Job Description:
Join QPS Engineering AG as an Automation Engineer (Pharma)
Become part of a future-focused team driving automation excellence in pharmaceutical manufacturing. In this role, you will plan, implement, and optimize automated systems in GMP-regulated environments, contributing directly to the efficiency, safety, and compliance of pharmaceutical production.
You’ll work on exciting, high-impact projects in close collaboration with cross-functional teams and bring your technical expertise to the heart of innovation. If you are passionate about automation and have at least 2 years of experience in the field, we look forward to your application!
Automation Engineer (Pharma)
Stein, Aargau, Switzerland
Full-time, Hybrid
QPS Engineering AG
Minimum 2 years
What We Offer
At QPS Engineering AG, you’ll play a central role in shaping modern pharmaceutical automation. We value innovation, teamwork, and technical excellence.
You'll be part of a motivated and collaborative team where your contributions directly impact project success and patient safety.
Benefits
- 💰 Competitive salary
- 📚 Opportunities for professional development and certifications
- 🏡 Hybrid work model
- 🤝 A supportive and inclusive work culture
Responsibilities:
- Designing, implementing, and optimizing automated systems for pharmaceutical production in compliance with GMP standards.
- Planning and documenting automation-related qualification and validation activities (e.g., FAT, SAT, IOQ).
- Developing and reviewing system and process specifications, functional design specifications (FDS), and control strategies.
- Collaborating with cross-functional teams including process engineering, QA, IT, and vendors to ensure seamless project execution.
- Managing project risks related to automation, ensuring safety, reliability, and product quality.
- Supporting system integration, troubleshooting, and performance optimization of PLC, SCADA, and DCS systems.
- Providing training and technical support on automation systems and compliance-related topics.
Preferred Qualifications:
- Bachelor’s or Master’s degree in Automation Engineering, Electrical Engineering, or a related technical field.
- Minimum of 2 years of experience in a comparable role within the pharmaceutical or biotechnology industry.
- Hands-on experience with GMP environments and good understanding of GAMP 5 and CSV principles.
- Solid knowledge of automation systems (e.g., Siemens, Allen-Bradley, Emerson DeltaV, or similar).
- Strong analytical and problem-solving skills, with an eye for technical and regulatory details.
- Fluent in German and English, both written and spoken.
