Senior Product Development Engineer II

Position Overview Product Development Engineer – Tissue Technologies. Reports to the Senior Director, R&D. Responsible for leading the Design Control process and managing the development, validation, and commercialization of medical devices across synthetic, xenograft, and allograft platforms. Responsibilities Understand and apply the basic principles of Design Controls. Lead and manage the Design Control process for medical device products. Assist with exploratory research and identification of new products. Use expertise to improve operational efficiencies and meet compliance requirements. Present data interpretation and recommendations at in‑house meetings. Summarize, interpret, and review data; draw conclusions; independently propose next steps. Manage processes and ensure that goals are achieved. Serve as a team leader and/or mentor junior professionals. Advises project team on resources needed for the scientific project. Collaborate with Manufacturing to transfer developmental products into manufacturing, sharing responsibility for Verification & Validation. Work with external vendors, consultants, and collaborators to facilitate project work. Interact with customers to assure design requirements are established and met. Specify and execute project work with a small team and prepare Quality System‑compliant documents for equipment, processes, product specifications, etc. Develop strategies and plans of execution using scientific knowledge to derive unique, cost‑effective solutions. Assist in planning and execution of safety and performance testing consistent with regulatory and clinical requirements. Establish priorities, checkpoints, and timelines for experimental work to support project objectives. Apply broad scientific knowledge and demonstrate high technical proficiency in own field. Demonstrate reasonable knowledge/expertise outside of own field. Employ interpersonal, communication, and negotiation skills with all personnel levels to facilitate information flow. Qualifications Bachelor’s degree with 8+ years of experience, Master’s degree with 5+ years, or Doctoral with 3+ years of experience, or equivalent education and experience. Minimum 4 years in the development of medical devices. Fully competent engineer in conventional aspects of the field and assignments. Hands‑on worker with secondary responsibility for instruction or supervision of others. Recognized leader within the team, manages and/or coordinates programs within the function. Strong interpersonal and organizational skills; multitasking capability; computer literate; independent work ability. Tools & Equipment Utilizes a computer, telephone, smartphone, and general office equipment. Strong computer skills are required. Physical Requirements Must be able to sit, listen, speak, write/type, and move throughout a manufacturing facility; may need to lift up to 25 pounds; may travel domestically and internationally by car or airplane as needed. EEO Statement Integra LifeSciences is an equal opportunity employer, committed to providing equal employment opportunities to all qualified applicants and employees regardless of race, marital status, color, religion, sex, age, national origin, sexual orientation, disability, or protected veteran status. The company provides reasonable accommodations for qualified individuals with disabilities in accordance with the ADA. #J-18808-Ljbffr INTEGRA LIFESCIENCES CORP