1

Internship Medical Device Engineer Intern Jobs in Boston, MA

Medical Device Assembler

Westford, MA · On-site

$19 - $21.51/hr

Medical Device Assembler Location : Westford, MA Employment Type : Full-Time| 6 Month contract | W2 ... technology, engineering, manufacturing, and project management. At BEPC , we are driven by ...

Be Seen First

Medical Device Assembler

Westford, MA · On-site

$19 - $21.50/hr

Medical Device Assembler Location : Westford, MA Employment Type : Full-Time| 6 Month contract | W2 ... technology, engineering, manufacturing, and project management. At BEPC , we are driven by ...

By submitting your interest, you'll be among the first to know when internship opportunities open ... Producing documentation to support medical device regulatory processes Who This Is For * Students ...

By submitting your interest, you'll be among the first to know when internship opportunities open ... Producing documentation to support medical device regulatory processes Who This Is For * Students ...

next page

Showing results 1-20

Internship Medical Device Engineer Intern information

See Boston, MA salary details

$12

$20

$32

How much do internship medical device engineer intern jobs pay per hour?

As of Sep 5, 2026, the average hourly pay for internship medical device engineer intern in Boston, MA is $20.98, according to ZipRecruiter salary data. Most workers in this role earn between $17.50 and $22.74 per hour, depending on experience, location, and employer.

What is the difference between Internship Medical Device Engineer Intern vs Medical Device Quality Assurance Intern?

AspectInternship Medical Device Engineer InternMedical Device Quality Assurance Intern
Required CredentialsEnrolled in engineering or related degree, some certifications beneficialEnrolled in quality assurance, engineering, or related degree, certifications like ISO or GMP helpful
Work EnvironmentDesign labs, R&D departments, product development teamsQuality labs, compliance departments, manufacturing settings
Employer & Industry UsageMedical device manufacturing companies, R&D firmsMedical device manufacturers, regulatory agencies, compliance firms
Common Search & ComparisonYesYes

The Internship Medical Device Engineer Intern focuses on product design, development, and engineering tasks within medical device companies. In contrast, the Medical Device Quality Assurance Intern concentrates on quality control, compliance, and regulatory standards. Both roles often require related educational backgrounds and are found in similar environments, but they serve different functions within the medical device industry.

Infographic showing various Internship Medical Device Engineer Intern job openings in Boston, MA as of August 2026, with employment types broken down into 20% Internship, 47% Full Time, 23% Part Time, and 10% Temporary. Highlights an 100% In-person job distribution, with an average salary of $43,645 per year, or $21 per hour.

Sr Staff Device Engineer

Scorpion Therapeutics

Lexington, MA • On-site

$170 - $210/hr

Other

Posted 6 days ago


Job description

Sr. Staff Device Engineer (Commercial Device Engineering - CDE)Responsibilities:
  • Serve as device SME for combination product device lifecycle management for on-market products.
  • Lead change controls, manufacturing process validation, device product complaint handling, and regular review of DHF.
  • Support post-market surveillance and provide input to MDR and post-market surveillance reports.
  • Act as commercial device technical lead with cross-functional teams to manage lifecycle of commercial combination products.
  • Conduct technical investigations; analyze manufacturing and commercial expansion technical aspects.
  • Oversee commercial device qualification; coordinate tech transfer (verification/validation) for new drug delivery devices; solve technical issues.
  • Lead gap assessments/remediation and guide risk management activities; lead projects within budget.
  • Manage design control activities: specifications, design verification/validation, design transfer, test protocols/reports.
  • Support manufacturing expansion and process validation; ensure quality regulation system alignment (DHF, MDR, ISO13485, ISO14971).
Minimum Qualifications:
  • PhD (3+ yrs), MS (5+ yrs), or BS (8+ yrs) in Mechanical/Electrical/Biomedical Engineering or related.
  • SME in medical devices, especially drug delivery systems (e.g., PFS, pen injectors, autoinjectors, needle safety devices) with technical leadership.
  • Knowledge of design controls and quality system requirements; cGMP and combination product guidance.
  • Strong understanding of manufacturing/process and packaging; experience drafting technical content; author URS, protocols, reports, and assessments.
  • Experience with technology transfer and test method development/validation; technical leadership in cross-functional settings.
  • Experience with medical device LCM change controls, complaint investigations, and post-market surveillance.
#J-18808-Ljbffr