Source description
About the role
We are currently looking for an experienced GLIMS Specialist to join a global pharmaceutical environment supporting laboratory and quality operations.
This role focuses on LabWare LIMS configuration, system support, and change management in a highly regulated setting. You will work closely with laboratories, quality teams, and global IT stakeholders to ensure the LIMS platform remains compliant, stable, and aligned with business needs.
Key Responsibilities
Act as a primary point of contact for LIMS-related support for laboratory and business users
Perform static data configuration in LabWare LIMS (analyses, specifications, calculations)
Manage and support change control activities in accordance with SDLC and validation requirements
Conduct impact assessments, prepare system requirements, and support UAT activities
Troubleshoot LIMS incidents and collaborate with global support and IT teams
Support documentation updates and training materials related to system changes
Ensure compliance with GMP/GxP and global data standards
Collaborate with distributed, international teams across multiple sites
Requirements
-
Bachelor’s degree in Chemistry, Biology, Computer Science, or a related field
-
4+ years of hands-on experience with LabWare LIMS in a pharmaceutical or regulated environment
-
Strong experience with static data configuration and LIMS system support
-
Good understanding of SDLC, validation, and change management
-
Familiarity with GMP/GxP and regulatory expectations
-
Experience working with SQL or LIMS querying tools for reporting
-
Strong communication skills and ability to work in a global environment
-
Fluent English (daily communication with international stakeholders)
-
Employment Details
-
Long-term contract until January 2027
-
Contract signed with an external partner, with day-to-day work performed within the client’s organization
-
Competitive hourly rate
-
Remote
-
Reference: 25-07511
More at eTeam