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Medical Device Internship Jobs in Puerto Rico (NOW HIRING)

Kelly Services

PR

$25/hr

Internship, co-op, or academic project experience within medical devices, manufacturing, quality, or packaging is considered as experience * Experience working in a regulated industry (Medical Device ...

Mentor Technical Group

Human Resources Intern

Caguas, PR · On-site

$14.75 - $19.50/hr

... medical device safety and efficacy guidelines. With offices in Caguas, PR, Boston, MA & San ... This internship will provide valuable hands-on experience in various HR functions, including talent ...

Jj

Finance Co-Op (12 Months)

Anasco, PR · Hybrid

$17.50 - $22.75/hr

Students with interest in the areas of finance and accounting on a medical device manufacturing ... internships. In addition to valuable work experience, students can also have the opportunity to ...

All JobsMedical Device JobsMedical Device Internship JobsMedical Device Internship Jobs in Puerto Rico

Medical Device Internship information

What is the difference between Medical Device Internship vs Medical Device Technician?

AspectMedical Device InternshipMedical Device Technician
Required CredentialsTypically pursuing or recent graduate in biomedical, mechanical, or related fieldsPost-secondary certification or associate degree in biomedical technology or related field
Work EnvironmentOffice, laboratory, or manufacturing settings; focus on learning and trainingClinical, hospital, or repair facilities; hands-on device maintenance and troubleshooting
Employer & Industry UsageMedical device companies, hospitals, research institutions; internship programsMedical device manufacturing, healthcare facilities, repair services
Common Search & Comparison IntentEntry-level learning experience, career explorationTechnical repair, device maintenance, troubleshooting skills

The main difference between a Medical Device Internship and a Medical Device Technician is that internships are training roles for students or recent graduates focusing on learning about medical devices, while technicians are trained professionals responsible for maintaining, repairing, and troubleshooting medical devices in clinical or manufacturing settings.

What is a Medical Device Internship?

A Medical Device Internship is a short-term position, typically for students or recent graduates, that provides hands-on experience in the medical device industry. Interns may work in various areas such as research and development, quality assurance, regulatory affairs, or engineering. The goal is to give participants practical exposure to how medical devices are designed, manufactured, tested, and brought to market while working alongside professionals in the field. This experience can help interns build valuable skills, network with industry experts, and improve their chances of securing a full-time role after graduation.

What are the key skills and qualifications needed to thrive as a Medical Device Intern, and why are they important?

To thrive as a Medical Device Intern, you need a background in biomedical engineering or a related field, strong analytical skills, and a basic understanding of medical device regulations. Familiarity with CAD software, laboratory equipment, and regulatory standards such as FDA or ISO is often required. Strong communication, teamwork, and problem-solving abilities help interns contribute effectively to multidisciplinary projects. These skills ensure that interns can support innovation, comply with industry standards, and work efficiently within development teams.

What types of projects and responsibilities can I expect during a Medical Device Internship?

As a Medical Device Intern, you will typically be involved in a variety of hands-on projects that support product development, testing, or regulatory compliance. Interns often assist with tasks such as prototyping, data analysis, documentation for regulatory submissions, and collaborating with engineers or quality assurance teams. You may also participate in cross-functional meetings, learn about industry standards, and contribute to process improvements. This experience provides valuable exposure to both technical and regulatory aspects of the medical device industry, helping you build a strong foundation for a future career.
What are the most commonly searched types of Medical Device jobs in Puerto Rico? The most popular types of Medical Device jobs in Puerto Rico are:
What are popular job titles related to Medical Device Internship jobs in Puerto Rico? For Medical Device Internship jobs in Puerto Rico, the most frequently searched job titles are:
What job categories do people searching Medical Device Internship jobs in Puerto Rico look for? The top searched job categories for Medical Device Internship jobs in Puerto Rico are:
Medical Device Internship jobs near you
Validation Specialist (Pack Engineering Support)

Validation Specialist (Pack Engineering Support)

Kelly Services

Anasco, PR

$25/hr

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 7 days ago

Job description

Think the best job opportunities are far away? Think again. Great opportunities are right here in your backyard.
Kelly® Engineering is looking for a Validation Engineering to work at a premier manufacturing client in Añasco, PR.
Let us help you grow at work and discover the next step in your career, all while being a vital part of your community.

