Philips Manufacturing Process engineer 

Israel, Haifa District, Haifa 

683119845

Manufacturing Process engineer

Manufacturing Process engineer
Your role:

As Manufacturing Engineer, you are responsible for the end-to- end manufacturing processes of CT detectors in the clean room environment, maintaining efficiency, reducing costs, improving sustainability, and maximizing profitability through tools and equipment of the manufacturing systems, leading to predictable, reliable, stable and efficient production processes.

In this position, you will play a crucial role in Haifa’s detection center, overseeing both established and new assembly processes and driving initiatives for manufacturing process optimization

Responsibilities:

• Monitoring both automated and manual assembly processes in clean room environment
• Support line-downs and troubleshoot problems associated with manufacturing processes
• Initiating and overseeing process technology development activities
• Accountable for process and manufacturing requirements based on Product Specifications
• Provides active inputs on improving the manufacturability of new products at the release stage.
• Identifying, designing, implementing and validating manufacturing processes, tools and equipment enabling quality and efficiency.
• Preparation & Release of Work instruction, PFMEA, Process validation docs etc.
• Executing processes with compliance to safety, regulatory- and environmental requirements as well as local laws, Philips General Business principles and other policies.

Education/Skills and Experience Requirements:

• BSc. or master’s degree in mechanical/Mechatronics/Material/Chemical/Biochemical Engineering
• 3+ years’ experience in similar role as process engineer
• Experience in problem solving and root cause analysis: Fishbone 8D, 4M methods
• Familiarity with statistical analysis and DOE (JMP, Minitab, proficiency in Excel)
• Excellent technical skills and knowledge of process-related standards
• Experience in Quality Management Systems (preferably in the medical industry), SAP, Windchill
• Preferably experience with process validation (PMAP, pFMEA, IQ, OQ, PQ)
• Continuous improvement mindset, result driven with quality approach
• Strong personal & communication skills in English

Indicate if this role is an office/field/onsite role.
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