Director of Materials Science - MedTech Surgery

Company: Disability Solutions
Location: Raritan
Posted on: October 25, 2024

Job Description:

Johnson and Johnson MedTech Surgery is seeking a Director of Materials Science to support our entire Surgery portfolio of products. The preferred location for this role is Raritan, NJ however candidates within a commutable distance of Cincinnati, OH will also be considered. This role will work a Flex/Hybrid schedule; there is NO remote option for this role. Relocation assistance is available for qualified candidates.\rAbout Johnson & JohnsonAt Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com/.\rThe Director of Materials Science will lead the development and execution of materials assessments, including toxicological and biocompatibility evaluations and materials management for surgical medical device products. This role will be pivotal in building capabilities to accelerate innovation, ensuring product safety and regulatory compliance, guiding cross-functional teams in the integration of materials insights into product development. This position will report directly to the Global VP, R&D Ethicon.\rJob Responsibilities:

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• Strategic Leadership: Develop and implement robust toxicology and biocompatibility strategies aligned with business goals
• Innovation: Develop enhanced capabilities leveraging new technology to advance and accelerate materials assessments. Identify and implement new ways of working to accelerate speed to market and ability to predict risks
• Regulatory Engagement: Engage with regulatory authorities to shape materials requirements, and ensure compliance with local and international regulatory standards, including FDA, EMA, and ISO guidelines for toxicological assessments.
• Team Management: Lead, mentor, and develop a team of toxicologists, biocompatibility, and materials specialists, fostering a culture of scientific excellence, continuous learning and inclusion
• Risk Assessment: Oversee the design and interpretation of toxicological studies, including in vitro and in vivo assessments, to identify potential risks associated with products.
• Cross-Functional Collaboration: Work closely with R&D, regulatory affairs, and clinical teams to integrate toxicology insights into product development processes.
• Scientific Communication: Prepare and present reports, presentations, and regulatory submissions to internal stakeholders and regulatory bodies, clearly communicating complex scientific data.
• Industry Engagement: Keep abreast of current trends and advancements in materials science, representing the company in relevant industry forums and conferences.\r\r

Keywords: Disability Solutions, Stratford , Director of Materials Science - MedTech Surgery, Executive , Raritan, Connecticut