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Internship R&D Engineer Medical Device Jobs in Gainesville, FL

Exactech

QA PM Specialist

Gainesville, FL · On-site

... Biomedical Engineering, highly preferred. * Minimum of 1 year of experience performing a complaint handling or post market surveillance role in a Medical Device or Pharmaceutical FDA regulated ...

Advita Ortho

QA PM Specialist

Gainesville, FL · On-site

... Biomedical Engineering, highly preferred. * Minimum of 1 year of experience performing a complaint handling or post market surveillance role in a Medical Device or Pharmaceutical FDA regulated ...

Evergen

Sr. Quality Engineer

Alachua, FL · On-site

$90K - $115K/yr

Supervises the Quality Assurance Engineering team including performance management, corrective ... Bachelor's degree in relevant technical discipline Experience * 6+ years of relevant medical device ...

Jacobs Management Group

Packaging Engineer

Alachua, FL · On-site

$65K - $80K/yr

Comfortable applying process validation methodology (IQ, OQ, PQ) and statistical tools (Gage R&R ... Understanding of regulatory requirements for packaging materials in a medical or life sciences ...

Jones Edmunds

Senior Engineer - Civil Engineering

Alachua, FL · On-site

$92K - $127K/yr

Direct the work of Project Engineers, Engineers, and Engineer Interns on a project-by-project basis ... Comprehensive Benefits Package including: - Medical, Dental, and Vision options - Employer paid ...

Exactech

VP of FP&A

Gainesville, FL

Serve as finance partner to functional leaders (Commercial, Operations, Engineering) to support ... Manufacturing and/or medical device industry experience preferred Functional/Technical Knowledge ...

Advita Ortho

VP of FP&A

Gainesville, FL · On-site

Serve as finance partner to functional leaders (Commercial, Operations, Engineering) to support ... Manufacturing and/or medical device industry experience preferred Functional/Technical Knowledge ...

Exactech

Corporate FP&A Manager

Gainesville, FL

$95K - $125K/yr

Act as a finance partner to functional leaders (e.g., Commercial, Operations, Engineering ... Background in manufacturing, healthcare, or medical device industry preferred Functional/Technical ...

Advita Ortho

Corporate FP&A Manager

Gainesville, FL · On-site

Act as a finance partner to functional leaders (e.g., Commercial, Operations, Engineering ... Background in manufacturing, healthcare, or medical device industry preferred Functional/Technical ...

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All JobsR&D Engineer Medical Device JobsInternship R&D Engineer Medical Device JobsInternship R&D Engineer Medical Device Jobs in Gainesville, FL

Internship R D Engineer Medical Device information

See Gainesville, FL salary details

$10

$17

$26

How much do internship r&d engineer medical device jobs pay per hour?

As of Aug 12, 2026, the average hourly pay for internship r&d engineer medical device in Gainesville, FL is $17.50, according to ZipRecruiter salary data. Most workers in this role earn between $14.62 and $18.94 per hour, depending on experience, location, and employer.

What does an internship R&D engineer 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 medical device?

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 medical device expect to work on?

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 near Gainesville, FL are hiring for Internship R&D Engineer Medical Device jobs? Cities near Gainesville, FL with the most Internship R&D Engineer Medical Device job openings:
Internship R D Engineer Medical Device jobs near you

QA PM Specialist

Exactech

Gainesville, FL • On-site

Full-time

Posted 7 days ago

Exactech rating

8.0

Company rating: 8.0 out of 10

Based on 6 frontline employees who took The Breakroom Quiz

Job description

The purpose of the QA Post Market Specialist is to perform complaint handling activities to ensure regulatory compliance and customer satisfaction. This role coordinates and submits regulatory reports to FDA and Country/Regional competent authorities.
  • Engaged in the receipt, documentation, investigation, and closure/resolution of customer complaints to ensure regulatory compliance (e.g., FDA, CMDR, ISO) and customer satisfaction.
  • Adhering to all Advita procedures and requirements. Assesses complaint events for regulatory reporting requirements.
  • Submits regulatory reports to FDA or Regional Competent Authority within regulatory timeframes.
  • Escalates high severity events and cases to Management.
  • Supports the completion of complaint activities in line with department metrics and key performance indicators.
  • Supports audits and audit requests for complaints.
  • Assists with continuous improvement activities and/or special projects, as assigned.
  • Assists in training complaint team members.
  • Assists in updates or creation of procedures, work instructions, forms, reports and letter templates to standardize departmental processes.
  • Knowing and applying Advita's Quality System and any appropriate FDA and international standards.
  • Assist and support other employees, teams, and sales personnel, as necessary.
Education:
  • Associate's Degree from an accredited institution required; Bachelor's Degree preferred.
 Experience:
  • Degree in Allied Health, Statistics, Epidemiology, Life Sciences or Biomedical Engineering, highly preferred.
  • Minimum of 1 year of experience performing a complaint handling or post market surveillance role in a Medical Device or Pharmaceutical FDA regulated environment.
  • In lieu of previous complaint handling experience, 2 years of experience in a quality assurance role in the Medical Device or Pharmaceutical FDA regulated environment.
  • Working knowledge of requirements of FDA, EU, and other global regulations related to complaint handling and Recalls/FSCA required.
  • Experience with FDA/ISO quality management system regulations required.
  • Experience with quality system management software highly preferred.
Functional/Technical Knowledge, Skills and Abilities Required:
  • Working knowledge/skill in Windows-based office productivity tools.
  • Excellent analytical skills and detail-oriented.
  • Strong organizational and time management skills.
  • Strong written, oral, and presentation communication skills. Ability to consistently meet high standards of input accuracy, produce quality documents, compile data, and perform simple analyses with accuracy. Self-directed; capable of setting own priorities and working independently to meet established deadlines.

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