Location: Bulle, Switzerland

Activity rate : 100%

Type of contract: Temporary contract (until 31.12.2025)

Start Date: 01.01.2025

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.

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.

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.