EyePoint
Director, Commercial Supply Chain – EyePoint
Develop and execute strategies for the global supply of DURAVYU through all stages of commercial manufacturing, including packaging, labeling, and distribution. Drive process improvements, enhance supply planning capabilities, and ensure compliance with global regulatory requirements while managing operations within a GxP environment.
Location Northbridge, MA (Materials Management & Supply Chain responsibilities across the Northbridge and Watertown facilities)
Compensation & Benefits Hybrid work schedule. Compensation includes equity and comprehensive benefits upon hire. Salary range:
Min $193,640.00 per year – Max $244,463.00 per year .
Responsibilities
Ensure safety, quality, and compliance in cGMP Materials Management / Logistics operations.
Establish and execute plans that enable operational and strategic initiatives.
Lead and coordinate resources to meet product quality standards and supply plans within budget.
Develop and implement metrics to track successful, timely accomplishment of goals, objectives, and projects.
Provide organizational leadership of the Commercial Supply Chain team, including talent management, performance, career development, and succession planning.
Develop short‑ and long‑term strategies, goals, objectives, and associated budgets for manufacturing operations and site deliverables.
Deliver results consistent with compliance requirements and core values.
Prepare and maintain department budget and workforce model.
Champion innovation and continuous improvement through process improvements, automation, and new technologies.
Lead Materials Management and Logistics investigations, ensuring consistency and compliance with external regulatory requirements.
Develop and implement commercial supply plans and manage Materials Management and GMP Warehouse Logistics functions.
Plan, establish, manage, and monitor forecast activities related to commercial clinical supply.
Manage vendors to ensure timely delivery of commercial product that meets regulatory and budgetary requirements, and ensure key project milestones are met.
Work with internal functions and external partners to manage complex projects, negotiate supply plans, and communicate timelines to stakeholders and partners.
Ensure regulatory, clinical, quality, and CMC plans and interdependencies are integrated for unified assurance of supply chain activities.
Maintain and comply with SOPs, identify gaps, recommend mitigations, and develop new SOPs with staff training.
Maintain a continuous‑improvement mentality to enhance commercial supply chain processes.
Recruit, retain, and develop high‑performing and diverse teams; build empowered teams that put patients and EyePoint first.
Serve as a role model, coach, and develop teams toward their fullest potential.
Represent the department to regulatory authorities as necessary.
Foster and maintain relationships with key site, company, and network partners.
Qualifications
Experience in small‑molecule drug product and/or combination drug‑device commercial supply chain.
Advanced knowledge of cGMP, associated CMC quality systems, and regulatory considerations in a pharmaceutical setting.
Demonstrated leadership, collaboration, and team‑building skills; ability to connect with all levels of the organization.
Deep knowledge of drug discovery, development, and commercialization processes.
Proven ability to manage multiple high‑priority projects effectively.
Ability to navigate and succeed in a fast‑paced, highly matrixed work environment.
Broad experience navigating cross‑functional teams through critical scientific, regulatory, and general development and global commercialization issues.
Strong collaboration, negotiation, analytical, and problem‑solving skills.
Strong written and verbal communication skills. Working knowledge of project controls in cost and financial assessments is desirable.
Ability to balance multiple priorities, work against tight timelines, and continually evaluate, measure, analyze, and report on collaboration success, potential risks or new opportunities.
Diverse, hands‑on operations experience.
Proven managerial experience and track record of compliance in a highly regulated GMP environment.
Understanding of regulatory requirements for global commercial supply distribution and labeling.
Understanding of cGMP, GCP, GDP and national/international transportation requirements for pharmaceutical materials.
Education and Experience
Bachelor’s degree in supply chain management, manufacturing, life sciences, or a related field.
Master’s degree & 7+ years of experience in a pharmaceutical Supply Chain / Operations field.
OR Bachelor’s degree & 9+ years of experience in a pharmaceutical Supply Chain / Operations field.
Minimum of 5 years of managerial experience directly leading people in a multi‑tiered (GMP) organization and/or leading teams, projects, programs or directing allocation of resources.
Prior experience developing and setting up a commercial supply chain infrastructure to support product launch.
Seniority Level Director
Employment Type Full‑time
EEO Statement EyePoint is proud to be an equal‑opportunity employer. All applicants will be considered for employment without attention to age, race, color, religion, sex, sexual orientation, gender identity, national origin, veteran, or disability status.
