Automation Engineer

BioTalent; Oberwallis; Vor Ort; CHF 100.000 - 150.000; Vollzeit

Zusammenfassung

BioTalent in Visp, Switzerland is seeking an experienced Automation Engineer to support MES automation and recipe development in a leading biopharmaceutical manufacturing environment. You will be involved in design, start-up, qualification and production, ensuring compliant and efficient manufacturing processes.

Work with project teams to author and troubleshoot recipes, optimise processes and maintain cGMP documentation, including eBRs and SOPs, while upholding safety, hygiene and quality

Qualifikationen

• Bachelor's or Master's degree in Engineering or related field.
• 3–5 years of hands-on recipe authoring in Emerson Syncade.
• Strong troubleshooting experience in MES environments.
• Process Engineering experience within BioPharma manufacturing.
• Experience creating flow paths in Bluebeam for CIP and SIP systems.
• Strong understanding of GMP-regulated environments.
• Excellent organisational and documentation skills.

Aufgaben

• Support and align product and production-specific requirements with the responsible project team.
• Design, test and modify manufacturing recipes under change control processes.
• Support design, commissioning, start-up, qualification and production activities.
• Develop and maintain cGMP-compliant documentation including eBRs, SOPs and operating procedures.
• Ensure compliance with safety, hygiene, environmental and quality standards.
• Continuously improve automation procedures and production processes.
• Troubleshoot MES and recipe-related issues during operational phases.
• Collaborate closely with manufacturing, engineering, validation and quality teams.

Kenntnisse

Automation engineering

Troubleshooting

Process engineering

Documentation

Ausbildung

Bachelor's or Master's in Engineering

Tools

Emerson Syncade

Bluebeam

eBR

Jobbeschreibung

We are seeking an experienced Automation Engineer to support MES automation and recipe development activities within a leading biopharmaceutical manufacturing environment in Visp, Switzerland. The successful candidate will play a key role throughout design, start-up, qualification, and production phases, ensuring compliant and efficient execution of manufacturing processes.

Working closely with project teams, the Automation Engineer will contribute to recipe authoring, troubleshooting, process optimisation, and GMP-compliant documentation within a highly regulated environment.

Responsibilities

• Support and align product and production-specific requirements with the responsible project team
• Design, test and modify manufacturing recipes under change control processes
• Support design, commissioning, start-up, qualification and production activities
• Develop and maintain cGMP-compliant documentation including eBRs, SOPs and operating procedures
• Ensure compliance with safety, hygiene, environmental and quality standards
• Continuously improve automation procedures and production processes
• Troubleshoot MES and recipe-related issues during operational phases
• Collaborate closely with manufacturing, engineering, validation and quality teams

Requirements

• Bachelor's or Master's degree in Engineering or related discipline
• 3-5 years of hands-on recipe authoring experience in Emerson Syncade
• Strong troubleshooting experience within MES environments
• Process Engineering experience within BioPharma manufacturing
• Experience creating flow paths in Bluebeam for CIP and SIP systems
• Strong understanding of GMP-regulated environments
• Excellent organisational and documentation skills
• Experience with electronic batch records (eBR)
• Knowledge of process control systems and manufacturing automation