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Entry Level Medical Device Engineer Jobs (NOW HIRING)

Aerotek

Medical Device Assembler

Lake Forest, CA · On-site

$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 ...

MagVenture

Be Seen First

Medical Device Customer Support Technician

Alpharetta, GA · On-site

$55K - $64K/yr

We are seeking an entry-level Medical Device Customer Support Technician to serve as the first ... Qualifications: * Background in biomedical engineering, life sciences, neuroscience, BMET or ...

Crown Medical, Inc.

Medical Device Rep

Albuquerque, NM · 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

Baton Rouge, LA · 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

Sarasota, FL · 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

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

Austin, TX · 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

Boca Raton, FL · 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 ...

onsemi

Device Engineer for Bucheon Site

Livonia, NY · On-site

The Entry-Level Device Engineer will support the development and improvement of semiconductor devices (Si/SiC MOSFET, IGBT). This role involves device analysis, simulation, and collaboration with ...

Arrow Electronics, Inc.

Device Engineer

Cedar Rapids, IA · On-site

$79K - $130K/yr

Device Engineer What You'll Be Doing: * Perform Development and Verification for Flight Management ... Medical, Dental, Vision Insurance * 401k, With Matching Contributions * Short-Term/Long-Term ...

Arrow Electronics

Device Engineer

Cedar Rapids, IA · On-site

$79K - $130K/yr

Device Engineer What You'll Be Doing: * Perform Development and Verification for Flight Management ... Medical, Dental, Vision Insurance * 401k, With Matching Contributions * Short-Term/Long-Term ...

SlingShot Connections

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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 ...

Bracco

Medical Device Assembler I

Eden Prairie, MN · On-site

$18.25 - $22.50/hr

The Medical Device Assembler I is responsible for performing a variety of production tasks related ... Instructions (WI), Engineering Prints and Bills of Materials (BOM). Primary Duties ...

Kelly Services

Medical Device Assembler

Irvine, CA · On-site

$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 ...

Bracco

Medical Device Assembler I

Eden Prairie, MN

$18.25 - $22.50/hr

The Medical Device Assembler I is responsible for performing a variety of production tasks related ... Instructions (WI), Engineering Prints and Bills of Materials (BOM). Primary Duties ...

Hearst Health

Medical Device Coder

Carmel, IN · On-site

$17.75 - $23.75/hr

Partnering with our information system developer and healthcare institution customers, you'll help ... Evaluates medical device content to ensure the accuracy of HCPCS mappings. * Follows up with ...

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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 Aug 6, 2026, the average hourly pay for entry level medical device engineer in the United States is $31.31, according to ZipRecruiter salary data. Most workers in this role earn between $27.40 and $34.62 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 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.
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What cities are hiring for Entry Level Medical Device Engineer jobs? Cities with the most Entry Level Medical Device Engineer job openings:
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Entry Level Medical Device Engineer jobs near you
Infographic showing various Entry Level Medical Device Engineer job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 15% Part Time, and 6% Contract. Highlights an 91% Physical, 1% Hybrid, and 8% Remote job distribution, with an average salary of $65,130 per year, or $31.3 per hour.

Engineer - Biotech Medical Device (Lifecycle Management, Design Controls, Documentation) - (JP15650)

3 Key Consulting

Thousand Oaks, CA • Hybrid

$40 - $46/hr

Full-time

Posted yesterday

New

Job description

Job Title: Engineer – Biotech Medical Device (Lifecycle Management, Design Controls, Documentation) - (JP15650)
Location: Thousand Oaks CA OR Cambridge MA 
Employment Type: Contract
Business Unit: Mechanical Autoinjectors Platform 
Duration: 16 months with likely extensions and/or conversion to permanent
Posting Date: 08/04/2026
Pay Rate: $40 - $46/hour W2 with benefits
Notes: Must be local - hybrid work schedule 3 onsite, 2 WFH - Urgent role to fill.
3 Key Consulting is hiring a Medical Device Engineer – Combination Products (Lifecycle Management, Design Control, Documentation) for a consulting engagement with our direct client, a leading global biopharmaceutical company.
Job Description:
The Engineer will support the lifecycle management (LCM) of commercial combination products, providing technical engineering support throughout the product lifecycle to ensure continued product quality, reliability, and compliance. This role partners with cross-functional teams including Manufacturing, Quality, Design Engineering, Reliability, Regulatory, and Supply Chain to investigate product performance, support product improvements, maintain design documentation, and execute Design Controls activities.
The successful candidate will apply engineering fundamentals, analytical problem-solving, and technical documentation skills to support commercial products through forensic investigations, trend analysis, engineering change management, and continuous improvement initiatives. The Engineer I will also support cross-functional initiatives to sustain commercial combination products through engineering investigations, risk assessments, Design Controls, and continuous product and process improvements.
Top Must Have Skill Sets:
1) Device Design Controls understanding and associated experience
2) Theoretical or practical experience in device failure more root cause analysis
3) Good documentation skills
Key Responsibilities
  • Support lifecycle management activities for commercial combination products throughout their commercial lifecycle.
  • Perform forensic evaluation of returned, retained, and engineering samples to support technical investigations.
  • Assemble and disassemble combination product samples for engineering analysis, troubleshooting, and failure investigations.
  • Lead and support structured root cause investigations using sound engineering methodologies and cross-functional collaboration.
  • Manage technical trend investigations by evaluating manufacturing, laboratory, complaint, and engineering data to identify product or process trends and recommend appropriate actions.
  • Support engineering investigations associated with deviations, CAPAs, nonconformances, and product complaints to identify root causes and implement effective corrective and preventive actions.
  • Support engineering change control activities, including technical assessments, risk evaluations, documentation updates, and implementation of product and process changes.
  • Support product risk management activities, including risk assessments, Design FMEA (dFMEA), Process FMEA (pFMEA), and evaluation of design or process changes throughout the commercial lifecycle.
  • Support Design Controls activities across the product lifecycle, including feasibility, characterization, verification, validation, design transfer, and post-market engineering support.
  • Support development, qualification, execution, and continuous improvement of engineering test methods used for characterization, verification, validation, and commercial lifecycle investigations.
  • Support development and maintenance of engineering specifications, test methods, and technical standards for commercial combination products.
  • Author, review, and maintain technical documentation including engineering assessments, protocols, reports, specifications, test methods, risk assessments, and Design Controls deliverables.
  • Support the development, maintenance, and continuous improvement of Design History Files (DHF) and Device Master Records (DMR).
  • Collaborate with Manufacturing, Quality, Regulatory, and Operations teams to support commercial production, technical investigations, product improvements, and continuous improvement initiatives.
  • Apply engineering principles and statistical methods to analyze engineering, manufacturing, laboratory, and complaint data to support technical decision making, product performance assessments, and issue resolution.
  • Support product complaint investigations and engineering assessments to identify potential failure mechanisms and corrective actions.
  • Ensure engineering documentation is complete, accurate, and compliant with applicable quality system requirements and company procedures.
  • Support multiple commercial programs while effectively managing priorities and project timelines.

