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Senior Process Development Engineer

CREGG
Department:Design
Type:ON-SITE
Region:Galway
Location:County Galway, Ireland
Experience:Mid-Senior level
Estimated Salary:€70,000 - €90,000
Skills:
PROCESS DEVELOPMENTLEANSIX SIGMAISO 13485FDADOEAUTOCADSOLIDWORKSRISK ANALYSISPROCESS VALIDATIONSTATISTICAL TECHNIQUES
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Job Description

Posted on: May 29, 2026

Senior Process Development Engineer

The successful candidate will be responsible for designing, developing, and validating robust, scalable processes & will provide direct line support to manufacturing operations, working closely with production teams to troubleshoot issues, stabilize processes, and maintain day-to-day performance.

Key Responsibilities:

  • Collaborate with engineers and production teams to develop and improve manufacturing processes.
  • Develop and implement manufacturing systems and strategies to achieve cost, quality, and time objectives while scaling up output to meet required annual growth rates.
  • Lead automation initiatives, from conceptual design through implementation, ensuring seamless integration with existing manufacturing processes and full compliance with quality and regulatory standards
  • Identify and drive implementation of process improvements using Lean methodologies.
  • Apply structured problem-solving techniques to process, material, or equipment issues, offering manufacturing or quality solutions from experience.
  • Develop and maintain operational processes and procedures that reflect industry best practices and comply with relevant regulatory requirements.
  • Perform process analysis and identify areas for improvement, including the evaluation and implementation of automation technologies (e.g., vision systems, robotics, digital monitoring) to enhance productivity, efficiency, and process reliability.
  • Develop complex experiments and validation protocols; analyse results, make recommendations, and prepare technical reports.
  • Analyse and resolve complex manufacturing and compliance issues (e.g., CAPA, non-conformances, audit observations).
  • Develop training materials and documentation (e.g., work instructions) to ensure effective knowledge transfer to production teams.
  • Work with internal stakeholders to explore and assess new technologies in terms of performance, cost, and reliability.
  • Actively engage in and support daily manufacturing operations.

Key Requirements:

  • Level 8 degree in Engineering or related discipline, with 5plus years of relevant experience.
  • Green Belt certification is a distinct advantage.
  • Proven experience in medical device process development, manufacturing, and project/program management.
  • Strong skills in risk analysis, problem-solving, and process validation (equipment and manufacturing).
  • Dynamic team player with proactive ownership of tasks and projects.
  • Excellent organizational and interpersonal skills.
  • Solid understanding of Lean principles and tools (e.g., DMAIC, Kaizen, Value Stream Mapping).
  • In-depth knowledge of ISO 13485 and FDA regulatory requirements.
  • Proficiency in statistical techniques (e.g., DOE, Six Sigma).
  • Competence in engineering design software (e.g., AutoCAD, SolidWorks)
Originally posted on LinkedIn

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