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Medical Device Product Development Jobs in Raleigh, NC

Merz North America

Senior Electrical Engineer

Raleigh, NC · On-site

$95K - $123K/yr

... products meet Medical Device safety requirements such as IEC 60601 and other Medical Device ... Responsible for electrical engineering design, development and support of products, sub-assemblies ...

Merz North America

Senior Electrical Engineer

Raleigh, NC

$95K - $123K/yr

... products meet Medical Device safety requirements such as IEC 60601 and other Medical Device ... Responsible for electrical engineering design, development and support of products, sub-assemblies ...

Baxter

Project Manager, R&D

Raleigh, NC · On-site

$120K - $165K/yr

  • Medical

  • Dental

  • Life

  • Retirement

  • PTO

Oversee the endtoend lifecycle of a software medical device product from discovery through requirements, development, verification, launch, and sustaining. * Engage regularly with all levels of ...

Oxford Global Resources

Electrical Engineer

Durham, NC · On-site

This Role will be responsible for the design, development, and testing of electrical systems and components for medical device products. You will contribute to various stages of the product lifecycle ...

Teleflex

Engineer 2, Sustaining, R&D

Morrisville, NC · On-site

$85K - $105K/yr

Experience and background requirements should focus on disposable medical device products. This ... development and implementation of related engineering activities to support changes and ...

Teleflex

Engineer 2, Sustaining, R&D

Morrisville, NC

$85K - $105K/yr

... D Engineer, based in Morrisville NC, is responsible for the sustaining engineering projects of ... Experience and background requirements should focus on disposable medical device products. This ...

Pentair

Product Development/Lab Technician

Apex, NC · On-site

$33/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Product Development/Lab Technician - Apex, NC At Pentair , you will workalongsidepassionate problem ... Medical, Dental, and Vision Insurance * 401(k) * Up to 5% 401K match starting day one of employment

Allucent

Sr. Director, CMC

Cary, NC · On-site +1

... development activities of drug, biologic or medical device products About the role As the Sr. Director, CMC, you will: * Lead end-to-end CMC strategy across drug substance, drug product, and ...

Allucent

Sr. Director, CMC

Cary, NC · Remote

... development activities of drug, biologic or medical device products About the role As the Sr. Director, CMC, you will: * Lead end-to-end CMC strategy across drug substance, drug product, and ...

Pentair

Product Development/Lab Technician

Apex, NC · On-site

$33/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Product Development/Lab Technician - Apex, NC At Pentair , you will work alongside passionate ... Medical, Dental, and Vision Insurance * 401(k) * Up to 5% 401K match starting day one of employment

Allucent

Sr. Director, CMC

Cary, NC · Remote

... development activities of drug, biologic or medical device products About the role As the Sr. Director, CMC, you will: * Lead end-to-end CMC strategy across drug substance, drug product, and ...

GILERO

Senior Design Quality Engineer - Medical Devices

Durham, NC · On-site

$100K - $140K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

As a Senior Design Quality Engineer at Gilero, A Sanner Company, you'll play a crucial role in ensuring the quality development of new medical device and combination products; from ideation through ...

GlaxoSmithKline

Device Engineer

Zebulon, NC

Lead early device development activities from concept through feasibility and engineering ... or medical product experience with hands-on experience using CAD tools for device design and ...

GSK

Device Engineer

Zebulon, NC · On-site

Lead early device development activities from concept through feasibility and engineering ... or medical product experience with hands-on experience using CAD tools for device design and ...

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Showing results 21-40

All JobsMedical Device Product Development JobsMedical Device Product Development Jobs in Raleigh, NC

Medical Device Product Development information

See Raleigh, NC salary details

$41.3K

$123.4K

$140.5K

How much do medical device product development jobs pay per year?

As of Aug 14, 2026, the average yearly pay for medical device product development in Raleigh, NC is $123,442.00, according to ZipRecruiter salary data. Most workers in this role earn between $111,300.00 and $139,000.00 per year, depending on experience, location, and employer.

What is a medical device product development?

A Medical Device Product Development job involves designing, testing, and bringing medical devices to market while ensuring compliance with regulatory standards. Professionals in this role work with cross-functional teams, including engineering, regulatory affairs, and manufacturing, to develop safe and effective healthcare solutions. They oversee the entire product lifecycle, from concept and prototyping to clinical validation and commercialization. Strong knowledge of FDA, ISO, and other regulatory requirements is essential.

What are some typical challenges faced in medical device product development roles?

Professionals in Medical Device Product Development often encounter challenges such as navigating complex regulatory requirements, managing cross-functional project teams, and ensuring that products meet both clinical needs and quality standards. Balancing innovative design with safety and compliance can require careful planning and solid problem-solving skills. Additionally, adapting to shifting project timelines and incorporating stakeholder feedback are common aspects of the job. Overcoming these challenges is rewarding and helps ensure the delivery of safe, effective devices to patients and healthcare providers.

What are the key skills and qualifications needed to thrive in medical device product development?

To thrive in Medical Device Product Development, you need a strong background in engineering or life sciences, product design, and an understanding of regulatory requirements like FDA and ISO standards. Proficiency with CAD software, project management tools, and knowledge of quality management systems (QMS) is commonly required, along with certifications such as Six Sigma or PMP being beneficial. Strong problem-solving abilities, collaboration skills, and effective communication are key soft skills for this role. These skills are important to ensure that devices are developed safely, efficiently, and in compliance with industry regulations while fostering innovation and teamwork.

