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Intern Medical Device Engineer Jobs in California

Device Engineer III

Foster City, CA · On-site

$117K - $152K/yr

We are seeking a highly motivated, detail-oriented Device Engineer III to support drug-device ... Development and manufacturing of medical devices in accordance with ISO 13485. * Risk management in ...

Device Engineer III

Foster City, CA · On-site

$117K - $152K/yr

We are seeking a highly motivated, detail-oriented Device Engineer III to support drug-device ... Development and manufacturing of medical devices in accordance with ISO 13485. * Risk management in ...

This person is primarily responsible for providing updates to the line lead/ engineers of build ... Benefit packages for this role will start on the 1st day of employment and include medical, dental ...

New

Be Seen First

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 ...

OLED Device Engineer

Cupertino, CA · On-site

$184.70 - $324.80/hr

Develop and define OLED device electrical and optical performance specifications with potential ... Comprehensive medical and dental coverage, retirement benefits, a range of discounted products and ...

Showing results 41-60

Intern Medical Device Engineer information

What does an intern medical device engineer do?

An Intern Medical Device Engineer assists in the design, development, and testing of medical devices under the supervision of experienced engineers. Their responsibilities may include conducting research, creating prototypes, analyzing data, and ensuring products meet regulatory standards. Interns often collaborate with cross-functional teams and gain hands-on experience in the medical device industry. This role provides valuable exposure to engineering processes and helps interns build skills required for a future career in biomedical engineering.

What types of projects and responsibilities can an intern medical device engineer expect during their internship?

As an Intern Medical Device Engineer, you can expect to participate in hands-on projects such as assisting in prototype development, performing laboratory testing, and collecting and analyzing data for product improvement. You'll often work closely with senior engineers, quality assurance teams, and regulatory specialists to ensure devices meet safety and compliance standards. Interns may also help prepare technical documentation and contribute to brainstorming sessions for new product features, providing a well-rounded exposure to the medical device development process. This collaborative environment offers valuable experience and networking opportunities for future career growth.

What are the key skills and qualifications needed to thrive as an intern medical device engineer?

To thrive as an Intern Medical Device Engineer, you need a solid background in biomedical engineering or a related field, along with foundational knowledge of device design and regulatory standards. Familiarity with CAD software, prototyping tools, and basic laboratory testing equipment is typically required, and coursework or certification in medical device regulations can be advantageous. Strong problem-solving, teamwork, and communication skills help interns contribute effectively to multidisciplinary projects and adapt to feedback. These competencies are crucial for ensuring safe, innovative device development and successful collaboration in a regulated industry.

What is the difference between Intern Medical Device Engineer vs Junior Medical Device Engineer?

AspectIntern Medical Device EngineerJunior Medical Device Engineer
CredentialsTypically pursuing or recently completed a relevant degreeBachelor's or Master's in biomedical, mechanical, or related engineering
Work EnvironmentInternship setting, supervised, learning-focusedEntry-level professional role, more independent tasks
Employer & Industry UsageMedical device companies, research labs, internshipsMedical device companies, manufacturing, R&D teams

Intern Medical Device Engineers are usually students or recent graduates gaining hands-on experience, while Junior Medical Device Engineers are entry-level professionals with some work experience. The internship focuses on learning and support, whereas the junior role involves more responsibility in product development and testing.

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 cities in California are hiring for Intern Medical Device Engineer jobs?

Cities in California with the most Intern Medical Device Engineer job openings:

Infographic showing various Intern Medical Device Engineer job openings in California as of August 2026, with employment types broken down into 27% Internship, 55% Full Time, and 18% Contract. Highlights an 100% In-person job distribution.

Manufacturing Engineer (medical device)

Stellent IT LLC

Camarillo, CA • On-site

$74K - $95K/yr

Other

Posted 13 days ago


Key responsibilities

  • Lead process development and process optimization of manufacturing equipment and processes.

  • Create and validate technical documentation, test methods, and validation activities to ensure compliance with GMP, FDA, and ISO standards.

  • Collaborate cross-functionally to support new product introductions, process improvements, and equipment validation activities.


