
1001 - 5000 Mitarbeiter
💊 Pharmazie
🏥 Gesundheitswesen
🧬 Biotechnologie
Pharmaceuticals • Healthcare • Biotechnology
Die Otsuka Pharmaceutical Companies (U. S. ) sind ein bedeutender Akteur in der Pharmaindustrie und widmen sich der Entwicklung innovativer Produkte für eine bessere Gesundheit weltweit. Das Unternehmen besteht aus zwei Hauptgesellschaften: Otsuka America Pharmaceutical, Inc. (OAPI), die auf die Vermarktung von Otsuka-entdeckten und lizenzierten Produkten in Nordamerika spezialisiert ist, und Otsuka Pharmaceutical Development & Commercialization, Inc. (OPDC), die sich auf die klinische Entwicklung und globale Zulassung innovativer Gesundheitslösungen, insbesondere im Bereich der Neurowissenschaften, konzentriert.
🕒 vor 1 Monat
🇺🇸 Vereinigte Staaten – Remote
💵 $249.973 - $388.125 / Jahr
⏰ Vollzeit
🔴 Experte
👔 Direktor
👻 Geisterscore 2%
🗣️🇺🇸🇬🇧 Englisch erforderlich
Woher diese Stelle stammt
Veröffentlicht auf der Karriereseite von Otsuka Pharmaceutical Companies (U.S.), nicht über eine Jobbörse
Von Remote Rocketship zum ersten Mal gesehen vor 1 Monat
Noch offen auf der Website von Otsuka Pharmaceutical Companies (U.S.). Geprüft vor 10 Stunden.

1001 - 5000 Mitarbeiter
💊 Pharmazie
🏥 Gesundheitswesen
🧬 Biotechnologie
Pharmaceuticals • Healthcare • Biotechnology
Die Otsuka Pharmaceutical Companies (U. S. ) sind ein bedeutender Akteur in der Pharmaindustrie und widmen sich der Entwicklung innovativer Produkte für eine bessere Gesundheit weltweit. Das Unternehmen besteht aus zwei Hauptgesellschaften: Otsuka America Pharmaceutical, Inc. (OAPI), die auf die Vermarktung von Otsuka-entdeckten und lizenzierten Produkten in Nordamerika spezialisiert ist, und Otsuka Pharmaceutical Development & Commercialization, Inc. (OPDC), die sich auf die klinische Entwicklung und globale Zulassung innovativer Gesundheitslösungen, insbesondere im Bereich der Neurowissenschaften, konzentriert.
• Lead a global team focused on R&D Quality • Ensure OAPI, OPDC, and affiliates are inspection ready • Oversee clinical trial and submission support • Lead the R&D audit program • Engage with regulatory authorities • Maintain clinical data integrity • Provide vision, guidance, strategic direction, and leadership for R&D Global Quality and the Global Quality function • Partner with business groups and global regions to assure end-to-end Quality and harmonize processes • Identify and mitigate Quality risks from development through commercial registration and product distribution • Inspire and develop Quality professionals and partner with key stakeholders • Ensure internal and external sites are inspection ready and provide resources during health authority inspections • Ensure findings are appropriately addressed and CAPAs are implemented and checked for effectiveness • Analyze findings and assess systemic trends • Lead clinical facility and system audits at facilities, investigator sites, and vendors • Establish standards and implement quality-management and compliance procedures • Report Quality Systems and Risks to Senior Management through Management Review • Ensure continuous inspection readiness across clinical trial sites and clinical and Pharmacovigilance operations • Oversee planning, execution, and follow-up of internal and external audits • Act as primary liaison with regulatory authorities • Ensure accuracy, consistency, and reliability of clinical and PV data • Lead, mentor, and develop QA professionals • Collaborate with stakeholders to align QA activities with business and regulatory requirements • Develop, implement, and maintain policies, systems, and procedures for quality and compliance • Lead systems for clinical vendor management and vendor oversight • Establish and maintain R&D Management Reviews • Develop and manage departmental budgets
• Bachelor’s degree and 15+ years of experience in a FDA regulated pharmaceutical and/or medical device industry environment • Strong knowledge of current global Good Clinical Practice (GCP) • Current and in-depth knowledge of audit techniques and government regulatory inspection procedures • Experience and successful interaction within a Japanese company, or a multinational with a Japanese arm • Previous experience working in the global pharmaceutical and medical device industry • Experience working with external service providers • Working knowledge of current Good Manufacturing Practice (cGMP) regulations • Strong project management, leadership, problem-solving, and organizational skills • High level of emotional intelligence • Exceptional leadership and team development skills • Excellent communication and interpersonal skills • Ability to work collaboratively with cross-functional teams • Strategic thinking and problem-solving abilities • Approximately 30% travel
• Incentive opportunity • Comprehensive medical coverage • Dental coverage • Vision coverage • Prescription drug coverage • Company-provided basic life insurance • Accidental death & dismemberment insurance • Short-term disability insurance • Long-term disability insurance • Tuition reimbursement • Student loan assistance • Generous 401(k) match • Flexible time off • Paid holidays • Paid leave programs • Other company-provided benefits
Jetzt BewerbenVerbessern Sie Ihre Chancen auf ein Vorstellungsgespräch, indem Sie Ihre Lebenslauf-Bewertung vor der Bewerbung überprüfen.
🕒 vor 1 Monat
Director leading APX project development for Westinghouse, a global nuclear energy solutions company. Driving federal customer growth, sales strategy, contracts, and executive government relationships.
🗣️🇺🇸🇬🇧 Englisch erforderlich
🕒 vor 1 Monat
Government affairs director shaping AstraZeneca’s pharmaceutical policy, reputation, and patient access across NY, NJ, and PA. Leading lobbying, payer policy, community engagement, and health equity initiatives.
🇺🇸 Vereinigte Staaten – Remote
💰 Post-IPO Debt im 2023-02
⏰ Vollzeit
🔴 Experte
👔 Direktor
🦅 H1B-Visum-Sponsor
🗣️🇺🇸🇬🇧 Englisch erforderlich
🕒 vor 1 Monat
Director growing Logic20/20’s utility consulting practice through client relationships, business development, and team building. Providing executive oversight for business and technology transformation engagements.
🗣️🇺🇸🇬🇧 Englisch erforderlich
🕒 vor 1 Monat
National Channel Director expanding Command|Link’s SaaS, network, voice, and IT security solutions through channel partners. Driving business development, partner enablement, and regional sales growth.
🗣️🇺🇸🇬🇧 Englisch erforderlich
🕒 vor 1 Monat
Clinical Development Director leading first-in-human and Phase 1 strategy for Enveda’s AI-enabled medicines. Advancing novel therapies across metabolism and autoimmune disease.
🇺🇸 Vereinigte Staaten – Remote
💵 $330.000 - $370.000 / Jahr
💰 €150.000.000 Series D - Enveda Biosciences im 2025-09
⏰ Vollzeit
🔴 Experte
👔 Direktor
🦅 H1B-Visum-Sponsor
🗣️🇺🇸🇬🇧 Englisch erforderlich