Associate Facilities Engineer
Core
Provide hands-on operational support and regulatory compliance for a manufacturing facility, including preventive maintenance, validation protocols, and documentation management.
Role type
Associate Facilities Engineer (Regulated Manufacturing)
Builds
Operational compliance and facility readiness for regulated manufacturing clients
Domain
Life Sciences / Regulated Manufacturing (Pharmaceuticals, Medical Devices, Semiconductors)
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
Preventive maintenance, troubleshooting, validation protocols, cleanroom certifications, CAPA management, work order systems, SOP/URS/QP documentation, cGMP, Design Control, regulatory writing
Preferred skills
Validation, Facilities, Quality, or Medical Device experience
Technologies
ServiceNow, Microsoft Office, Outlook, Teams
Responsibilities
Perform preventive maintenance and troubleshooting; Execute validation protocols and cleanroom certifications; Document and report corrective actions for nonconformances; Manage work order and ticket systems; Update facilities documentation and create change orders
Seniority
Mid-level, hands-on IC
