In this role, you will support automation projects in a dynamic life sciences environment, focusing on either DeltaV or MES PharmaSuite systems. You will lead automation development, testing, and troubleshooting activities, ensuring seamless integration and compliance. Your expertise will drive process improvements and technological advancements in manufacturing operations.
Start Date: 15/09/2025
Duration: 12 Months
Place of Work: Visp
Key Responsibilities
* Develop, review, and update automation specifications and documentation
* Perform offline and online coding, testing, and peer reviews of automation software
* Manage the design, development, and execution of Automation Change Records (ACRs), Quality Change Records, and validation protocols
* Lead automation activities for unit operations, resolving issues efficiently and implementing changes on complex projects
* Evaluate proposed modifications and investigate discrepancies during manufacturing processes
* Troubleshoot process, equipment, and system malfunctions or failures
* Contribute to establishing policies, standards, and best practices for automation systems
* Implement innovative automation solutions to enhance quality, efficiency, and compliance
Candidate Profile
* Proven experience with automation systems in the pharmaceutical or biotech industry
* Strong knowledge of either DeltaV or MES PharmaSuite, with a preference for candidates specialized in one of these platforms
* Solid understanding of automation development, validation, and troubleshooting processes
* Ability to interpret and develop technical specifications and documentation
* Excellent problem-solving skills and attention to detail
* Fluent in English, with strong communication skills
Job ID 41181094
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