Labvantage LIMS Consultant (SME/ Admin)

Job Description

Position We are seeking a LabVantage LIMS Administrator to support the Pilot Bioproduction Facility. (ONLY apply if you have expertise in configuring and troubleshooting Labvantage LIMS) Responsibilities This independent self-starter will be asked to set up Labvantage LIMS for this burgeoning highly technical pharmaceutical/ med device clients and training SysAdmins to use LV LIMS in regulated GxP IT environments. This candidate: Leads LIMS implementation projects, ensuring adherence to project timelines and budgets. Collaborates with stakeholders to gather requirements and design effective LIMS solutions. Configures LabVantage to meet specific business needs, including workflows, security settings, and reporting. Oversees the creation, maintenance, and accuracy of master data within the LIMS system. Customizes and configures LabVantage modules, workflows, and reports to fit the laboratory's unique requirements. Develops and implements data governance policies and procedures. Ensures data integrity and consistency across the organization. Provides end-user support for quality control activities, including data validation, review, and approval processes. Assists in the development and implementation of quality control standards and procedures. Monitors and troubleshoots quality control issues. Performs routine maintenance, updates, and upgrades to the LabVantage LIMS to ensure optimal performance and reliability. Identifies potential risk and mitigation strategies. Coordinates with cross-functional teams to ensure project success. Provides technical support to end-users, resolving issues and answering questions related to LabVantage functionality. Maintains and updates LIMS documentation and training materials. Stays current with the latest LabVantage updates and best practices. Manages application vendor support agreements. Qualifications Bachelor's degree in Computer Science, Information Technology, or a related field, and ten (10) years of relevant experience Minimum of five (5) years of experience in LabVantage 8 LIMS coding, development, and implementation. CGMP Quality Control, Environmental Monitoring, or Manufacturing experience. Experience in laboratory environments and understanding of laboratory workflows. Strong understanding of LIMS implementation methodologies and best practices. Familiarity with LabVantage LIMS architecture and database schema. Demonstrates proficiency in master data management and data governance principles. Excellent problem-solving and troubleshooting skills. Strong communication and interpersonal skills. Ability to work independently. Preferred Certifications in LabVantage or related LIMS technologies. Experience with LIMS validation and compliance requirements. Knowledge of scripting languages (e.g., Python, SQL). Experience with other cGMP or biopharmaceutical software applications. Show more Show less