Executive Director, Commercial Quality Systems

Overview The Executive Director, Commercial Quality Systems is responsible for the strategic leadership, development, and continuous improvement of Celldex Therapeutics' Quality Management System (QMS) to support commercial and late-stage clinical products. This role ensures quality systems are compliant with global regulatory requirements, industry standards, and company objectives while fostering a culture of quality and operational excellence. The Executive Director oversees key quality processes, including deviations, CAPA, change control, complaint management, document control, training, and inspection readiness programs. As a senior quality leader, this position partners closely with Regulatory Affairs, Manufacturing, Supply Chain, IT, and Technical Operations to ensure a robust and sustainable quality infrastructure across the organization. Responsibilities Responsible for the management and development of a growing team of (4) Quality leaders. This includes Quality Management, Quality Inspection Management, and Quality Medical Device Management. Responsible for the strategic quality leadership of designing, maintaining, and keeping current Celldex's commercial Quality Systems. Responsible for the development and implementation of the electronic systems utilized for the facilitation of Celldex's Quality Systems. Development of the Inspection Management System for Celldex and its CDMOs to ensure successful Health Authority Inspections. Partnering with Operations to ensure Celldex develops and maintains appropriate standards for Medical Devices. Trend and present Commercial Quality Metrics for Management Review Committee meetings. As a part of the Quality Leadership Team, work within the team to drive Strategic Quality initiatives across the organization. Develop departmental budgets for the QA department, including defining resources and personnel needs. Qualifications BS in a scientific discipline required; advanced degree preferred Experience supporting commercial biologics and product lifecycle quality activities. Expertise with eQMS platforms, quality metrics, and continuous improvement programs. Extensive expertise developing and managing enterprise Quality Management Systems (QMS). Strong knowledge of FDA, EMA, ICH, and global GxP regulatory requirements. Proven experience with deviations, CAPA, change control, complaints, document control, and training systems. Demonstrated success leading regulatory inspections, audit readiness, and compliance initiatives. Proven success leading and developing high-performing quality organizations, including direct management of managers and cross-functional team Compensation Statement The expected base salary for this position is: $233631.00 to $303417.00. We are committed to compensating employees equitably based on several factors including experience, education, licensure/certifications, skill level, location of the position, and availability of similar talent in a competitive market. Subject to eligibility and applicable plan terms, compensation includes base salary, annual discretionary bonus, long term incentive, 401(K) plan with employer contribution, health care and other insurance benefits (for employee and family), paid holidays, vacation, and sick days. A summary of our benefits can be found on our careers page Celldex is proud to be an equal opportunity employer that strives to foster a culture of diversity, equity, and inclusion. We are committed to promoting a diverse environment through development, recruiting and community outreach. #J-18808-Ljbffr Celldex Therapeutics, Inc.