Overview
In this role, you will lead GMP-compliant control systems design, delivery, and validation to support biotech manufacturing processes. You will shape system architectures, standards, and traceability across projects within a regulated environment. You’ll drive automation improvements, coordinate commissioning and validation activities, and collaborate with cross-functional teams to enable manufacturing excellence. This is a chance to influence site-wide control system strategy in a fast-paced biotech setting.
Pay / Benefits
- competitive benefits
- ongoing professional development
- opportunity to work on complex, high-value capital projects
Responsibilities
- Lead design, delivery, and lifecycle management of GMP-compliant control systems (PLC, SCADA, and HMI)
- Define architectures and standards with traceability from requirements to deployment
- Oversee automation development, configuration, and software validation in regulated context
- Manage commissioning, qualification, validation, and system handovers; coordinate audits with regulators and vendors
- Lead automation improvement initiatives, support digital transformation strategies, and manage change control
Key requirements
- A degree or higher in engineering or a science discipline (e.g., Electrical, Mechanical, Automation Engineering)
- Proven experience in automation system design, validation, and lifecycle management in pharmaceutical, biotech, or similar regulated environments
- Extensive knowledge of PLC, SCADA (Siemens, Allen-Bradley), GMP, data integrity, and validation standards
- Cross-functional collaboration
- Leadership and project management
- Strong communication and regulatory liaison
- PLC
- SCADA
- HMI
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