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Internship R&D Engineer Medical Device Jobs in Florida

Program Manager - Engineering - I&R

Naples, FL · On-site

$121K/yr

Program Manager - Engineering - I&R Arthrex, Inc. is a global medical device company and a leader in new product development and medical education in orthopedics. Arthrex is actively searching for a ...

Program Manager - Engineering - I&R

Naples, FL · On-site

$121K/yr

Program Manager - Engineering - I&R Arthrex, Inc. is a global medical device company and a leader in new product development and medical education in orthopedics. Arthrex is actively searching for a ...

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Internship R D Engineer Medical Device information

What does an Internship R&D Engineer in Medical Device do?

An Internship R&D Engineer in Medical Device assists in the research and development of new medical technologies and products. Their responsibilities typically include supporting senior engineers in designing, testing, and improving medical devices, conducting experiments, collecting and analyzing data, and preparing technical documentation. Interns also learn about regulatory standards and industry best practices while working as part of a multidisciplinary team. This role is ideal for students or recent graduates looking to gain hands-on experience in medical device innovation.

What are the key skills and qualifications needed to thrive as an Internship R&D Engineer in Medical Devices, and why are they important?

To thrive as an Internship R&D Engineer in Medical Devices, you generally need a background in biomedical engineering or a related field, with strong analytical and problem-solving abilities. Familiarity with CAD software, lab equipment, and basic knowledge of regulatory standards like ISO 13485 is important, and prior internships or relevant coursework can be advantageous. Attention to detail, effective communication, and collaborative teamwork skills help you contribute meaningfully to projects and navigate cross-functional environments. These skills ensure you can support innovative product development while adhering to strict safety and quality standards in the medical device industry.

What is the difference between Internship R&D Engineer Medical Device vs R&D Engineer Medical Device?

AspectInternship R&D Engineer Medical DeviceR&D Engineer Medical Device
QualificationsEnrolled in or recent graduate of engineering/biomedical programsBachelor's or Master's in engineering/biomedical fields
Work EnvironmentInternship programs, entry-level projects, supervised tasksFull-time, independent project work, team collaboration
ResponsibilitiesAssisting in research, testing, and documentationDesign, develop, and improve medical device products
Industry UsageCommonly used for training and entry-level experienceCore role in product development and innovation

In summary, the Internship R&D Engineer Medical Device is an entry-level position designed for students or recent graduates gaining initial industry experience. The R&D Engineer Medical Device is a full-time professional role with greater responsibilities in product development and innovation within the medical device industry.

What types of projects or tasks can an Internship R&D Engineer expect to work on in the medical device industry?

As an Internship R&D Engineer in the medical device industry, you can expect to be involved in a variety of projects such as prototyping new device concepts, conducting laboratory experiments, performing data analysis, and supporting design verification and validation activities. Interns often collaborate closely with multidisciplinary teams, including senior engineers, regulatory specialists, and clinicians, to help solve real-world problems and improve patient outcomes. This hands-on experience provides valuable insight into the product development lifecycle and offers opportunities to contribute to meaningful projects that can enhance your technical and professional skills.
What cities in Florida are hiring for Internship R&D Engineer Medical Device jobs? Cities in Florida with the most Internship R&D Engineer Medical Device job openings:
Sr. Engineer I (Mechanical) - Product Improvement - I&R

Sr. Engineer I (Mechanical) - Product Improvement - I&R

ARTHREX

Ave Maria, FL • On-site

Other

Medical, Dental, Vision, Life, Retirement, PTO

Posted 5 days ago


Arthrex rating

8.3

Company rating: 8.3 out of 10

Based on 74 frontline employees who took The Breakroom Quiz

64th of 516 rated manufacturers


Job description

Requisition ID:                       65083                          Title: Sr. Engineer I (Mechanical) - Product Improvement - I&R

Arthrex, Inc. is a global medical device company and a leader in new product development and medical education in orthopedics. Arthrex is actively searching for a Sr. Engineer I - Product Improvement. This individual will be responsible for ongoing product improvement and sustainment engineering support for medical devices, including analysis, design enhancements, implementation, verification, and sustaining activities to ensure product quality, reliability, and compliance throughout its lifecycle. Join our talented team at a global medical device company focused on Helping Surgeons Treat Their Patients Better.