Job description

Job details:

Job title:Manufacturing Engineer (medical device)

Location: Camarillo. CA

Long Term Contract

Job Description:

6+ years of experience in life sciences and medical device industries, excelling in New Product Introduction (NPI), process development, equipment validation (IQ/OQ/PQ), test method validation (TMVs) and continuous improvement in GMP, FDA, and ISO 13485 environments driving process efficiency and compliance.

EDUCATION

  • M.S., Engineering preferred (but not required)
  • B.S., Engineering Could be Biomedical, Mechanical, Industrial, Manufacturing, Aerospace

RELEVANT EXPERIENCE

Sr. Manufacturing Process Engineer New Product Introduction (NPI)

  • Led process development and process optimization of semi-automated equipment using Design of Experiments (DOE), statistical analysis and control charts (Minitab) to improve yield by 23%
  • Authored comprehensive technical documentation including URS, IQ/OQ/PQ, SOPs, MPIs, Engineering Reports, BOMs, and Work Instructions in support of GMP/FDA/ISO 9001 compliance
  • Created and validated functional and destructive Test Methods; conducted Test Method Validation (TMV)-Attribute and Variable using Gage R&R to ensure high reliability and repeatability
  • Executed Sterilization Validation (EO/Gamma) for subassembly level components per ISO standards and regulations
  • Collaborated cross-functionally with R&D, Quality, Supply Chain, and Suppliers to develop material specifications for raw materials, subassemblies, and finished goods
  • contributing to a 15% reduction in material non-conformances and improved first-pass yield.
  • Designed tooling and fixtures in SolidWorks, driving production efficiency, cost reduction, and improved throughput by identifying bottlenecks and reduced scrap rate by 15%
  • Managed facility expansion projects, performing impact/risk assessments, coordinating equipment calibration, preventive maintenance, and equipment qualification for seamless integration
  • Supported DFM activities and Design Verification & Validation (V&V) builds for New Product Introductions (NPI), ensuring manufacturability and quality from concept through scale-up
  • Spearheaded technology transfer of capital equipment that increasing operator efficiency by 30%, moving from single-pill to multi-pill packaging and managing validation activities
  • Engineered and supported manufacturing of injection-molded plastic and silicone components by introducing and optimizing capital equipment, leveraging strong GD&T knowledge to interpret detailed mechanical drawings and ensure design intent
  • Conducted and maintained pFMEAs, cycle time, and yield analyses, leading to a 20% reduction in equipment downtime
  • Drove compliance by partnering with Quality to ensure GxP alignment; owned ECOs/DCOs for process changes via QMS-PLM (Arena)

TECHNICAL SKILLS

  • Manufacturing & Quality: DOE, Gage R&R, SPC, ANOVA, TMV, GMP, IQ/OQ/PQ, CAPA, pFMEA, Aseptic Manufacturing, Root Cause Analysis (5 Whys, Fishbone), Sterilization (EO, Gamma), Injection Molding, Thermoforming, Serialization, Packaging
  • Tools & Software: Microsoft Office, Minitab, JMP, SolidWorks, Visio, SAP ERP, MES, Arena, JIRA, Agile, Windchill, Microsoft ProjectMethods & System: Lean Manufacturing, Six Sigma (DMAIC), 5S, A3, 8D, PDCA, Gemba Walk, VSM
  • Project & Program Management: Project Management, Team Management, Project Planning, Stakeholder Communication, Risk Management, Budget Management, RACI Matrice

Sandip Kumar
Sr. Tech Recruiter

Email:

Address:
505 Knolle Court
Saint Augustine, FL 32092

Telephone:
+1


Stellent IT logo

About Stellent IT

Sourced by ZipRecruiter

Stellent IT, based in St Augustine, Florida, USA, is a renowned company in the IT sector whose primary focus is providing top-tier IT consulting and staffing services. Stellent IT's expertise lies not just in fulfilling IT staffing needs but in offering comprehensive technological solutions that enhance and drive business performance. Despite the limited information about their founding history, the company has earned a name for itself in the IT industry due to its commitment to quality and consistent delivery. With a mission centered around helping businesses efficiently navigate the IT landscape by providing strategic technology-inspired solutions, Stellent IT prides itself as a leader in its field.

Industry

Recruiting and staffing services

Company size

11 - 50 Employees

Headquarters location

St Augustine, FL, US

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