Otsuka Pharmaceutical
Associate Director, Global Supplier Quality
Otsuka Pharmaceutical, Princeton, New Jersey, United States
The Associate Director of Global Supplier Quality will be responsible for the execution of supplier quality audit and monitoring across the company’s global network of contract manufacturing organizations (CMOs). This role supports the qualification, monitoring, and compliance of external manufacturing partners to ensure the quality and reliability of pharmaceutical products, including small molecules and biologics.
Job Description Supplier Quality Execution
Support the qualification and ongoing monitoring of CMOs and critical suppliers. Execute supplier audits and ensure timely follow-up and resolution of findings. Maintain and update quality agreements in collaboration with internal stakeholders. Conduct risk assessments and support mitigation plans for supplier-related quality issues.
Compliance & Documentation
Ensure supplier compliance with global regulatory requirements (e.g., FDA, EMA, ICH). Prepare documentation and support internal and external audits and inspections. Maintain accurate records of supplier performance and audit outcomes.
Cross-Functional Collaboration
Collaborate with Procurement, Manufacturing, Regulatory Affairs, and Technical Operations to ensure supplier quality is integrated into business processes. Serve as a point of contact for operational supplier quality issues and escalations.
Metrics & Reporting
Track and report key performance indicators (KPIs) related to supplier quality. Provide regular updates to leadership on supplier performance and compliance status
.
Team & Project Support
May supervise or mentor junior quality staff or contractors. Support continuous improvement initiatives within the supplier quality function.
Qualifications Required Bachelor’s degree in a scientific or engineering discipline. 6+ years of experience in pharmaceutical quality, with 2+ years in supplier or external manufacturing quality. Strong knowledge of GMP regulations for small molecules and/or biologics. Experience conducting audits and managing supplier documentation. Strong communication and problem-solving skills. Ability to travel internationally as needed. Preferred Experience working with global CMOs. Familiarity with digital tools and systems for supplier management. Exposure to regulatory inspections and remediation activities.
Job Description Supplier Quality Execution
Support the qualification and ongoing monitoring of CMOs and critical suppliers. Execute supplier audits and ensure timely follow-up and resolution of findings. Maintain and update quality agreements in collaboration with internal stakeholders. Conduct risk assessments and support mitigation plans for supplier-related quality issues.
Compliance & Documentation
Ensure supplier compliance with global regulatory requirements (e.g., FDA, EMA, ICH). Prepare documentation and support internal and external audits and inspections. Maintain accurate records of supplier performance and audit outcomes.
Cross-Functional Collaboration
Collaborate with Procurement, Manufacturing, Regulatory Affairs, and Technical Operations to ensure supplier quality is integrated into business processes. Serve as a point of contact for operational supplier quality issues and escalations.
Metrics & Reporting
Track and report key performance indicators (KPIs) related to supplier quality. Provide regular updates to leadership on supplier performance and compliance status
.
Team & Project Support
May supervise or mentor junior quality staff or contractors. Support continuous improvement initiatives within the supplier quality function.
Qualifications Required Bachelor’s degree in a scientific or engineering discipline. 6+ years of experience in pharmaceutical quality, with 2+ years in supplier or external manufacturing quality. Strong knowledge of GMP regulations for small molecules and/or biologics. Experience conducting audits and managing supplier documentation. Strong communication and problem-solving skills. Ability to travel internationally as needed. Preferred Experience working with global CMOs. Familiarity with digital tools and systems for supplier management. Exposure to regulatory inspections and remediation activities.