Senior Technician USP (m/f/d) Job in Fenil-sur-Corsier, Waadt

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veröffentlicht am 24. april 2026

Referenznummer: 25045

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Jobdetails

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.
...

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)

We are currently looking a Senior Technician USP for a 6-month assignment for our client based in Coreir-sur-Vevey.

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)

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Jobdetails

Zusammenfassung

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