial Endotoxin Test, Low Bioburden, and Identification) per
    established procedures in GLP/GxP environments; deliver results within
    defined timelines and complete tasks as assigned.
  • Review results and perform
    data entry using the LIMS.
  • Conduct Growth Promotion
    testing and Method Suitability assessments.
  • Manage sample/material
    receipt and testing, applying quality, EHS, and safety procedures,
    guidelines, and standards.
  • Initiate deviations, OOS
    events, or other relevant events; perform lab investigations and
    define/implement CAPA as needed.
  • Write/update microbiology lab
    procedures and participate in continuous improvement activities.
  • Serve as technical referent
    during external/internal audits.
  • Collaborate with colleagues
    and other departments while adhering to established standards, including
    Good Documentation Practices; escalate events that may impact operations.
  • Manage own workload and
    contribute technically and scientifically by exchanging ideas succinctly;
    engage in training programs focused on performance and personal
    development; be available for on-call rotations (on-site/off-site) as
    needed.
Show more

This role supports
GLP/GMP microbiology analyses within a flagship biotech development program,
leveraging advanced analytical technologies in a flexible, agile, and
collaborative lab environment.

Reporting to the Lab
Manager, Global Analytical Development, this position contributes to the
microbiology laboratory by executing GLP and GMP analyses. It interfaces with
QA, GAD (all functions), and manufacturing colleagues to enable smooth analysis
execution, documentation management, and problem solving, while supporting
growth, simplification, and change initiatives to deliver the biotech pipeline
to patients.

Key responsibilities

  • Execute tests (Bioburden,
    Bacterial Endotoxin Test, Low Bioburden, and Identification) per
    established procedures in GLP/GxP environments; deliver results within
    defined timelines and complete tasks as assigned.
  • Review results and perform
    data entry using the LIMS.
  • Conduct Growth Promotion
    testing and Method Suitability assessments.
  • Manage sample/material ...
receipt and testing, applying quality, EHS, and safety procedures,
guidelines, and standards.
  • Initiate deviations, OOS
    events, or other relevant events; perform lab investigations and
    define/implement CAPA as needed.
  • Write/update microbiology lab
    procedures and participate in continuous improvement activities.
  • Serve as technical referent
    during external/internal audits.
  • Collaborate with colleagues
    and other departments while adhering to established standards, including
    Good Documentation Practices; escalate events that may impact operations.
  • Manage own workload and
    contribute technically and scientifically by exchanging ideas succinctly;
    engage in training programs focused on performance and personal
    development; be available for on-call rotations (on-site/off-site) as
    needed.
  • Show more
    • Qualification

      Who you are

      • Minimum CFC or equivalent
        diploma; Bachelor's or Master's degree in microbiology or related field.
      • Strong knowledge of
        microbiological and analytical techniques; proven experience in
        GMP-regulated pharmaceutical environments.
      • Practical experience with and
        knowledge of LIMS systems.
      • Results-oriented, proactive,
        with a sense of urgency.
      • Strong collaboration skills
        and a team-oriented mindset.
      • Team player with good
        communication skills in English; French is a plus.
      • Able to perform on-call
        duties according to business needs.
    get in touch

    we are here to help you with your questions.

    C

    Clelia Liberatore

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