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Project Engineer Medical Device Jobs in California

... Systems Engineer you will be part of a small, agile team; responsible for medical device ... Grit to drive challenging projects to completion in a fast-pace environment. * Enjoy working in a ...

... Systems Engineer you will be part of a small, agile team; responsible for medical device ... Grit to drive challenging projects to completion in a fast-pace environment. * Enjoy working in a ...

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Senior Mechanical Engineer - Medical Device San Diego, CA (Onsite) 130,000-180,000 DOE Join a growing medical-device team developing and improving a precision electromechanical product. This is an ...

Staff Engineer - Medical Device

Brea, CA · On-site

$115K - $160K/yr

Projects may include travel to conduct or witness tests at client sites. * Initiates communication with clients to promote and explain the benefits of new and existing services. Follows up on ...

Staff Engineer - Medical Device

Brea, CA · On-site

$115K - $160K/yr

Projects may include travel to conduct or witness tests at client sites. * Initiates communication with clients to promote and explain the benefits of new and existing services. Follows up on ...

Staff Engineer - Medical Device

Brea, CA · Hybrid

$115K - $160K/yr

Projects may include travel to conduct or witness tests at client sites. * Initiates communication with clients to promote and explain the benefits of new and existing services. Follows up on ...

Staff Engineer - Medical Device

Brea, CA · Hybrid

$115K - $160K/yr

Projects may include travel to conduct or witness tests at client sites. * Initiates communication with clients to promote and explain the benefits of new and existing services. Follows up on ...

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Project Engineer Medical Device information

What does a project engineer do in the medical device industry?

A Project Engineer in the medical device industry is responsible for planning, coordinating, and managing projects related to the development and manufacturing of medical devices. They oversee project timelines, budgets, and resources, ensuring that all technical and regulatory requirements are met. Their work involves collaborating with cross-functional teams, such as design, quality assurance, and regulatory affairs, to bring safe and effective medical devices to market. Project Engineers also help resolve technical challenges and ensure products comply with industry standards and government regulations.

What are the key skills and qualifications needed to thrive as a project engineer in the medical device industry?

To excel as a Project Engineer in medical devices, you need a solid background in engineering (typically a degree in biomedical, mechanical, or electrical engineering), experience with product development, and knowledge of regulatory standards like FDA and ISO 13485. Familiarity with CAD software, project management tools, and validation protocols is highly valuable, along with certifications such as PMP or Six Sigma. Strong problem-solving abilities, collaboration, and effective communication are essential soft skills for leading cross-functional teams and resolving technical challenges. These skills and qualifications ensure safe, compliant, and innovative device development that meets patient and market needs.

How does a project engineer in the medical device industry typically collaborate with cross-functional teams during product development?

As a Project Engineer in the medical device field, you’ll work closely with cross-functional teams such as R&D, quality assurance, regulatory affairs, and manufacturing. Collaboration involves coordinating project timelines, ensuring design requirements are met, and facilitating communication between departments to address technical challenges and regulatory compliance. Regular meetings and clear documentation are essential to keep all stakeholders aligned, and you may often serve as a bridge between engineering and non-engineering teams. This collaborative environment fosters innovation and helps ensure the successful and timely launch of safe, effective medical devices.

What is the difference between Project Engineer Medical Device vs Quality Engineer Medical Device?

AspectProject Engineer Medical DeviceQuality Engineer Medical Device
Required CredentialsBachelor's in Engineering, certifications like PMP beneficialBachelor's in Engineering or Science, certifications like CQE preferred
Work EnvironmentDesign, development, and project management teams in manufacturing or R&DQuality assurance, compliance, and inspection teams in manufacturing
Employer & Industry UsageMedical device companies focusing on product development and project executionMedical device companies ensuring product quality and regulatory compliance
Common Search & Comparison IntentUnderstanding project management roles in medical device industryUnderstanding quality assurance roles in medical device industry

The Project Engineer Medical Device focuses on managing product development projects, coordinating teams, and ensuring timely delivery. In contrast, the Quality Engineer Medical Device concentrates on maintaining product quality, compliance with regulations, and conducting inspections. Both roles are essential in medical device companies but serve different functions within the product lifecycle.

Infographic showing various Project Engineer Medical Device job openings in California as of August 2026, with employment types broken down into 67% Full Time, and 33% Contract. Highlights an 100% In-person job distribution.

Engineer - Senior Project (Medical)

Intertek

Lake Forest, CA • On-site

$120K - $140K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 7 days ago


Intertek rating

7.9

Company rating: 7.9 out of 10

Based on 78 frontline employees who took The Breakroom Quiz

50th of 120 rated laboratories


Job description

Senior Project Engineer-Medical - Lake Forest, California

Intertek, a leading provider of quality and safety solutions to many of the world's top-recognized brands and companies, is actively seeking a Senior Project Engineer-Medical to join our Electrical team in Lake Forest, California in the medical device compliance industry.  

Intertek's Electrical business line applies more than 100 years of product testing expertise to quickly and efficiently help clients meet safety, performance, environmental and quality requirements for every market. Spanning a wide range of industries such as Medical, Lighting, Renewable Energy, HVACR, Appliances & Electronics, Hazardous Locations, Industrial Equipment, Life Safety & Security, IT & Telecom Equipment, Intertek's global network of laboratories employ world-class experts in their fields who deliver quality, accurate testing and certification that continually exceeds our clients' expectations and helps to clear a path for their product's success. Intertek is continually innovating and evolving to reduce risk for consumers, brands and organizations in every sector and industry around the world. We go beyond Testing, Inspection and Certification of products: we are a Total Quality Assurance Provider to industries worldwide. Our Purpose: Bringing quality, safety, and sustainability to life.

