Hybrid Medical Device Manufacturing Validation Engineer

CREGG; Tipperary; Hybrid; EUR 55,000 - 75,000; Full time

Job summary

CREGG seeks a Manufacturing Engineer for our Clonmel site with hybrid work options. You will support daily operations, validate new equipment, implement process improvements, and lead equipment transfers between clean rooms in a highly regulated medical devices environment.

You will collaborate with engineering, QA, EHS and production teams to ensure quality, compliance and on-time production goals. 2–5 years in engineering is preferred.

Qualifications

• NFQ Level 8 in a Technical Discipline (Science, Biomedical, Mechanical, Manufacturing, etc.).
• Minimum 2–5 years’ experience at an Engineering level, ideally in Medical Device industry or other highly regulated environment.
• Automated Manufacturing equipment experience advantageous.

Responsibilities

• Introduction and validation of new equipment.
• Analyze process, product, material or equipment specs and performance requirements.
• Collaborate with cross-functional teams to resolve production/engineering issues.
• Summarize, analyze and draw conclusions from test results for technical resolution.
• Transfer and validate equipment between clean rooms.
• Continuous Improvement & Yield Analysis.
• Drive improvements in process equipment design, layout and performance.
• Engage with technicians and cross-functional teams for process success.
• Root cause analysis using Lean tools and techniques.
• Write and improve process procedures.
• Apply validation techniques and regulatory requirements.
• Promote cross-functional teamwork.
• Evaluate environmental impact of new equipment/processes/chemicals.
• Provide technical guidance to Associate Engineers and technicians.

Skills

Root cause analysis

Lean tools

Validation procedures

Education

NFQ Level 8 in a Technical Discipline

Tools

Automated Manufacturing equipment

Job description

CREGG seeks a Manufacturing Engineer for our Clonmel site with hybrid work options. You will support daily operations, validate new equipment, implement process improvements, and lead equipment transfers between clean rooms in a highly regulated medical devices environment.

You will collaborate with engineering, QA, EHS and production teams to ensure quality, compliance and on-time production goals. 2–5 years in engineering is preferred.