Qureos Mentor

CAIRE Inc

<div><p><b>Summary/Objective</b></p><p>
Successful candidate will join CAIRE&rsquo;s Research &amp; Development team at the global headquarters in Georgia. This individual will work on CAIRE&rsquo;s oxygen therapy medical devices, with a focus on electronic embedded system design, as part of larger cross-disciplinary electro-mechanical design teams. This senior level electrical engineer will integrate into the full product life cycle, from design and development to transfer to manufacturing and sustaining activities.</p><p>
This on-site position is a hands-on engineering position with time spent in the office, laboratory and manufacturing floor for product launch support. Limited travel may be required to visit/support key suppliers or certified external laboratories. This position will be based out of the Canton/Ball Ground location of CAIRE, which is approximately 30 minutes north of the greater Atlanta, GA area.</p><p><b>
Essential Functions</b><br>
<br>
Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.</p><ul><li>
Perform development and sustaining tasks for electro-mechanical medical devices with the cross functional design team.</li><li>
Design and develop innovative solutions to meet engineering and marketing requirements.</li><li>
Troubleshoot and determine corrective measures for prototype designs and quality defects.</li><li>
Develop and perform test protocols to evaluate design changes, product improvements and cost reduction opportunities.</li><li>
Design and fabricate prototypes, tooling fixtures, and test benches as required.</li><li>
Work with Supply Chain to optimize material supply chain for cost and design for manufacturability.</li><li>
Determine product/component costing and BOM (Bill of Materials) management through centralized document management system.</li><li>
Identify and resolve product assembly issues to improve product consistency and eliminate variance in conjunction with production and manufacturing engineering.</li><li>
Work within a greater team to ensure that all aspects of new product introduction, and changes to existing products, are effectively communicated to production personnel. Prepare and communicate ECO and/or TDD changes to production.</li><li>
Interface with various departments in coordinating technical information relating to specific projects or regarding quality issues.</li><li>
Sustain existing products, which may include identifying alternates for EOL components, design improvements, cost down efforts.</li><li>
Develop control and power management solutions to optimize power consumption, system reliability and performance.</li><li>
Develop test and diagnostics test hardware to support bench testing, production testing and field service.</li><li>
Perform electrical component selection and create PCB schematics. Perform and/or oversee PCBA layout.</li><li>
Observe and practice safety procedures and policies.</li><li>
Other duties and responsibilities as assigned by management.</li></ul><p><b>
Competencies/Success Factors</b></p><ul><li>
Business or Job-Specific Knowledge</li><li>
Learning Ability</li><li>
Analytical Skills</li><li>
Results Focus / Output Orientation</li><li>
Team Orientation</li><li>
Interpersonal Communication</li><li>
Problem-Solving</li><li>
Strategic Skills</li></ul><p><b>
Supervisory Responsibility</b><br>
<br>
This position has no supervisory responsibilities</p><p><b>
Work Environment</b><br>
<br>
This job operates in a professional office and lab environment. This position will require the ability to move around the engineering lab and production floor to address production</p><p><b>
Physical Demands</b><br>
<br>
The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job.</p><ul><li>
Frequent standing, sitting, walking, bending, stooping, twisting and occasional crawling.</li><li>
Occasional lifting up to 50 lbs., occasional heavier lifting.</li><li>
Occasional pushing, pulling and handling of materials.</li></ul><p><b>
Travel</b><br>
<br>
Limited travel, less than 10%</p><p><b>
Required Education and Experience</b></p><ul><li>
BS Degree in Engineering &ndash; Electrical or Computer, or equivalent</li><li>
Minimum 6 years professional engineering experience, preferably in the design and manufacturing of electro-mechanical products.</li><li>
Working knowledge of Electrical CAD software. Altium experience is preferred.</li><li>
Working knowledge of computers, including MS Word, Excel, and Office Suite programs.</li><li>
Strong communication and organizational skills</li><li>
Ability to work both independently and in team settings.</li><li>
Sound understanding of and demonstrated success applying fundamentals within electrical design: analog and digital circuits, digital communication, controls, energy consumption, PCBAs, prototyping and troubleshooting.</li><li>
Experience testing and troubleshooting utilizing multimeter and oscilloscope.</li><li>
Experience prototyping electrical assemblies and soldering PCB surface-mount components.</li></ul><p>
 <b>Preferred Education and Experience</b></p><ul><li>
Experience with electrical design for embedded systems using microcontrollers.</li><li>
Experience with control systems, such as brushless DC motor control and electro-pneumatic systems.</li><li>
Experience with power management (AC and battery power) for low voltage devices.</li><li>
Experience implementing wireless solutions for Bluetooth, WIFI, and/or Cellular.</li><li>
Experience with serial communication protocols, such as UART, I2C, SPI, USB.</li><li>
Basic software programming knowledge, such as using languages such as C/C++.</li><li>
Medical Device background a plus</li><li>
Understanding of production metrics and Six Sigma.</li><li>
Understanding of Medical Device design control processes and associated ISO standards compliance (60601, 13485, 9001, etc.) preferred</li><li>
Demonstrated success leading small and medium sized engineering projects or subsystem designs.</li></ul><p><b>
Additional Eligibility Qualifications</b><br>
<br>
None required for this position.</p><p>
Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities and activities may change at any time with or without notice.</p><p>
 CAIRE is committed to providing equal employment opportunity without regard to race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, age, disability, veteran status, or membership in any other class protected by federal, state, or local law.</p></div>

