eLIMS QC Analyst — Global Master Data

Johnson & Johnson MedTech; Malvern (Chester County); On-site; USD 90,000 - 130,000; Full time

Job summary

Johnson & Johnson is seeking a Quality Systems Analyst (Analyst eLIMS CoE) to support master data configuration in eLIMS (LabVantage) across a global QC network. The role emphasizes compliant, standardized configurations in a GxP environment and collaboration with laboratories, quality teams, and cross-functional partners.

You will lead master data governance, participate in change controls, and contribute to paperless lab workflows while driving continuous improvement and regulatory compliance

Qualifications

• Bachelor’s degree or equivalent in a relevant field or experience in a regulated environment.
• 2–4 years of experience in a regulated environment.
• Hands-on experience with eLIMS / LabVantage in QC operations.
• Strong knowledge of cGMP / GxP requirements, quality systems, and risk management.

Responsibilities

• Create, review, approve, and maintain complex master data in eLIMS (LabVantage).
• Ensure accuracy, completeness, and traceability of master data and documentation.
• Configure master data across Release, Stability, Raw Materials, Packaging Materials, COA processes.
• Support harmonized eLIMS configurations across sites and processes.
• Translate requirements into effective system configurations for QC operations.
• Support change control activities and UAT, upgrades, and implementations.
• Drive continuous improvement in QC processes across a global network.

Skills

English communication

Stakeholder management

Cross-functional collaboration

Independent work

Analytical thinking

Attention to detail

Problem solving

Ownership & accountability

Education

Bachelor’s degree

Tools

eLIMS (LabVantage)

TruVault EDMS

COMET

Job description

Johnson & Johnson is seeking a Quality Systems Analyst (Analyst eLIMS CoE) to support master data configuration in eLIMS (LabVantage) across a global QC network. The role emphasizes compliant, standardized configurations in a GxP environment and collaboration with laboratories, quality teams, and cross-functional partners.

You will lead master data governance, participate in change controls, and contribute to paperless lab workflows while driving continuous improvement and regulatory compliance