This position will be based out of our manufacturing facility in Ave Maria, FL.

Essential Duties and Responsibilities:

  • Designs components and/or functional systems primarily by modifying existing designs to develop or improve product functionality and durability while facilitating manufacturing operations to meet engineering design intent.
  • Analyzes customer feedback to identify common issues and areas for enhancement, reviews failure modes on the operations lines and of returned devices, and performs root cause investigations to recommend design and development alterations to improve product quality and/or procedures.
  • Acts as the primary mechanical design resource on multifunctional product support teams, as assigned by the Engineering Manager, through project technical feasibility analysis, initiation, planning, execution, verification, release, and sustaining, adhering closely to project timeline and budget. 
  • Works closely with cross-functional teams, including Design, Manufacturing, Service, Repair, Quality, Supply Chain, etc., to ensure the design considers the needs of internal stakeholders.
  • Supports the creation of Manufacturing and Service processes (assembly/disassembly/rework), ensuring design intent is maintained.
  • Determines the necessity of testing and performs or oversees rigorous verification testing and validation of product improvements to ensure they meet safety, quality, and regulatory standards for assigned products.
  • Maintains comprehensive documentation of all product changes and improvements, including design specifications, test results, and validation reports.
  • Works with Systems Engineering to maintain an accurate design history file for assigned projects, adhering to Arthrex design control procedures.
  • Works with project management and extended team to determine timelines for assigned projects and reports the progress of assigned projects on a timely basis. 
  • Provides Regulatory department technical support for assigned projects as needed.
  • Supports Marketing and Product Management with technical information for training and marketing assigned products.
  • Implements continuous improvement methodologies to enhance product development processes and outcomes.
  • Attends surgical observations (live surgery, wet labs, and/or dry labs) to gather input from end users and identify opportunities for product improvements, and may be required to travel to attend trade shows and/or training events.

Education/ Experience:

  • Bachelor's Degree in Mechanical Engineering or equivalent is required (MS Preferred).
  • 5 Years of full-time job experience in Mechanical Engineering (excluding internships and/or academic programs).

Skills:   

  • Knowledgeable of FDA and ISO guidelines for the development of medical devices required.
  • Manufacturing process knowledge required.
  • Project management and communication skills required.
  • Working knowledge of anatomy from an orthopedic standpoint preferred.
  • Expert in designing products using a 3D-CAD program required (SolidWorks preferred).
  • Expert level application of latest ASME Y14.5 standard.
  • Expert level application of tolerance analysis (stack-up) methods.
  • Technical knowledge in development methodologies, design, and project implementation required.
  • Knowledge of orthopedic surgery principles, theories, products, and historical perspective preferred.
  • Expert level application of one or more design simulation and/or analysis tool (FEA, CFD, optical ray tracing, etc.) and appropriate methods to validate results.
  • Proficient with Design for Quality tools such as FTA, FMEA, HALT/HASS.

Knowledge:

  • Complete understanding and application of principles, concepts, practices, and standards.  Full knowledge of industry practices and regulations.
  • Develops design solutions to complex problems at system level, which require the regular use of analysis, ingenuity, and innovation. Ensures solutions are consistent with organization objectives.

Arthrex Benefits

  • Medical, Dental and Vision Insurance
  • Company-Provided Life Insurance
  • Voluntary Life Insurance
  • Flexible Spending Account (FSA)
  • Supplemental Insurance Plans (Accident, Cancer, Hospital, Critical Illness)
  • Matching 401(k) Retirement Plan
  • Annual Bonus
  • Wellness Incentive Program
  • Free Onsite Medical Clinics
  • Free Onsite Lunch
  • Tuition Reimbursement Program
  • Trip of a Lifetime
  • Paid Parental Leave
  • Paid Time Off
  • Volunteer PTO
  • Employee Assistance Provider (EAP)

All qualified applicants will receive consideration for employment without regard to race, color, religion, age, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other status protected by law.


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