Facilities Engineer – GMP, Utilities & Asset Reliability

7266-Janssen Biologics B.V. Legal Entity; Amsterdam; On-site; EUR 45,000 - 71,000; Full time

Benefits offered by this job

Annual bonus

Vacation days

Well-being reimbursement

Job summary

Johnson & Johnson's Leiden Bio site seeks an FM Engineer to ensure safe, compliant, and cost-effective operation of facility infrastructure, building assets, and utilities. You will lead asset maintenance, reliability programs, and CAPA investigations in a highly regulated pharma setting.

You will specialize in one of three tracks and collaborate across Operations, Quality, EHS&S, and Maintenance to drive continuous improvement and data integrity across SAP/CMMS systems.

Qualifications

• Bachelor's degree in Engineering, Facilities Management, Asset Management, or related discipline.
• Minimum 2+ years in facilities engineering, maintenance engineering, utilities, asset management, or reliability engineering.
• Experience within GMP-regulated or highly regulated environment preferred.
• Experience with SAP or CMMS systems.
• Knowledge of GMP, EHS&S, CAPA, Change Control, and quality systems (preferred).

Responsibilities

• Ensure safe, compliant, reliable operation of facility infrastructure, building assets and utility systems.
• Provide technical leadership in asset maintenance, reliability improvement, and regulatory compliance.
• Collaborate with Operations, Quality, EHS&S, Engineering, Maintenance, and Project Delivery teams.
• Develop maintenance strategies and lead data integrity initiatives in SAP/CMMS.

Skills

Facility Engineering

Facility Management

Data Savvy

Project Schedule

Quality Assurance (QA)

Education

Bachelor's degree in Engineering / Facilities Management / Asset Management

Tools

SAP / CMMS systems

Job description

Johnson & Johnson's Leiden Bio site seeks an FM Engineer to ensure safe, compliant, and cost-effective operation of facility infrastructure, building assets, and utilities. You will lead asset maintenance, reliability programs, and CAPA investigations in a highly regulated pharma setting.

You will specialize in one of three tracks and collaborate across Operations, Quality, EHS&S, and Maintenance to drive continuous improvement and data integrity across SAP/CMMS systems.