LIMS Data Analyst 2

Join our Quality team in Portsmouth, NH to play a vital role in setting up, loading, and maintaining master data within our global Laboratory Information Management System (gLIMS) to support site Quality Control and manufacturing operations.

This is a site-based role during regular office hours. Working closely with local Quality Control, Manufacturing, and global IT teams supports the technical precision, data integrity, and compliance needed to manufacture medicines to the highest standards.

• An agile career and dynamic working culture.

• An inclusive and ethical workplace.

• Exposure to enterprise quality systems (TrackWise, gLIMS) and global data management frameworks.

• Competitive hourly rate.

• Master Data Setup & Management: Build, configure, and input initially required master data into the global LIMS system, including consumables, sampling plans, specifications, parameter lists, test methods, and LES templates.

• Data Integrity & Cleansing: Perform local data cleansing to ensure master data quality, accuracy, and adherence to global guidelines and data principles.

• SOP & Work Instruction Authoring: Develop clear, concise local work instructions detailing how global LIMS processes are executed at the Portsmouth site level.

• Quality Systems Compliance: Adhere to cGMP guidelines and maintain working knowledge of Quality System workflows, including deviations, CAPAs, change controls, and OTNs using TrackWise.

• Cross-Functional Support: Collaborate closely with local Quality Control (QC), Manufacturing Operations, Validation, and the global gLIMS project team to establish local ongoing data management support.

• Education: Bachelor of Science (B.S.) in a science-related discipline or equivalent relevant experience.

• Experience: Entry Level (0–4 years) of experience in Quality Control (QC), enterprise systems, or validation within a cGMP regulated biotech/pharma environment.

• LIMS Expertise: Hands-on proficiency using LIMS or similar laboratory data management systems, specifically with master data loading and setup processes.

• QC & Validation Knowledge: Understanding of QC lab operations, sampling plans, parameter lists, and computer system/equipment validations.

• Technical Skills: Strong proficiency with Microsoft Office Suite (MS Project, Word, Excel, PowerPoint) and quality tracking tools like TrackWise.

Founded in 1897 in the Swiss Alps, our business has embraced innovation and kept pace with a fast-changing world for more than 125 years.

We are the CDMO that opened the door to a new era of medicine – one where breakthroughs could be produced at scale and made available around the world. Our contributions have led the way in drug approvals in our industry.

The therapies we help bring to life reach up to 100 million people each year, and we contribute to around one in every ten medicines that are newly approved by the FDA.

Political, regulatory, or economic disruption in one region doesn’t put the brakes on our business as our global network of 30+ sites across five continents provides resilience against global instability.

We are a community of big thinkers and bold doers. We focus on what matters, and together we make it happen. We are constantly pushing ourselves to make things better, never stopping until we make it right.

Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity or expression, national origin, age, disability, protected veteran status, genetic information, or any other characteristic protected by applicable federal, state, or local law.

At Lonza, we are committed to building an inclusive workplace where diverse perspectives are valued and respected. We believe that diversity strengthens our teams, drives innovation, and helps us better serve our employees, customers, and communities. Reasonable accommodations are available for qualified individuals with disabilities throughout the recruitment process.