Compensation : From $25 by hr and up, based on experience
Shift                  : Admin, Monday through Friday. Available weekends, alternate shifts, after-hours activities when needed
Location           : On Site | Añasco, Puerto Rico
This job might be an outstanding fit if you have the following qualifications:
  • Bachelor’s Degree in Engineering or a related technical discipline (required).
  • Internship, co-op, or academic project experience within medical devices, manufacturing, quality, or packaging is considered as experience
  • Experience working in a regulated industry (Medical Device, Pharmaceutical, Biotechnology, etc.). Experience with tray-sealing processes (required).
  • Available for working in ISO Class 7 cleanroom environments and following strict gowning requirements.
  • Demonstrate strong documentation, organizational, and communication skills.
  • Fluent in English (read, write, speak, and understand).
  • Proficient in Microsoft Office (Excel, Word, PowerPoint).
  • Thrive in a fast-paced, collaborative manufacturing environment with a strong willingness to learn.
    • Preferred Requirements
      • At least 4+ years of engineering or manufacturing experience.
      • Experience with packaging validation, laboratory testing, or engineering projects.
      • Knowledge of FDA QSR, ISO 13485, ISO 9001, GMP, and medical device regulations.
      • Exposure to sterile barrier systems and validation methodologies.
What’s a typical day as Validation Engineering? You’ll be:
  • Supporting packaging validation and testing activities for sterile and non-sterile medical device packaging systems.
  • Executing validation protocols, engineering studies, and testing activities in close collaboration with Packaging and Project Engineers.
  • Collecting, analyzing, and documenting testing data and validation results.
  • Preparing and maintaining technical documentation, including protocols, reports, and test summaries.
  • Coordinating with cross-functional teams such as Quality, Operations, Regulatory, and Engineering.
  • Supporting troubleshooting, risk assessments, process improvements, and packaging line trials.
  • Ensuring compliance with internal procedures and applicable regulatory requirements.
Why you should apply to be Validation Engineering:
  • Opportunity to work in a regulated medical device manufacturing environment.
  • Competitive pay rate with room to grow based on experience.
  • Collaborate with engineering, quality, and regulatory professionals on impactful validation projects.
  • Work for a respected industry leader focused on safety, compliance, and continuous improvement.
  • Gain valuable hands-on experience in packaging validation and technical documentation.
  • Access to the following benefits:
    • Weekly pay (W2)
    • Sick, Vacations & Holidays paid*
    • Christmas bonus*
      • * Must comply with minimum established requirements to qualify.
What happens next

Once you apply, you’ll proceed to next steps if your skills and experience look like a good fit. But don’t worry—even if this position doesn’t work out, you’re still in our network. That means all of our recruiters will have access to your profile, expanding your opportunities even more.

Helping you discover what’s next in your career is what we’re all about, so let’s get to work.
Apply to be Validation Engineering today!
 


As part of our promise to talent, Kelly supports those who work with us through a variety of benefits, perks, and work-related resources. Kelly offers eligible employees voluntary benefit plans including medical, dental, vision, telemedicine, term life, whole life, accident insurance, critical illness, a legal plan, and short-term disability. As a Kelly employee, you will have access to a retirement savings plan, service bonus and holiday pay plans (earn up to eight paid holidays per benefit year), and a transit spending account. In addition, employees are entitled to earn paid sick leave under the applicable state or local plan. Click here for more information on benefits and perks that may be available to you as a member of the Kelly Talent Community.

Why Kelly® Engineering?

Your engineering skills are in demand, but how do you find the right fit? Easy. At Kelly Engineering, our team creates expert talent solutions to solve the world’s most critical challenges. We connect you with leading organizations where you can collaborate on innovative projects, work with cutting-edge technologies and accelerate your growth. Whether you prefer the variety and flexibility of short-term projects or are looking for a long-term opportunity, we’re here to guide you to the next step in your engineering career.

About Kelly

Work changes everything. And at Kelly, we’re obsessed with where it can take you. To us, it’s about more than simply accepting your next job opportunity. It’s the fuel that powers every next step of your life. It’s the ripple effect that changes and improves everything for your family, your community, and the world. Which is why, here at Kelly, we are dedicated to providing you with limitless opportunities to enrich your life-just ask the 300,000 people we employ each year.
Kelly is committed to providing equal employment opportunities to all qualified employees and applicants regardless of race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or any other legally protected status, and we take affirmative action to recruit, employ, and advance qualified individuals with disabilities and protected veterans in the workforce. Requests for accommodation related to our application process can be directed to the Kelly Human Resource Knowledge Center. Kelly complies with the requirements of California’s state and local Fair Chance laws. A conviction does not automatically bar individuals from employment. Kelly participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S.
Kelly may use AI-powered tools during the recruitment and hiring process. For full details, including how Kelly uses AI, your rights, and how to request a reasonable accommodation, visit the Recruitment Artificial Intelligence Notice.

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