LIMS System and Data Administrator, Quality Control

About Forge  

Forge, a member of Ajinomoto Bio-Pharma Services, is a gene therapy development engine, focused on enabling access to life changing gene therapies and helping bring them from idea into reality. We partner with innovators in the gene therapy community: scientists, physicians, biotech/pharma companies, and patient groups. We bring expertise in gene therapy manufacturing and therapeutics development to the table, helping to champion teams that are navigating the long road from the lab bench to the bedside. Our goal is simple but vital to patients living with disease, and we take it seriously. With a patient-first approach, we are forging new models for working together to better accelerate these transformative medicines to reach those who need them the most.  

Forge is based in Columbus, Ohio, in a 200,000 square foot facility known affectionately by team members as, the Hearth. The Hearth, is a custom-designed cGMP facility dedicated to AAV manufacturing and hosts scalable, end-to-end manufacturing services.  

About the Role: 

The LIMS System and Data Administrator role will be the primary business Administrator for the Veeva Laboratory Information Management System (LIMS) within the Quality Control (QC) group. This role is responsible for entering sample and specification requirements into LIMS to support in-process, release, and stability testing for AAV, plasmid, cell bank, buffer, and raw materials, along with generation of electronic Certificate of Analysis (COA) and Certificate of Testing (COT) documents needed to support batch release or disposition. The LIMS System and Data Administrator will also provide user input and prioritization for system enhancements and new module implementations.  This role provides an opportunity to play a significant impact in the success of client gene therapy programs.

What You'll Do:

• Oversee daily operations of the LIMS system for logging batches, entering QC testing results, and issuing electronic COAs and COTs.
• Maintain data integrity, security, and compliance within the LIMS system, ensuring adherence to GMP and regulatory requirements.
• Develop user requirements and test scripts for custom scripts, code, or automation tools to support LIMS integration with analytical instruments and other enterprise systems.
• Optimize workflows within the LIMS to improve data capture, reporting, and traceability by collaborating with IT and Vendor Managed Services.
• Implement quality control checks within the system to ensure accurate and compliant data entry.
• Provide business leadership for the implementation of new LIMS modules, system updates, and enhancements to support QC testing needs.
• Work closely with IT, QA, and QC leadership to configure system settings, user roles, and permissions.
• Collaborate with laboratory staff to identify system improvements and customize LIMS functionalities.
• Provide power user support, troubleshooting issues, and resolving system-related queries within QC.
• Train QC personnel on LIMS functionalities, data entry procedures, and reporting workflows.
• Develop SOPs, training materials, and documentation for LIMS system use and best practices.
• Ensure LIMS operations comply with GMP, FDA 21 CFR Part 11, USP, and data integrity requirements.
• Support internal and external regulatory audits and inspections by providing LIMS documentation and system access as required.
• Collaborate on periodic system reviews and validations to maintain compliance with regulatory standards.
• Partner with QC, QA, IT, and Manufacturing teams to ensure seamless integration of the LIMS system into broader operations.
• Work with external vendors and internal stakeholders to support ongoing LIMS improvements and upgrades.
• Assist in integrating LIMS with ELN (Electronic Lab Notebook), ERP (Enterprise Resource Planning), and CDS (Chromatography Data Systems).

What You'll Bring:

• BS or MS in Life Sciences, Biotechnology, or a related field is preferred, with degrees in Computer Science or a related field to be considered as well.
• Experience administering LIMS in a GMP-regulated QC laboratory (biologics, gene therapy, or pharmaceuticals preferred).
• Experience with Veeva LIMS or other enterprise LIMS platforms (LabWare, LabVantage, STARLIMS, etc.).
• Understanding of QC analytical methods, sample types, and AAV manufacturing processes, or viral vector manufacturing is highly desirable.
• Familiarity with