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Process Engineer Medical Device Jobs (NOW HIRING)

We are seeking an experienced Manufacturing Process Engineer to support a growing medical device manufacturing operation specializing in silicone component manufacturing . This role is responsible ...

Staff Engineer - Medical Device

Brea, CA ยท On-site

$115K - $160K/yr

Resolves engineering issues associated with Variation Notices by analyzing and reporting on the ... This position also provides health benefits such as medical, dental and vision; wellness benefits ...

Staff Engineer - Medical Device

Brea, CA ยท On-site

$115K - $160K/yr

Resolves engineering issues associated with Variation Notices by analyzing and reporting on the ... This position also provides health benefits such as medical, dental and vision; wellness benefits ...

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

Process Engineer

Torrington, CT ยท 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 ...

Showing results 41-60

Process Engineer Medical Device information

See salary details

$49.5K

$92K

$142.5K

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

As of Aug 16, 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 skills and qualifications are needed to thrive as a process engineer medical device?

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 does a process engineer medical device do?

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?

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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What cities are hiring for Process Engineer Medical Device jobs?

Cities with the most Process Engineer Medical Device job openings:

What states have the most Process Engineer Medical Device jobs?

States with the most job openings for Process Engineer Medical Device jobs include:

Infographic showing various Process Engineer Medical Device job openings in the United States as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $92,018 per year, or $44.2 per hour.

Senior Electrical Engineer - Medical Device

Kforce Technology Staffing

Carlsbad, CA โ€ข On-site

$111K - $145K/yr

Other

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 20 days ago


Job description

RESPONSIBILITIES:
Kforce's client in Carlsbad, CA is looking for a Senior Electrical Engineer - Medical Device (Individual Contributor). This role does not involve managing or leading other engineers. The focus is deep technical contribution, not people leadership. This position is an individual contributing position which entails a combination of design and sustaining work.
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
REQUIREMENTS:
* Bachelor's degree in Electrical Engineering, Computer Engineering or similar field
* At least 5-8+ years of electrical engineering design and sustaining experience in Class II or III medical devices
* Experience owning designs from concept through production and sustaining
* Experience working within regulated design control environments
* Experience supporting verification, validation, and compliance testing
* Strong working knowledge of IEC 60601, electrical safety, and EMC/EMI compliance
* Proficiency with schematic capture and PCB design tools (Altium, OrCAD, DxDesigner, PADS)
* 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:
* Master's degree
* Experience with DSP based systems and signal processing
* Background in small or fast-paced companies
* Familiarity with ISO 14971 risk management
The pay range is the lowest to highest compensation we reasonably in good faith believe we would pay at posting for this role. We may ultimately pay more or less than this range. Employee pay is based on factors like relevant education, qualifications, certifications, experience, skills, seniority, location, performance, union contract and business needs. This range may be modified in the future.
We offer comprehensive benefits including medical/dental/vision insurance, HSA, FSA, 401(k), and life, disability & ADD insurance to eligible employees. Salaried personnel receive paid time off. Hourly employees are not eligible for paid time off unless required by law. Hourly employees on a Service Contract Act project are eligible for paid sick leave.
Note: Pay is not considered compensation until it is earned, vested and determinable. The amount and availability of any compensation remains in Kforce's sole discretion unless and until paid and may be modified in its discretion consistent with the law.
This job is not eligible for bonuses, incentives or commissions.
Kforce is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, pregnancy, sexual orientation, gender identity, national origin, age, protected veteran status, or disability status.
By clicking ?Apply Today? you agree to receive calls, AI-generated calls, text messages or emails from Kforce and its affiliates, and service providers. Note that if you choose to communicate with Kforce via text messaging the frequency may vary, and message and data rates may apply. Carriers are not liable for delayed or undelivered messages. You will always have the right to cease communicating via text by using key words such as STOP.