Facilities & Equipment Systems Improvement Specialist

What We Are Looking For

The 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 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 ROLE

• Lead 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 management

Your Background

• Required Qualifications:
• 10+ 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 Qualifications:
• Experience in sterile manufacturing environments and contamination control strategies.
• Practical knowledge of cleanroom operations, sterilization technologies, and equipment lifecycle management.

Reason to Join US

• Competitive salary
• Continued personal development
• Joining a global leader in diagnostic and interventional imaging
• Commitment to offering innovative solutions to improve the quality of patients' lives worldwide
• Joining a diverse and inclusive company

Pay

This role is eligible for Guerbet benefits.

Schedule

N/A