Analytical Transfer & QC Readiness Expert.

  • Bulle, Fribourg
  • veröffentlicht vor 1 Tagen
  • läuft am 21. Dezember 2024 ab
bewerben

Job Details

zusammenfassung.

  • Branche
    Life sciences
  • Kontakt
    Laetitia Stirer
  • Referenznummer
    209836-177

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Job Details

Location: Bulle, Switzerland

Activity rate : 100%

Type of contract: Temporary contract (until 31.12.2025 with possible extensions)

Start Date: 03.02.2025

You care about customers? UCB does as well! As a patient-centric company, UCB is searching for the right fit for their Patient Supply Quality Control department.

As part of a project to introduce a new molecule, you will manage analytical method transfers, validation and QC readiness wihtin a regulated cGMP-compliant environment.

Your key responsibilities:

  • Organize/ validate analytical tests; ensure accuracy and compliance with protocols;
  • Draft, review, and update validation protocols, risk assessments, and quality documentation;
  • Coordinate closely with QC to ensure seamless knowledge transfer and lab readiness;
  • Act as a Subject Matter Expert (SME) on analytical methods, new equipment qualification, providing expertise across teams;
  • Ensure strict adherence to cGMP and HSE standards; actively participate in CAPA, deviation investigations, and safety improvements;
  • Promote HSE policies within the team, ensure safe lab practices, and report any incidents or near-misses to maintain a safe work environment.

Location: Bulle, Switzerland

Activity rate : 100%

Type of contract: Temporary contract (until 31.12.2025 with possible extensions)

Start Date: 03.02.2025

You care about customers? UCB does as well! As a patient-centric company, UCB is searching for the right fit for their Patient Supply Quality Control department.

As part of a project to introduce a new molecule, you will manage analytical method transfers, validation and QC readiness wihtin a regulated cGMP-compliant environment.

Your key responsibilities:

  • Organize/ validate analytical tests; ensure accuracy and compliance with protocols;
  • Draft, review, and update validation protocols, risk assessments, and quality documentation;
  • Coordinate closely with QC to ensure seamless knowledge transfer and lab readiness;
  • Act as a Subject Matter Expert (SME) on analytical methods, new equipment qualification, providing expertise across teams;
  • Ensure strict adherence to cGMP and HSE standards; actively participate in CAPA, deviation investigations, and safety improvements;
  • Promote HSE policies within the team, ensure safe lab practices, and report any incidents or near-misses to maintain a safe work environment.

  • Qualifikationen

    What will make you successful:

    • Bachelor's or Master's degree with hands-on laboratory experience;
    • Fluency in French and English, both spoken and written;
    • Practical knowledge of analytical methods (HPLC/UPLC, GC, KF, RMN a plus) and equipment troubleshooting; mandatory expertise in Empower software;
    • Skilled in MS Office and basic statistical analysis;
    • Excellent communication skills, with a solution-oriented and customer-focused mindset;
    • Highly organized, pragmatic, proactive, and a responsible team player with a critical mindset.

    We can offer you a new challenge in a diverse and innovative environment that gives temporary contrats the opportunity to step aside for a long period.

    Have we sparked your interest? Then we look forward to receiving your online application.

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UCB Pharma
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Einsatzort

1630 Bulle, Fribourg

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LS

Laetitia Stirer

  • Randstad UCB Bulle

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