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LIMS Administrator

Job in Seattle, King County, Washington, 98127, USA
Listing for: 1872 Consulting
Full Time position
Listed on 2025-12-20
Job specializations:
  • IT/Tech
    Database Administrator, IT Consultant, Data Analyst, Systems Administrator
Job Description & How to Apply Below

Position Summary

In this role you will manage and maintain our Laboratory Information Management System (LIMS). The ideal candidate will have a strong background in LIMS administration within a regulated environment, preferably within the pharmaceutical industry. This role is critical to ensuring the efficient operation of our laboratory and the integrity of our data. The LIMS Administrator will play a key role in system maintenance, user support, data management, and continuous improvement initiatives related to the LIMS.

Responsibilities
  • System Administration: Perform daily administration of the LIMS, including user management, security settings, data backups, and system upgrades.
  • Troubleshooting and Support: Provide technical support to LIMS users, troubleshoot system issues, and resolve user inquiries.
  • Data Management: Ensure data integrity and accuracy within the LIMS. Develop and implement data management procedures, including data entry, validation, and reporting.
  • System Enhancement: Identify opportunities for system improvement and automation. Collaborate with IT and laboratory personnel to implement enhancements and new functionalities.
  • Validation and Compliance: Maintain system validation documentation and ensure compliance with relevant regulatory requirements, including 21 CFR Part 11, EU Annex 11, and ISO 9001 standards.
  • Training: Develop and deliver training materials for LIMS users.
  • Vendor Management: Liaise with LIMS vendors for technical support, system upgrades, and maintenance contracts.
  • Documentation: Maintain comprehensive system documentation, including SOPs, validation protocols, and training materials.
Requirements
  • 8+ years of demonstrated experience in administering a LIMS within a regulated laboratory environment.
  • Proven experience with vendor selection, system implementation, and system integration projects for LIMS.
  • Prior experience in a pharmaceutical Quality Assurance role is required. ASQ CQA, CMQ/OE, or other relevant certifications are a plus.
  • Experience with 21 CFR Part 11, EU Annex 11, and ISO 9001 quality management system standards.
  • Documentation and Records Management experience, ideally in a laboratory setting
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