
1001 - 5000 employees
π Pharmaceuticals
π₯ Healthcare
𧬠Biotechnology
Pharmaceuticals β’ Healthcare β’ Biotechnology
Otsuka Pharmaceutical Companies (U. S. ) is a prominent player in the pharmaceutical manufacturing industry, dedicated to creating innovative products for better health worldwide. The company comprises two main entities: Otsuka America Pharmaceutical, Inc. (OAPI), which is focused on commercializing Otsuka-discovered and in-licensed products in North America, and Otsuka Pharmaceutical Development & Commercialization, Inc. (OPDC), which specializes in the clinical development and global registration of innovative healthcare solutions, particularly in the field of neuroscience.
π₯ 1 minute ago
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1001 - 5000 employees
π Pharmaceuticals
π₯ Healthcare
𧬠Biotechnology
Pharmaceuticals β’ Healthcare β’ Biotechnology
Otsuka Pharmaceutical Companies (U. S. ) is a prominent player in the pharmaceutical manufacturing industry, dedicated to creating innovative products for better health worldwide. The company comprises two main entities: Otsuka America Pharmaceutical, Inc. (OAPI), which is focused on commercializing Otsuka-discovered and in-licensed products in North America, and Otsuka Pharmaceutical Development & Commercialization, Inc. (OPDC), which specializes in the clinical development and global registration of innovative healthcare solutions, particularly in the field of neuroscience.
β’ Lead execution of supplier quality management strategies β’ Assist with supplier management activities (qualification, audits, risk management, compliance oversight) β’ Oversee supplier performance oversight activities (KPIs, supplier scorecards, governance) β’ Manage critical supplier relationships and drive continuous improvement initiatives β’ Develop supplier quality metrics and provide management-level insights regarding supplier quality performance
β’ Bachelorβs degree in a scientific, engineering, or health-related discipline (e.g., Chemistry, Biology, Pharmacy, etc.) required β’ Advanced degree (MS, MBA) preferred β’ Minimum of 8 years of progressive experience within the pharmaceutical, biopharmaceutical, or medical device industry β’ Minimum of 5 years of direct managerial experience managing, developing, and evaluating quality professionals in a global or matrixed environment β’ Hands-on experience with TrackWise Digital strictly required β’ Knowledge of global GxP regulations (FDA 21 CFR 210/211/11, EU GMP, EudraLex Volume 4, ICH guidelines Q7, Q9, Q10) β’ Certification or proven track record exhibiting lead auditor capabilities β’ Advanced analytical capabilities β’ Exceptional communication skills β’ Demonstrated conflict resolution & negotiation abilities
β’ Comprehensive medical, dental, vision, prescription drug coverage β’ Company provided basic life, accidental death & dismemberment β’ Short-term and long-term disability insurance β’ Tuition reimbursement β’ Student loan assistance β’ A generous 401(k) match β’ Flexible time off β’ Paid holidays β’ Paid leave programs as well as other company provided benefits
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