The Director of Product & Pipeline Communications at Otsuka will lead communications for marketed products and late-stage pipeline candidates. Responsibilities include developing communication strategies, coordinating with global teams, overseeing PR agencies, and evaluating communications effectiveness. The role requires strong skills in written communication, analytical thinking, and an understanding of the healthcare industry.

The Senior Manager of Catalog Management oversees supplier catalogs on the SAP Ariba platform, ensuring data accuracy and compliance with procurement policies. They collaborate with suppliers, support procurement teams, and optimize catalog processes while also handling data audits and user training.

The Director, Corporate Counsel will provide legal expertise in employment law, corporate governance, and litigation management. This role includes developing legal strategies, ensuring compliance with laws affecting operations, and collaborating with senior leadership on policy implementation.

The Associate Director of HCP Engagement Operations will lead and optimize HCP engagement processes, ensuring compliance with regulations while managing relationships with third-party service providers. They will oversee operational activities including documentation, payment processes, and reporting, as well as providing strategic direction and continuous improvement initiatives.

The Regional Sales Manager will lead a cross-functional team to develop and execute a strategy that enhances customer satisfaction and improves patient care. Responsibilities include driving commercial strategy, managing relationships within the healthcare ecosystem, and fostering a collaborative, patient-centric culture to meet performance targets.

As a Quality Risk Management Intern at Otsuka, you will support the establishment of a standard risk management framework, assess current practices, research industry standards, and help create risk management templates. You'll work closely with experienced professionals while gaining hands-on experience in the pharmaceutical industry.

The internship focuses on developing a future-ready workforce within the Global Quality organization at Otsuka. Interns will collaborate with leadership to standardize learning and development plans, assess training needs, and create role-based curricula in the pharmaceutical industry.

The Supplier Assurance Specialist at Otsuka Pharmaceutical Europe will manage the quality system to ensure compliance with regulations. Responsibilities include performing GxP audits, maintaining supplier quality, preparing GMP documentation, and supporting various quality initiatives. The role requires collaboration with suppliers and participation in internal and regulatory audits.

The Associate Director, Promotion Compliance will oversee the review, revision, and approval of promotional labeling for pharmaceuticals and medical devices. They will ensure compliance with regulatory standards, provide training, communicate with regulatory bodies, and manage contracts and policies related to promotional materials.

The Cloud Engineer will manage public cloud environments (AWS, Azure, Oracle), focusing on automation and compliance. Responsibilities include developing automation scripts, ensuring security standards, managing audits, integrating directory services, and overseeing containerized applications. Strong communication skills are essential for stakeholder interactions.

The Director of Quantitative Pharmacology, Pharmacometrics leads all pharmacometrics activities for clinical projects, overseeing study design, analysis, and reporting. Responsibilities include managing pharmacometrics activities, authoring submission documents, and collaborating with development teams for regulatory filings and pediatric development plans.

The Associate Director of Quality Control for Biologics will manage analytical method development and oversee quality control testing of biologic products. Responsibilities include compliance with regulatory guidelines, leading pharmaceutical stability studies, developing technical documentation, and managing project budgets while collaborating with cross-functional teams and training staff.

The Director of IT Strategic Sourcing oversees the Sourcing process for IT category spend, partners with IT leadership for value optimization, and ensures compliance with sourcing policies. Responsibilities include managing vendor relationships, leading contract negotiations, identifying cost-saving opportunities, and mentoring the sourcing team to achieve operational excellence.

The Associate will support financial transparency reporting by collecting and validating data, managing data quality errors, and ensuring compliance with regulations. Responsibilities include data analysis, collaboration with stakeholders, monitoring financial transparency trends, and assisting with reporting and process improvements.

The Director of Commercial Advanced Analytics will generate and deliver data-driven insights to support strategic decisions across brands and therapeutic areas, utilizing advanced statistical analysis and machine learning methods. Responsibilities include leading the interpretation of AI/ML models, collaborating with diverse stakeholders, and enhancing data science capabilities to drive business impact.

The Associate Director for Combination Product Development will lead the design and management of combination products while balancing engineering, regulatory, and quality needs. Responsibilities include managing design history files, facilitating risk assessments, ensuring compliance, and developing tactical and strategic activities in conjunction with various departments. This role requires strong leadership and communication skills to manage projects and teams effectively.

The Senior Manager of Legal Operations will lead and improve the legal department's operational culture by implementing process and technology improvements. Key responsibilities include project management, data analysis, and cross-functional collaboration to enhance the efficiency and effectiveness of legal workflows and operations.

In this role, the Associate Director, Payer Analytics will provide actionable insights by leveraging advanced statistical techniques to support drug development and commercial insights. The position involves managing teams, leading analytics on contracting, communicating findings to stakeholders, and collaborating across market access, marketing, and sales teams.

The Senior Director of Public Policy will lead Otsuka's public policy agenda, ensuring alignment with strategic goals. Responsibilities include developing policy strategies, collaborating across departments, engaging with key healthcare policy leaders, and managing a public policy team while fostering relationships with trade organizations.

The Sr Manager, Global Product Quality - API/DP oversees quality management of clinical and commercial pharmaceutical products. Responsibilities include quality oversight of contract manufacturers, reviewing batch records, managing audits, and collaborating with multiple departments to ensure compliance with regulatory requirements. They maintain quality metrics to drive continuous improvement and write standard operating procedures.