Viridian Therapeutics, Inc.
Sr. Manager, QC LIMS Administrator
Viridian Therapeutics, Inc., Waltham, Massachusetts, United States, 02254
Overview
Sr. Manager, QC LIMS Administrator at Viridian Therapeutics, Inc. Join to apply for the Sr. Manager, QC LIMS Administrator role at Viridian Therapeutics, Inc. This position reports to the Executive Director, Quality Control and will serve as a subject matter expert responsible for configuring, maintaining, and optimizing the LIMS platform to support Quality Control laboratory operations. The role collaborates with IT, Analytical Development, Quality Control, Quality Assurance, and Computer System Validation to ensure compliant, efficient, and user-friendly system solutions. The LIMS Administrator leads system configuration projects, supports data integrity initiatives, manages routine updates, and provides user training to enable reliable and streamlined laboratory operation. This role is based in our Waltham, MA headquarters. Office-based employees are required to work in the office three days per week.
Responsibilities
Lead the configuration, maintenance, and enhancement of QC workflows within the LIMS platform.
Translate user and business requirements into effective, compliant system solutions and workflows.
Develop and execute projects and plans to ensure timely delivery of enhancements.
Own and manage change controls, deviations, and other quality records related to LIMS.
Serve as QC lead for metadata management, reporting, and data structure updates.
Author and deliver end-user procedures, training materials, and hands-on training sessions.
Support system upgrades, validation activities, and ensure ongoing system compliance with regulatory requirements.
Generate and manage LIMS data reporting and support data queries from business partners.
Partner with IT and vendors to troubleshoot, escalate, and resolve LIMS issues.
Support internal and external audits by ensuring data integrity and system compliance with applicable regulations.
Qualifications
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 industry.
Strong understanding of QC laboratory workflows, analytical instrumentation, and data management principles.
In-depth knowledge of data integrity regulations and guidelines (e.g., 21 CFR Part 11, Computer System Validation, ALCOA).
Proven hands-on experience in LIMS administration, configuration, implementation, and validation.
Ability to translate user requirements into efficient system workflows and develop creative solutions within platform constraints.
Excellent communication skills with the ability to train and support staff across multiple levels and functions.
Demonstrated project management experience and ability to work in a fast-paced, collaborative environment.
Comfortable in an adaptable small company environment with minimal direction and ability to adjust workload based on changing priorities.
Strong commitment to ethical standards.
Proficient with Microsoft Office suite (Word, PowerPoint, Excel, Outlook, SharePoint, etc.).
Ability to travel up to 5%.
The salary range for this position is commensurate with experience.
Benefits
Competitive pay and stock options for all employees.
Medical, dental, and vision coverage with 100% of premiums paid by Viridian for employees and their eligible dependents.
Fertility and mental health programs.
Short- and long-term disability coverage.
Life, Travel and AD&D.
401(k) company match with immediate vesting.
Employee Stock Purchase Plan.
Generous vacation plan and paid company holiday shutdowns.
Various mental, financial, and proactive health programs.
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 accommodation. Viridian Therapeutics, Inc participates in E-Verify, the federal program for electronic verification of employment eligibility.
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Sr. Manager, QC LIMS Administrator at Viridian Therapeutics, Inc. Join to apply for the Sr. Manager, QC LIMS Administrator role at Viridian Therapeutics, Inc. This position reports to the Executive Director, Quality Control and will serve as a subject matter expert responsible for configuring, maintaining, and optimizing the LIMS platform to support Quality Control laboratory operations. The role collaborates with IT, Analytical Development, Quality Control, Quality Assurance, and Computer System Validation to ensure compliant, efficient, and user-friendly system solutions. The LIMS Administrator leads system configuration projects, supports data integrity initiatives, manages routine updates, and provides user training to enable reliable and streamlined laboratory operation. This role is based in our Waltham, MA headquarters. Office-based employees are required to work in the office three days per week.
Responsibilities
Lead the configuration, maintenance, and enhancement of QC workflows within the LIMS platform.
Translate user and business requirements into effective, compliant system solutions and workflows.
Develop and execute projects and plans to ensure timely delivery of enhancements.
Own and manage change controls, deviations, and other quality records related to LIMS.
Serve as QC lead for metadata management, reporting, and data structure updates.
Author and deliver end-user procedures, training materials, and hands-on training sessions.
Support system upgrades, validation activities, and ensure ongoing system compliance with regulatory requirements.
Generate and manage LIMS data reporting and support data queries from business partners.
Partner with IT and vendors to troubleshoot, escalate, and resolve LIMS issues.
Support internal and external audits by ensuring data integrity and system compliance with applicable regulations.
Qualifications
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 industry.
Strong understanding of QC laboratory workflows, analytical instrumentation, and data management principles.
In-depth knowledge of data integrity regulations and guidelines (e.g., 21 CFR Part 11, Computer System Validation, ALCOA).
Proven hands-on experience in LIMS administration, configuration, implementation, and validation.
Ability to translate user requirements into efficient system workflows and develop creative solutions within platform constraints.
Excellent communication skills with the ability to train and support staff across multiple levels and functions.
Demonstrated project management experience and ability to work in a fast-paced, collaborative environment.
Comfortable in an adaptable small company environment with minimal direction and ability to adjust workload based on changing priorities.
Strong commitment to ethical standards.
Proficient with Microsoft Office suite (Word, PowerPoint, Excel, Outlook, SharePoint, etc.).
Ability to travel up to 5%.
The salary range for this position is commensurate with experience.
Benefits
Competitive pay and stock options for all employees.
Medical, dental, and vision coverage with 100% of premiums paid by Viridian for employees and their eligible dependents.
Fertility and mental health programs.
Short- and long-term disability coverage.
Life, Travel and AD&D.
401(k) company match with immediate vesting.
Employee Stock Purchase Plan.
Generous vacation plan and paid company holiday shutdowns.
Various mental, financial, and proactive health programs.
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 accommodation. Viridian Therapeutics, Inc participates in E-Verify, the federal program for electronic verification of employment eligibility.
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