Senior Manager, Clinical Product Supply Quality Assurance

Role: Senior Manager, Clinical Product Supply Quality Assurance, providing strategic QA leadership for AbbVie's clinical development pipeline. Responsibilities include overseeing quality strategy, risk management, and compliance for clinical supplies from drug substance to finished product, ensuring timely and high-quality delivery aligned with development milestones and regulatory standards. The role involves representing QA on cross-functional CMC teams, managing supply and manufacturing risks, facilitating integration activities such as licensing and external partnerships, and supporting due diligence assessments. Additional duties encompass overseeing investigations, deviations, product recalls, and inspection readiness, as well as influencing decision-making to mitigate compliance and supply risks while maintaining timelines. Requirements: Bachelor's degree in life sciences, chemistry, biology, engineering, or related field; 8+ years in Quality Assurance or pharmaceutical manufacturing, with experience supporting clinical supply, GMP compliance, and regulatory interactions. Preferred qualifications include advanced degrees, project management certification, and experience with global GMP requirements, due diligence, and external collaborations. The candidate should demonstrate strong strategic, communication, and influencing skills, with the ability to operate effectively across global teams. This hybrid role is based in North Chicago, IL; Worcester, MA; Irvine, CA; or San Francisco, CA.