Analyst eLIMS CoE QC Operations

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 MedTech, 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.

About Innovative Medicine

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.

Why This Role Matters

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.

Responsibilities

• Create, review, approve, and maintain complex master data in eLIMS (LabVantage).
• 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.

Requirements

• 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 / LabVantage.
• 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 level; C1 preferred.
• Strong stakeholder management and cross-functional collaboration skills.
• Ability to work independently and lead domain-specific initiatives.

Preferred Qualifications

• Advanced experience in eLIMS master data configuration across multiple data types.
• Strong understanding of iLABs / paperless laboratory processes and New Product Introduction workflows.
• Experience with Stability Master Data Management and COA configuration.
• Experience with Enterprise Quality Systems such as COMET.
• Experience in change control assessment and execution ownership.
• Experience with EDMS solutions, for example TruVault.
• Previous Johnson & Johnson experience is preferred.
• Experience in the pharmaceutical industry is preferred.
• Understanding of multi-site configurations across Biotherapeutics, Synthetics, and Advanced Therapies.

Skills

• Advanced analytical thinking.
• High attention to detail.
• Structured problem-solving.
• Strong ownership and accountability.
• Stakeholder influence and collaboration.
• Ability to manage complexity in regulated environments.

Pay

• Netherlands – The anticipated base pay range for this position is 44,700 - 70,840 EUR.
• Ireland – The anticipated base pay range for this position is 42,400 - 67,965 EUR.