Overview
In this role you will lead engineering projects to strengthen manufacturing capabilities within Cytiva, on-site in Ilfracombe. You will work with cross-functional teams to apply validated methods and drive improvements in regulated environments. Your work supports faster, reliable production of life-science solutions, contributing to the Danaher system of continuous improvement. This is a chance to shape manufacturing processes that have real impact on patients and healthcare outcomes.
Responsibilities
- Lead engineering projects and process improvement activities to enhance manufacturing capabilities
- Own structured problem solving within the project engineering team
- Collaborate with Operations, Manufacturing Engineering/Product Engineering, and Quality
- Research and learn processes, tools, and technologies to achieve project objectives
Key requirements
- Proven experience in an engineering project environment
- Knowledge of project management techniques
- Proactive use of structured problem solving tools (DMAIC, PSP)
- Strong communication to update stakeholders
- Experience in a regulated (GMP) environment and change control including risk assessment (dFMEA/pFMEA)
- Formally qualified in Mechanical/Production Engineering (or equivalent) (if specified)
- Proactive and enthusiastic attitude
- Clear communicator
- Cross-functional collaboration
- IQOQPQ validation methods
- DMAIC, PSP (problem-solving frameworks)
- dFMEA/pFMEA (risk assessment)
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