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This Process Engineer supports manufacturing and production improvement projects in the area of Industry 4.0 for the Hägendorf, Balsthal and Tuttlingen production sites. The role sits within the Master Data pillar of the Engineering Department, as part of the Digital Manufacturing team, and provides a broad range of manufacturing and production project opportunities to help shape the Factory of the Future.

Tasks

  • Configure and implement the MES product portfolio, including intake files, master data, recipes, workflows, and test work orders, to support a smooth production go-live and enable connected manufacturing, real-time data visibility, advanced analytics, and predictive, adaptive processes.
  • Support the transition from BabtecQ CAQ to Critical Manufacturing CAQ and contribute to related system and process changes.
  • Support master data preparation, cleansing, migration, and verification activities related to MES, CAQ.
  • Provide MES shopfloor and post-go-live support, including hypercare, user guidance, issue escalation, operator feedback follow-up and production coordination.
  • Maintain compliance and business continuity by troubleshooting CM MES issues and deviations, performing root cause analysis, supporting system recovery, defining workarounds, and escalating when needed.
  • Drive MES-related procedure updates and support user engagement through training materials, hands-on coaching, knowledge transfer, and competency assessments.
  • Collaborate with Engineering, Quality, Operations, Planning, and IT to align MES activities with production and business needs.
  • Use MES, Industry 4.0 solutions, and data-driven methods to monitor, analyze, and improve medical device manufacturing and production processes.
  • Identify continuous improvement opportunities, implement new digital technologies, and acquire data from manufacturing systems such as CNC machines, finishing equipment, and heat treatment systems.
  • Support engineering projects by planning and executing activities, tracking progress and costs, preparing status reports, maintaining documentation, and meeting agreed goals and timelines.

Requirements

  • Engineering degree (FH/University, Bachelor-s or Master-s), preferably in Industrial Engineering, Manufacturing / Production Engineering, Mechanical Engineering, Automation / Mechatronics, Process Engineering, Business Information Systems / Computer Science, or equivalent.
  • 0 to 5 years of experience in a regulated industry, such as medical devices, combined with a strong affinity for data and data analysis.
  • General knowledge of manufacturing technologies and processes such as turning, milling, drilling, grinding, erosion, heat treatment, cleaning, shot peening, bead blasting, electropolishing, passivation, plastic injection molding, and laser marking.
  • Good IT skills, especially in Microsoft Excel, with experience in digital tools, business applications, manufacturing systems, and ERP, MES, PLM, or CAQ systems such as SAP, Critical Manufacturing, Agile, Windchill, or BabtecQ.
  • Experience in MES implementation projects, including design, configuration, testing, deployment, and support, is an advantage.
  • Fluent business communication in English and German.
  • Advocates change and communicates effectively through meeting facilitation, data presentation, decision-making, cross-level communication, and people development.
  • Demonstrates Jabil-s core behavioral competencies, including agility, decisiveness, self-development and development of others, resilience, and building trusting relationships.
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Über uns
Jabil Switzerland Manufacturing GmbH fertigt medizintechnische Produkte, insbesondere orthopädische Implantate und chirurgische Instrumente. Die Gesellschaft hat ihren Sitz in Hägendorf und betreibt sieben Standorte in der Schweiz. Sie gehört zum internationalen Jabil-Konzern.
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