Bio Process Engineer (6119)
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Position: Bioprocess Engineer
Location: Valais, Switzerland
Contract Duration: Until June 2025 (High chance of extension)
Overview:
We are seeking a highly skilled Bioprocess Engineer to join our client’s operational team in the Valais region of Switzerland. This is a contract role with the potential for extension. As a Bioprocess Engineer, you will be responsible for executing manufacturing processes, ensuring compliance with safety, quality, and delivery standards. You will also support CAPEX projects, contribute to process improvement, and be a key resource for the successful execution of manufacturing campaigns.
General Functional Responsibilities:
- Ensure compliance with the client's safety, quality, and code of conduct standards
- Adhere to GMP standards for the production of Mammalian products and intermediates
- Maintain GMP-compliant documentation of processes and tasks
Project-Specific Responsibilities:
- Represent manufacturing in CAPEX projects and provide input for manufacturing suite and equipment setup, commissioning, and qualification, including automation
- Prepare and execute risk assessments in SHE, EM, Operations, and Cleaning for assigned products
- Create and update training documents, and provide support and training for production staff
- Oversee production campaigns, ensuring safety, quality, and on-time delivery, including troubleshooting and issue resolution
- Ensure timely preparation, creation, and review of production documentation (Recipes, EBRs, SOPs) in line with local procedures
- Prepare and review quality records (change requests, deviations, investigations, CAPAs)
- Collaborate with MSAT to enhance process robustness and improvements in routine manufacturing
- Work inter-departmentally to resolve work orders, preventative maintenance, QC, and documentation issues before production
- Act as SME, liaising with vendors and suppliers as necessary
- Participate in on-call service for troubleshooting outside of regular hours (Pikett)
Requirements:
- Proficiency in English is mandatory; German is a strong plus
- Strong understanding of GMP, safety, and quality standards in a manufacturing environment
- Experience in process optimization, documentation, and cross-functional collaboration
How to Apply:
Interested in learning more about this opportunity with CTC? Please click the 'apply now' button or email your application to: vanessa.gilardoni@ctcresourcing.com.