QC LabVantage LIMS Data Migration Specialist

Location: Portsmouth, New Hampshire - Lonza

Job ID: 1660

Compensation: W2, Contract

Position Summary

Seeking a hands-on LabVantage LIMS specialist with pharmaceutical or biotech QC experience. The role involves configuring and loading specifications, test methods, sampling plans, parameter lists, consumables, and LES templates.

Key Responsibilities

• Set up and load local master data in accordance with global guidelines, governance standards, and data principles.
• Build, configure, and load required master data into the global LabVantage LIMS platform, including consumables, sampling plans, specifications, parameter lists, test methods, and Laboratory Execution System (LES) templates.
• Map and align master data across LIMS and related source or destination platforms, identifying gaps, inconsistencies, and dependencies.
• Cleanse, review, and verify local data to improve completeness, consistency, accuracy, and readiness for migration or production use.
• Support data reconciliation, issue resolution, and quality checks before and after data loads.
• Develop clear local work instructions that describe how global master data processes will be executed at the site level.
• Collaborate with Quality Control, the global gLIMS team, Manufacturing Operations, and other cross-functional stakeholders.
• Track assigned deliverables, communicate risks or data-quality issues promptly, and complete work with limited supervision.
• Maintain documentation and records in accordance with applicable quality, data-integrity, and regulatory requirements.

Required Qualifications

• Direct, minimum five years of recent hands-on LabVantage experience
• LIMS master-data configuration, migration, or loading
• Pharmaceutical, biotech, or regulated laboratory experience
• Understanding of specifications, methods, parameters, sampling plans, or LES

Education

• Bachelor's degree in a scientific, technical, information systems, or related discipline is preferred. Relevant hands-on experience may be considered in place of a degree.

Preferred Qualifications

• Experience supporting a global or multi-site LIMS implementation.
• Experience authoring site work instructions, SOPs, or controlled process documentation.
• Experience supporting validated computerized systems in a GxP environment.

Key Competencies

• Data accuracy and quality focus; structured problem-solving; ownership and accountability; cross-functional collaboration; clear communication; adaptability; and the ability to prioritize multiple deliverables.

Quality and Safety Expectations

• Follow all applicable site safety procedures, required training, quality policies, and cGMP expectations. Promptly identify and escalate data-integrity, quality, compliance, or safety concerns through the appropriate channels.