Location:

Portsmouth, New Hampshire 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, 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.

Pay:

$80.00 - $100.00 per hour Expected hours: 40.0 per week Application Question(s): 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.

Work Location:

In person