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Associate Quality Control
- Contract
- Good Manufacturing Practice (GMP)
- Switzerland
This vacancy has now expired. Please see similar roles below...
Join a dynamic team at a leading Contract Manufacturing Organisation (CMO) and contribute to groundbreaking projects and cutting-edge solutions.
Proclinical is seeking an Associate Quality Control professional to join our client's team in Switzerland. In this role, you will ensure that all operations comply with cGMP regulations and provide reactive support for discrepancy identification. You will be involved in supporting quality key metrics and analysis, working cross-functionally within the Luterbach Quality and site organization, as well as collaborating with various departments such as QC, Corporate Quality, and QA.
Please note that to be considered for this role you must have the right to work in this location or hold an EU passport.
Responsibilities:
- Ensure operations meet or exceed cGMP regulations.
- Provide reactive support for discrepancy identification.
- Support quality key metrics and analysis.
- Collaborate across various departments including QC, Corporate Quality, and QA.
- Work cross-functionally within the Luterbach Quality and site organization.
Key Skills and Requirements:
- Proficiency in German and English, with a minimum B1 level in English.
- Basic knowledge of Microbiology and Chemistry.
- Skills in buffer and solution preparation are preferred.
- Experience in aseptic working environments.
- Strong organizational skills and ability to work independently.
- Effective communication skills with management, peers, contractors, and external partners.
- Experience with productivity software such as Word, Excel, and Outlook.
- Familiarity with LabWare LIMS and Oracle systems is advantageous.
If you are having difficulty in applying or if you have any questions, please contact Ashley Bennett at a.bennett@proclinical.com.
Apply Now:
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