Project Engineer specialized in Automation (fluent English)

2 permanent positions – Based in Switzerland


QUALIFICATIONS

• Engineering degree or manufacturing engineering
• Experience in manufacturing and equipment engineering.
• Previous work experience in the medical device or pharmaceutical industry is a strong plus
• Experience leading a cross functional project team and strong demonstrated project management skills to achieve quality improvements and cost reductions required.
• Relevant experience in automation of manufacturing processes (PLC, vision system, material handling, inspection in-line)
• Experience in equipment, process, and computer system validation (CSV) requirements and execution
• Process Excellence Six Sigma or Lean certification highly desirable
• Demonstrated vendor management experience is required to communicate user requirements for new equipment, monitor equipment build status, and test equipment against user requirements.

TASKS RESPONSABILITIES

• Assess and improve medical manufacturing processes and equipment to achieve cost reductions and quality improvements
• Manage cost improvement, technology or automation projects in the plant
• Provide engineering input to solve complex manufacturing process problems including a continuous focus on plant equipment and manufacturing processes
• Use Process Excellence methodologies to improve manufacturing processes e.g. Six Sigma
• Specify, select, install, and validate new automated medical manufacturing assembly equipment
• Provide detailed financial evaluations of manufacturing processes, including analyses of capital purchases, assessments of vendor costs, calculations of product standard costs, analysis of cost-savings initiatives to satisfy company financial commitments
• Review / create user requirement specifications for new automation equipment
• Manage the technical interface with key equipment vendors through the process of machine design, procurement, design reviews, and installation of new manufacturing equipment.
• Complete equipment factory acceptance tests (FATs) at vendor locations for new equipment
• Coordinate equipment installation and validation activities and requirements with all functional site departments
• Create & execute validation strategies for medical device assembly processes, writing validation protocols and reports, executing process tests, analyzing the resulting data from validation activities
• Use automation expertise to design/troubleshoot/optimize automation solutions
• Ensure all Health, Safety and Environment requirements are met and new standards are implemented


Excellent salary package for the right candidate!

Please send your CV in a WORD format in English to sophie@approachpeople.com

Envoyez votre CV à eddy@approachpeople.com