Medical Implants Design jobs

Design and develop components and assemblies using first principles, Lead development of product or sub-systems for complex electromechanical products and analyze / simulate design to understand key parameters and sensitivities. Establish design feasibility by testing circuit and demonstrating statistical capability for critical functions.

Define design inputs (i.e., product requirements), develop design outputs (i.e., product specifications), define technical strategies for an adequate verification and validation approach. Drive successful verification and validation testing.

Ideate, conceptualize, and build concepts and prototypes to aid incubation of new opportunities or down-select wining solutions for new product developments, upgrades, or improvements.

Create simulation and mathematical models as appropriate to demonstrate functional feasibility of technical solution based on experimental, numerical, statistical, and/or finite-elements tools and techniques.

Participate in troubleshooting, root-cause analysis and devise solutions and approaches for solving technical problems (solution gameplan) and overcoming development challenges in an inclusive and collaborative fashion.

Develop test methods and fixtures for products, components, and systems simulation, evaluation, and verification testing including creating formal Verification test protocols, run tests, and write Verification test reports.

May communicate key technical content to parties within and outside of own function (R&D). May have responsibility for communicating with parties external to the organization and manage external development partners to meet project deliverables on time.

Deliver agreed project outcomes on-time and on-budget per project plan.

Manage your assigned project tasks, workstreams, and deliverables ensuring full alignment with the overall project plan and business objectives.

Report to Project lead on your assigned tasks, ensuring early escalation and identification of project risks.

Participate in design review and DFMA activities.

Aid in the effective cross-functional collaboration ensuring timely and efficient delivery of target business outcomes.

Contribute to the assessment of new opportunities, acquisition targets, competitive products, and Intellectual Properties (IP’s) to aid competitiveness and differentiation of our business offerings.

Support scoping, project planning and product requirement definition for new product development, upgrades, or line extensions as appropriate.

Contribute to the selection, evaluation, and implementation of new tools, techniques, and best practices to ensure state-of-the-art product development capabilities and best practices.

Effectively and timely communicate (written and verbal) progress status updates associated with project issues.

Ensure adherence to medical devices design control compliance by ensuring all applicable safety, quality and regulatory guidelines and policies are followed to develop safe and effective products.

Maintain technical documentation for project and products as applicable per company quality standards, policies, and procedures and well as engineering best practices and functional excellence requirements.