Facilities & Equipment Systems Improvement Specialist

WHAT WE ARE LOOKING FORThe Facilities & Equipment Systems Improvement Specialist will be Operating in full compliance with applicable hygiene, safety, quality, and regulatory standards, and in alignment with the organization’s framework, company’s procedures, and the defined scope of responsibility the role is accountable for. This role is a contract role for 18-24 months and will be eligible for Guerbet's benefits, etc. This role focuses on improving the performance, reliability, and compliance of facility infrastructure, utilities, and process equipment by turning regulatory requirements, system evaluations, and operational insights into practical, sustainable improvements. Working collaboratively with Engineering, Production, Quality, and Validation, the Specialist ensures systems remain compliant, efficient, and operationally robust. It is a hands-on position dedicated to implementing meaningful improvements and driving measurable operational impact.YOUR ROLELead and actively implement CAPAs and improvement initiatives for facilities and equipment.Translate regulatory and operational requirements into clear, actionable improvements.Collaborate with cross-functional teams to ensure improvements are embedded into daily operations and maintenance practices.Verify effectiveness through structured follow-up, trending, and operational observations.Strengthen facility maintenance, HVAC/cleanroom systems, and critical utilities to meet GMP expectations.Improve sterility assurance practices, including HEPA filtration, environmental monitoring, and utility performance.Enhance equipment qualification (IQ/OQ/PQ) programs, maintenance schedules, and cleaning validation.Partner with Validation and Production to ensure equipment and systems operate reliably, safely, and in compliance with GMP.Performs other duties as assigned by managementYOUR BACKGROUNDRequired Qualifications10+ years of experience in facilities engineering, equipment qualification, or maintenance within GMP-regulated environments.Experience working with HVAC systems, critical utilities, and facility/equipment systems in regulated settings.Strong cross-functional collaboration, problem-solving, and hands-on operational implementation skills.Preferred QualificationsExperience in sterile manufacturing environments and contamination control strategies.Practical knowledge of cleanroom operations, sterilization technologies, and equipment lifecycle management.