Jobdescription
Location : Bulle, Switzerland
Activity rate : 100%
Type of contract : Temporary contract (until 31.12.2026)
Start Date : ASAP
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.
In that role you will support analytical method transfers, validation, and QC readiness within a regulated, cGMP-compliant environment.
Your key responsibilities :
* Conduct and 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.
* Lead and contribute to continuous improvement initiatives and cross-functional projects.
* Act as a Subject Matter Expert (SME) on analytical methods, 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
* Proficiency in both French and English (spoken and written)
* Good knowledge in analytical methods (LAL, endotoxin, bioburden, etc.)
* Skilled in MS Office and basic statistics
* Strong communicator with clear and structured thinking
* Highly organized, solution-oriented, and customer-focused
* Pragmatic, responsible, and proactive
* 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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