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Entry Level Medical Device Engineer Jobs in California

Aerotek

Medical Device Assembler

Lake Forest, CA

$19.25 - $23.50/hr

... device assembly and packaging for medical device products. This role requires strong manual ... Read and interpret manufacturing procedures, engineering drawings, and inspection procedures ...

New

Aerotek

Medical Device Assembler

Carlsbad, CA

$18.50 - $22.50/hr

Medical Device Manufacturing Technician This role focuses on the manufacturing and assembly of ... Collaborate with engineers to develop and refine process documentation for manufacturing and ...

Crown Medical, Inc.

Medical Device Rep

Santa Barbara, CA · On-site

$82K - $113K/yr

Medical Sales Territory Representative - Entry Level We are a leading Medical Device and Equipment company focused on 5 innovative segments of the U.S Healthcare market. We are a fully integrated ...

Crown Medical, Inc.

Medical Device Rep

Carlsbad, CA · On-site

$82K - $113K/yr

Medical Sales Territory Representative - Entry Level We are a leading Medical Device and Equipment company focused on 5 innovative segments of the U.S Healthcare market. We are a fully integrated ...

SlingShot Connections

Be Seen First

Medical Device Assembler

San Clemente, CA · On-site

$20.25/hr

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 ...

Kelly Services

Medical Device Assembler

Irvine, CA

$24/hr

As a Medical Device Assembler, you will play a key role in developing and assembling innovative ... engineers in resolving product and process problems. * Complete documentation such as Device ...

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Entry Level Medical Device Engineer information

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How much do entry level medical device engineer jobs pay per hour?

As of Jul 26, 2026, the average hourly pay for entry level medical device engineer in California is $30.90, according to ZipRecruiter salary data. Most workers in this role earn between $27.07 and $34.18 per hour, depending on experience, location, and employer.

What does an entry level medical device engineer do?

An entry level medical device engineer assists in designing, developing, and testing medical devices such as implants, diagnostic equipment, or surgical tools. They often work as part of a team under the supervision of experienced engineers, ensuring products meet regulatory standards and function safely and effectively. Responsibilities may also include documenting results, conducting research, and supporting manufacturing or quality assurance processes. This role provides hands-on experience with engineering principles in the healthcare industry and often serves as a starting point for more specialized or senior positions.

What is the difference between Entry Level Medical Device Engineer vs Quality Assurance Technician?

AspectEntry Level Medical Device EngineerQuality Assurance Technician
Required CredentialsBachelor's in engineering, biomedical or related fieldBachelor's in science, engineering, or related field; certifications optional
Work EnvironmentDesign labs, manufacturing facilities, R&D teamsManufacturing plants, quality control labs
Employer & Industry UsageMedical device companies, biotech firmsManufacturers, healthcare device companies

Entry Level Medical Device Engineers focus on designing and developing medical devices, while Quality Assurance Technicians ensure products meet quality standards. Both roles are essential in the medical device industry and often work closely to ensure product safety and compliance.

What Does an Entry-Level Medical Device Engineer Do?

As an entry-level medical device engineer, your duties include the research, design, and development of medical devices and healthcare products and equipment. An entry-level engineer works as part of a research and development team. You typically have specific tasks such as performing research on materials or testing a device in a laboratory setting or during a clinical trial. In addition to responsibilities related to design and development, entry-level engineers often document tests and trials, collect and organize data, and create drawings and plans using computer-aided design software.

What types of projects and responsibilities can an entry level medical device engineer expect during their first year on the job?

As an entry level medical device engineer, you can expect to work closely with cross-functional teams—including design, quality, and manufacturing—to support product development and improvements. Your responsibilities may include assisting in prototyping, conducting testing and data analysis, and maintaining detailed documentation to ensure regulatory compliance. You’ll likely gain hands-on experience troubleshooting devices, collaborating in design reviews, and participating in validation activities. This role provides an excellent foundation for learning industry standards and building technical and teamwork skills essential for career advancement.

What are the key skills and qualifications needed to thrive as an Entry Level Medical Device Engineer, and why are they important?

To thrive as an Entry Level Medical Device Engineer, you need a bachelor's degree in biomedical, mechanical, or electrical engineering, along with a solid understanding of engineering principles and medical device regulations. Familiarity with CAD software, prototyping tools, and knowledge of FDA or ISO standards is typically required. Strong problem-solving skills, attention to detail, and effective teamwork and communication abilities help you stand out in this role. These competencies are critical for ensuring the safe design and development of innovative medical devices that meet regulatory standards and patient needs.
More about Entry Level Medical Device Engineer jobs
What are the most commonly searched types of Medical Device Engineer jobs in California? The most popular types of Medical Device Engineer jobs in California are:
What are popular job titles related to Entry Level Medical Device Engineer jobs in California? For Entry Level Medical Device Engineer jobs in California, the most frequently searched job titles are:
What job categories do people searching Entry Level Medical Device Engineer jobs in California look for? The top searched job categories for Entry Level Medical Device Engineer jobs in California are:
What cities in California are hiring for Entry Level Medical Device Engineer jobs? Cities in California with the most Entry Level Medical Device Engineer job openings:
Entry Level Medical Device Engineer jobs near you
Infographic showing various Entry Level Medical Device Engineer job openings in California as of July 2026, with employment types broken down into 78% Full Time, 14% Part Time, and 8% Contract. Highlights an 93% Physical, 2% Hybrid, and 5% Remote job distribution, with an average salary of $64,277 per year, or $30.9 per hour.
Engineer, Drug Device Combination Product - Prefilled Syringes (JP15357)

