Associate Director, Global Product Quality

divh2Associate Director, Global Product Quality - Biologics/h2pThe 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 Otsukas 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./ph3Job Description/h3pResponsible for directing quality oversight of GMP contract manufacturers of Otsuka clinical and commercial products./ppDevelops comprehensive quality strategies for complex biologic development programs that address unique manufacturing challenges./ppEstablishes and maintain the effectiveness of Quality Systems for managing the batch record review and release process Quality Management Activities supporting all phases of clinical development as well as Commercial Product (API, drug product, and final finished product)./ppTransforms biologic manufacturing quality challenges through innovative approaches that maintain product integrity while optimizing operational efficiency./ppWorks collaboratively within the Global Quality Dept. and other functions within OAPI and OPDC to assure Compliance to ensure continuous improvement and compliance./ppManages reports and trends to the Management Representative to help in the preparation of Management reviews and/or other ad hoc reporting requests./ppEstablishes and maintains Standard Operating Procedures, work instructions, forms, templates and other documents associated with the systems noted above./ppImproves supplier quality performance for batch record review and release process for OAPI GMP release of Contract Manufacturers operations supporting clinical and commercial products./ppInterfaces with Contract Manufacturers/Laboratories, Tech Ops, Technical Services and Supply Chain Sourcing to drive Quality improvements that minimize the Costs of Quality, specifically component, materials or finished product deviations, OOS incidents, rejects, etc./ppRepresents global quality during execution of product technical transfer activities to ensure all aspects of the transfer are conducted per cGMP./ppAssists 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./ppResponsible for reviewing, drafting, and augmenting existing Quality agreements with external service providers to assure that full compliance and best practices as identified by Otsuka are communicated and continuously met./ppServes 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./ph3Qualifications/h3pRequired:/ppBachelors degree in Chemistry, Biology or other Physical Sciences./ppTen years of combined and/or pharmaceutical manufacturing, QA or QC assurance roles managing and directing quality oversight of commercial product and development project activities./ppSeven 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./ppProven experience with biologics GMP manufacturing, including upstream (cell culture, bioreactors) and downstream (purification, filtration, formulation) processes./ppExpertise in conducting root cause investigations and driving CAPA implementation./ppAbility to supervise multiple direct reports and projects in a fast-paced environment./ppDemonstrated success in working on and leading cross-functional teams./ppExperience with Pre Approval Inspections for NDAs and BLAs./ppExperience in driving continuous improvement projects./ppTrackWise Experience./ppExcellent interpersonal and communication skills./ppPosition requires approximately 20% domestic travel; Occasional international travel may also be expected./ppPreferred:/ppAdvanced degree in Biology or other Physical Sciences./ppExperience with quality oversight of controlled substances./ph3Competencies/h3pAccountability for Results - Stay focused on key strategic objectives, be accountable for high standards of performance, and take an active role in leading change./ppStrategic Thinking Problem Solving - Make decisions considering the long-term impact to customers, patients, employees, and the business./ppPatient Customer Centricity - Maintain an ongoing focus on the needs of our customers and/or key stakeholders./ppImpactful Communication - Communicate with logic, clarity, and respect. Influence at all levels to achieve the best results for Otsuka./ppRespectful Collaboration - Seek and value others perspectives and strive for diverse partnerships to enhance work toward common goals./ppEmpowered Development - Play an active role in professional development as a business imperative./ppSalary: 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 candidates 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./ppCompany benefits: 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./ppOtsuka 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)./ppStatement 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. We do not require any financial, credit card or bank account information and/or any payment of any kind to be considered for employment. We will also not offer you money to buy equipment, software, or for any other purpose during the job application process. If you are being asked to pay or offered money for equipment fees or some other application processing fee, even if claimed you will be reimbursed, this is not Otsuka. These claims are fraudulent and you are strongly advised to exercise caution when you receive such an offer of employment. Otsuka will also never ask you to download a third-party application in order to communicate about a legitimate job opportunity. Scammers may also send offers or claims from a fake email address or from Yahoo, Gmail, Hotmail, etc, and not from an official Otsuka email address. Please take extra caution while examining such an email address, as the scammers may misspell an official Otsuka email address and use a slightly modified version duplicating letters. To ensure that you are communicating about a legitimate job opportunity at Otsuka, please only deal directly with Otsuka through its official Otsuka Career website https://vhr-otsuka.wd1.myworkdayjobs.com/en-US/External. Otsuka will not be held liable or responsible for any claims, losses, damages or expenses resulting from job recruiting scams. If you suspect a position is fraudulent, please contact Otsukas call center at: 800-363-5670. If you believe you are the victim of fraud resulting from a job recruiting scam, please contact the FBI through the Internet Crime Complaint Center at: https://www.ic3.gov, or your local authorities./p/div