Sr. Manager, QC LIMS Administrator

At Viridian, we are focused on developing best-in-class medicines for people living with autoimmune and rare diseases. Leveraging our team’s expertise in antibody discovery and engineering, we have created a robust pipeline of differentiated investigational therapeutic candidates for well-validated targets.

Reporting to the Executive Director, Quality Control, the Sr. Manager, QC LIMS Administrator will serve as a key subject matter expert responsible for configuring, maintaining, and optimizing the LIMS platform to support Quality Control laboratory operations. This role will collaborate closely with stakeholders across IT, Analytical Development (AD), Quality Control (QC), Quality Assurance (QA), and Computer System Validation (CSV) to ensure compliant, efficient, and user-friendly system solutions.

The LIMS Administrator will lead system configuration projects, support data integrity initiatives, manage routine updates, and provide user training to enable reliable and streamlined laboratory operation.

• o):
  
  Lead the configuration, maintenance, and enhancement of QC workflows within the LIMS platf
• orm Translate user and business requirements into effective, compliant system solutions and workfl
• ows Develop and execute projects and implement plans to ensure timely delivery of enhanceme
• ntsOwn and manage change controls, deviations, and other quality records related to L
• IMSServe as QC lead for metadata management, reporting, and data structure upda
• tes Author and deliver end-user procedures, training materials, and hands-on training sessi
• ons Support system upgrades, validation activities, and ensure ongoing system compliance with regulatory requireme
• nts Generate and manage LIMS data reporting and support data queries from business partn
• ers Partner with IT and vendors to troubleshoot, escal
• ate, resolve LIMS iss
• ues Support internal and external audits by ensuring data integrity and system compliance with applicable regulati

• ns:
  
  Requires a Bachelor’s degree in Life Sciences, Computer Science, Information Technology, or a related field with 8+ years of relevant experience in the life sciences, biotech, or pharmaceutical indus
• try Strong understanding of QC laboratory workflows, analytical instrumentation, and data management princip
• lesIn-depth knowledge of data integrity regulations and guidelines (21 CFR Part 11, Computer System Validation, ALCOA
• ++)Proven hands-on experience in LIMS administration, configuration, implementation, and validat
• ion Ability to translate user requirements into efficient system workflows and develop creative solutions within platform constrai
• nts Excellent communication skills with the ability to train and support staff across multiple levels and functi
• ons Demonstrated project management experience and ability to work in a fast-paced, collaborative environm
• ent Comfortable in an adaptable small company environment with minimal direction and able to adjust workload based upon changing priorit
• ies Strong commitment to ethical standa
• rds Proficient with Microsoft Office suite (i.e., Word, PowerPoint, Excel, Outlook, SharePoint, etc.)
• Ability to travel up to 5%
• The salary range for this position is commensurate with experie
• nce

Viridian Therapeutics, Inc. provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination, harassment, or retaliation of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by Federal, State, and Local laws. Viridian will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment.

Please contact us to request accommodat

i

on. Viridian Therapeutics, Inc participates in E-Verify, the federal program for electronic verification of employment eligibil

ity.

Mid‑Senior level

Full‑time

Quality Assurance