Sr. Mechanical Engineer - Compressor

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Provides technical expertise in new product design and development projects. The engineer will be tasked design and development activities as well as sustaining and manufacturing support type tasks. The engineer will be part of a cross‑functional design team and will be responsible for supporting projects and products throughout the entire life cycle.

This position will focus on designing and developing high‑quality oxygen concentrators, leveraging modern design methodologies such as design quality, statistical analysis, tolerance analysis, design‑to‑cost, and design for manufacturability, serviceability, and sustainability. This role requires familiarity with key medical device standards and expertise in system architecture, integration, and design verification.

• Design and develop oxygen concentrators, focusing on functional and performance excellence.
• Apply advanced engineering methodologies, including statistical analysis, tolerance analysis, and design quality techniques, to ensure product reliability and robustness.
• Ensure compliance with ISO
  13485, IEC
  60601, IEC
  80601, and other medical device standards as required by FDA and other regulatory agencies.
• Collaborate cross‑functionally with electrical engineers, industrial designers, and other stakeholders to optimize designs for manufacturability and serviceability.
• Integrate cost‑conscious strategies, balancing functionality with design‑to‑cost initiatives.
• Design plastic components, working closely with injection molding suppliers to achieve high‑quality production standards.
• Develop system architecture and oversee system integration efforts to ensure cohesive product functionality.
• Conduct design verification activities, including simulations and tests, to validate designs and ensure adherence to regulatory and safety standards.
• Support the production team by ensuring smooth transitioning from prototype to mass manufacturing while maintaining quality.
• Utilize feedback from customers and service teams to improve product designs and enhance user experience.
• Incorporate insights from designs by other manufacturers into the development process for continuous improvement.
• Document design processes, analysis results, and lessons learned for knowledge management and ongoing enhancement.

• Mechanical Skills
• Project/Task Management
• Analytical Skills
• Team Orientation
• Coaching/Developing Others
• Problem‑Solving
• Leadership

Responsible for leading, coaching, and directing other engineers.

This job operates in a professional office environment.

• Frequent standing, sitting, walking, bending, stooping, twisting and occasional crawling.
• Occasional lifting up to 50 lbs., occasional heavier lifting.
• Occasional pushing, pulling and handling of materials.

Occasional travel as needed, such as international travel to other sites and locations for training and collaboration purposes.

• Bachelor’s or Master’s degree in Mechanical Engineering or a related field.
• 5‑8 years of experience in product design and development, particularly in medical devices or similar industries.
• Proficiency in modern design methodologies, including tolerance analysis, statistical analysis, design‑to‑cost, and design for manufacturability.
• Strong experience with CAD software (e.g., Solid Works, CATIA, or equivalent) and simulation tools.
• Familiarity with regulatory requirements and standards for medical devices, including ISO
  13485, IEC
  60601, IEC
  80601, and FDA requirements.
• Expertise in designing plastic parts and collaborating with injection molding suppliers.
• Proven ability in system architecture development and system integration.
• Experience in design verification processes, including simulation and testing.
• Ability to incorporate knowledge from designs by other manufacturers into development workflows.
• Exceptional problem‑solving skills, attention to detail, and ability to manage multiple projects.
• Excellent communication and documentation…