LIMS Lead - Validation, Compliance & System Ownership

Curia Aalborg ApS; Albuquerque (NM); On-site; USD 95,000 - 135,000; Full time

Benefits offered by this job

Paid training

Vacation and holidays

401K program

Education reimbursement

Learning platform

Job summary

Curia in Albuquerque, NM seeks a Senior Specialist LIMS to own and administer the LabVantage LIMS, ensuring data integrity and regulatory compliance across QC, QA, IT and manufacturing teams.

Responsibilities include validation coordination, user training and continuous improvement, with a focus on audits, change control and system upgrades. A bachelor's degree and hands-on LIMS experience are required.

Qualifications

• Bachelor's degree in a relevant science or engineering field.
• Minimum 5 years of experience in GMP-regulated pharma or biotech.
• At least 2 years in LIMS administration or system ownership.

Responsibilities

• Lead LIMS administration, configuration and master data management.
• Coordinate validation activities and ensure cGMP compliance.
• Collaborate with QC, QA, IT and manufacturing to optimize workflows.
• Support audits, inspections and data governance.
• Develop training materials and provide user support for LIMS.

Skills

LIMS Administration

Data integrity

GMP knowledge

Project management

Cross-functional collaboration

Education

Bachelor’s degree in Chemistry, Biology, Life Sciences, Engineering, Computer Science or related field

5+ years GMP pharma/biotech experience

Tools

LabVantage LIMS

SQL

Reporting tools

Job description

Curia in Albuquerque, NM seeks a Senior Specialist LIMS to own and administer the LabVantage LIMS, ensuring data integrity and regulatory compliance across QC, QA, IT and manufacturing teams.

Responsibilities include validation coordination, user training and continuous improvement, with a focus on audits, change control and system upgrades. A bachelor's degree and hands-on LIMS experience are required.