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Medical Device Embedded System Engineer Jobs in Bonifay, FL

Senior Drainage Engineer

Chipley, FL · On-site

$86K - $119K/yr

Using computer engineering software to design stormwater management and storm drain systems, as ... Medical, Dental, & Vision * 401(k) retirement savings plan + employer matching * Paid Time Off (PTO ...

Nuclear Engineer

Vernon, FL

$85K - $102K/yr

Key Responsibilities Provide technical direction in areas such as reactor and fluid systems design ... Meeting medical, vision, and dental standards, including body composition and physical fitness ...

Nuclear Engineer

Bonifay, FL

$82K - $98K/yr

Key Responsibilities Provide technical direction in areas such as reactor and fluid systems design ... Meeting medical, vision, and dental standards, including body composition and physical fitness ...

Nuclear Engineer

Hartford, AL

$88K - $106K/yr

Key Responsibilities Provide technical direction in areas such as reactor and fluid systems design ... Meeting medical, vision, and dental standards, including body composition and physical fitness ...

Nuclear Engineer

Graceville, FL

$88K - $106K/yr

Key Responsibilities Provide technical direction in areas such as reactor and fluid systems design ... Meeting medical, vision, and dental standards, including body composition and physical fitness ...

Nuclear Engineer

Marianna, FL

$92K - $110K/yr

Key Responsibilities Provide technical direction in areas such as reactor and fluid systems design ... Meeting medical, vision, and dental standards, including body composition and physical fitness ...

Nuclear Engineer

Cottondale, FL

$87K - $104K/yr

Key Responsibilities Provide technical direction in areas such as reactor and fluid systems design ... Meeting medical, vision, and dental standards, including body composition and physical fitness ...

Nuclear Engineer

Chipley, FL

$81K - $97K/yr

Key Responsibilities Provide technical direction in areas such as reactor and fluid systems design ... Meeting medical, vision, and dental standards, including body composition and physical fitness ...

INSPECTOR III - 55006068

Marianna, FL · On-site

$45K - $59K/yr

Use various engineering tools, equipment, Instruments and computers for performing technical ... device usage, installation/placement and materials to ensure safe work zones. Reviews work site ...

INSPECTOR III - 55006068

Marianna, FL · On-site

$45K - $59K/yr

Use various engineering tools, equipment, Instruments and computers for performing technical ... device usage, installation/placement and materials to ensure safe work zones. Reviews work site ...

INSPECTOR III - 55006068

Marianna, FL · On-site

$45K - $59K/yr

Use various engineering tools, equipment, Instruments and computers for performing technical ... device usage, installation/placement and materials to ensure safe work zones. Reviews work site ...

... valve device, using positive-end expiratory pressure respirators, performing cricothyrotomy for ... Medical Services System in which they function: (1) patient assessment; (2) basic life support ...

... valve device, using positive-end expiratory pressure respirators, performing cricothyrotomy for ... Medical Services System in which they function: (1) patient assessment; (2) basic life support ...

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Showing results 1-20

Medical Device Embedded System Engineer information

See Bonifay, FL salary details

$52.3K

$114.8K

$160.6K

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

As of Aug 24, 2026, the average yearly pay for medical device embedded system engineer in Bonifay, FL is $114,799.00, according to ZipRecruiter salary data. Most workers in this role earn between $93,200.00 and $136,700.00 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 Bonifay, FL are hiring for Medical Device Embedded System Engineer jobs?

Cities near Bonifay, FL with the most Medical Device Embedded System Engineer job openings:

