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.
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.