Facilitiies Specialist
Core
Central technical and administrative resource for sustaining compliant pharmaceutical operations, managing facility maintenance, calibration, vendor coordination, and quality system documentation.
Role type
Facilities Specialist (GMP/Pharma)
Builds
Compliant pharmaceutical manufacturing environment
Domain
Biopharma / Pharmaceutical Manufacturing
Deliverable
infrastructure
Required skills
GMP compliance, vendor management, shutdown planning, equipment lifecycle management, quality system documentation, inventory management, access control systems
Preferred skills
Aseptic manufacturing environment experience
Technologies
CMMS, GMP documentation systems
Responsibilities
Drive timely completion and documentation of Quality System Events (Events, Deviations, CAPAs, NCRs); Coordinate and maintain vendor relationships for maintenance and calibration services; Develop and execute semiannual shutdown plans; Source and procure maintenance and calibration tools, spare parts, and equipment; Support departmental CMMS needs and asset decommissioning; Lead special projects for complex equipment lifecycle management; Manage and administer badge access control systems.