Senior R+D Electrical Engineer - Diagnostics at Midmark Corporation in Cincinnati, OH | Kablio

Role

Description

regulatory compliance

hardware design

wireless integration

system architecture

pcb design

quality assurance

Own the hardware compliance strategy, ensuring designs meet all requirements for FDA (21 CFR 820), ISO 13485, and IEC 60601-1, and act as a key technical resource during regulatory reviews.
Identifies opportunities for cost savings without compromising quality.
Serve as the technical authority for all hardware design aspects, from concept to manufacturing, including simulation, validation, and complex troubleshooting.
Drive the technology selection and integration strategy for next-generation wireless, including advanced BLE features and other innovative communication hardware.
Provides leadership, coaching, and/or mentoring to level II and level III engineers.
Mentor other hardware engineers and provide technical oversight on all designs.
Own the architecture for the entire system, optimizing for battery life, efficiency, thermal performance, and electrical safety.
Applies domain mastery to the application and advancement of engineering methods and tools.
Manage technical relationships with hardware component vendors and contract manufacturers.
Ensures that documentation complies with company standards and industry regulations.
Design complex PCB assemblies and test fixtures to support development, verification, and manufacturing needs.
Establishes and enforces quality standards; participates in quality improvement initiatives.
Lead the hardware architecture for systems utilizing high-performance, ARM-based solutions.

Requirements

technical lead

altium designer

dfm

signal integrity

medical standards

system architecture

Demonstrated ability to lead technical projects, mentor engineers, and make critical architectural decisions.
Expert-level proficiency with Altium Designer.
Deep expertise in design for manufacturing (DFM).
Mastery of high-speed digital design, signal integrity (SI), and power integrity (PI).
Expert-level knowledge and application of medical device hardware standards (IEC 60601-1) and development within a 21 CFR 820 compliant QMS.
A strong system-level perspective, with the ability to manage complex technical trade-offs.

Benefits

Information not given or found

Training + Development

Information not given or found

Interview process

Information not given or found

Visa Sponsorship

Information not given or found

Security clearance

Information not given or found

Company

Overview

Founded 1915

Year Established

The company has been a pioneering force in healthcare solutions from its inception.

Designs and manufactures medical equipment that enhances the patient care experience.
Offers a wide range of products including examination tables, diagnostic equipment, and sterilization systems.
Serves various healthcare facilities like hospitals, clinics, and dental offices with tailored solutions.
Known for innovative products that improve workflows and patient outcomes in medical environments.
Has a global presence with operations extending across multiple countries and healthcare markets.
Consistently focused on integrating cutting-edge technology into their products for efficiency and safety.

Culture + Values

Commitment to improving the quality of care for people and the efficiency of care delivery.
Continuous improvement and innovation to meet evolving customer needs.
Integrity and transparency in all interactions.
Collaboration and teamwork for achieving shared goals.
Passion for customer success through quality products and services.
Accountability for actions and decisions to achieve organizational goals.

Environment + Sustainability

2050

Net Zero Emissions Target

Sets a goal to achieve net zero emissions by the specified year.

Focus on energy efficiency through sustainable product designs and operations.
Implementation of recycling and waste reduction programs in manufacturing.
Reduction of greenhouse gas emissions as part of sustainability initiatives.
Tracking and reporting of environmental performance to ensure continuous improvement.

Inclusion & Diversity

Articles

Careers

Press Releases

Newsroom

Role

Description

regulatory compliance

hardware design

wireless integration

system architecture

pcb design

quality assurance

Own the hardware compliance strategy, ensuring designs meet all requirements for FDA (21 CFR 820), ISO 13485, and IEC 60601-1, and act as a key technical resource during regulatory reviews.
Identifies opportunities for cost savings without compromising quality.
Serve as the technical authority for all hardware design aspects, from concept to manufacturing, including simulation, validation, and complex troubleshooting.
Drive the technology selection and integration strategy for next-generation wireless, including advanced BLE features and other innovative communication hardware.
Provides leadership, coaching, and/or mentoring to level II and level III engineers.
Mentor other hardware engineers and provide technical oversight on all designs.
Own the architecture for the entire system, optimizing for battery life, efficiency, thermal performance, and electrical safety.
Applies domain mastery to the application and advancement of engineering methods and tools.
Manage technical relationships with hardware component vendors and contract manufacturers.
Ensures that documentation complies with company standards and industry regulations.
Design complex PCB assemblies and test fixtures to support development, verification, and manufacturing needs.
Establishes and enforces quality standards; participates in quality improvement initiatives.
Lead the hardware architecture for systems utilizing high-performance, ARM-based solutions.

Requirements

technical lead

altium designer

dfm

signal integrity

medical standards

system architecture

Demonstrated ability to lead technical projects, mentor engineers, and make critical architectural decisions.
Expert-level proficiency with Altium Designer.
Deep expertise in design for manufacturing (DFM).
Mastery of high-speed digital design, signal integrity (SI), and power integrity (PI).
Expert-level knowledge and application of medical device hardware standards (IEC 60601-1) and development within a 21 CFR 820 compliant QMS.
A strong system-level perspective, with the ability to manage complex technical trade-offs.

Benefits

Information not given or found

Training + Development

Information not given or found

Interview process

Information not given or found

Visa Sponsorship

Information not given or found

Security clearance

Information not given or found