Head of Quality Assurance, Drug Product, GMP QA

Job Summary

Leads a team of 5-7 MSMQ’s that are responsible for leading an independent QA function, with authority for final batch disposition, QA oversight of manufacturing/testing, and independence from production per Daiichi Sankyo’s GMP Quality Manuals.

Responsibilities

• Resolve issues in internal and external manufacturing site quality performance escalated from MSMQs in collaboration and negotiation with Tech Unit Senior Leaders (L-2 Leaders) and other internal peer groups, and escalate issues to GMQ Head as necessary for resolution and approval.
• Ensure the local QMS remains fully compliant with the global Quality Manual by managing key pillars such as CAPA, change control, and data integrity. Use a risk-based approach to drive periodic reviews and maintain rigorous policy oversight.
• Provide hands-on leadership to ensure the seamless execution of Quality Assurance (QA) functions, including complaint management, root-cause investigations, and the reporting of critical GMP issues to senior management.
• Direct the batch release process by overseeing complex jurisdiction controls and cross-functional data integration, ensuring all disposition decisions align with Daiichi Sankyo’s Quality digital roadmap and analytics strategy.
• Drive a culture of Continuous Improvement (CI) across the site, spearheading initiatives to systematically reduce deviations, shorten manufacturing cycle times, and enhance the robustness of the CAPA (Corrective and Preventive Action) system.
• Supports the enhancement of a robust Integrated Risk Management (IRM) framework, identifying potential risks throughout the product lifecycle and implementing proactive mitigation strategies to ensure patient safety and product efficacy.
• Represent Quality Assurance in internal and (potentially) external leadership forums and strategic initiatives.

Qualifications

• Education Qualifications: Bachelor's Degree in a science-related discipline required. An Advanced Degree strongly preferred.
• Experience Qualifications: 10 or more years of experience in a specific technical area as Quality Assurance and/or biologics manufacturing in a large multinational pharmaceutical organization required. 10 or more years of experience managing a team (preferably global teams covering various countries/time zones), being able to lead across different cultures, build effective teams, develop talents required. Must have extensive experience in audit readiness (including HA audit preparation, conduct mock audits), and risk management required. Proven expertise in Quality Assurance HA communication, inspection management support for CMO manufacturing at a biologics company required. Demonstrated experience overseeing CMOs (including understanding CMO expectations, capabilities, and challenges) required. Demonstrated experience in one or more of the following: Formulated Bulk, Filling and Finish, secondary packaging processes, current industry best practices for inspection (visual and automated) and their associated materials (e.g. Vials, Syringes, Device Delivery systems, secondary packaging) required. Must have expert knowledge of manufacturing and GMP QA requirements for a specific technical area. Proven ability to problem-solve on quality and supply assurance (including root cause identification and analysis, preventive actions and investigation) required. Ability to conduct knowledge transfer (including transfer of institutionalized knowledge, setting up formal structures, onboarding, convening communities of practice, ensuring access to expertise) required. Business level English must be strong both written and oral. Must be able to work cross functionally as a strong collaborator with ability to partner with internal and external stakeholders across multiple global regions. Proen abiity to use sound risk judgment to escalate issues when needed.
• Travel Requirements: Ability to travel up to 30% of the time globally. Requires flexibility of increased travel dependent on the level of frequency of manufacturing activities at a given CMO.

Company Information

Daiichi Sankyo, Inc. is an equal opportunity/affirmative action employer. Qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected veteran status, age, or any other characteristic protected by law.

Salary Range: USD$226,275.00 - USD$377,125.00