Bioprocess Engineer
- Schweiz
- Freiberuflich
- Vollzeit
- Job type:
Manufacturing * Location:
SwitzerlandVisp, SchweizPosting date: 11 Aug 2025Reference: 66602Ready to step into a pivotal role at a global CMO and help shape the future of healthcare manufacturing?Proclinical is seeking a dedicated and experienced engineer to support manufacturing operations in a biopharmaceutical environment. This role focuses on downstream processing, ensuring compliance with cGMP guidelines, and contributing to the preparation and execution of production campaigns. You will play a key role in troubleshooting, documentation, and process improvement while collaborating across teams to maintain high-quality standards.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:
- Oversee and support the execution of manufacturing campaigns in downstream processing.
- Prepare and execute risk analyses for safety, health, and environmental operations, implementing and monitoring defined measures.
- Develop, review, and manage production documentation, including electronic batch records.
- Perform manufacturing activities in compliance with cGMP guidelines, troubleshoot equipment, and resolve issues.
- Review production documentation, address deviations, manage change requests, and implement CAPAs to uphold GMP standards.
- Act as a production expert in capital investment projects, contributing to the setup, commissioning, and qualification of manufacturing suites and equipment.
- Prepare, modify, and review MES-DeltaV recipes for equipment and facility components.
- Coordinate with engineering teams and workshops for campaign preparation and facility changeovers.
- Lead innovation and improvement projects related to manufacturing processes.
- Train operators on manufacturing processes for assigned products.
- Represent the production unit during customer audits and visits.
- Perform other duties as assigned.
- Academic background in Biotechnology, Biochemistry, or related disciplines (Bachelor's, Master's, or PhD).
- Strong knowledge of biotechnology and/or biotechnical engineering, particularly in downstream processing.
- Solid understanding of cGMP guidelines and practices.
- Proficiency in English; German language skills are a plus.
- Familiarity with MES and DeltaV systems is highly desirable.
- Excellent communication skills and ability to collaborate across teams.
- Structured, organized, and solution-oriented working style with a proactive mindset.
- On-site presence required; remote work is not available for this role.