Viridian Therapeutics
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 Sr. Director, Commercial Supply Chain, the Manager, Logistics will be responsible for pre‑clinical, clinical, and commercial logistics across our global network of contract manufacturing organizations and vendors. You will partner with cross‑functional teams to supply on time deliveries of medical device components, drug substance, drug product, and combination products to downstream production facilities that match the needs of the business and ensure supply to our patients.
This role may be based in our Waltham, MA headquarters, which would be a hybrid role, or it can also be fully remote. Our office‑based employees are required to work in the office three (3) days a week. If remote, travel to headquarters for meetings would be required at the discretion of management.
Responsibilities
Coordinate pre‑clinical, clinical, and commercial global logistics activities for temperature‑controlled GMP materials including scheduling, tracking, and performing quality checks across the supply chain to ensure compliance
Execute international shipments including import / export document generation and trade compliance activities
Maintain processes and systems to track and monitor shipping and receiving processes with direction from other Logistics subject matter experts
Serve as the relationship manager for couriers, trade compliance advisors, GMP storage facilities, and customs brokers to handle all global logistics activities
Author and maintain documents to ensure effective product handling, including SOP’s, shipping and receiving forms, visual work instructions, and information sheets in accordance with GDP
Review temperature data captured from monitored shipments against established product retest temperature and time limits; trend excursions and propose corrective actions
Support the execution of shipping validation studies to support global movement of GMP materials (master and working cell banks, drug substance, drug product, medical device components and assembled combination products, such as autoinjectors)
Collaborate with couriers worldwide to set up and maintain shipping lanes and pricing for all products
Provide support in supply chain and external manufacturing budgeting including PO and invoice management
Qualifications
Requires a Bachelor’s degree life sciences, supply chain, or related discipline with 5+ years of experience in the Biotechnology/Pharmaceutical industry with a minimum of 3+ years of experience in Supply Chain and/or cGMP Commercial Manufacturing Operations
Demonstrated strong written and verbal communication skills
Proven mindset of proactive continuous improvement
Efficient independent worker with ability to focus and drive for results
Strong attention to detail
Ability to work in a fast‑paced environment and to handle multiple tasks
Strong commitment to ethical standards
Proficient with Microsoft Office suite (i.e., Word, PowerPoint, Excel, Outlook, SharePoint, etc.)
Ability to travel domestically and internationally up to 15%
The salary range for this position is commensurate with experience
Benefits
Competitive pay and stock options for all employees
Competitive medical, dental, and vision plans
Fertility and mental health programs
Short‑ and long‑term disability coverage
Life, Travel and AD&D
401(k) Company Match with immediate company vest
Employee Stock Purchase plan
Generous vacation plan and paid company holiday shutdowns
Various mental, financial, and proactive physical health programs covered by Viridian
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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Reporting to the Sr. Director, Commercial Supply Chain, the Manager, Logistics will be responsible for pre‑clinical, clinical, and commercial logistics across our global network of contract manufacturing organizations and vendors. You will partner with cross‑functional teams to supply on time deliveries of medical device components, drug substance, drug product, and combination products to downstream production facilities that match the needs of the business and ensure supply to our patients.
This role may be based in our Waltham, MA headquarters, which would be a hybrid role, or it can also be fully remote. Our office‑based employees are required to work in the office three (3) days a week. If remote, travel to headquarters for meetings would be required at the discretion of management.
Responsibilities
Coordinate pre‑clinical, clinical, and commercial global logistics activities for temperature‑controlled GMP materials including scheduling, tracking, and performing quality checks across the supply chain to ensure compliance
Execute international shipments including import / export document generation and trade compliance activities
Maintain processes and systems to track and monitor shipping and receiving processes with direction from other Logistics subject matter experts
Serve as the relationship manager for couriers, trade compliance advisors, GMP storage facilities, and customs brokers to handle all global logistics activities
Author and maintain documents to ensure effective product handling, including SOP’s, shipping and receiving forms, visual work instructions, and information sheets in accordance with GDP
Review temperature data captured from monitored shipments against established product retest temperature and time limits; trend excursions and propose corrective actions
Support the execution of shipping validation studies to support global movement of GMP materials (master and working cell banks, drug substance, drug product, medical device components and assembled combination products, such as autoinjectors)
Collaborate with couriers worldwide to set up and maintain shipping lanes and pricing for all products
Provide support in supply chain and external manufacturing budgeting including PO and invoice management
Qualifications
Requires a Bachelor’s degree life sciences, supply chain, or related discipline with 5+ years of experience in the Biotechnology/Pharmaceutical industry with a minimum of 3+ years of experience in Supply Chain and/or cGMP Commercial Manufacturing Operations
Demonstrated strong written and verbal communication skills
Proven mindset of proactive continuous improvement
Efficient independent worker with ability to focus and drive for results
Strong attention to detail
Ability to work in a fast‑paced environment and to handle multiple tasks
Strong commitment to ethical standards
Proficient with Microsoft Office suite (i.e., Word, PowerPoint, Excel, Outlook, SharePoint, etc.)
Ability to travel domestically and internationally up to 15%
The salary range for this position is commensurate with experience
Benefits
Competitive pay and stock options for all employees
Competitive medical, dental, and vision plans
Fertility and mental health programs
Short‑ and long‑term disability coverage
Life, Travel and AD&D
401(k) Company Match with immediate company vest
Employee Stock Purchase plan
Generous vacation plan and paid company holiday shutdowns
Various mental, financial, and proactive physical health programs covered by Viridian
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.
#J-18808-Ljbffr