Key Skills

Job Description

Who We Are: Catalyx is a machine vision and automation company that integrates technology and people to help global manufacturers and logistics companies achieve next-generation levels of quality and throughput. For over thirty years, the minds behind Catalyx have been at work maximizing operational processes across highly regulated industries by inventing new technology applications and supporting companies with technical experts. With 9 global offices, over 550 team members, and 3,000 projects under our belt (and counting), we have the capabilities and reach to solve unique process problems at scale – and the vision to keep doing what’s never been done before. For more information visit www.catalyx.ai. The Role: Catalyx is seeking an experienced Systems Engineer to support / upgrade laboratory systems operating within regulated GLP and GMP environments. Key Responsibilities Execute Windows 11 upgrades on business-critical laboratory and manufacturing PCs Perform system assessments to determine compatibility and upgrade readiness Support validation activities in GLP/GMP-regulated environments Develop and execute test protocols (IQ/OQ support as required) Coordinate with Lab IT, QA, Automation, and site stakeholders Minimize operational disruption during upgrade execution Support rollback and remediation plans if required Ensure cybersecurity and data integrity standards are maintained Participate in change control processes and deviation management Requirements 5+ years of IT infrastructure or endpoint engineering experience Direct experience supporting systems in GLP, GMP, or GxP regulated environments Experience with Windows OS migrations (Windows 10 to Windows 11 preferred) Familiarity with validated systems and computer system validation (CSV) Understanding of 21 CFR Part 11, data integrity, and audit trail requirements Experience supporting laboratory instrumentation PCs (analytical systems preferred) Strong documentation skills in regulated environments Experience working with Change Control systems Preferred Experience Experience supporting pharmaceutical or biotechnology companies Exposure to validated lab applications (e.g., chromatography systems, LIMS, Empower, etc.) Knowledge of manufacturing systems (MES, SCADA, DCS interfaces) Familiarity with SCCM, Intune, or enterprise deployment tools Experience in regulated packaging or manufacturing environments Why Join Catalyx? At Catalyx we understand that our people are our greatest asset. For this reason and many others, we take care of them. The team in Catalyx benefits from a Total Rewards package. This includes great personal benefits and professional growth opportunities. Catalyx is an Equal Opportunity Employer. We are committed to creating a diverse and inclusive workplace where all individuals are valued, respected, and supported. We do not discriminate on the basis of race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), national origin, age, disability, veteran status, genetic information, or any other characteristic protected by applicable law. We encourage applications from all qualified candidates, regardless of background, and strive to create a welcoming environment for everyone. At Catalyx, we are committed to attracting the best global talent. We proudly support our international employees by offering assistance with Critical Skills Visa applications for eligible candidates.

Core Responsibilities

Upgrade business-critical laboratory and manufacturing PCs to Windows 11, assess system compatibility, and support validation activities in regulated environments. Coordinate with site stakeholders, minimize operational disruption, maintain cybersecurity and data integrity, and support change control, remediation, and rollback activities.

Requirements

Requires at least five years of IT infrastructure or endpoint engineering experience, including direct support for GLP, GMP, or other GxP-regulated systems and Windows OS migrations. Candidates should understand computer system validation, 21 CFR Part 11, data integrity, audit trails, laboratory instrumentation PCs, and regulated documentation and change control.

Benefits

• Personal Benefits
• Professional Growth Opportunities
• Critical Skills Visa Application Assistance for Eligible Candidates