Facilities & Utilities Engineer

MCS Group; Mid and East Antrim District; On-site; GBP 40,000 - 55,000; Full time

Job summary

A leading Medical Device Manufacturer in Northern Ireland is seeking a Facilities and Utilities Engineer to support their pharmaceutical manufacturing site. The successful candidate will manage projects related to site utilities and infrastructure, ensuring compliance with regulatory standards. Responsibilities include overseeing maintenance activities, leading project work, and coordinating with stakeholders. Ideal candidates will have a degree in Engineering and proven experience in project management within a regulated environment. Competitive package and opportunities for career growth are provided.

Qualifications

• Proven experience managing engineering projects and working within CDM regulations.
• Excellent communication and stakeholder management skills.
• Knowledge of GMP, validation, and regulatory compliance.

Responsibilities

• Oversee the operation, maintenance, and continuous improvement of site utilities.
• Lead and support capital and non-capital engineering projects.
• Manage the installation and commissioning of new manufacturing and support equipment.
• Develop and implement preventative and corrective maintenance strategies.

Skills

Project management

Stakeholder management

Communication

Proficient in AutoCAD

Proficient in MS Project

Proficient in CMMS systems

Education

Degree in Mechanical, Electrical, or Building Services Engineering

Tools

AutoCAD

MS Project

CMMS systems

Job description

MCS Group is proud to be working as an Exclusive Partner to a leading Medical Device Manufacturing company based in Larne to recruit a Facilities & Utilities Engineer to join their growing team.

Want to get 2026 off to a cracker?

We are seeking a proactive and experienced Facilities and Utilities Engineer to support the operational integrity and strategic development of our clients pharmaceutical manufacturing site.

This role is critical in ensuring that all site utilities, infrastructure, and facilities meet regulatory standards and support production needs.

The successful candidate will lead and support project work, equipment installations, building infrastructure maintenance, and new building developments, while ensuring compliance with CDM (Construction Design and Management) regulations.

Key Responsibilities

• Oversee the operation, maintenance, and continuous improvement of site utilities including HVAC, compressed air, steam, water systems, and electrical distribution.
• Ensure all systems operate efficiently and reliably to support GMP manufacturing.
• Lead and support capital and non-capital engineering projects from concept through to commissioning and handover.
• Develop project scopes, budgets, timelines, and risk assessments.
• Coordinate with internal stakeholders and external contractors to ensure timely and compliant project delivery.
• Manage the installation and commissioning of new manufacturing and support equipment.
• Ensure validation and qualification activities are completed in line with pharmaceutical standards.
• Develop and implement preventative and corrective maintenance strategies for site buildings and infrastructure.
• Coordinate with maintenance teams and contractors to ensure timely resolution of issues.
• Support site expansion and refurbishment projects including feasibility studies, design coordination, and construction oversight.
• Liaise with architects, engineers, and regulatory bodies to ensure compliance with building codes and pharmaceutical standards.
• Supervision of Technical team members, contractors and suppliers in completion of facilities maintenance activities.

Qualifications & Experience

• Degree in Mechanical, Electrical, or Building Services Engineering (or equivalent).
• Proven experience managing engineering projects and working within CDM regulations.
• Excellent communication and stakeholder management skills.
• Proficient in AutoCAD, MS Project, and CMMS systems.

Desirable Skills

• NEBOSH or IOSH certification.
• Experience with cleanroom environments and HVAC design.
• Familiarity with sustainability and energy efficiency initiatives.
• Experience working within a pharmaceutical, biotech or highly regulated manufacturing environment
• Strong knowledge of GMP, validation, and regulatory compliance.

Full details will be discussed upon application.

To speak in absolute confidence about this opportunity please send an up to date CV via the link provided or contact Alan Montgomery, Specialist Consultant at MCS Group

028 96 935492

Even if this position is not right for you, we may have others that are. Please visit MCS Group to view a wide selection of our current jobs www.mcsgroup.jobs

All conversations will be treated in the strictest of confidence.

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