Job Description Reporting to the Director of Combination Product Development, the Associate Director - Device Development is the technical expert in the field of combination products & drug delivery devices who can effectively navigate and balance complex engineering, regulatory, quality and commercial needs while developing the best product for the user and patient. You are responsible for the creation and management of design history files and technical dossiers for combination and device projects for new and existing products. Additional responsibilities include facilitation of risk assessments, coordination of human factors usability studies, creation and management of product and component specifications, design control documents, engineering protocols and reports and frequent presentations to project teams and management. This position will frequently require management of outside resources as well as assigned and/or unassigned leadership of project teams in a matrix organization. Support the vision for the Device Development & Technology function: Support and implement a vision with appropriate strategies that supports the OPDC objectives and aligns with the business and OPCJ/OPDC/MDD development programs. Work with the Director of Device Development and other functions including Packaging, Supply Chain, Clinical Supplies Operations, Quality Control, and Quality Management to support strategies for product and process improvements. Support the development of flexible and compliant product development process. Develop and support the strategic activities of the department: Support and implement appropriate filing strategies working with OPCJ, OPDC, MDD and OAPI departments to support registration of all new products and life-cycle management products. Initiate and manage the development and implementation of policies, procedures, and standards for the Device Technology department. Evaluate and recommend strategic directions for new and innovative delivery device technologies to support new and life-cycle management projects. Develop and perform the tactical activities: Ensure efficient transfer of products and on-going product support all products to CMO's from device perspective. Develop and maintain departmental knowledge, experience, and expertise in state-of-the-art devices for pharmaceutical products. Assure adherence to latest worldwide regulatory rules and guidance concerning devices and work to develop device risk mitigation. Create, maintain, and update device related documents required for regulatory filings and compliance Facilitate studies as required. Write protocols, reports, specifications, procedures, change control requests, technical assessments, etc. Program management of Device projects: Develop project plans and corresponding project managements tools to support the execution of all projects Manage cross functional teams (including 3rd party resources). Execute Human Factors Engineering & Usability activities. Qualifications/ Required Knowledge/ Experience and Skills: This position requires 6-10 years of applicable experience in the pharmaceutical, biotechnology or medical device industries. Primary expertise should be demonstrated in engineering, device regulatory, device quality systems (cfr 820, ISO 13485), human factors engineering principals, risk management for medical devices (ISO 14971), etc. You should demonstrate strong technical writing and presentation skills and be able to translate technical information to non-technical audiences. Demonstrated leadership skills especially the management of high-visibility project teams. Demonstrated knowledge of parenteral delivery devices (syringes, self/ or auto-injectors), etc. In-depth understanding of device verification including functional testing, process validation/verification, quality assurance, and regulatory requirements as they pertain to and devices. Ability to work strategically and independently with internal and external groups on multiple projects. Excellent written and verbal communication skills with demonstrated ability to establish and maintain effective communications internally and with external manufacturing partners. Competency in use of business and project management computer software (such as MSProject and MSOffice). Travel (approximately 20 - 25%) Educational Qualifications Bachelor's degree in a related Engineering discipline (Mechanical, Electrical, Biomedical, etc.) Masters or advanced degree preferred Competencies Accountability for Results - Stay focused on key strategic objectives, be accountable for high standards of performance, and take an active role in leading change. Strategic Thinking & Problem Solving - Make decisions considering the long-term impact to customers, patients, employees, and the business. Patient & Customer Centricity - Maintain an ongoing focus on the needs of our customers and/or key stakeholders. Impactful Communication - Communicate with logic, clarity, and respect. Influence at all levels to achieve the best results for Otsuka. Respectful Collaboration - Seek and value others' perspectives and strive for diverse partnerships to enhance work toward common goals. Empowered Development - Play an active role in professional development as a business imperative. Come discover more about Otsuka and our benefit offerings; https://www.otsuka-us.com/careers-join-otsuka . Disclaimer: This job description is intended to describe the general nature and level of the work being performed by the people assigned to this position. It is not intended to include every job duty and responsibility specific to the position. Otsuka reserves the right to amend and change responsibilities to meet business and organizational needs as necessary. Otsuka is an equal opportunity employer . All qualified applicants are encouraged to apply and will be given consideration for employment without regard to race, color, sex, gender identity or gender expression, sexual orientation, age, disability, religion, national origin, veteran status, marital status, or any other legally protected characteristic . 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