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Process Engineer

Morgan McKinley
Department:Operations
Type:ON-SITE
Region:Limerick
Location:Cashel, County Tipperary, Ireland
Experience:Associate
Estimated Salary:€45,000 - €65,000
Skills:
PROCESS ENGINEERINGMANUFACTURINGPHARMAMEDICAL DEVICEPROCESS VALIDATIONCONTINUOUS IMPROVEMENTROOT CAUSE ANALYSISGMPREGULATORY COMPLIANCENPIEQUIPMENT TROUBLESHOOTINGSOPSBATCH RECORDSCAPA
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Job Description

Posted on: April 2, 2026

Process Engineer – Manufacturing (Pharma/Med Device)

📍 Tipperary | 🕒 Permanent

We are currently partnering with a leading, highly regulated manufacturing organisation to recruit a Process Engineer to join their growing team. This is an excellent opportunity to join a site that is investing heavily in new technology, equipment, and continuous improvement initiatives.

This role will suit someone who enjoys being hands-on on the production floor, working closely with operations to drive process performance, troubleshoot issues, and support new product introductions.

The Role

As Process Engineer, you will play a key role in supporting day-to-day manufacturing while also driving improvements across processes, equipment, and product quality.

Key responsibilities include:

  • Provide hands-on technical support to manufacturing operations
  • Troubleshoot process and equipment issues to minimise downtime and improve performance
  • Support and lead process validation activities (IQ/OQ/PQ)
  • Work on continuous improvement initiatives to optimise yield, efficiency, and cost
  • Support new product introduction (NPI) and equipment implementation projects
  • Collaborate cross-functionally with Operations, Quality, and Engineering teams
  • Drive root cause analysis (RCA) and implement effective CAPAs
  • Ensure compliance with GMP, regulatory, and quality standards
  • Support documentation including SOPs, batch records, and validation protocols

About You

We are looking for a practical, solutions-driven engineer who enjoys working in a fast-paced manufacturing environment.

  • Degree in Engineering (Mechanical, Manufacturing, Chemical or similar)
  • 2+ years’ experience in a regulated manufacturing environment (pharma or medical device preferred)
  • Strong hands-on process / manufacturing support experience
  • Experience with process validation (IQ/OQ/PQ)
  • Proven ability in problem-solving, RCA, and continuous improvement
  • Comfortable working closely with production teams on the floor
  • Strong communication and teamwork skills

What’s on Offer

  • Competitive salary + bonus
  • Healthcare & pension
  • Opportunity to work in a highly collaborative, hands-on environment
  • Strong exposure to NPI, validation, and process improvement projects
  • Clear career progression opportunities
Originally posted on LinkedIn

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