Medical Devices Analyst jobs in London

Based in Slough, this is an exciting opportunity to play a hands-on role in configuring, loading master data, and implementing a brand-new global LIMS platform within a high-performing Quality Control environment on a 6-month contract.

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.

The hourly rate for this position in the United Kingdom is expected to range between £16 and £20. Initial salary placement within this range will be determined based on role‑related factors such as experience, qualifications, and expected contribution.

What you will do:

• Perform local master data setup and load in alignment with global guidelines and data principles to ensure strict data integrity.

• Build and input all initially required master data into the global LIMS system, including consumables, sampling plans, specifications, parameter lists, test methods, and LES templates.

• Conduct local data cleansing to ensure high data quality and accuracy across the laboratory platforms.

• Develop clear and concise local work instructions to detail the execution of global data processes at the site level.

• Collaborate with global and local Quality Control (QC) stakeholders to align master data structures.

• Potentially transition into a permanent role within the local LIMS Office, providing ongoing master data support and leadership at the Slough site.

What we are looking for:

• Proven experience in data management, specifically around master data setup, migration, and loading processes.

• Direct knowledge of QC laboratory operations, testing methods, and related data requirements.

• Strong proficiency in using a Laboratory Information Management System (LIMS) or similar complex database systems.

• Demonstrated ability to develop clear, technical local work instructions and documentation.

• Exceptional attention to detail and sharp analytical skills to maintain data accuracy and quality.

• Prior exposure to or familiarity with Laboratory Execution System (LES) templates is highly advantageous.

About Lonza

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

Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we 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.