Automation Engineer (Biotech Process Automation)
Lucerne
Key information
- Publication date:18 August 2025
- Workload:100%
- Contract type:Temporary
- Place of work:Lucerne
Our client, an internationally renowned pharmaceutical company is currently looking for a Automation Engineer available from the 1. October for Lucerne area, to join an international team for a period of 12 months.
Depending on the selected candidate's performance and motivation, the possibility of an extension or a permanent take over.
Our client, an internationally renowned pharmaceutical company is currently looking for a Automation Engineer available from the 1. October for Lucerne area, to join an international team for a period of 12 months.
Depending on the selected candidate's performance and motivation, the possibility of an extension or a permanent take over.
Description
- Foster diversity and inclusion by building strong collaborations within cross-functional teams across different cultures and backgrounds
- Act as Subject Matter Expert for the implementation of control strategies on new equipment to optimize manufacturing processes in a GMP environment
- Drive the adoption of innovative technologies, software, control strategies, and instruments to streamline production and administrative processes
- Provide automation support for systems such as DCS (DeltaV), MES (PAS-X), PLC, SCADA, and OEM systems
- Lead and support continuous improvement initiatives, including automation reviews of equipment specifications, P&IDs, and system lifecycle documentation
- Troubleshoot complex automation and equipment issues to improve manufacturing performance (e.g. yield improvements), adapt systems for new products, and ensure compliance with cGMP requirements
- Manage process technology transfers from early-stage pipeline facilities to full GMP operations, ensuring readiness for commercial supply
- Lead automation-related investigations into deviations and implement effective corrective actions
- Coordinate with external partners for spare parts, service visits, and system support
- Support qualification of new systems by writing, reviewing, and executing test documentation
- Collaborate closely with Operations, Quality, Validation, and Technical teams to resolve complex issues
- Contribute to digital transformation projects, including system integrations, data connectivity, data analysis/modeling, validation strategies, and process optimization via control systems
- Flexibility to support off-shift work as needed for projects, operations, and qualification activities
Profile
- Bachelor's degree in Life Sciences or equivalent with at least 5 years' practical experience in automation controls (DeltaV DCS)
- Strong knowledge of computer validation/SDLC requirements and automation change control procedures (e.g., GAMP 5)
- Excellent oral and written communication skills in English (C1); German is an advantage
- Proven expertise with DeltaV DCS, DeltaV Batch, and standards such as ISA S95 and S88
- Minimum 3 years' experience in Automation or Engineering within Biologics, Food, Medical Devices, or Pharmaceutical industries
- Demonstrated experience in developing and implementing industrial controls such as DCS (DeltaV), MES (PAS-X), and Historian (PI)
- Knowledge of I/O networking (Ethernet/IP, OPC, Profinet, ModBus) is a plus
- Basic networking skills desirable
- Hands-on experience in commissioning, qualification, and test protocol development and execution
Job Offer
Join a global pharmaceutical leader and shape the future of automation in GMP manufacturing.
Take ownership of innovative projects, drive digital transformation, and contribute to life-saving medicines in a highly regulated environment.
Are you ready to bring your expertise to the next level? We look forward to receiving your application!
About company
Michael Page
Lucerne
Reviews
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