Senior Biomaterials Scientist/Engineer

Company: Disability Solutions
Location: Raritan
Posted on: September 28, 2024

Job Description:

Ethicon, a member of Johnson & Johnson's family of companies, is recruiting for an Biomaterials Scientist/Engineer located in Raritan, NJ.At Johnson & Johnson MedTech, we're changing the trajectory of health for humanity, using robotics to enhance healthcare providers' abilities and improve patients' diagnoses, treatments, and recovery times. Johnson & Johnson Robotics was established in 2020 with the integration of Auris Health, Verb Surgical, C-SATS, and Ethicon. It comprises three key med-tech platforms: Flexible Robotics (MONARCH---), Surgical Robotics (OTTAVA---), and Digital Solutions. Join our collaborative, rapidly growing teams in the San Francisco Bay Area (Redwood City and Santa Clara), Cincinnati, and Seattle. You'll collaborate on breakthrough medical technologies that unite multiple subject areas to build a connected digital ecosystem that advances medical professionals' skills and improves patient outcomes.OverviewEstablished and productive individual contributor in a scientific/technology field. Contributes to the planning and ensuring that materials performance is aligned with patient safety guidelines and the specific intentions of the user. Confers with superiors in ensuring materials integrity, accuracy, and consistency across selection and specification. Collaborates with multidisciplinary teams to affect the flow of materials and materials information from client to release for manufacturing.Develop, optimized, innovative stability analytic techniques for medical devices according to established procedures, ensuring quality standards are met. Responsible for leading engineering activities for medical device product stability laboratory program for Ethicon Raritan sites in New Jersey.Key Responsibilities:

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• Responsible for stability chambers maintenance, calibration, and validation activities
• Track, monitor, and drive optimization projects.
• Implementation of protocols, reports, and other stability documents in LIMS
• Act as Project Manager using 6 sigma approaches for all aspects of new stability equipment required in GMP stability laboratory, includes but not limited to procurement, qualifications/validations and all associated quality documents.
• Successful update and release of Stability documents
• Has confirmed experience in standard Medical Device environmental chamber, photo chamber, packaging and physical testing equipment IQ/OQ/PQ.
• Implement initiatives to improve efficiency, cycle times and productivity, including creation and improvement of document templates.
• Bring a multidisciplinary view to solving problems that involve data, algorithms and statistical models.
• Data Sourcing: Acquire data from diverse data lakes, data clusters, cloud data services and more
• Consults with technical teams.
• Responsible and accountable for progressing applied research activities.
• Stays on top of current scientific developments and new techniques to apply theories and concepts to improve stability capabilities and stability compliance.
• Responsible for communicating business related issues or opportunities to next management level
• Responsible for following all Company guidelines related to Health, Safety and Environmental practices as applicable.
• For those who supervise or manage a staff, responsible for ensuring that subordinates follow all Company guidelines related to Health, Safety and Environmental practices and that all resources needed to do so are available and in good condition, if applicable
• Responsible for ensuring personal and Company compliance with all Federal, State, local and Company regulations, policies, and procedures
• Performs other duties assigned as needed\r\r

Keywords: Disability Solutions, New Brunswick , Senior Biomaterials Scientist/Engineer, Engineering , Raritan, New Jersey