What are the most commonly searched types of Medical Device Product Development jobs in Raleigh, NC?

The most popular types of Medical Device Product Development jobs in Raleigh, NC are:

What are popular job titles related to Medical Device Product Development jobs in Raleigh, NC?

For Medical Device Product Development jobs in Raleigh, NC, the most frequently searched job titles are:

What job categories do people searching Medical Device Product Development jobs in Raleigh, NC look for?

The top searched job categories for Medical Device Product Development jobs in Raleigh, NC are:

Medical Device Product Development jobs near you
Infographic showing various Medical Device Product Development job openings in Raleigh, NC as of August 2026, with employment types broken down into 1% As Needed, 75% Full Time, 18% Part Time, and 6% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $123,442 per year, or $59.3 per hour.

Senior Electrical Engineer

Merz North America

Raleigh, NC • On-site

$95K - $123K/yr

Full-time

Re-posted 27 days ago

Job description

About Us
Founded in 1908, Merz is a successful, family-owned specialty healthcare company with a rich history. As a leading global aesthetics business, our award-winning portfolio of injectables, devices, and skincare products empowers healthcare professionals to enhance confidence through aesthetic medicine. Our purpose is to fuel confidence by helping people look better, feel better, and live better. We believe you do not have to choose between living life and making a living. Live your best life with Merz Aesthetics.
A Brief Overview
The Senior Electrical Engineer will lead the design, development, and analysis of electronic hardware and embedded firmware for both new and existing products within the R&D Product Development organization. This role requires deep expertise in mixed-signal PCBA design, embedded C/C++ firmware development, and system-level engineering. You will work hands-on in the lab to prototype, debug, and validate designs, while collaborating closely with internal hardware/software teams and external design partners to meet technical requirements, project schedules, and cost targets. Key responsibilities include developing system and subsystem requirements, translating them into robust hardware and firmware architectures, and executing verification and validation activities to ensure design compliance. Strong analytical and troubleshooting abilities are essential for solving complex electrical and embedded system challenges. Experience with IEC 60601 electrical safety and EMC standards is required to ensure products meet all regulatory and quality expectations
What You Will Do
  • Verification Testing:
    • Complete system integration and verification test planning using high-level verification test plans.
  • Electrical Root Cause Analysis:
    • Lead root cause investigations for product quality issues and implement correction plans
  • Electrical Engineering:
    • Properly plan and execute scheduled electrical and firmware work packages collaborating with internal and external design resources to meet project milestones.
    • Delivering electrical and embedded products in a timely fashion with integrity and meeting all applicable standard for medical device quality.
    • Provide electrical and firmware engineering support ensuring current and new products meet Medical Device safety requirements such as IEC 60601 and other Medical Device standards.
    • Ensure duties are completed according to Merz SOPs and enhance necessary SOPs to improve efficiency and quality.
    • Responsible for electrical engineering design, development and support of products, sub-assemblies, board level circuits with a strong emphasis on digital and some analog based circuits containing HIFU amplifiers, linear regulators and buck power supplies.
    • Write and develop associated firmware designs to support hardware functionality. Experience in FPGA and Micro Controller designs and able to write in Verilog and VHDL code.
    • Responsible for verifying electrical and firmware design requirements through engineering analysis and testing.
    • Write and conduct engineering studies for root cause analysis on product enhancements and failures.
    • Provide broad electrical and firmware engineering technical expertise through various phases of product life cycle.
    • Provide electrical and firmware engineering analysis, feasibility reports and studies to assist the product development team.
    • Maintain/improve existing product designs in support of Manufacturing activities.
    • Follow design control procedures and enhance existing procedures as needed.

Minimum Requirements
  • Bachelor of Science (B.S.) in Electrical Engineering, Systems Engineering or a related field.
  • 5+ years of engineering experience in the medical device industry and/or highly regulated engineering environments
  • 7+ years of proven experience in mixed signal designs utilizing FPGAs
  • Exposure to software development practices and IEC 62304

Preferred Qualifications
  • Master's Degree of engineering experience in the medical device industry and/or highly regulated engineering environments

Technical & Functional Skills
  • Demonstrated ability to author and manage systems, sub-assembly and board level requirements and specifications in a highly methodical and organized manner
  • Experience with mixed signal technology designs
  • Good understanding of high-speed PCB layout considerations such as parasitic, crosstalk isolation, power supply noise, grounding, and EMI consideration
  • Familiarity with common manufacturing methods, both for electrical and mechanical and components
  • Experience with Altium Designer, OrCAD, Cadence Allegro, PADs schematic and layout tools or equivalent
  • Strong comprehension of risk management and risk analysis techniques, consistent with ISO 14971, applied to medical devices
  • Thorough understanding of verification strategy and test planning.
  • Experience in Verilog for FPGA designs.
  • Experience with Altera, Xilinx or Lattice FPGA development environments.
  • Experience with engineering analysis tools such as MATLAB and Signal Integrity tools, Hyperlinx or other similar tools.

Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities
This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor.

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