Manufacturing Process Optimization Specialist

6 hours ago

Galway, Galway, Ireland beBeeProductivity Full time €80,805 - €102,245
Job Title: Production Engineering Specialist

The successful candidate will play a pivotal role in enhancing and maintaining existing manufacturing processes to ensure consistent production of high-quality medical devices.

Key Responsibilities:
  • Provide day-to-day technical support to resolve production challenges, minimize downtime, and ensure stable operations.
  • Analyse root causes of production issues and implement corrective actions to address defects or inefficiencies.
  • Identify and implement opportunities to improve yields, reduce waste, and enhance overall production efficiency using Lean Manufacturing, Six Sigma, and other methodologies.
  • Lead or support engineering changes (ECOs) to existing products, processes, or equipment, and validate and document changes to ensure they meet quality, compliance, and operational requirements.
  • Ensure the continued functionality of production equipment through preventative maintenance programs, and support equipment upgrades or replacements to improve reliability and performance.
  • Partner with cross-functional teams, including Quality, Operations, NPD, and Supply Chain, to address process deviations, non-conformances, and supplier issues.
Requirements:
  • Preferably a minimum of 3 years' experience in a similar role.
  • Strong problem-solving and troubleshooting skills.
  • Ability to prioritize tasks and manage multiple ongoing projects.
  • Excellent communication and collaboration skills to work with cross-functional teams.
  • Catheter assembly experience, including braided/coiled shaft assembly and reflow, tip bonding, and handle assembly, is a definite advantage.
  • Must be able to plan, organize, and implement multiple concurrent tasks and projects.
  • Jigs & Fixtures design and maintenance experience would be an advantage.
  • Demonstrate a practical understanding of lean manufacturing principles and statistics.
  • Equipment and Process Validation experience with working knowledge of Minitab software.
  • SolidWorks/AutoCAD skills would be an advantage.
  • Knowledge of ISO & FDA compliance.
  • Demonstrate a dynamic, motivated & flexible approach to work with results-oriented attitude.

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