Engineer, Drug Device Combination Product - Prefilled Syringes (JP15357)

3 Key Consulting

Thousand Oaks, CA

$40 - $46/hr

Full-time

Posted 19 days ago

Job description

Job Title: Engineer, Drug Device Combination Product – Prefilled Syringes (JP15357)
Location: Thousand Oaks, CA
Business Unit: Prefilled Syringes And Lyo Kit Platforms
Employment Type:  Contract
Duration: 12 months with likely extensions or conversion to perm
Rate: $40-46/hours W2 with benefits
Posting Date: 5/7/2026
Target Start Date: 6/1/2026
3 Key Consulting is hiring!  We are recruiting an Engineer for a consulting engagement with our direct client, a leading global biotechnology company.
Ideal Candidate: has hands-on experience in engineering environments, particularly with tools like Instron systems and optical measurement methods, as well as proficiency in technical documentation and teamwork. They should have experience in regulated industries, preferably biopharma, biomedical, or medical devices, though aerospace or mechanical disciplines are acceptable. Proficiency in Microsoft Office is required, and CAD/SolidWorks skills are a plus. Entry-level candidates with practical experience, such as internships, are preferred, while overqualification (e.g., PhD or advanced degrees with extensive experience) is less desirable. Packaging engineering knowledge is a bonus but not mandatory.
Job Description:.
The Device Engineer will participate in the design, development, and lifecycle management design control activities for commercialized drug delivery devices. This role includes technical operations support for combination product development to global launch, clinical and commercial manufacturing, failure investigation, design change evaluation, development and execution of test procedures, and continuous improvement initiatives.
Scope includes mechanical delivery devices, such as; Prefilled syringes. The qualified candidate will be part of a sustaining device engineering team that ensures design history files of these mechanical delivery devices are maintained. The engineer will participate in cross functional teams, leading device design activities such as the development of product enhancements, analytical failure analysis and implementation of design solutions, assessment of proposed changes, support product launches, defend inspection and ensure the follow through of commitments.
Essential skills and Responsibilities:
 
  • Adheres to strict documentation practices in a GMP regulated environment
  • Fully competent engineer in all conventional aspects of the subject matter, functional area, and assignments, plans and conduct work requiring judgment in the independent evaluation, selection, and substantial adaptation and modification of standard techniques, procedures and criteria and devises new approaches to problems encountered.
  • Authors and reviews technical documentation including protocols, reports, and technical assessments
  • Analyze and trend generated data by applying relevant statistical techniques to enable senior staff to make informed decisions
  • Coordinates and executes laboratory testing to support characterization, verification, design transfer, and fill-finish efforts
  • Maintains combination product design history files for assigned products
  • Develops characterization test methods through fixture prototyping, reference sample creation, and GR&R analysis
  • Provides functional subject matter expertise to actively participate in cross-functional activities including system level root cause analysis, design changes, and change control assessments
  • Provide general laboratory support including inventory management, sample shipments, and cleanup.
  • Works with Scientists and Engineers, to assess and develop appropriate design and manufacturing specifications
  • Individual contributor with Leadership attributes to effectively represent device engineer within a large network/matrix organization
  • At a minimum familiar with the following standards and regulations:
  • Quality System Regulation – 21CFR820
  • Risk Management – ISO 14971
  • EU Medical Device requirements – Council Directive 93/42/EEC

Preferred Qualifications:
  • Bachelor’s Degree or higher in relevant engineering or scientific field (Mechanical, Biomedical, Bioengineering)
  • Minimum 2 year of scientific or engineering experience in a GMP regulated environment
  • Statistical Analysis software (Minitab or JMP)
  • Strong technical writing skills
  • CAD fixturing software (SolidWorks)
  • Tolerance Stack-Ups (2D, 3D, RSS)
  • Instron force tester using BlueHill Universal
  • Experience with design controls; including (but not limited to) verification and design transfer
  • Understanding of risk assessments including hazard and probability analysis
  • Background in medical device development, commercialization and knowledge of manufacturing processes (fill-finish)
  • Ability to work independently and dynamically across functional teams
  • Excellent written and verbal communication skills
  • Ability to support complex workstreams under demanding timelines

Top Must Have Skill Sets:
  • Technical Writing and Succinct Communication of Technical Topics
  • In-Lab Testing
  • Tolerance Stack-Ups

Day to Day Responsibilities:
Documentation, Testing, Organization of Timelines and management of deliverables, cross-functional collaboration.
Basic Qualifications:
Master degree OR Bachelor degree and 2 years of experience OR Associate degree and 6 years of experience OR High school diploma / GED and 8 years of experience
 
Red Flags:
Overly Timid, Non-Succinct Communication, Lack of Technical Basis
Additional stand-alone red flag: inability to be present on site/support onsite based activities. This is a hybrid role, NOT fully remote.
Interview Process:
Virtual - 1:1 with the manager and Panel Interview
We invite qualified candidates to send your resume to recruiting@3keyconsulting.com.  If you decide that you’re not interested in pursuing this particular position, please feel free to take a look at the other positions on our website www.3keyconsulting.com/careers. You are also welcome to share this opportunity with anyone you think might be interested in applying for this role.