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Process Engineer Medical Device Jobs (NOW HIRING)

Intellectt INC

Industrial Engineer | Med Device

Raynham, MA

$72K - $95K/yr

Key Skills Required: 3+ years of Medical Device or regulated manufacturing experience Strong SAP / MRP / PP&L experience Supply Chain Planning & Inventory Management Windchill or PLM systems exposure ...

System One Holdings, LLC

Process Engineer

Waltham, MA · On-site

$45 - $51/hr

Process Engineer Location: Waltham, Massachusetts Type: Contract Compensation: $45.00 - $51.00 per ... Support medical device manufacturing process development, transfer, optimization, and validation ...

Agiliad

Medical Test Engineer

Boston, MA · On-site

Test Engineer - Medical Devices (Cardiovascular Domain) Job Title: Test Engineer / Senior Test ... Understand device design, system architecture, and core technologies to support effective test ...

Aptyx

Process Engineer

Torrington, CT · On-site

... medical device manufacturing environment. This role serves as the technical owner of injection ... The Process Engineer partners closely with Quality, Production, Tooling, Maintenance, Engineering ...

Aptyx

Process Engineer

Torrington, CT · On-site

$80K - $115K/yr

... medical device manufacturing environment. This role serves as the technical owner of injection ... The Process Engineer partners closely with Quality, Production, Tooling, Maintenance, Engineering ...

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How much do process engineer medical device jobs pay per year?

As of Jun 5, 2026, the average yearly pay for process engineer medical device in the United States is $92,018.00, according to ZipRecruiter salary data. Most workers in this role earn between $74,500.00 and $103,000.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in the Process Engineer Medical Device position, and why are they important?

A Process Engineer in Medical Devices typically requires a degree in engineering (such as chemical, biomedical, or mechanical engineering) and experience with manufacturing processes, quality systems, and regulatory compliance. Familiarity with tools like CAD software, statistical analysis programs, lean manufacturing techniques, and knowledge of standards such as ISO 13485 are common requirements. Strong problem-solving abilities, project management skills, and excellent communication facilitate successful interactions with cross-functional teams. These skills ensure efficient, high-quality, and compliant manufacturing processes critical to patient safety and company success.

What are some common projects or responsibilities I might take on as a Process Engineer in the medical device industry?

As a Process Engineer in the medical device industry, you'll commonly work on projects such as optimizing manufacturing processes, implementing new technologies, and ensuring compliance with strict quality and regulatory standards. Your daily tasks may include designing and validating production methods, troubleshooting process issues, and collaborating closely with quality assurance, R&D, and production teams. You may also be involved in documentation, process scale-up for new products, and continuous improvement initiatives. The role is highly collaborative, requiring you to coordinate with both technical and non-technical staff to meet quality, efficiency, and regulatory goals.

What is a Process Engineer Medical Device job?

A Process Engineer in the medical device industry is responsible for designing, implementing, and optimizing manufacturing processes to ensure efficiency, quality, and compliance with regulatory standards. They work to improve production procedures, troubleshoot issues, and develop new process technologies. Their role involves collaborating with cross-functional teams, such as design, quality, and regulatory, to ensure medical devices meet industry requirements. Additionally, they analyze data, validate processes, and support continuous improvement initiatives to enhance product reliability and manufacturing scalability.

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Process Engineer Medical Device jobs near you
Infographic showing various Process Engineer Medical Device job openings in the United States as of May 2026, with employment types broken down into 82% Full Time, 9% Temporary, and 9% Contract. Highlights an 93% Physical, 2% Hybrid, and 5% Remote job distribution, with an average salary of $92,018 per year, or $44.2 per hour.

Senior Electrical Engineer - Medical Device Carlsbad, CA

ESR Healthcare

Carlsbad, NM • On-site

$175K/yr

Full-time

Posted 2 days ago

Job description

Job Description: Senior Electrical Engineer - Medical Device Up to: $175000/Annually Refer & Earn $1000 View Referral Details JOB DESCRIPTION client in Carlsbad, CA is looking for a Senior Electrical Engineer - Medical Devices (Individual Contributor). This role does not involve managing or leading other engineers. The focus is deep technical contribution, not people leadership.

Overview: We are partnered directly with the hiring manager to identify a Senior Electrical Engineer who will play a critical, hands on role in the design, development, integration, and sustaining of advanced Class II medical device systems. This role spans early-stage R&D, NPI, and sustaining engineering, offering exposure across the full product lifecycle. The company offers a competitive compensation package, including base salary, and an annual bonus.

This position is 100% onsite. Responsibilities: Design and develop electrical subsystems for complex medical platforms, ensuring compliance with IEC 60601, EMC/EMI, and regulatory design controls Work hands on to debug, test, and implement electrical solutions at the board and system level Support sustaining engineering activities, including product improvements, issue resolution, and field support Participate in early-stage R&D, NPI, and design transfer activities Translate user and system requirements into robust electrical designs, including component selection and manufacturability considerations Develop and execute verification and validation strategies (simulation, prototyping, bench testing, performance testing) Author and maintain technical documentation supporting DHF, regulatory submissions, and continuous improvement Optimize existing designs for cost, manufacturability, reliability, and performance Perform root cause analysis and implement corrective actions for electrical failures This position is an individual contributing position Bachelor's degree in Electrical Engineering; Master's preferred At least 5+ years of electrical engineering experience in Class II or III medical devices Experience owning designs from concept through production and sustaining Strong working knowledge of IEC 60601, electrical safety, and EMC/EMI compliance Experience working within regulated design control environments Proficiency with schematic capture and PCB design tools (Altium, OrCAD, DxDesigner, PADS) Experience supporting verification, validation, and compliance testing Comfortable working across R&D, NPI, and sustaining phases Hands on experience with some of the following would be ideal: Power supply design Low noise system design SPI, I-C, UART, Ethernet ADC/DAC, PLL, DDS Nice to Haves: Experience with DSP based systems and signal processing Background in small or fast paced companies Familiarity with ISO 14971 risk management Working Place: Carlsbad, California, United States Company : ESR Healthcare

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