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.