SIRE® Life Sciences 🧬 logo

Senior Facilities Engineer

SIRE® Life Sciences 🧬

Leiden
Full-time
5-10 years experience
On-site

Key Skills

Facilities Engineering
Facility Utilities
Building Infrastructure
Preventive Maintenance
Equipment Reliability
GMP Compliance
GxP Compliance
EHS
Quality Management Systems
CAPA
Change Control
Contractor Management
Project Coordination
Troubleshooting
Stakeholder Management
Continuous Improvement

Job Description

About the Company Join a global healthcare organization at a state-of-the-art manufacturing site in Leiden. As part of the Facilities team, you will play a key role in ensuring the reliability, safety, and compliance of facility infrastructure, utilities, and manufacturing support systems within a highly regulated GMP environment. Role Description As a Facilities Engineer, you will oversee the operation, maintenance, and continuous improvement of building services, utilities, and facility systems. Working closely with Engineering, Maintenance, EHS, Quality, and external contractors, you will ensure equipment reliability, regulatory compliance, and operational excellence while supporting site improvement projects. Key Responsibilities Coordinate the maintenance and operation of facility systems, utilities, and building infrastructure Ensure compliance with GMP, GxP, EHS, and quality standards Lead equipment reliability and preventive maintenance initiatives Support facility upgrades, maintenance projects, and infrastructure improvements Supervise contractors and monitor service quality, budgets, and project progress Identify operational risks and implement mitigation actions Drive continuous improvement initiatives focused on safety, reliability, and efficiency Support CAPA implementation, change controls, and regulatory compliance activities Monitor energy usage and contribute to sustainability and cost-saving initiatives Collaborate with cross-functional teams to support manufacturing operations Requirements 5+ years of experience in Facilities Engineering, Maintenance, or Technical Operations Experience within a GMP-regulated manufacturing environment (pharmaceutical, biotechnology, medical devices, or similar) Strong knowledge of facility utilities, maintenance systems, and infrastructure Experience with preventive maintenance, contractor management, and project coordination Good understanding of EHS, Quality Management Systems, and CAPA processes Strong troubleshooting and problem-solving skills Excellent communication and stakeholder management abilities Fluent in English

Core Responsibilities

Coordinate the operation, maintenance, and improvement of facility systems, utilities, and building infrastructure while ensuring GMP, GxP, EHS, and quality compliance. Lead reliability and preventive maintenance efforts, support facility projects and compliance activities, manage contractors, and contribute to safety, efficiency, and sustainability improvements.

Requirements

Requires at least five years of experience in facilities engineering, maintenance, or technical operations, including work in a GMP-regulated manufacturing environment. Candidates should have strong knowledge of utilities and infrastructure, preventive maintenance, contractor and project coordination, EHS, quality systems, and CAPA, along with strong communication and problem-solving skills and fluency in English.

About SIRE® Life Sciences 🧬

Industry: Biotechnology Research

Company size: 201-500 employees

SIRE® Life Sciences is the market-leading partner for Life Sciences consultancy, project management, and secondment services in the Netherlands. We specialize in connecting expert consultants and project managers with leading biotech, pharmaceutical, medical device, clinical research, and food technology organizations. Our services include: - Life Sciences recruitment & executive search - Interim management & secondment - SOW-based project outsourcing & delivery - RPO (Recruitment Process Outsourcing) - MSP workforce management & vendor-neutral solutions - GMP, GCP, GLP compliance staffing - Clinical research & regulatory affairs resourcing With 100,000+ professionals in our network and 25+ years of experience, SIRE® Life Sciences delivers measurable results for regulated organizations across the Netherlands and Europe. We work with pharma, biotech, medical device, CDMO, CRO, and food technology companies at every stage of the product lifecycle. What sets us apart: - Deep domain expertise in Life Sciences & regulated industries - Full compliance with GxP, ISO, WAADI, and Dutch labour law - Flexible engagement models: permanent, interim, project (SOW), and managed services - Proven delivery track record across Pharma, Biotech, MedTech & Food Science Based in Leiden Bio Science Park, Netherlands. www.sire-search.com

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