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Medical Device Embedded System Engineer Jobs in Springfield, IL

Danaher

Software Engineer Internships

Springfield, IL · On-site

Supporting the development of console and embedded software systems * Troubleshooting issues and ... Producing documentation to support medical device regulatory processes Who This Is For * Students ...

Danaher

Software Engineer Internships

Springfield, IL · On-site

Supporting the development of console and embedded software systems * Troubleshooting issues and ... Producing documentation to support medical device regulatory processes Who This Is For * Students ...

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All JobsMedical Device Embedded System Engineer JobsMedical Device Embedded System Engineer Jobs in Springfield, IL

Medical Device Embedded System Engineer information

See Springfield, IL salary details

$61.9K

$136.1K

$190.3K

How much do medical device embedded system engineer jobs pay per year?

As of Jul 6, 2026, the average yearly pay for medical device embedded system engineer in Springfield, IL is $136,053.00, according to ZipRecruiter salary data. Most workers in this role earn between $110,500.00 and $162,000.00 per year, depending on experience, location, and employer.

What does a Medical Device Embedded System Engineer do?

A Medical Device Embedded System Engineer designs, develops, and maintains the embedded software and hardware used in medical devices such as pacemakers, infusion pumps, and diagnostic equipment. They ensure that the systems meet strict safety, reliability, and regulatory standards required in the healthcare industry. Their work involves programming microcontrollers, integrating sensors and communication modules, and collaborating with cross-functional teams to ensure the final product is safe, effective, and compliant with medical regulations.

How does a Medical Device Embedded System Engineer typically collaborate with cross-functional teams during product development?

As a Medical Device Embedded System Engineer, you’ll work closely with teams such as hardware engineers, software developers, quality assurance, regulatory affairs, and clinical experts. Collaboration is essential to ensure the embedded system meets safety, performance, and regulatory requirements. This often involves participating in design reviews, troubleshooting integration issues, and providing technical documentation. Effective communication and teamwork are key, as you’ll be translating clinical needs into technical solutions and ensuring compliance with medical standards.

What are the key skills and qualifications needed to thrive as a Medical Device Embedded System Engineer, and why are they important?

A Medical Device Embedded System Engineer typically needs a strong background in electrical or computer engineering, experience with embedded C/C++ programming, and a solid understanding of medical device regulations. Familiarity with microcontrollers, real-time operating systems (RTOS), and compliance standards like IEC 62304 is highly valuable, and certifications in embedded systems or medical device software can be advantageous. Strong problem-solving skills, attention to detail, and effective teamwork are essential soft skills for excelling in this position. These competencies ensure the development of safe, reliable, and regulatory-compliant medical devices that improve patient outcomes.

What is the difference between Medical Device Embedded System Engineer vs Medical Software Engineer?

AspectMedical Device Embedded System EngineerMedical Software Engineer
CredentialsBachelor's or higher in Electrical, Computer Engineering, or related; knowledge of embedded systemsBachelor's or higher in Computer Science, Software Engineering, or related; programming skills
Work EnvironmentDesigning and testing embedded hardware/software for medical devicesDeveloping medical software applications, often on PCs or servers
Industry UsageUsed in medical devices like pacemakers, imaging equipment, and monitorsUsed in healthcare software, EHR systems, and medical data analysis

The Medical Device Embedded System Engineer focuses on developing embedded hardware and firmware for medical devices, ensuring safety and compliance. In contrast, the Medical Software Engineer primarily develops software applications used in healthcare settings. Both roles require technical expertise but differ in their focus on hardware versus software development within the medical industry.

What cities near Springfield, IL are hiring for Medical Device Embedded System Engineer jobs? Cities near Springfield, IL with the most Medical Device Embedded System Engineer job openings:
Medical Device Embedded System Engineer jobs near you

Facilities Engineer

Stark Pharma Solutions Inc

Springfield, IL • On-site

Contractor

Posted 5 days ago

Be an early applicant

Job description

Hi,

My name is Sravani Dasari from Stark Pharma Solutions Inc. We are hiring talent for our client and are currently working on a Facilities Engineer position. Please send me your updated resume if you have relevant experience and are interested in this opportunity. The detailed job description is as follows.

Job Title: Facilities Engineer
Location: Springfield, IL
Duration: Long Term

Position Overview

We are seeking an experienced Facilities Engineer to support facility operations within a regulated pharmaceutical, biotechnology, or medical device manufacturing environment. This role will focus on maintaining, optimizing, and improving facility infrastructure and critical utility systems while ensuring compliance with quality, safety, and regulatory requirements. The ideal candidate will have strong expertise in facility engineering, preventive maintenance, HVAC and utility systems, equipment reliability, and continuous improvement initiatives to support efficient manufacturing operations.

Key Responsibilities

• Maintain, troubleshoot, and optimize facility infrastructure, utility systems, and building operations to ensure reliable manufacturing support.

• Support HVAC systems, clean utilities, water systems, compressed air systems, and other critical facility equipment.

• Develop and execute preventive and corrective maintenance programs to maximize equipment reliability and minimize operational downtime.

• Coordinate equipment installation, commissioning, qualification, and facility upgrade projects.

• Monitor facility performance and recommend improvements to enhance operational efficiency, reliability, and energy utilization.

• Perform root cause analysis for equipment failures and implement effective corrective and preventive actions (CAPA).

• Collaborate with Manufacturing, Quality, Validation, Maintenance, Environmental Health & Safety (EHS), and Engineering teams to support production objectives.

• Maintain engineering documentation, maintenance records, SOPs, and equipment history in accordance with company quality systems.

• Support internal audits and regulatory inspections while ensuring compliance with GMP, FDA, OSHA, and environmental regulations.

• Drive continuous improvement initiatives to improve facility performance, safety, and operational excellence.

Required Qualifications

• Bachelor's Degree in Mechanical Engineering, Electrical Engineering, Industrial Engineering, Civil Engineering, or a related engineering discipline.

• 3+ years of Facilities Engineering experience within pharmaceutical, biotechnology, medical device, or other regulated manufacturing environments.

• Hands-on experience supporting HVAC systems, clean utilities, water systems, compressed air systems, facility infrastructure, and preventive maintenance programs.

• Experience with equipment installation, commissioning, qualification, troubleshooting, and facility improvement projects.

• Strong knowledge of GMP, FDA, OSHA, and applicable regulatory requirements.

• Familiarity with CMMS (Computerized Maintenance Management Systems), maintenance planning, and engineering documentation.

• Experience with reliability engineering, root cause analysis, CAPA, and continuous improvement methodologies such as Lean Manufacturing or Six Sigma is preferred.

• Knowledge of facility validation, engineering change management, energy management, and utility optimization is an added advantage.

• Experience working within pharmaceutical, biotechnology, or medical device manufacturing facilities is highly preferred.

• Professional Engineer (PE), Certified Facility Manager (CFM), or other relevant engineering certifications are a plus.

• Excellent problem-solving, communication, technical documentation, organizational, and cross-functional collaboration skills.

I am actively connecting with professionals for current and upcoming opportunities. If you are open to exploring new roles or would like to stay informed about relevant positions, please send me your updated resume along with the best number and time to reach you.

Please follow Stark Pharma Solutions on LinkedIn for the latest job updates: https://www.linkedin.com/company/99455976/