CPL are looking for a 12-month contract Automation Engineer to join a Global Pharmaceutical Manufacturing company based in Visp, in the canton of Valais in Switzerland.
Accountabilities
1. Support and align the product and production-specific requirements in coordination with the responsible project team.
2. Designing, testing, and changing recipes (under change control) during the design, start-up, qualification, and production phase.
3. Ensuring the cGMP-compliant documentation (eBR; SOP; operating regulations, etc.).
4. Constantly improving procedures and processes in compliance with safety, hygiene, environmental, and quality requirements in the area of responsibility.
Candidate Profile
1. Education: Master’s or Bachelor’s degree in relevant engineering discipline.
2. Expertise in the area of Bioprocess Automation (Emerson MES Syncade).
3. 3-5 years of hands-on recipe authoring in Syncade / troubleshooting experience mandatory.
4. Structured, focused, and well-organized work ethic; solution-oriented and open-minded for new ideas.
5. Impeccable team and social skills; very good understanding of IT / process control systems with a view for operational optimization potential.
6. Ability to communicate internally and externally at higher levels; strong business understanding and strong team orientation.
7. Working responsibly, especially with the owned system.
8. Languages: English fluent.
If you are interested and have the right to work in Switzerland, please get in touch.
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