
1001 - 5000 employés
💊 Pharmaceutique
🏥 Santé
🧬 Biotechnologie
Pharmaceuticals • Healthcare • Biotechnology
Les Entreprises Pharmaceutiques Otsuka (États-Unis) sont un acteur de premier plan dans l'industrie de la fabrication pharmaceutique, dédiées à la création de produits innovants pour améliorer la santé mondiale. La société se compose de deux entités principales : Otsuka America Pharmaceutical, Inc. (OAPI), qui se concentre sur la commercialisation des produits découverts par Otsuka et sous licence en Amérique du Nord, et Otsuka Pharmaceutical Development & Commercialization, Inc. (OPDC), spécialisée dans le développement clinique et l'enregistrement mondial de solutions de santé innovantes, particulièrement dans le domaine des neurosciences.
🕒 il y a 11 jours
🇺🇸 États-Unis – Télétravail
💵 $169 222 - $253 000 / an
⏰ Temps Plein
🟠 Senior
👔 Directeur
👻 Score fantôme 0%
🗣️🇺🇸🇬🇧 Anglais requis
Améliorez vos chances d'obtenir un entretien en vérifiant votre score de CV avant de postuler.

1001 - 5000 employés
💊 Pharmaceutique
🏥 Santé
🧬 Biotechnologie
Pharmaceuticals • Healthcare • Biotechnology
Les Entreprises Pharmaceutiques Otsuka (États-Unis) sont un acteur de premier plan dans l'industrie de la fabrication pharmaceutique, dédiées à la création de produits innovants pour améliorer la santé mondiale. La société se compose de deux entités principales : Otsuka America Pharmaceutical, Inc. (OAPI), qui se concentre sur la commercialisation des produits découverts par Otsuka et sous licence en Amérique du Nord, et Otsuka Pharmaceutical Development & Commercialization, Inc. (OPDC), spécialisée dans le développement clinique et l'enregistrement mondial de solutions de santé innovantes, particulièrement dans le domaine des neurosciences.
• Provide strategic and scientific leadership for outsourced bioanalytical activities supporting clinical development programs • Oversee bioanalytical method development, qualification, validation, and sample analysis activities • Conduct scientific troubleshooting and optimization • Develop and maintain partnerships with bioanalytical CROs and external vendors • Monitor vendor performance and adherence to study timelines, quality standards, contractual obligations, and regulatory requirements • Ensure bioanalytical activities comply with global regulatory guidance and industry best practices • Serve as the bioanalytical subject matter expert on cross-functional project teams • Provide scientific recommendations and risk assessments to support decision making • Support regulatory submissions through submission-related documents, agency-question responses, and inspection-readiness activities • Evaluate emerging analytical technologies, biomarker strategies, and innovative measurement approaches • Drive continuous improvement, digital solutions, and operational efficiencies within bioanalysis
• Ph.D. with a minimum of 5 years of relevant industry experience in regulated bioanalysis; or M.S. or B.S. degree with a minimum of 8 years of relevant industry experience • Demonstrated expertise in regulated bioanalysis supporting clinical development, including pharmacokinetic and biomarker assays • Strong knowledge of global bioanalytical regulatory guidance and industry standards • Hands-on experience and understanding of LC-MS/MS, ELISA, ECL, flow cytometry, and other relevant platforms • Experience with immunogenicity assays, including anti-drug antibody (ADA) and neutralizing antibody (NAb) assays, is a plus • Experience managing CROs and external partnerships, including oversight of deliverables, budgets, timelines, quality, and compliance • Strong project management skills with the ability to prioritize and manage multiple complex programs simultaneously • Excellent verbal, written, and presentation skills • Ability to communicate complex scientific information effectively to technical and non-technical stakeholders • Demonstrated ability to work collaboratively in cross-functional teams and influence decision making
• Comprehensive medical, dental, vision, and prescription drug coverage • Company-provided basic life insurance • Accidental death and dismemberment insurance • Short-term and long-term disability insurance • Tuition reimbursement • Student loan assistance • Generous 401(k) match • Flexible time off • Paid holidays • Paid leave programs • Incentive opportunity
Postuler Maintenant🕒 il y a 11 jours
Senior Director leading ABB’s West US electrification service operations and nationwide digital controls center. Owning P&L, service execution, growth strategy, and multifunctional teams.
🇺🇸 États-Unis – Télétravail
💵 $163 500 - $261 600 / an
💰 €545 852 720 Post-IPO Debt - ABB en 2023-11
⏰ Temps Plein
🟠 Senior
👔 Directeur
🗣️🇺🇸🇬🇧 Anglais requis
🕒 il y a 11 jours
Associate Director guiding analytics transformation for Merkle’s data-driven marketing clients. Auditing digital ecosystems and developing AI, privacy, and MarTech roadmaps.
🗣️🇺🇸🇬🇧 Anglais requis
🕒 il y a 11 jours
Senior Director governing Oxford's global staffing vendor strategy, vendor economics, and nearshore/offshore operations. Building structured delivery programs, controls, and strategic partnerships across global supply channels.
🗣️🇺🇸🇬🇧 Anglais requis
🕒 il y a 11 jours
Senior Director leading Waters Corporation’s global service organization for analytical technologies and scientific instruments. Driving customer experience, service growth, operational excellence, and profitability across worldwide regions.
🗣️🇺🇸🇬🇧 Anglais requis
🕒 il y a 11 jours
Senior Director strengthening carrier partnerships for Trucordia’s nationwide insurance brokerage. Optimizing appointments, negotiations, profitability, and complex P&C insurance growth.
🗣️🇺🇸🇬🇧 Anglais requis