Staff Mechanical Design Engineer

Job Title: Staff Mechanical Design Engineer
Location: This position is based in our Campbell, California offices.

Why Telos Health?
At Telos Health we are developing novel robotic-assisted technologies and interventional capabilities that will forever change the disparate outcomes of ischemic stroke a disease that impacts close to a million people a year in the U.S., and 10 million worldwide. Not only is Telos changing the way stroke is treated, but also bringing this treatment to the greater population who is currently without. We are actively building a team who is focused on developing novel solutions for this complex disease a disease in which one in four adults will face in their lifetime.

What You ll Do:
As a key member of our engineering team, you will play a critical role in developing an integrated fluidics assembly of injection-molded components that seamlessly interfaces with our robotic system. Your expertise in designing single use components such as syringes, valves, and manifolds, and ensuring their compatibility with external motion systems, will be essential for success. These components are high user touchpoints and must withstand significant loads during use. Your experience of bringing prototype systems all the way through production, including verification, validation and transfer to manufacturing, is key for this role. Your ability to transition smoothly from detailed design work to collaborating cross-functionally with our industrial design team will be important as well. Your responsibilities will span from conceptualization through verification and validation testing, ultimately supporting the transition to manufacturing for commercial release.

Key Responsibilities:

• Mechanical Design: Lead the design and development of critical components that ensure system functionality, focusing on high-pressure pumping, flow control within sensor-driven architectures, and the development of innovative hardware to improve safety and reliability. You will be proficient in the use of FEA to ensure adequate safety factors and generate drawings using GD&T.
• User Experience Integration: Work closely with user-experience and industrial design teams to ensure that our products not only meet but exceed customer expectations for ease of use and functionality, directly influencing the overall user experience.
• Vendor Management: identify and manage vendors that can prototype and eventually manufacture subcomponents or components and work with them through the verification process.
• Innovation and Intellectual Property: Lead innovation sessions to generate cutting-edge ideas, and collaborate with our legal team to protect these innovations through patents, ensuring the safeguarding of our intellectual property.
• Testing and Data-Driven Improvement: Plan, execute, and oversee rigorous testing protocols, analyze test data, and apply insights to enhance and optimize designs. Ensure comprehensive documentation to facilitate continuous improvement and effective knowledge transfer.
• Comprehensive Documentation: Take full responsibility for the creation and maintenance of detailed design drawings, test reports, and other critical documentation, ensuring that all processes are meticulously organized and transparent.

What You ll Bring:

• Bachelor s degree in Engineering (Mechanical, Biomedical, or related discipline) with 8+ years of related experience or 6+ years with MS or Advanced degree; or equivalent combination of education and work experience in the medical device or related regulated industry.
• 5+ years previous experience in a technical innovation role, with specific focus on the design, development, manufacturing, and testing of sterile, single use medical device related injection molded consumable components, devices, and/or assemblies.
• Strong understanding of fabrication methods, in particular injection molding.
• Experience and familiarity with statistical methods such as such as SPC, SQC, and DOE and use and implementation of Statistical Analysis Software (Minitab or similar).
• Proficiency using SolidWorks, for designing and documenting device designs, tooling, and fixtures.
• Extensive experience in full R&D product life cycle (concept through regulatory approval/market release).
• Experience with Design Control procedures and requirements and working under regulated quality systems such as GMPs, ISO 13485, and MDR.
• Demonstrated excellent written and verbal communications skills as a member of a cross functional team.

Supervisory Responsibilities:

• May supervise or provide guidance to more junior engineering or technician staff

Employee Benefits include a stake in our collective success with stock options, competitive salaries, a 401k plan, health benefits, generous PTO, and a parental leave program.

Salary Range: $154,000-$173,000/annually

Please note that the salary information is a general guideline only. Imperative Care considers factors such as scope and responsibilities of the position, candidate's work experience, education/training, key skills, and internal equity, as well as location, market and business considerations when extending an offer.

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