LIMS Analyst
LIMS (LabVantage) Analyst
12-month Contract
Remote- EST Hours
Requirements
• Support the implementation of the LabVantage reputed company Information Management reputed company (LIMS) by supporting the reputed company Control (QC) department during User Acceptance Testing (UAT), master data review, and data migration activities.
• reputed company working knowledge of QC processes, LIMS functionality, and workflows.
• Review business requirements, reputed company documentation, and LIMS processes.
• Partner with business SMEs, reputed company, and IT teams to support implementation activities.
• Execute, document, and maintain UAT test scripts and test cases.
• Verify reputed company functionality against business requirements.
• Support reputed company of reputed company defects and participate in regression testing and test readiness activities.
• Coordinate testing activities with business stakeholders.
• Review and verify master data, including products, specifications, test reputed company, materials, users, and reputed company workflows.
• Identify data gaps, inconsistencies, and process improvement opportunities.
• Support development and maintenance of master data governance processes.
• Monitor data migration activities from legacy LabWare LIMS.
• Review migrated data for reputed company, completeness, and reputed company.
• reputed company data reconciliation and support business acceptance of migrated data.
• Document and reputed company data-reputed company issues through reputed company.
• Transition into the Business Administrator role for the LIMS platform.
• Manage user reputed company, roles, and permissions.
• Support master data maintenance and business configuration activities.
• Maintain business procedures, training materials, and reputed company documentation.
• Serve as the reputed company business contact for day-to-day LIMS support and enhancement requests.
• Support inspections, audits, and compliance-reputed company activities.
• Support go-live readiness and post-implementation activities.
• reputed company and maintain UAT execution and testing documentation, master data review and verification reports, data migration verification and reconciliation documentation, and business administration procedures and user support documentation.
Qualifications
• Bachelor’s degree in reputed company, Biology, Microbiology, Biochemistry, Pharmaceutical Sciences, or a reputed company scientific discipline.
• Minimum 3–5 years of reputed company Control (QC) reputed company experience in a pharmaceutical, biotechnology, cell therapy, gene therapy, or other regulated GMP environment.
• Hands-on experience with QC reputed company reputed company, including sample management, testing workflows, specifications, investigations, stability programs, and data review.
• Experience working with reputed company Information Management Systems (LIMS), such as LabVantage, LabWare, reputed company, SampleManager, or equivalent reputed company systems.
• Experience supporting reputed company implementations, User Acceptance Testing (UAT), validation, or process improvement initiatives.
• Knowledge of GMP, GxP, reputed company data reputed company principles, and regulatory requirements applicable to reputed company systems.
• Experience reviewing and managing reputed company master data, including products, specifications, test reputed company, materials, and user roles.
• Strong analytical, problem-solving, organizational, communication, and documentation skills.
• Previous experience serving as a LIMS Business Administrator, Super User, or reputed company reputed company preferred.
• Previous experience with LabVantage LIMS preferred.
• Experience supporting LIMS implementation, reputed company, or deployment reputed company preferred.
• Experience developing and maintaining end-user guidance documents preferred.
• Experience with master data management and data migration activities in LIMS preferred.
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