Facilities Engineer
Core
Support reliable operation, maintenance, and continuous improvement of facility and utility systems for aseptic pharmaceutical manufacturing.
Role type
Facilities Engineer (Regulated Manufacturing)
Builds
Production continuity for aseptic pharmaceutical manufacturing
Domain
Biopharmaceuticals / Regulated Manufacturing
Deliverable
physical/clinical work
Required skills
HVAC systems, clean utilities, cGMP compliance, validation principles, deviation management, change control, CAPA processes, CMMS systems, root cause analysis, risk assessment
Preferred skills
aseptic manufacturing experience, cleanroom environments
Technologies
CMMS, engineering documentation tools
Responsibilities
Monitor system performance for environmental and operational compliance, support qualification and validation activities, participate in root cause analysis and CAPA implementation, review maintenance data for reliability improvements, support capital projects for facility upgrades, partner with Quality and Manufacturing teams, oversee vendor work, conduct risk assessments for contamination control.
Seniority
Mid-level, hands-on IC