#J-18808-Ljbffr
Location Northbridge, MA (Materials Management & Supply Chain responsibilities across the Northbridge and Watertown facilities)
Compensation & Benefits Hybrid work schedule. Compensation includes equity and comprehensive benefits upon hire. Salary range:
Min $193,640.00 per year – Max $244,463.00 per year .
Responsibilities
Ensure safety, quality, and compliance in cGMP Materials Management / Logistics operations.
Establish and execute plans that enable operational and strategic initiatives.
Lead and coordinate resources to meet product quality standards and supply plans within budget.
Develop and implement metrics to track successful, timely accomplishment of goals, objectives, and projects.
Provide organizational leadership of the Commercial Supply Chain team, including talent management, performance, career development, and succession planning.
Develop short‑ and long‑term strategies, goals, objectives, and associated budgets for manufacturing operations and site deliverables.
Deliver results consistent with compliance requirements and core values.
Prepare and maintain department budget and workforce model.
Champion innovation and continuous improvement through process improvements, automation, and new technologies.
Lead Materials Management and Logistics investigations, ensuring consistency and compliance with external regulatory requirements.
Develop and implement commercial supply plans and manage Materials Management and GMP Warehouse Logistics functions.
Plan, establish, manage, and monitor forecast activities related to commercial clinical supply.
Manage vendors to ensure timely delivery of commercial product that meets regulatory and budgetary requirements, and ensure key project milestones are met.
Work with internal functions and external partners to manage complex projects, negotiate supply plans, and communicate timelines to stakeholders and partners.
Ensure regulatory, clinical, quality, and CMC plans and interdependencies are integrated for unified assurance of supply chain activities.
Maintain and comply with SOPs, identify gaps, recommend mitigations, and develop new SOPs with staff training.
Maintain a continuous‑improvement mentality to enhance commercial supply chain processes.
Recruit, retain, and develop high‑performing and diverse teams; build empowered teams that put patients and EyePoint first.
Serve as a role model, coach, and develop teams toward their fullest potential.
Represent the department to regulatory authorities as necessary.
Foster and maintain relationships with key site, company, and network partners.
Qualifications
Experience in small‑molecule drug product and/or combination drug‑device commercial supply chain.
Advanced knowledge of cGMP, associated CMC quality systems, and regulatory considerations in a pharmaceutical setting.
Demonstrated leadership, collaboration, and team‑building skills; ability to connect with all levels of the organization.
Deep knowledge of drug discovery, development, and commercialization processes.
Proven ability to manage multiple high‑priority projects effectively.
Ability to navigate and succeed in a fast‑paced, highly matrixed work environment.
Broad experience navigating cross‑functional teams through critical scientific, regulatory, and general development and global commercialization issues.
Strong collaboration, negotiation, analytical, and problem‑solving skills.
Strong written and verbal communication skills. Working knowledge of project controls in cost and financial assessments is desirable.
Ability to balance multiple priorities, work against tight timelines, and continually evaluate, measure, analyze, and report on collaboration success, potential risks or new opportunities.
Diverse, hands‑on operations experience.
Proven managerial experience and track record of compliance in a highly regulated GMP environment.
Understanding of regulatory requirements for global commercial supply distribution and labeling.
Understanding of cGMP, GCP, GDP and national/international transportation requirements for pharmaceutical materials.
Education and Experience
Bachelor’s degree in supply chain management, manufacturing, life sciences, or a related field.
Master’s degree & 7+ years of experience in a pharmaceutical Supply Chain / Operations field.
OR Bachelor’s degree & 9+ years of experience in a pharmaceutical Supply Chain / Operations field.
Minimum of 5 years of managerial experience directly leading people in a multi‑tiered (GMP) organization and/or leading teams, projects, programs or directing allocation of resources.
Prior experience developing and setting up a commercial supply chain infrastructure to support product launch.
Seniority Level Director
Employment Type Full‑time
EEO Statement EyePoint is proud to be an equal‑opportunity employer. All applicants will be considered for employment without attention to age, race, color, religion, sex, sexual orientation, gender identity, national origin, veteran, or disability status.
#J-18808-Ljbffr