What are we looking for?

The Senior Project Engineer - Medical is responsible for independently performing testing and evaluation on a variety of products to the provisions of U.S., Canadian and other International product safety standards, writing reports and communicating with clients. This position is also responsible for providing local expertise in one or more product categories and mentoring and training less senior technical personnel. This position has the potential for 15% travel.

Salary & Benefits Information 

The base wage or salary range for this position is $120K to $140K. Individual compensation packages are based on a variety of factors unique to each candidate including skill set, experience, qualifications, and other job-related reasons.  

In addition to competitive compensation packages, when working with Intertek you can expect benefits including medical, dental, vision, life, disability, 401(k) with company match, generous vacation / sick time (PTO), tuition reimbursement and more. 

What you'll do:

  • Read and determine applicability of national codes and standards clauses for the EUT (equipment under test.)
  • Perform testing of products in accordance with standards. Core tests include, but are not limited to: rating, leakage current, dielectric, temperature, pressure, stability, mechanical hazard, flammability, abnormal and fault insurance, rain, radiation, sound, and laser.
  • Mentor less senior technical personnel.
  • Supply information for quotes such as length of project, site needed, rental equipment, samples, and standards that will be used.
  • Set up and operate standard test equipment including, but not limited to: spectrum analyzer, oscilloscope, multi-meter, dielectric strength tester, ground continuity tester, digital multi-meter, surge generator, over-voltage tester, environmental condition chamber, and articulated probes. Use hand tools to build/calibrate test fixtures.
  • Provide local technical expertise and maintain reviewer status in one or more product categories. 
  • Proactively develop and communicate test procedures, new test fixtures and report shells for local office. 
  • Investigate technical complaints for the local office and support accreditations efforts by performing technical audits locally. 
  • Demonstrate enough product and/or standards knowledge to be considered an expert in multiple product categories for the local office. 
  • Provide quotations for a large array of standards and complex projects and products. 
  • Actively represent Intertek by participating on standards/industry committees and/or associations. 
  • Perform preliminary design reviews (PDR) both on and off site.
  • Perform field labeling jobs.
  • Follow sample handling procedures, ensuring that sample is logged in and out of the system.  Move equipment as needed through the facility. Properly package sample for shipment. 
  • Provide complex sales support such as giving presentations during client visits. 
  • Communicate project status and test results to client, sales personnel, and management throughout testing. Provide on-going support to clients as needed. 
  • Within policy guidelines, identify, properly document, and recommend engineering judgments. 
  • Perform other work as required.

This position outline is a general guideline and does not represent all encompassing details. The position assumes that the incumbent has both the mental and physical requirements to carry out the above defined duties. 

Minimum Requirements & Qualifications:

  • Bachelor's Degree in Engineering
  • 4+ years' experience in directly related field
  • Experience with IEC/UL/CSA safety certification standards (60601-1 and its collaterals and particulars, 61010-1, 62368-1, etc.)
  • Must have a valid unrestricted driver's license and safe driving record
  • Model Intertek's 10X Energies at all times within the work place, practicing business the right way
  • Be aware of, and adhere to, safety practices and policies to ensure your own safety, as well as the safety of others who may be affected by your actions at work 
  • Ability to work in fast-paced, multi-tasking environment with shifting priorities and demanding deadlines
  • Microsoft Office software experience is a must have
  • Must be customer focused and quality driven
  • Ability to travel as business needs dictate, up to 15%

Preferred Requirements & Qualifications:

  • Bachelor's degree in electrical or biomedical engineering
  • Engineer in Training (EIT)
  • Prior project management experience
  • Experience with U.S., Canadian, and other international product safety standards i.e., ANSI, CSA, UL, EN, IE

Intertek: Total Quality. Assured.

Intertek is a world leader in the Quality Assurance market, with a proven, high-quality business model and a global network of customer-focused operations and highly engaged subject matter experts. With passion, pace, and precision we work to exceed our customers' expectations, while engaging with our employees to be 10X in their performance and professional growth.

Intertek is a drug-free workplace. As a condition of employment, certain positions may be required to pass a pre-employment drug test based on the type of work that will be performed.

We Value Diversity

Intertek's network of phenomenal people are our greatest assets, and the diversity they bring fuels our success. Intertek is an Equal Employment Opportunity Employer that values inclusion and diversity. We take affirmative action to ensure all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or other legally protected characteristics.

For individuals with disabilities who would like to request accommodation, or who need assistance applying, please email intertekhrusa@intertek.com or call 1-877-694-8543 (option #5) to speak with a member of the HR Department.

#LI-AS1 

*Intertek does not accept unsolicited approaches from agencies and will not pay a fee for any placement resulting from the receipt of an unsolicited resume. 

Intertek is a leading Total Quality Assurance provider to industries worldwide. Our network of more than 1,000 laboratories and offices in more than 100 countries, delivers innovative and bespoke Assurance, Testing, Inspection and Certification (ATIC) solutions for our customers' operations and supply chains. Working at Intertek means joining a global network of state-of-the-art facilities and passionate people who deliver superior customer service with a purpose of bringing quality, safety, and sustainability to life. 

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