Associate Director, Global Product Quality

Associate Director, Global Product Quality - BiologicsThe Associate Director, Global Product Quality - Biologics is responsible for directing quality oversight of clinical and commercial products at CMOs under contract by Otsuka to ensure that they are manufactured, packed, labelled, stored, and transported in a controlled way that is in accordance with regulatory expectations and applicable cGMP/GDP quality standards. This role will direct Biologics Quality Assurance support, including oversight of upstream and downstream biologics manufacturing processes, ensuring compliance with biologics-specific GMP requirements. This role has global responsibility for directing clinical and commercial product quality to ensure global supply for Otsuka's patients. This role will also work collaboratively with other functional departments across Otsuka Affiliates and Subsidiaries to maintain the effectiveness of the Otsuka Quality Systems that support OPDC-sponsored clinical studies as well as drive continuous improvement.Responsibilities include:Developing comprehensive quality strategies for complex biologic development programs that address unique manufacturing challenges.Establishing and maintaining the effectiveness of quality systems for managing the batch record review and release process.Transforming biologic manufacturing quality challenges through innovative approaches that maintain product integrity while optimizing operational efficiency.Working collaboratively within the Global Quality Dept. and other functions within OAPI and OPDC to assure compliance and continuous improvement.Managing reports and trends to the Management Representative to help in the preparation of management reviews and/or other ad hoc reporting requests.Establishing and maintaining standard operating procedures, work instructions, forms, templates, and other documents associated with the systems noted above.Improving supplier quality performance for batch record review and release process for OAPI GMP release of contract manufacturers operations supporting clinical and commercial products.Representing global quality during execution of product technical transfer activities to ensure all aspects of the transfer are conducted per cGMP.Assisting in conducting audits of contract manufacturers/laboratories (as part of an audit team) to ensure compliance with OAPI and OPDC requirements as well as applicable regulatory requirements.Responsible for reviewing, drafting, and augmenting existing quality agreements with external service providers to assure that full compliance and best practices are communicated and continuously met.Serving as a global quality product champion with a focus on ensuring the quality of our biologics products, monitoring, and escalation of any situations with potential negative impacts on clinical study supplies, supply chain for commercial products, or patient safety.Qualifications:Required: Bachelor's degree in Chemistry, Biology or other Physical Sciences. Ten years of combined and/or pharmaceutical manufacturing, QA or QC assurance roles managing and directing quality oversight of commercial product and development project activities. Seven years of product quality experience performing batch review and release activities of suppliers or contract manufacturers or equivalent preferred supporting commercial products and/or development projects. Proven experience with biologics GMP manufacturing, including upstream (cell culture, bioreactors) and downstream (purification, filtration, formulation) processes. Expertise in conducting root cause investigations and driving CAPA implementation. Ability to supervise multiple direct reports and projects in a fast-paced environment. Demonstrated success in working on and leading cross functional teams. Experience with Pre Approval Inspections for NDAs and BLAs. Experience in driving continuous improvement projects. TrackWise Experience. Excellent interpersonal and communication skills. Position requires approximately 20% domestic travel; occasional international travel may also be expected.Preferred: Advanced degree in Biology or other Physical Sciences. Experience with quality oversight of controlled substances.Competencies:Accountability for Results - Stay focused on key strategic objectives, be accountable for high standards of performance, and take an active role in leading change.Strategic Thinking & Problem Solving - Make decisions considering the long-term impact to customers, patients, employees, and the business.Patient & Customer Centricity - Maintain an ongoing focus on the needs of our customers and/or key stakeholders.Impactful Communication - Communicate with logic, clarity, and respect. Influence at all levels to achieve the best results for Otsuka.Respectful Collaboration - Seek and value others' perspectives and strive for diverse partnerships to enhance work toward common goals.Empowered Development - Play an active role in professional development as a business imperative.Salary: Minimum $146,955.00 - Maximum $219,650.00, plus incentive opportunity: The range shown represents a typical pay range or starting pay for individuals who are hired in the role to perform in the United States. Other elements may be used to determine actual pay such as the candidate's job experience, specific skills, and comparison to internal incumbents currently in role. Typically, actual pay will be positioned within the established range, rather than at its minimum or maximum. This information is provided to applicants in accordance with states and local laws.Company benefits include comprehensive medical, dental, vision, prescription drug coverage, company provided basic life, accidental death & dismemberment, short-term and long-term disability insurance, tuition reimbursement, student loan assistance, a generous 401(k) match, flexible time off, paid holidays, and paid leave programs as well as other company-provided benefits.Otsuka is an equal opportunity employer. All qualified applicants are encouraged to apply and will be given consideration for employment without regard to race, color, sex, gender identity or gender expression, sexual orientation, age, disability, religion, national origin, veteran status, marital status, or any other legally protected characteristic. If you are a qualified individual with a disability or a disabled veteran, you may request a reasonable accommodation, if you are unable or limited in your ability to apply to this job opening as a result of your disability. You can request reasonable accommodations by contacting Accommodation Request (EEAccommodations@otsuka-us.com).Statement Regarding Job Recruiting Fraud Scams: At Otsuka we take security and protection of your personal information very seriously. Please be aware individuals may approach you and falsely present themselves as our employees or representatives. They may use this false pretense to try to gain access to your personal information or acquire money from you by offering fictitious employment opportunities purportedly on our behalf. Please understand, Otsuka will never ask for financial information of any kind or for payment of money during the job application process. 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