Preferred Qualifications and Experience
Experience in one or more of the following areas:
  • Combination products or medical device development, commercialization, or lifecycle management.
  • Lifecycle management (LCM) of commercial medical devices or combination products.
  • Mechanical system design, testing, and analysis.
  • Mechanical failure analysis and root cause investigations.
  • Product complaint investigations and forensic engineering analysis.
  • Experience performing computed tomography (CT) scanning, X-ray imaging, or comparable non-destructive forensic analysis techniques for medical devices or plastic injection molded components.
  • Experience performing forensic analysis of plastic injection molded components, including dimensional, cosmetic, structural, or material-related investigations to support root cause analysis and product performance assessments.
  • Assembly and disassembly of medical devices for engineering evaluation.
  • Engineering change control and product lifecycle documentation.
  • Experience supporting deviations, CAPAs, nonconformances, and engineering investigations within a regulated quality system.
  • Design Controls activities including feasibility, characterization, verification, validation, design transfer, and post-market support.
  • Development and maintenance of Design History Files (DHF) and Device Master Records (DMR).
  • Experience participating in Design FMEA (dFMEA), Process FMEA (pFMEA), and engineering risk assessments.
  • Risk management in accordance with FDA Quality System Regulation, ISO 13485, and ISO 14971 principles.
  • Statistical analysis and interpretation of engineering, manufacturing, laboratory, or complaint data.
  • Experience using statistical software such as Minitab, JMP, or equivalent for engineering and data analysis.
  • Familiarity with Design of Experiments (DOE), Statistical Process Control (SPC), process capability analysis, and engineering statistics.
  • Trend analysis using manufacturing, laboratory, or complaint data to identify product or process performance trends.
  • Technical documentation, engineering reports, protocols, and scientific writing.
  • Laboratory instrumentation and test equipment.
  • Mechanical testing and characterization of medical devices or plastic injection molded components.
  • Test method development, verification, validation, and qualification.
  • Prototype fabrication and mechanical evaluation.
  • Test fixture design and development.
  • SolidWorks or equivalent 3D CAD software.
  • Ability to interpret engineering drawings, geometric dimensioning and tolerancing (GD&T), specifications, and technical standards.
  • Cross-functional collaboration with Manufacturing, Quality, Regulatory, Reliability, and Design Engineering teams.
Basic Skills
  • Strong analytical, troubleshooting, and problem-solving skills.
  • Ability to perform structured root cause investigations using sound engineering methodologies.
  • Excellent written and verbal communication skills.
  • Strong technical writing skills for engineering documentation, reports, and Design Controls deliverables.
  • Ability to analyze complex technical data and communicate engineering conclusions effectively.
  • Ability to read, interpret, and apply engineering drawings, specifications, technical procedures, and applicable quality system requirements.
  • Strong organizational skills with the ability to manage multiple assignments and priorities in a fast-paced, regulated environment.
  • Ability to work independently while collaborating effectively within cross-functional teams.
  • High attention to detail and commitment to quality.
  • Comfortable working in laboratory, manufacturing, and office environments while following applicable safety procedures.
Work Environment
This position includes laboratory, manufacturing, and office-based activities supporting commercial combination products. Responsibilities include handling and evaluating drug delivery devices, performing engineering evaluations, operating laboratory equipment, and supporting investigations involving prefilled syringe-based combination products in accordance with applicable safety procedures.
This is a contingent worker position supporting engineering activities within company Combination Product Engineering organization.
Why is the Position Open?
Supplement additional workload on team
Day to Day Responsibilities:
Ability to support RCAs from rejected units from assembly site sites. Maintenance of trend evaluations across the LCM network and ability to support LCM and some development documentation related to design controls such as verification plans and DHF maintenance.
Value Proposition: Unique industry opportunity, career growth, experience
Red Flags:
  • Lack of experience in the design controls process.
  • No ability to perform testing at ATO or AMA site
  • Minimal to no experience or understanding of combination products or drug delivery devices.
  • Bad communication skills.
  • Uncomfortable with a hybrid working environment.

Interview process:
  • Interviews to be begin ASAP
  • Two virtual interviews
  • Final onsite interview

We invite qualified candidates to send your resume to resumes@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.