Job title: Research And Development Engineer
Company: Katalyst Healthcares & Life Sciences
Job description: Responsibilities:
- Research, design, and develop stepper motor systems for use in medical devices, ensuring compliance with industry standards and regulatory requirements.
- Collaborate with cross-functional teams including electrical engineers, mechanical engineers, and software developers to integrate stepper motor technology into medical device platforms.
- Conduct feasibility studies and performance evaluations of stepper motor solutions, identifying opportunities for optimization and enhancement.
- Lead prototype development and testing activities, utilizing rapid prototyping techniques to validate stepper motor designs.
- Participate in design reviews, providing technical expertise and recommendations to optimize stepper motor performance, reliability, and manufacturability.
- Generate technical documentation including specifications, test plans, and reports to support regulatory submissions and product commercialization.
- Stay current with emerging trends and advancements in stepper motor technology, applying knowledge to drive innovation and maintain competitive advantage.
- Collaborate with external vendors and research partners to explore new technologies and potential collaborations for advancing stepper motor applications in medical devices.
- Provide technical support to manufacturing and operations teams during product scale-up and transfer to production, ensuring smooth transition and adherence to design specifications.
- Contribute to intellectual property development through patent disclosures and invention disclosures related to stepper motor innovations in medical devices.
Requirements:
- Bachelor’s degree in electrical engineering, Mechanical Engineering, or a related field; advanced degree preferred.
- Minimum of 4 years of experience in research and development roles within the medical devices industry, with a focus on stepper motor technology.
- Proficiency in stepper motor design, control algorithms, and integration within complex electromechanical systems.
- Strong understanding of regulatory requirements and standards applicable to medical devices (e.g., FDA QSR, ISO 13485).
- Experience with CAD software for design and simulation (e.g., SolidWorks, ANSYS) is preferred.
- Excellent problem-solving skills with the ability to analyse and troubleshoot complex technical issues.
- Effective communication and collaboration skills, with the ability to work cross-functionally in a team environment.
- Demonstrated project management abilities, with the capability to prioritize tasks and meet project milestones effectively.
- Knowledge of manufacturing processes and practices related to medical device production is desirable.
- Ability to adapt to a fast-paced, dynamic work environment and thrive in a culture of innovation and continuous improvement.
Expected salary:
Location: Saint Louis, MO
Job date: Sun, 06 Oct 2024 07:10:31 GMT
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