LIMS Support Specialist Position Available In Cabarrus, North Carolina
Tallo's Job Summary: The LIMS Support Specialist position at a Large Pharmaceutical Manufacturer in Concord, NC entails ensuring LabVantage LIMS system functionality aligns with internal and regulatory standards. Responsibilities include data verification, system configuration, and collaborating with key stakeholders. Qualifications include a Bachelor's degree in Computer Science or related field, experience with laboratory IT systems, and prior work in GMP-regulated environments.
Job Description
Title:
LIMS Analyst Client:
Large Pharmaceutical Manufacturer Type:
~12-month contract, potential for extension/full-time conversion
Location:
Concord, NC (hybrid schedule)
Schedule:
8-5 Monday-Friday, onsite Position Summary The LIMS Support Specialist is responsible for supporting laboratory operations by ensuring the LabVantage LIMS system functions as intended and complies with both internal and regulatory requirements. The role focuses on system configuration, master data management, and ensuring system usability for end users. Key Responsibilities & Deliverables Create and verify master data in LabVantage LIMS, including specifications, sampling plans, product variants, and storage records. Support site deployment and upgrades of the LabVantage LIMS platform. Perform non-terminal record monitoring to ensure data integrity. Investigate and support resolution of audit trail discrepancies identified during system audit trail reviews. Contribute to quality system improvements, including: Creating or revising worksheets Updating Laboratory Execution System (LES) documentation Updating laboratory methods Maintaining other laboratory documentation systems Collaborate with key stakeholders including the Global Quality Laboratory Network , Global IT , and Site IT teams. Required Qualifications Bachelor’s degree in Computer Science , Life Science , Applied Science , or a related field. Experience with laboratory IT systems , including: System installation and qualification Business requirement gathering Master data population System configuration Hands-on experience working in a GMP-regulated laboratory environment . Prior experience operating or implementing LabVantage LIMS or equivalent laboratory information systems. Preferred Qualifications Master’s degree in a relevant scientific or technical discipline. Familiarity with compliance requirements and regulatory expectations in GMP lab environments. Strong oral and written communication skills , with experience in documentation and presenting technical content.
Additional Information Standard work schedule:
Monday to Friday, 8-hour days onsite May require occasional support during weekends or off-hours due to 24/7 manufacturing operations.
