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Process Engineer Medical Device Jobs in California

Process Engineer

Lake Forest, CA · On-site

$71K - $80K/yr

Applied Medical is a new-generation medical device company with a proven business model and ... Position Description As a Process Engineer at Applied Medical, you'll lead cross-functional ...

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Perform in-process quality inspections and provide timely feedback regarding quality or production ... Medical device, Petrochemical and Clinical Research.

Pay: $22-26/hour Position Summary The Medical Device Assembly Technician is responsible for ... Perform in-process quality inspections and provide timely feedback regarding quality or production ...

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Support engineering tests by executing defined test methods * Record and maintain documentation as ... Comfortable working in a regulated environment (medical device experience is a plus) * Ability to ...

Medical Device Assembler

Irvine, CA

$19 - $23.25/hr

Communicate any defects, issues, or process concerns to the appropriate team members to support ... Minimum of 2 years of medical device assembly experience, preferably in a clean room environment.

Applies subject matter knowledge in the area of Medical Device and Manufacturing Engineering ... Models processes and units operations. Ensures proper sequence of operation and prepares ...

Applies subject matter knowledge in the area of Medical Device and Manufacturing Engineering ... Models processes and units operations. Ensures proper sequence of operation and prepares ...

Applies subject matter knowledge in the area of Medical Device and Manufacturing Engineering ... processes and units operations. • Ensures proper sequence of operation and prepares ...

Showing results 41-60

Process Engineer Medical Device information

See California salary details

$48.9K

$90.8K

$140.6K

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

As of Aug 11, 2026, the average yearly pay for process engineer medical device in California is $90,813.00, according to ZipRecruiter salary data. Most workers in this role earn between $73,500.00 and $101,700.00 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.

Infographic showing various Process Engineer Medical Device job openings in California 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 $90,813 per year, or $43.7 per hour.

Process Engineer

Applied Medical

Lake Forest, CA • On-site

$71K - $80K/yr

Full-time

Life, Retirement, PTO

Re-posted 9 days ago


Applied Medical rating

8.0

Company rating: 8.0 out of 10

Based on 23 frontline employees who took The Breakroom Quiz


Job description

Applied Medical is a new-generation medical device company with a proven business model and commitment to innovation fueled by rapid business growth and expansion. Our company has been developing and manufacturing advanced surgical technologies for over 35 years and has earned a strong reputation for excellence in the healthcare field. Our unique business model, combined with our dedication to delivering the highest quality products, enables team members to contribute to a larger capacity than is possible in typical positions.


Position Description

As a Process Engineer at Applied Medical, you’ll lead cross-functional improvement initiatives that drive consistency, efficiency, and scalability across a wide range of manufacturing systems. From component assembly to process validations and documentation, this role combines hands-on process ownership with strategic collaboration. You’ll bridge the gap between design and production, ensuring our processes are compliant, optimized, and ready to scale.

Key Responsibilities:

  • Cross-Process Improvement: Analyze, document, and improve existing workflows for component-level manufacturing, including assembly, bonding, testing, and sub-processes beyond plastics.

  • Validation & Compliance: Lead and support equipment and process validations (IQ/OQ/PQ), working with quality and documentation teams to ensure regulatory alignment.

  • Tooling & Fixture Coordination: Collaborate with design and tooling engineers to evaluate or improve manufacturing fixtures and workflows.

  • Documentation Mastery: Own and maintain process documentation including SOPs, work instructions, validation protocols, and technical reports.

  • Project Ownership: Manage validation timelines, trials, and change implementation across multiple teams, including operations, tooling, and quality.

  • Technician Support: Train floor technicians on updated processes, documentation, or new procedures as workflows evolve.


Position Requirements
  • Bachelor’s degree in Mechanical, Chemical, Bioengineering, or a related field
  • More than one year of industry experience in manufacturing, injection molding, or process engineering
  • Exposure to plastics manufacturing, component-level production, or contract manufacturing environments
  • Interest in process planning, optimization, and cross-team coordination
  • Proficiency with CAD software for basic design collaboration and documentation
  • Ability to communicate across departments and work in technician-facing environments
  • Strong analytical and documentation skills for recipe development, SOPs, and technical reporting
  • Project coordination mindset with a focus on execution and follow-through

Preferred
  • Hands-on experience with injection molding systems or plastics process development

  • Familiarity with validation protocols (IQ/OQ/PQ) and regulated manufacturing environments

  • CAD design ability beyond basics with SolidWorks, CATIA, or equivalent

  • Minitab or Excel-based data analysis for performance metrics or capability studies

  • Experience collaborating with cross-functional engineering and quality teams

  • Interest in developing scalable solutions for scrap reduction, cycle time efficiency, and process sustainability

  • Comfort with root-cause analysis, data collection, and continuous improvement techniques

If you’re passionate about bringing order to complex workflows, documenting technical change, and working cross-functionally to refine how products are made, the Process Engineer role offers an exciting opportunity to make scalable impact in medical manufacturing.


Benefits
  • Competitive compensation range: $71,000 - $80,000 / year (California).
  • Comprehensive benefits package.
  • Training and mentorship opportunities.
  • On-campus wellness activities.
  • Education reimbursement program.
  • 401(k) program with discretionary employer match.
  • Generous vacation accrual and paid holiday schedule.

Please note that the compensation range may be adjusted in the future, and bonus and incentive compensation plans may apply.

Our total reward package reflects our commitment to employee growth and well-being, as we invest in your development and offer a range of benefits designed to enhance your career and life.

All compensation and benefits are subject to plan documents and written agreements.

Equal Opportunity Employer

Applied Medical is an Equal Employment Opportunity employer. All qualified applicants will receive consideration for employment without regard to age, ancestry, color, disability (mental and physical), exercising the right to family care and medical leave, gender, gender expression, gender identity, genetic information, marital status, medical condition, military or veteran status, national origin, political affiliation, race, religious creed, sex (including pregnancy, childbirth, breastfeeding and related medical conditions), or sexual orientation, or any other basis protected by federal, state or local laws in the locations where Applied Medical operates. 

Qualifications:
  • Bachelor’s degree in Mechanical, Chemical, Bioengineering, or a related field
  • More than one year of industry experience in manufacturing, injection molding, or process engineering
  • Exposure to plastics manufacturing, component-level production, or contract manufacturing environments
  • Interest in process planning, optimization, and cross-team coordination
  • Proficiency with CAD software for basic design collaboration and documentation
  • Ability to communicate across departments and work in technician-facing environments
  • Strong analytical and documentation skills for recipe development, SOPs, and technical reporting
  • Project coordination mindset with a focus on execution and follow-through
Education:UNAVAILABLEEmployment Type: FULL_TIME

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