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 (Pharmaceutical Manufacturing)
Builds
Compliant pharmaceutical manufacturing environments and equipment lifecycle management
Domain
Biopharma / Pharmaceutical Manufacturing
Deliverable
infrastructure
Required skills
Facilities maintenance, calibration services, vendor management, GMP documentation, quality system event management, shutdown planning, asset lifecycle management, inventory management, access control administration
Preferred skills
Aseptic manufacturing environment experience
Technologies
CMMS, GMP documentation systems
Responsibilities
Drive completion and documentation of Quality System Events (Events, Deviations, CAPAs, NCRs); Coordinate and maintain vendor relationships for maintenance and calibration; Develop and execute semiannual shutdown plans; Source and procure maintenance tools, spare parts, and equipment; Support departmental CMMS needs and asset decommissioning; Lead special projects for complex equipment lifecycle management; Manage badge access control systems and conduct routine audits.