The actual location of this job is in Visp, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed. You will be responsible for the implementation, optimization, and ongoing support of Manufacturing Execution Systems (MES) and Emerson DeltaV process control systems within biopharmaceutical manufacturing facilities. You will play a key role in ensuring efficient production operations, regulatory compliance, and adherence to the highest quality standards. This is a fully site-based role. Working together in person supports close, real-time collaboration and the technical precision needed to manufacture medicines to the highest quality and safety standards.
Tasks
- Design, implement, and validate MES recipes and DeltaV control strategies that support robust and compliant biopharmaceutical manufacturing processes.
- Partner closely with Manufacturing, Process Development, Automation, Engineering, and Quality teams to ensure seamless system integration and operational excellence.
- Troubleshoot and resolve MES and DeltaV system issues, minimizing production disruptions and supporting reliable plant operations.
- Develop and maintain technical documentation, including specifications, work instructions, and validation records in accordance with GMP requirements.
- Support end users through training, technical guidance, and ongoing system expertise.
- Drive continuous improvement initiatives, identifying opportunities to optimize manufacturing processes, automation strategies, and system performance.
- Contribute to the implementation of new technologies and digital manufacturing solutions that enhance productivity, compliance, and operational efficiency.
Requirements
- Experience working in the pharmaceutical, biopharmaceutical, biotechnology, or other highly regulated manufacturing environments.
- Strong knowledge of Manufacturing Execution Systems (MES), ideally including Werum PAS-X, Rockwell PharmaSuite, or comparable platforms.
- Experience with Emerson DeltaV or other distributed control systems used in process manufacturing.
- Understanding of GMP regulations, computerized system validation, and qualification activities in regulated industries.
- Ability to analyze complex technical issues, identify root causes, and implement effective solutions.
- Strong communication and collaboration skills, with the ability to work effectively across multidisciplinary teams.
- A degree in Bioprocess Engineering, Biotechnology, Automation Engineering, Electrical Engineering, or a related technical discipline, or equivalent experience demonstrating these capabilities.
Benefits
- An agile career with opportunities for professional growth in a global life sciences organization.
- A collaborative, inclusive, and ethical workplace where diverse perspectives are valued.
- Competitive compensation and recognition programs that reward high performance.
- Access to a wide range of local and global benefits, depending on role and location.
- Opportunities to work with cutting-edge technologies in biopharmaceutical manufacturing and automation.
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