Manager, QC LIMS

Position OverviewThe Manager, QC Laboratory Information Management System (LIMS) is responsible for developing strategic plans for implementing FDB's global Laboratory Information Management System (LIMS). This role harmonizes processes across all current and future FDB sites and leads the transition of QC into a paperless environment. The Manager, QC LIMS guides a team of LIMS experts to translate global and site-specific needs into user requirements, system design, configuration, and implementation plans. This role acts as the primary subject matter expert (SME) for LIMS and focuses on maintaining and continuously enhancing the global LIMS system.Company OverviewFollow Your Genki to North America's largest, state-of-the-art Life Science Manufacturing Facility & CDMOThe work we do at FUJIFILM Diosynth Biotechnologies has never been more important—and we are looking for talented candidates to join us. We are growing our locations, our capabilities, and our teams, and looking for passionate, mission-driven people like you who want to make a real difference in people’s lives. Join FUJIFILM Diosynth Biotechnologies and help manufacture the next vaccine, cure, or gene therapy in partnership with some of the most innovative biopharma companies across the globe. We are proud to cultivate a culture that will fuel your passion, energy and drive - what we call Genki.Join usWe are growing our locations and are investing more than $2 billion into establishing a new large-scale manufacturing site for biopharmaceuticals in the United States to accelerate the growth of our Bio CDMO (Contract and Development Manufacturing Organization) business. This will be the largest end-to-end cell culture CDMO provider in North America.The new site will offer end-to-end solutions to our customers looking to manufacture biopharmaceuticals in the US. In addition to drug substance manufacture, it will also provide automated fill-finish and assembly, packaging, and labeling services. The new state-of-the-art facility is located in Holly Springs, North Carolina, United States.Job DescriptionWhat You'll Do Provides cross-functional leadership as the recognized LIMS expert Develops strategic implementation plans, recruits LIMS staff, and manages project budgets Ensures data integrity principles are at the core of LIMS implementation Directs the LIMS team to:o Establish user requirements and best practices to enhance laboratory operations, reduce cycle times, and boost efficiencyo Identify and assess opportunities for improving the LIMS implementation processo Develop, implement,, and review validation protocols, SOPs, test scripts, and training materials for LIMSo Configure, customize, maintain, and upgrade the LIMS systemo Develop Master Data templates for LIMSo Provide support and training to new users for data entry and reporting Manages and prioritizes the workload and responsibilities of the LIMS team Provides guidance and support to less experienced team members Identifies and implements system improvements Integrates quality and regulatory compliance into LIMS design Prepares and delivers presentations to both internal and external stakeholders Manages and develops direct reports from LIMS team Administers company policies such as time off, shift work, and inclement weather that directly impact employees Completes required administrative tasks (e.g., timecard approvals, time off approvals, expense reports etc.) Coaches and guides direct reports to foster professional development Participates in the recruitment process and retention strategies to attract and retain talent, as needed Addresses performance gaps, employee questions and concerns, and partners with HR as needed for resolution Performs other duties, as assigned.Minimum Requirements: Bachelor’s degree with 7+ years of experience in a GMP environment and LIMS experience in pharmaceutical industry OR Master’s degree with 5+ years of experience in a GMP environment and LIMS experience in pharmaceutical industry OR PHD with 3+ years of experience in a GMP environment and LIMS experience in pharmaceutical industry 2-5 years of people management experience Proven experience in full life cycle implementation of multi-site LIMS Proven experience in connecting analyzers to the LIMS and ability to provide a roadmap from Development to QC. Extensive knowledge of GMPs, computer system software development and validation, with the ability to apply to non-routine situations. Deep understanding and command of LIMS requirements.Preferred Requirements: Experience in LabWare v8Physical and Work Environment Requirements:Ability to discern audible cues.Ability to ascend or descend ladders, scaffolding, ramps, etc.Ability to stand for prolonged periods of time up to 120 minutesAbility to sit for prolonged periods of time up to 120 minutesAbility to conduct activities using repetitive motions that include writs, hands and/or fingers.Ability to conduct work that includes moving objects up to 10 pounds.To all agencies: Please, no phone calls or emails to any employee of FUJIFILM about this requisition. All resumes submitted by search firms/employment agencies to any employee at FUJIFILM via-email, the internet or in any form and/or method will be deemed the sole property of FUJIFILM, unless such search firms/employment agencies were engaged by FUJIFILM for this requisition and a valid agreement with FUJIFILM is in place. In the event a candidate who was submitted outside of the FUJIFILM agency engagement process is hired, no fee or payment of any kind will be paid.EEO InformationFujifilm is committed to providing equal opportunities in hiring, promotion and advancement, compensation, benefits, and training regardless of nationality, age, gender, sexual orientation or gender identity, race, ethnicity, religion, political creed, ideology, national, or social origin, disability, veteran status, etc.ADA InformationIf you require reasonable accommodation in completing this application, interviewing, completing any pre-employment testing, or otherwise participating in the employee selection process, please direct your inquiries to our HR Department (FDBNPNC@fujifilm.com).Job Locations US-NC-Holly SpringsPosted Date 14 hours ago (2/28/2025 9:21 AM)Requisition ID 2025-33593Category Quality ControlCompany (Portal Searching) FUJIFILM Diosynth Biotechnologies