Jobs · Information Technology · New York

LIMS Master Data Specialist III

Curia · Rensselaer, NY · 2 wk ago
Information Technology$100k–$125k/yrFull-time

About the role

The LIMS Master Data Specialist III plays a crucial role in ensuring the accuracy and integrity of laboratory data within the LabVantage LIMS platform. This position requires a deep understanding of analytical testing and techniques, as well as experience working in a GMP-regulated environment.

Responsibilities

  • Create and revise master data elements in the LabVantage LIMS platform, including test methods, specifications, analytical procedures, sampling plans, product parameters, and instrument mapping.
  • Enforce data integrity standards, version control, and data accuracy across all laboratory processes. Ensure compliance with global corporate policies and regulatory standards (e.g., FDA 21 CFR Part 11, cGMP, ISO 17025).
  • Partner with lab subject matter experts (SMEs) to gather business requirements and map existing workflows to system capabilities. Partner with IT System Admin to develop, test and implement new functionality.
  • Serve as the first line of support for end-user issues, troubleshoot master data anomalies, and assist with data migration during system upgrades. Support routine troubleshooting of data-related issues and escalate technical problems to System Admin or vendor as needed.
  • Own and update Master Data Standard Operating Procedures (SOPs), data maps, and validation documentation associated with LIMS.
  • Build and maintain test definitions, sampling plans, specifications, and stability protocols in LIMS, in collaboration with QC SMEs.
  • Support internal and external regulatory audits and inspections by providing LIMS documentation and system access as required.
  • Execute validation test scripts associated with LIMS.
  • Work with QC leadership to support ongoing LIMS improvements and upgrades.

Requirements

  • Associate’s or Bachelor’s degree in Life Sciences, Engineering, or a related STEM field.
  • Minimum of 2–5 years of experience in a GMP-regulated pharmaceutical or life sciences laboratory environment.
  • Understanding of analytical testing and techniques.
  • PREFERRED: Experience with LIMS as an end user and/or participation in an LIMS implementation.

Qualifications

  • Education, experience, location and tenure may be considered along with internal equity when job offers are extended.
  • We do not accept unsolicited assistance from any headhunters or recruitment firms for any of our job openings.
  • All interested applicants must apply online. Please be aware of scammers. Curia will only send offer letters and requests for sensitive personal information from a curiaglobal.com email address.
  • Curia is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability.
  • Curia is an E-Verify employer.

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