We are currently looking a Senior Technician USP for a 6-month assignment for our client based in Coreir-sur-Vevey.
Your role
As a Senior Technician in Clinical Manufacturing, you will play a key role in supporting large-scale biomanufacturing operations and contributing to the development of innovative biotechnological processes.
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Your main responsibilities will include:
- Supporting the scale-up of purification processes from 200L to 2000L for pre-clinical and clinical manufacturing
- Producing biological materials at both large and small scale to support clinical studies and laboratory activities
- Ensuring equipment performance, compliance, and proper maintenance
- Contributing to the implementation of new technologies and continuous improvement initiatives
- Managing deviations, investigations, and quality-related documentation in line with GMP requirements
- Ensuring full traceability of activities (protocols, reports, SOPs, batch records, etc.)
- Collaborating closely with Engineering, Technology, and Quality teams
- Maintaining high standards in quality, safety (EHS), and regulatory compliance
- Actively participating in operational excellence projects and identifying improvement opportunities
- Staying up to date with emerging technologies in the field
Your profile:
- MSc, Engineering degree, or technical degree with at least 5 years of relevant industry experience
- Hands-on experience in biomanufacturing, ideally in GMP environments
- Strong understanding of quality standards and GxP regulations
- Ability to work in a structured, detail-oriented, and compliant manner
- Proactive mindset with a continuous improvement approach
- Good communication skills and ability to work effectively in cross-functional teams
- Comfortable managing priorities and working under deadlines
- Basic project management skills
- Fluent French required, English (minimum B1 level)
