19.04.25 | Vollzeit | Corsier-sur-Vevey | JobLeads GmbH | CHF 80’000 - CHF 100’000 Analytical Dev&Innovation Biochemistry Lab Manager - m/f/d, Corsier-sur-Vevey Job Description In the “Analytical Dev. and Innovation” organization of Global Analytical Development, this role represents an opportunity to significantly contribute to the startup of high-tech analytical laboratories
Später ansehen19.04.25 | Vollzeit | Corsier-sur-Vevey | JobLeads GmbH | CHF 100’000 - CHF 125’000 Analytical Op&QC Lab Scientist - All Genders, Corsier-sur-Vevey Client Location Job Category Other Job Reference 2f860d7bd565 Job Views 3 Posted 02.04.2025 Expiry Date 17.05.2025 Job Description An exciting new opportunity has risen at our State-Of-The-Art Biotech Development Facility
Später ansehen29.04.25 | Vollzeit | Corsier-sur-Vevey | Randstad Schweiz AGWithin the Drug Substance Development (DSD) - Manufacturing department, we are looking for a "DSP Manufacturing Senior Technician " who will support the DSP large-scale operations (GMP and pilot). You will be part of a team of technicians, engineers and scientists specialized in the production
Später ansehen24.04.25 | Vollzeit | Corsier-sur-Vevey | Randstad Schweiz AGYour role Within the Drug Substance Development (DSD) - Manufacturing department, we are looking for a "Media&Buffer - Technician" who will support the preparation of Media&Buffer at large-scale (GMP). You will be part of a team of technicians, engineers and scientists specialized
Später ansehen23.04.25 | Vollzeit | Corsier-sur-Vevey | Randstad Schweiz AGJoin our team as an Analytical Project Manager and help drive the success of innovative molecules from early-stage development to commercialization! Key Responsibilities - Collaborate with Analytical Leads to streamline processes and support product launches. - Track actions and assist senior
Später ansehen15.04.25 | Vollzeit | Corsier-sur-Vevey | Randstad Schweiz AGAnd reports from BPS/MFG related to process development and validation - Follow deviations and change control linked to validation/qualification projects Who you are - University postgrade degree in Science or Engineering - Knowledge of cGMP regulations - At least 2 years’ experience in a quality environment
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