Sr. Electrical Engineer

<div><div><b>Summary/Objective</b></div><div>
MGC Diagnostics is seeking a skilled and driven Project Manager to lead the development of cardiorespiratory diagnostic medical devices.</div><div></div><div><br>
This role is responsible for cross-functional leadership of product development from concept through global commercialization, managing internal teams across multiple locations and supporting engagement with technical and operational external partners.</div><div></div><div><br>
The successful candidate will drive execution within a structured, stage-gate development environment while ensuring compliance with global regulatory and quality standards.</div><div></div><div><b><br>
Essential Functions</b></div><div>
Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.</div><ul><li>
Lead full lifecycle project management of new product development (NPD) for Class II FDA-regulated medical devices, from concept through design transfer and commercial launch.</li><li>
Develop and maintain integrated project plans, timelines, resource forecasts, risk registers, and budgets aligned to program objectives.</li><li>
Ensure compliance with global medical device regulations including FDA (21 CFR Part 820), ISO 13485, ISO 14971, IEC 60601, and other applicable international standards.</li><li>
Drive execution of product development through a stage-gate process, ensuring quality system deliverables and DHF completeness.</li><li>
Coordinate activities across cross-functional internal teams, including R&amp;D, QA/RA, Operations, Marketing, and Clinical Affairs, located in multiple geographic regions.</li><li>
Collaborate with external partners and suppliers, supporting technical and operations leads to manage vendor deliverables and timelines.</li><li>
Facilitate formal design reviews, technical documentation review, and risk management activities.</li><li>
Prepare and deliver regular program status updates to senior leadership, including project health, milestones, and risk mitigation strategies.</li><li>
Support regulatory submission activities (e.g., 510(k), technical file, global registrations) in collaboration with Regulatory Affairs.</li><li>
Promote a culture of accountability, continuous improvement, and cross-functional problem-solving.</li></ul><div></div><div><b><br>
Competencies/Success Factors</b></div><ul><li>
Detail Orientation</li><li>
Project/ Task Management</li><li>
Results Focus/ Output Orientation</li><li>
Personal Energy/ Enthusiasm</li><li>
Team Orientation</li><li>
Interpersonal Communication</li><li>
Leadership</li><li>
Problem Solving</li></ul><div></div><div><b><br>
Supervisory Responsibility</b></div><div>
None.</div><div></div><div><b><br>
Work Environment</b></div><div>
This job operates in a professional office environment. This role routinely uses standard office equipment such as computers, phones and photocopiers.</div><div></div><div><b><br>
Physical Demands</b></div><div>
The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job.</div><ul><li>
Frequent standing, sitting, walking, bending, stooping, twisting and occasional crawling.</li><li>
Occasional lifting up to 50 lbs., occasional heavier lifting.</li><li>
Occasional pushing, pulling and handling of materials.</li></ul><div></div><div><b><br>
Travel</b></div><div>
Very limited travel&lt; than 5%</div><div></div><div><b><br>
Required Education and Experience</b></div><ul><li>
Bachelor&rsquo;s degree in Engineering, Biomedical Sciences, or a related technical field.</li><li>
Minimum of 5 years of experience in medical device product development with at least 3 years in a dedicated project or program management role.</li><li>
Strong understanding of medical device design controls, regulatory requirements, and product development life cycle in a highly regulated environment.</li><li>
Proven success leading projects involving electromechanical systems, embedded software, and firmware.</li><li>
Expertise in waterfall development methodologies and stage-gate execution.</li><li>
Proficient in project management tools (e.g., MS Project, Smartsheet) and MS Office Suite.</li><li>
Exceptional organizational, leadership, communication, and stakeholder management skills.</li></ul><div></div><div><b><br>
Preferred Education and Experience</b></div><ul><li>
PMP certification or equivalent project management training.</li><li>
Experience with global regulatory markets, including FDA, EU MDR, Health Canada, ANVISA, PMDA, TGA, and MHRA.</li><li>
Experience with cybersecurity, data privacy, and interoperability considerations in connected medical devices.</li><li>
Familiarity with IEC 62304, ISO 14971, and ISO 10993 standards.</li><li>
Knowledge of design for manufacturing (DFM), design for reliability (DfR), and working with contract manufacturers.</li></ul><div></div><div><b><br>
Additional Eligibility Qualifications</b></div><div>
None required for this position.</div><div></div><div><br>
Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities and activities may change at any time with or without notice.</div><div></div><div><br>
MGC Diagnostics is committed to providing equal employment opportunity without regard to race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, age, disability, veteran status, or membership in any other class protected by federal, state, or local law.</div></div>

Project Manager

Join CAIRE Inc and explore 2   exciting career opportunities. They're hiring for various roles with options for remote or on-site work. Apply today and become part of their innovative team.

CAIRE Inc

ABOUT_COMPANY

Sr. Electrical Engineer

Project Manager