Quality and Process Improvement Engineer

Professional Products

Defuniak Springs, FL • On-site

Full-time

Medical, Retirement, PTO

Re-posted 6 days ago


Job description

Job Description
Position: Quality and Process Improvement Engineer
Modality: Full-Time, Salary, In-Person
Location: Defuniak Springs, FL
Industry: Medical Device, Class 1, Manufacturing
**Professional Products, Inc. does not sponsor employment visas for this position.**
Company Profile:
Since starting in a single-window store in the Florida panhandle in 1963, Professional Products Inc. (PPI) has grown into an international medical device manufacturing and distribution corporation. Our products are the market leader in integrated cold therapy, user-comfort-based material science, and patient safety through advanced antimicrobial technology. PPI enables innovation with vertically integrated domestic U.S. operations, a spirit of entrepreneurship, and operational agility.
Our Culture:
Professional Products is a family-owned company built on integrity, innovation, and accountability. We value a collaborative culture in which all functions-Production, Quality, Regulatory, Finance, and Operations-actively participate in executing our strategic vision. We encourage initiative and independent problem-solving, empowering our team members to take ownership and translate company goals into tangible, measurable results.
The Position
The Quality and Process Improvement Engineer will be responsible for maintaining and advancing PPI's ISO 13485:2016 Quality Management System (QMS) and driving cross-functional process improvement initiatives.
This role balances 50% quality management and 50% process improvement, serving as a key bridge between operational functions. In addition to sustaining QMS compliance, the engineer will lead initiatives that enhance business processes such as medical billing for insurance reimbursement, operational compliance, and data-driven improvement projects.
The position supports Production, Purchasing, Product Realization, Finance, and Regulatory Compliance, while fostering collaboration across all company functions.
The PPI team comprises collaborative, diverse, and passionate professionals who take great pride in their work and are committed to helping others grow and develop. You'll have a platform to engage directly with decision-makers and influence both operational and strategic outcomes.
Required Knowledge
  • Strong working knowledge of the ISO 13485:2016 or ISO 9001 standards.
  • Understanding of Quality Management System concepts, including RCCA, CAPA, Process Validation, and Process Control.
  • Familiarity with Power BI, SQL, Excel, and Microsoft Business Central for data analysis and reporting.
  • Strong professional proficiency in the Microsoft Suite (Outlook, Word, Excel).

Skills / Abilities:
  • Strong initiative and ability to drive independent projects to completion.
  • Quality-oriented and attentive to detail while balancing speed and practicality.
  • Excellent analytical, communication, and cross-functional collaboration skills.
  • Ability to translate strategic objectives into actionable improvement projects.
  • Strong organizational, time management, and problem-solving abilities.

Job Description
The Quality and Process Improvement Engineer reports to the Chief Commercial and Operations Officer.
Internal relationships include Production, Purchasing, Research and Design, Programming, Finance, and Executive Management in DeFuniak Springs, FL.
External relationships may include commercial collaborations with partners, distributors, customers, and suppliers.The
Key Responsibilities:
  • Maintain and continually improve PPI's ISO 13485:2016 certification and QMS as the Management Representative.
  • Lead Corrective and Preventive Action (CAPA) processes: initiation, root cause analysis, action implementation, and validation.
  • Drive process improvement initiatives across Quality, Operations, and Administrative workflows-including medical billing and insurance compliance.
  • Manage responses for customer complaints, investigations, and returns analysis.
  • Coordinate with suppliers for Supplier Corrective Action Reports (SCARs).
  • Perform quality containment for defective products and communicate quality alerts.
  • Assess and disposition non-conformances in production.
  • Provide quality and compliance training and coaching to other departments.
  • Manage calibration records and ensure equipment compliance with QMS requirements.
  • Conduct internal quality system, product, and process audits supporting continual improvement.
  • Establish and track Quality KPIs and lead Management Review data preparation.
  • Partner with cross-functional teams to identify, implement, and measure process improvement outcomes.

The Successful Applicant
  • Minimum 3 years of experience in Quality or Manufacturing Engineering.
  • Minimum 3 years of experience working within ISO 13485 or ISO 9001 systems.
  • 1-3 years of manufacturing experience, preferably in process or quality engineering.
  • Bachelor's degree in an Engineering-related field.
  • Demonstrated ability to work independently and cross-functionally in a dynamic environment.
  • Interest in professional growth toward a Quality & Compliance Manager or Continuous Improvement Lead role.

Benefits
  • Bonus Compensation
  • Paid Holidays
  • Vacation
  • 401k
  • Health Insurance

Professional Products is an equal opportunity employer.
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other characteristic protected by law.
Professional Products, Inc. does not sponsor employment visas for this position.
Skills Required
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More Details
Employment Type: Full Time Location: DeFuniak Springs, FL, USA , Florida , United States Experience Required: Associate Date Published: 22 Oct 2025