LIMS Analyst at Cambrex – High Point, North Carolina

Cambrex
LIMS Analyst

US-NC-High Point

Job ID: 2026-4615
Type: Regular Full-Time
# of Openings: 1
Category: Quality Control
Cambrex - High Point

Overview

The LIMS Coordinator will configure, support, maintain and administer the LIMS database, collecting and storing data for pharmaceutical operations. The position will interpret needs of the business through analysis to create LIMS set up needs. ROLE WILL BE ON-SITE (NO REMOTE)

Responsibilities

• Configure and maintain LIMS modules to support QC testing, inventory management, raw material testing/release/stability, instrumentation, cleaning validation and integration with other computerized site systems.
• Provide sound technical subject matter expertise on local and multi-site LIMS projects.
• Experience with data migration into LIMS.
• Configure static and master data within LIMS.
• Conduct validation of LIMS subroutines, analyses and other code-based functionality.
• Assist with writing and execution of test scripts.
• Primary contact for users to troubleshoot LIMS issues.
• LIMS trainer for site personnel.
• Ensure system is compliant with 21 CFR Part 11 and data integrity best practices for pharmaceutical environments.
• Implement CAPAs to address LIMS related corrections and ensure CAPAs are completed within assigned time frame.
• Write/update LIMS related SOPs, Work Instructions, Protocols, and other system specific documentation.
• Ordering and receiving of inventory.

Qualifications / Skills

• Excellent oral and written communication skills
• Excellent organizational, problem-solving, interpersonal and time management skills
• Strong attention to detail and a proven ability to multi-task and prioritize.

Qualifications

• Bachelor’s or master’s Degree in life science or computer science/IT.
• 3+ years of experience preferred in configuration and administration of Laboratory Information Management Systems (LIMS).
• Experience supporting and integrating lab applications in a regulated industry.
• Experience with 21 CFR Part 11, data integrity best practices and computerized system regulatory compliance.
• Knowledge of cGMP manufacturing.