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Entry Level Medical Device Engineer Jobs in Boston, MA

restor3d

Manufacturing Engineer I

Wilmington, MA · On-site

$80K - $85K/yr

Required Education and Experience: - 1-3 years of experience in manufacturing process support and development in the medical device industry. - Bachelor's Degree in Engineering required Preferred ...

restor3d

Manufacturing Engineer I

Wilmington, MA · On-site

$80K - $85K/yr

Required Education and Experience: - 1-3 years of experience in manufacturing process support and development in the medical device industry. - Bachelor's Degree in Engineering required Preferred ...

Analog Devices

Engineer, Quality Engineering

Wilmington, MA · On-site

$78K - $101K/yr

We are seeking a motivated Quality Systems Engineer to join our team. This role supports the ... Understanding quality management principles and regulatory requirements in the medical device ...

Analogdevices

Engineer, Quality Engineering

Wilmington, MA · On-site

$78K - $101K/yr

We are seeking a motivated Quality Systems Engineer to join our team. This role supports the ... Understandingquality management principles and regulatory requirements in the medical device ...

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All JobsMedical Device Engineer JobsEntry Level Medical Device Engineer JobsEntry Level Medical Device Engineer Jobs in Boston, MA

Entry Level Medical Device Engineer information

See Boston, MA salary details

$15

$34

$55

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

As of Aug 7, 2026, the average hourly pay for entry level medical device engineer in Boston, MA is $34.02, according to ZipRecruiter salary data. Most workers in this role earn between $29.76 and $37.60 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 are popular job titles related to Entry Level Medical Device Engineer jobs in Boston, MA? For Entry Level Medical Device Engineer jobs in Boston, MA, the most frequently searched job titles are:
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Entry Level Medical Device Engineer jobs near you
Infographic showing various Entry Level Medical Device Engineer job openings in Boston, MA as of August 2026, with employment types broken down into 85% Full Time, and 15% Contract. Highlights an 92% In-person, and 8% Hybrid job distribution, with an average salary of $70,757 per year, or $34 per hour.

Manufacturing Engineer I

restor3d

Wilmington, MA • On-site

$80K - $85K/yr

Full-time

Re-posted 25 days ago

Job description

Job Summary: The Manufacturing Engineer I will be responsible for the selection, development, qualification, and scale-up of production processes and equipment across different manufacturing departments. Process objectives are the high quality, high volume production of patient-tailored implants and associated instruments.

Duties and responsibilities:

-       Develop and maintain strong, internal working relationships across restor3d.

-       Understand the objectives, responsibilities, and mission of the Operations department and works towards those goals.

-       Prioritize and plan work activities; adapt for changing conditions.

-       Initiation, execution, and documentation of IQ, OQ, & PQ activities

-       Optimization of manufacturing processes (5S) for Lean Manufacturing

-       Development of formal training programs for the production personnel

-       Day-to-day production support activities such as NCRs and CAPAs

-       Processing of engineering change orders from originator to final approval

-       Developing and updating preventative maintenance programs

-       Writing and executing process validation plans and reports, using sound, data/stats supported results.

-       Play a major role in the CNC process for the manufacturing of implants

-       Using Statistical tools for alternative material evaluations and validations projects

-       Support of material handling and control system

-       Conduct time studies and process flow mapping.

-       Assure compliance with the requirements set forth by US FDA QSR and ISO regulations

-       Documentation of manufacturing processes and inspection criteria within the company’s documentation procedures.

-       Evaluate and recommend capital equipment to best suit needs of company’s selected fabrication processes.

-       Participation on project teams as a key contributor bringing proactive solutions and execution.

-       Other responsibilities as assigned.

 

Required Education and Experience:

-       1-3 years of experience in manufacturing process support and development in the medical device industry.

-       Bachelor’s Degree in Engineering required

 

Preferred Education and Experience:

-       Previous experience in orthopedics strongly preferred

-       Previous experience working with CNC machines preferred

-       Medical Device/GMP experience preferred

 

Required Skills:  

-       Excellent written and verbal communication skills.

-       Able to work accurately in medical device regulated environment with strong attention to detail.

-       Demonstrated ability to monitor own work to ensure quality, accuracy and thoroughness.

-       Strong organizational, analytical and time-management skills.

-       Able to self-motivate and work both independently and as part of a team.

-       Understanding of ISO 13485 and QSR regulations

-       Knowledge of statistical analysis (Green Belt preferred)

-       Experience working with CNC manufacturing processes

-       Knowledge of computer aided design (SolidWords preferred)

Physical Requirements: 

-       Working at a desk for prolonged periods of time.

-       Working with CNC machines/equipment.