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Based in Slough, this role is a fantastic opportunity to play a vital part in ensuring data integrity and establishing local support structures for ongoing LIMS master data management.
Site-based with limited flexibility
This role is primarily based on site. Working together in person supports close, real-time collaboration and the technical precision needed to manufacture medicines to the highest quality and safety standards. We offer flexibility to work remotely for no more than 20% of your time. Requests are considered on a case-by-case basis, in line with business needs.
What you will get:
- An agile career and dynamic working culture.
- An inclusive and ethical workplace.
- Competitive hourly rate / compensation package.
Compensation for this role will be determined by the candidate’s qualifications, skills, experience, and relevant knowledge.
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.
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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.
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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.
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