eLIMS Master Data Analyst

eLIMS Master Data Analyst iLABS – QC Operations

Location: Schaffhausen (hybrid working - 3 days onsite, 2 days remote),

Duration: until Dec 2026

Hours: 40

Essential: Experience in setting up eLIMS Master Data elements eg specifications, work items, sample template, sample plant etc, experience in the linked paperless method execution.Fluent English, strong GMP experience in Pharma, Medtech or Food industry, previous experience of eLIMS, iLAB, QC  

Imagine your next project driving the digital transformation of quality control by bridging the gap between laboratory science and advanced data systems.

The Janssen Supply Group, a member of the Johnson & Johnson family of companies, is recruiting for an eLIMS CoE master data Analyst iLABS, QC Operations. This position works within the eLIMS CoE and is an expert in data setups in the eLIMS system to support lab processes including paperless (iLAB), product release and CofA generations.

roles and responsibilities.

You will independently maintain and review high quality data setups, integrate instruments and applications, and translate specifications within the eLIMS system using current business processes.

This will involve:

• Performing expert data setups in the eLIMS system to support paperless lab processes (iLAB).

• Reviewing and testing system updates and creating system-related documentation.

• Identifying and driving process improvements within QC Operations.

• Interacting with IT and translating technical requirements into business language.

• Mentoring, leading, and training team members on master data requirements.

• Managing implementation activities of change controls and participating in project activities.

• Maintaining system documentation in TruVault, COMET, Confluence, or q-Test.

how to succeed.

You are a detail-oriented professional with a strong background in regulated medical industries e.g. pharma, biotech, medical devices or food - and a passion for laboratory informatics and process harmonization.

You will also bring:

• A minimum bachelor's degree or equivalent education.

• 3 years plus experience in a regulated medical industry (Pharmaceutical, Medical Devices, or Diagnostics or Food - a highly regulated GMP environment).

• Knowledge and experience with LIMS, iLABS, and Quality systems.

• Broad knowledge of cGMPs and applicable regulations (FDA, ICH Q8, 9, 10).

• Strong written and verbal communication skills in English essential, German nice to have (A2, B1 level)

• Ability to manage multiple issues, prioritize effectively, and lead projects.

• Flexibility in adapting to urgent needs and maintaining strong relationships with local laboratories.

benefits.

This role offers a very competitive hourly rate. This contract will run until the end of 2026

you are welcome here.

Johnson & Johnson is working to create an inclusive environment where diverse backgrounds, perspectives, and experiences are valued and each and every one of our people feels that they belong and can reach their potential. No matter who they are.

application process.

We are looking to process the first round of applications within the next 2 working days.

We do not accept applications via email.

Diversity, Equity & Inclusion.

Johnson & Johnson is an Affirmative Action and Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status