The Director of Supplier Quality is responsible for overseeing the quality assurance processes related to suppliers and ensuring that all products meet the company’s quality standards. This role involves developing supplier quality strategies, conducting audits, managing supplier relationships, and collaborating with cross-functional teams to drive continuous improvement initiatives.  This role will partner closely with business stakeholders to ensure identification and mitigation of risks, alignment with regulatory and commercial strategy and continuing support of Fusion’s clinical development pipeline. The Director, Supplier Quality will report directly to the Vice President, Quality.

Responsibilities

• Develop and implement a comprehensive supplier quality strategy aligned with organizational goals
• Evaluate and select suppliers based on quality performance, capabilities, and risk assessments
• Establish and maintain strong relationships with key suppliers to drive quality improvements
• Oversee supplier audits and assessments, ensuring adherence to quality standards and regulations.
• Develop and implement quality metrics to monitor supplier performance.
• Collaborate with suppliers and internal teams to identify areas for quality improvement.
• Drive initiatives such as root cause analysis and corrective action plans for quality issues.
• Work closely with procurement, engineering, and manufacturing teams to align supplier quality goals with operational needs.
• Facilitate training and knowledge sharing regarding quality standards and processes.
• Prepare quality reports for senior management, highlighting trends and areas of concern.

Qualifications

• Bachelor’s degree in Engineering, Quality Assurance, Supply Chain Management, or a related field; Master’s degree preferred
• Minimum of 10-12 years of experience in supplier quality management
• Prior experience with radiopharmaceuticals is desired
• Phase 1/Phase 2 supplier quality management experience in a Biotech/Pharma setting desired
• Strong knowledge of quality management systems (e.g., ISO 9001, IATF 16949) and quality tools (e.g., Six Sigma, Lean)
• Excellent analytical, problem-solving, and decision-making skills
• Strong communication and interpersonal skills, with the ability to work collaboratively across functions.
• Demonstrated ability to effectively lead professional staff and teams

• Familiarity with supplier risk management and assessment methodologies
• Proficiency in quality management software and data analysis tools

• Approximately 20-30% business travel required to external Contract Development Manufacturing Organization (CDMO) / Business Partner sites, or to attend professional development training seminars – as needed / directed

All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.