Analyst eLIMS CoE QC Operations

• Job title Analyst eLIMS CoE QC Operations
• Function Quality
• Sub function Quality Systems
• Category Analyst, Quality Systems (P4 – E24)
• Location Schaffhausen / Ringaskiddy / Raritan / Horsham / Malvern / Leiden / Switzerland / Ireland / United States of America / Netherlands
• Work pattern Hybrid Work

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and Med Tech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.

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As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.

Quality

Quality Systems

Professional

Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow.

Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.

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• Schaffhausen, Switzerland
• Leiden, South Holland, Netherlands
• Ringaskiddy, Cork, Ireland
• Horsham, Pennsylvania, United States of America
• Malvern, Pennsylvania, United States of America
• Raritan, New Jersey, United States of America

This role offers you the opportunity to contribute to the future of digital QC laboratories by enabling compliant, reliable, and efficient eLIMS configurations across Johnson & Johnson’s global network. You will help strengthen standardization, support paperless laboratory workflows, and contribute to continuous improvement within a global Center of Excellence.

In this role, you will support the configuration, governance, and lifecycle management of complex master data within the eLIMS (Lab Vantage) system. You will ensure compliant, accurate, and standardized system configurations in a GxP environment that support QC Operations across a global network. As part of the eLIMS Center of Excellence, you will collaborate with laboratories, quality organizations, system owners, and cross‑functional partners to enable efficient paperless laboratory processes, drive continuous improvement, and maintain regulatory compliance.

• Create, review, approve, and maintain complex master data in eLIMS (Lab Vantage).
• Ensure accuracy, completeness, compliance, and traceability of master data and related documentation.
• Configure master data supporting Release, Stability, Raw Materials, Packaging Materials, and COA‑related processes.
• Support harmonized and standardized eLIMS configurations across multiple sites and processes.
• Translate laboratory and business requirements into effective system configurations.
• Execute and support change control activities, including impact assessments and implementation planning.
• Support User Acceptance Testing (UAT), system upgrades, enhancements, and new implementations.
• Drive continuous improvement initiatives and identify opportunities to optimize QC business processes.

• Bachelor’s degree or equivalent combination of education and experience.
• 2 to 4 years of experience in a regulated environment.
• Hands-on experience with eLIMS / Lab Vantage.
• Solid knowledge of cGMP / GxP requirements, quality systems, compliance processes, and risk management principles.
• Demonstrated ability to manage complex topics independently, prioritize effectively, and escalate appropriately.
• Strong communication skills in English, minimum B2…