Master Data Specialist

Master Data Specialist

Are you ready to shape the future of medicine manufacturing by driving data excellence in cutting-edge QC and LIMS systems? Join our team in Portsmouth, NH, and play a pivotal role in maintaining high-impact master data integrity across gLIMS, Syncade (DeltaV MES), and SAP!

This is a fully site‑based role. Working together in person supports close, real‑time collaboration and the technical precision needed to manufacture medicines to the highest quality and safety standards.

What you will get:

• An agile career and dynamic working culture.

• An inclusive and ethical workplace.

• Competitive hourly rate

What you will do:

• Ensure high quality and accuracy of local QC master data across LabVantage LIMS (gLIMS), Syncade (DeltaV MES), and SAP platforms.

• Perform local master data setup, cleansing, and validation aligned with global guidelines and cGMP data principles.

• Build and input core master data including consumables, sampling plans, specifications, parameter lists, test methods, and LES templates.

• Develop and refine clear local work instructions detailing global process execution at the site level.

• Partner closely with local Quality Control SMEs, Manufacturing Operations, and global gLIMS project teams to support go-live readiness.

• Maintain rigorous data integrity and compliance across the complete project lifecycle in a cGMP environment.

• Drive continuous improvement by identifying opportunities to streamline data management and system integration processes.

What we are looking for:

• Proven experience in master data management, data cleansing, and validation processes within a regulated industry.

• Strong working knowledge of QC laboratory operations, Quality Systems (e.g., TrackWise, CAPAs, deviations), and cGMP regulations.

• Hands-on experience or proficiency with LIMS (specifically LabVantage/gLIMS) or similar enterprise systems (e.g., MES, SAP).

• Bachelor of Science in a science-related discipline or equivalent relevant experience in the field.

• High attention to detail, strong analytical capabilities, and excellent written communication skills for creating work instructions.

• Demonstrated ability to collaborate effectively across cross-functional teams and manage structured deliverables on schedule.

About Lonza

At Lonza, their people are their greatest strength. With 30+ sites across five continents, their globally connected teams work together every day to manufacture the medicines of tomorrow. Their core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who they are and how they work together. Everyone’s ideas, big or small, have the potential to improve millions of lives, and that’s the kind of work they want you to be part of.

Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, they value diversity and are committed to creating an inclusive environment.

As Lonza’s talent acquisition partner, please note, Randstad is responsible for the engagement and contracting of this contingent role.

Ready to play your part in shaping the future of life sciences? Apply now.