
1001 - 5000 funcionários
💊 Farmacêutico
🏥 Saúde
🧬 Biotecnologia
Pharmaceuticals • Healthcare • Biotechnology
As Empresas Farmacêuticas Otsuka (EUA) são um ator proeminente na indústria de fabricação farmacêutica, dedicadas a criar produtos inovadores para uma melhor saúde em todo o mundo. A empresa é composta por duas entidades principais: a Otsuka America Pharmaceutical, Inc. (OAPI), que se concentra na comercialização de produtos descobertos e licenciados pela Otsuka na América do Norte, e a Otsuka Pharmaceutical Development & Commercialization, Inc. (OPDC), que é especializada no desenvolvimento clínico e registro global de soluções inovadoras em saúde, particularmente na área de neurociências.
🕒 Julho 23
🗣️🇺🇸🇬🇧 Inglês obrigatório
Melhore suas chances de conseguir uma entrevista verificando sua pontuação de currículo antes de se candidatar.

1001 - 5000 funcionários
💊 Farmacêutico
🏥 Saúde
🧬 Biotecnologia
Pharmaceuticals • Healthcare • Biotechnology
As Empresas Farmacêuticas Otsuka (EUA) são um ator proeminente na indústria de fabricação farmacêutica, dedicadas a criar produtos inovadores para uma melhor saúde em todo o mundo. A empresa é composta por duas entidades principais: a Otsuka America Pharmaceutical, Inc. (OAPI), que se concentra na comercialização de produtos descobertos e licenciados pela Otsuka na América do Norte, e a Otsuka Pharmaceutical Development & Commercialization, Inc. (OPDC), que é especializada no desenvolvimento clínico e registro global de soluções inovadoras em saúde, particularmente na área de neurociências.
• Serve as the central point of contact and business partner for CDMOs, ensuring alignment between partner actions and company goals • Contract Negotiation to structure agreements, manage terms, and collaborate with legal and internal stakeholders • Standardize Governance and Business Review structure with CDMO executive leadership to ensure long-term collaboration • Define, set, and monitor key performance indicators (KPIs) to hold CDMOs accountable for delivery and quality • Support comprehensive risk assessments focused on stable supply chains and quality assurance at partner sites • Facilitate discussions and drive the implementation of improvement measures based on KPI performance data and identified risks • Conduct business-side assessments during GMP audits led by the Quality Team to ensure commercial and operational viability • Support the internal decision-making process regarding new CDMO selections and major capital investments • Act as the lead for cross-departmental coordination when major incidents occur • Collaborate with internal departments to identify supply risks stemming from regulatory shifts, demand volatility, or manufacturing deviations, and lead the execution of countermeasures at the CDMO level
• Bachelor’s degree in Science, Engineering, Business, or a related field (MBA or advanced degree preferred) • 8–12+ years of experience in alliance management, strategic sourcing, or external manufacturing within the pharmaceutical or biotech industry • Proven ability to influence and collaborate with cross-functional stakeholders in a complex, matrixed organization • Strong background in risk management, business continuity planning, and performance analytics (KPIs) • Exceptional negotiation and communication skills • Knowledge of CDMO landscape and manufacturing processes across one or multiple modalities (e.g., small molecule, biologics, sterile fill-finish, etc.) • Thorough knowledge of GMPs (CFR title 21, parts 210-211 and Part 600), along with EU, MHRA and other global health authority regulations • Strong, proven supplier relationship management skills • Negotiation and contract management skills a plus
• 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 • Paid leave programs as well as other company provided benefits
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