LIMS Data Analyst 2

Lonza; Portsmouth (NH); On-site; Confidential; Full time

Benefits offered by this job

Competitive hourly rate

Job summary

Lonza is seeking a Site-based LIMS Data Analyst 2 to support Quality Control and manufacturing operations in Portsmouth, NH (onsite). You will help ensure data integrity within gLIMS by setting up, loading, and maintaining master data used across the quality workflow, aligning site execution with enterprise standards.

You will collaborate with local QC, Manufacturing Operations, Validation, and the global gLIMS project team to establish ongoing data management support in a cGMP environment.

Qualifications

• Bachelor of Science in a science-related discipline or equivalent experience.
• Entry level (0–4 years) experience in QC, enterprise systems, or validation within a cGMP regulated biotech/pharma setting.
• Hands-on proficiency using LIMS or similar laboratory data management systems, with emphasis on master data loading and setup.
• Understanding of QC lab operations, including sampling plans and parameter lists, and computer system/equipment validation concepts.
• Strong proficiency with Microsoft Office Suite including MS Project, Word, Excel, and PowerPoint, plus experience with TrackWise.

Responsibilities

• Build, configure, and initially load required master data into gLIMS, including consumables, sampling plans, specifications, parameter lists, test methods, and LES templates.
• Perform local data cleansing to maintain master data quality, accuracy, and adherence to global guidelines and data principles.
• Create clear local work instructions documenting how global gLIMS processes are executed at the Portsmouth site level.
• Work in accordance with cGMP guidelines and maintain working knowledge of Quality System workflows, including deviations, CAPAs, change controls, and OTNs using TrackWise.
• Collaborate with local Quality Control, Manufacturing Operations, Validation, and the global gLIMS project team to establish ongoing local data management support.

Skills

LIMS data management

Master data loading

Data cleansing

QC operations understanding

Microsoft Office Suite

Education

B.S. in science

Tools

LIMS

TrackWise

MS Project

Word

Excel

PowerPoint

Job description

Lonza is seeking a Site-based LIMS Data Analyst 2 to support Quality Control and manufacturing operations in Portsmouth, NH (onsite). In this role, you will help ensure technical accuracy and data integrity within the global Laboratory Information Management System (gLIMS) by setting up, loading, and maintaining key master data used across the quality workflow. You will work closely with local QC, Manufacturing, and global IT stakeholders to align site execution with enterprise standards, supporting compliance in a cGMP-regulated biotech/pharma environment.

What you’ll be doing

• Build, configure, and initially load required master data into gLIMS, including consumables, sampling plans, specifications, parameter lists, test methods, and LES templates.
• Perform local data cleansing to maintain master data quality, accuracy, and adherence to global guidelines and data principles.
• Create clear local work instructions that document how global gLIMS processes are executed at the Portsmouth site level.
• Work in accordance with cGMP guidelines and maintain working knowledge of Quality System workflows, including deviations, CAPAs, change controls, and OTNs using TrackWise.
• Collaborate with local Quality Control, Manufacturing Operations, Validation, and the global gLIMS project team to establish ongoing local data management support.

What you bring

• Bachelor of Science (B.S.) in a science-related discipline or equivalent relevant experience.
• Entry level (0–4 years) experience in Quality Control (QC), enterprise systems, or validation within a cGMP regulated biotech/pharma setting.
• Hands-on proficiency using LIMS or similar laboratory data management systems, with emphasis on master data loading and setup.
• Understanding of QC lab operations, including sampling plans, parameter lists, and computer system/equipment validation concepts.
• Strong proficiency with Microsoft Office Suite including MS Project, Word, Excel, and PowerPoint, plus experience with quality tracking tools such as TrackWise.

Systems you’ll work with

gLIMS, LIMS, TrackWise, Microsoft Office Suite (MS Project, Word, Excel, PowerPoint), and Quality System workflows.

Benefits

• An agile career and dynamic working culture.
• Inclusive and ethical workplace environment.
• Exposure to enterprise quality systems including TrackWise and gLIMS, plus global data management frameworks.
• Competitive hourly rate.