Analyst eLIMS CoE QC Operations

Johnson & Johnson Innovative Medicine•Horsham, PA

9d•€42,400 - €70,840•Hybrid

About The Position

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. Learn more at https://www.jnj.com/innovative-medicine We are searching for the best talent to join us as Analyst eLIMS CoE (QC Operations) at one of the following locations: 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 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. Purpose: In this role, you will support the configuration, governance, and lifecycle management of complex master data within the eLIMS (LabVantage) 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.

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.

Nice To Haves

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.

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.