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Senior Process Engineer

Cpl Healthcare

Limerick

On-site

EUR 65,000 - 85,000

Full time

Today
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Job summary

A leading healthcare solutions provider is seeking a Senior Process Engineer in County Limerick. This technical role focuses on driving process improvements, resolving complex manufacturing challenges, and supporting product transfers. The ideal candidate will have at least 7 years of experience in a GMP-regulated environment and a Level 8 B.Sc./B.Eng in relevant fields. Strong problem-solving and project management skills are essential.

Qualifications

  • Minimum 7 years’ engineering experience within a GMP-regulated environment.
  • Experience with process validation in medical device or pharmaceutical environments.

Responsibilities

  • Provide technical leadership to drive process improvements and enhance product quality.
  • Identify and implement corrective actions for manufacturing issues.
  • Lead and coordinate multiple projects in a matrix environment.

Skills

Technical leadership
Project management
Problem-solving
Interpersonal skills

Education

Level 8 B.Sc./B.Eng. in relevant field

Tools

MS Office
Statistical tools (DOE, capability analysis)
Job description
Senior Process Engineer

A senior technical role responsible for driving process improvements, resolving complex manufacturing issues, and supporting product transfers within a defined value stream. The position provides technical leadership, ensuring high-quality, efficient, and compliant production operations.

Responsibilities
  • Provide technical leadership within the value stream, driving continuous improvement initiatives that enhance product quality and overall equipment effectiveness.
  • Identify, investigate, and implement corrective and preventive actions related to process quality or manufacturing issues.
  • Apply data-driven problem-solving and strong analytical methods to resolve equipment, system, and process challenges.
  • Lead and coordinate multiple projects in a matrix environment, including change management through quality systems.
  • Support delivery of new and innovative products across multiple product value streams in a timely and cost-effective manner.
  • Conduct process validation activities for new or existing production lines.
  • Communicate findings clearly across the organisation and collaborate effectively with cross-functional teams.
  • Stay current with process engineering advancements and implement new technologies that raise performance standards.
Requirements
Essential
  • Level 8 B.Sc./B.Eng. in Physics, Chemistry, Biological Science, Mechanical, Materials, or Process Engineering.
  • Minimum 7 years’ engineering experience within a GMP-regulated environment.
Desirable
  • Strong project management skills (FPx or equivalent), with proven ability to lead cross-functional teams.
  • Excellent interpersonal and collaborative skills, capable of influencing across teams.
  • Strong problem-solving capabilities and ability to manage multiple priorities.
  • High level of self-motivation and proficiency with MS Office tools.
  • Experience with advanced statistical tools such as DOE, capability analysis, and hypothesis testing, alongside DMAIC methodologies.
  • Familiarity with process validation in medical device or pharmaceutical environments.
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