Facilities Engineer

We are seeking an experienced  Facilities Engineer  to oversee the operation, maintenance, and continuous improvement of facility systems and utilities at our Leiden site.
This role is responsible for ensuring full compliance with  GMP, EHS, Quality, and environmental regulations , while supporting operational reliability and project execution.
The Facilities Engineer will act as a technical subject matter expert, support capital and improvement projects, and ensure facilities services meet production and compliance standards.

Key Responsibilities   Manage facilities operations in compliance with  GxP, EHS, and Quality regulations
Oversee maintenance, repair, and installation of utility and facility systems
Supervise contractors and subcontractors to ensure compliance with company standards
Ensure environmental management systems are implemented, monitored, and maintained
Identify operational and compliance risks and implement mitigation plans
Maintain and update Standard Operating Procedures (SOPs)
Act as Subject Matter Expert (SME) for audits, deviations, area improvements, and capital justifications
Support and lead facilities-related projects and cross-functional initiatives
Manage assigned budgets and drive cost optimization
Promote continuous improvement and innovative solutions
Ensure compliance with all federal, local, and corporate regulatory requirements
Support the Facilities Supervisor and collaborate across departments as needed
Bachelor’s degree in Engineering, Facilities Management, or related technical field
5–7 years of relevant experience in facilities engineering or technical operations
Strong knowledge of:
EHS & Environmental regulations
Facilities utilities (GMP and non-GMP systems)
Experience managing contractors and service providers
Strong troubleshooting and problem-solving skills
Excellent written and verbal communication skills in English
Ability to work independently and prioritize effectively
Strong compliance mindset with high integrity
Nice to Have    Master’s degree (MS or MBA)
Professional Engineer (PE) certification
Experience supporting regulatory audits
Experience in pharmaceutical, biotech, or highly regulated environments
Familiarity with CAPA systems
Practicalities    Work Model:  Onsite (due to operational and compliance requirements)
Contract Duration:  6 months
Extension:  Possible based on performance and business needs

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