Sr Stability Scientist/Engineer - Raritan New Jersey

Company: Disability Solutions
Location: Raritan, New Jersey
Posted On: 02/06/2025

Ethicon, a member of Johnson & Johnson's family of companies, is recruiting for an Biomaterials Scientist/Engineer located in Raritan, NJ.At 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/.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 More...

      

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