On-Site Facilities Engineer — GMP & Continuous Improvement Lead

PCI TRGR Penn Pharmaceutical Services Ltd; Stamullen; On-site; EUR 45,000 - 70,000; Full time

Job summary

A global pharmaceutical services provider is seeking a Facilities Engineer to join their Stamullen team. This on-site role requires a degree in Engineering and 2-5 years of experience in GMP-regulated manufacturing. Responsibilities include managing maintenance, ensuring compliance with GMP standards, and collaborating with the engineering team on improvements. Candidates should have strong communication and budgeting skills, along with knowledge of CMMS and AutoCAD. This position offers an opportunity for impactful work in a supportive environment.

Qualifications

• 2-5 years' experience in a similar role in GMP-regulated manufacturing.
• Experience with facilities equipment maintenance best practices.
• Excellent written and verbal communication skills.

Responsibilities

• Manage and maintain all facilities, utility, equipment, and grounds.
• Ensure compliance with GMP guidelines.
• Prepare and manage budgets for maintenance and facilities.

Skills

Communication skills

Collaboration

Budget management

Continuous Improvement

Education

Degree in Engineering (mechanical/electrical)

Tools

CMMS

Microsoft Office

AutoCAD

Job description

A global pharmaceutical services provider is seeking a Facilities Engineer to join their Stamullen team. This on-site role requires a degree in Engineering and 2-5 years of experience in GMP-regulated manufacturing. Responsibilities include managing maintenance, ensuring compliance with GMP standards, and collaborating with the engineering team on improvements. Candidates should have strong communication and budgeting skills, along with knowledge of CMMS and AutoCAD. This position offers an opportunity for impactful work in a supportive environment.