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Internship Medical Device Testing Jobs (NOW HIRING)

Device Testing Engineer

San Jose, CA · On-site

$100K - $250K/yr

Support ReRAM device characterization, testing report and reliability report. Qualifications ... medical condition, disability, genetic information, military or veteran status, or any other ...

Pay: $22-26/hour Position Summary The Medical Device Assembly Technician is responsible for ... and testing fixtures. * Perform in-process quality inspections and provide timely feedback ...

Major Skill: u Micro controllers u C Programming u White box testing u Embedded Device testing u Medical domain u Wi-Fi Additional Information All your information will be kept confidential according ...

This is pure device testing Position. Understand the design developed in C language for micro-controller based on Non-RTOS and RTOS environment for a highly safety critical handheld medical device.

This is pure device testing Position. * Understand the design developed in C language for micro-controller based on Non-RTOS and RTOS environment for a highly safety critical handheld medical device.

This is pure device testing Position. * Understand the design developed in C language for micro-controller based on Non-RTOS and RTOS environment for a highly safety critical handheld medical device.

This is pure device testing Position. * Understand the design developed in C language for micro-controller based on Non-RTOS and RTOS environment for a highly safety critical handheld medical device.

Analytical Development, Analytical Testing, GMP Laboratory, GMP Testing, Interdisciplinary Collaboration, Mechanical Testing, Medical Device Management, Medical Devices, Medical Device Technologies ...

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Internship Medical Device Testing information

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How much do internship medical device testing jobs pay per hour?

As of Aug 12, 2026, the average hourly pay for internship medical device testing in the United States is $19.31, according to ZipRecruiter salary data. Most workers in this role earn between $16.11 and $20.91 per hour, depending on experience, location, and employer.

What types of projects and hands-on experiences can I expect during a medical device testing internship?

As a Medical Device Testing intern, you can expect to participate in a variety of projects that involve evaluating the safety, functionality, and reliability of medical devices. Typical responsibilities may include assisting with test setup, executing test protocols, recording and analyzing data, and collaborating with engineers and regulatory teams to ensure compliance with industry standards. Interns often gain exposure to specialized lab equipment, quality assurance practices, and regulatory documentation, all while working closely with experienced professionals in a team-oriented environment. This hands-on experience is valuable for building technical skills and understanding the product development lifecycle in the medical device industry.

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

AspectInternship Medical Device TestingMedical Device Quality Assurance Intern
Required CredentialsTypically enrolled in related health sciences or engineering programsSimilar educational background, often in quality management or engineering
Work EnvironmentLaboratory and testing facilities, hands-on testing activitiesQuality management departments, documentation, and compliance tasks
Employer & Industry UsageManufacturers, testing labs, R&D departmentsManufacturers, regulatory agencies, compliance teams
Search & Comparison IntentUnderstanding testing roles in medical device developmentExploring quality assurance internship opportunities in medical devices

Internship Medical Device Testing focuses on hands-on testing and validation of medical devices, while Medical Device Quality Assurance Interns concentrate on ensuring compliance, documentation, and quality standards. Both roles are essential in the medical device industry and often overlap in skills and environment, but they serve different aspects of product development and regulation.

What are the key skills and qualifications needed to thrive in a medical device testing internship?

To thrive in a Medical Device Testing internship, you need a solid background in biomedical engineering, life sciences, or a related field, often supported by coursework in device regulations and laboratory methods. Familiarity with testing equipment, data analysis software, and relevant standards like ISO 13485 or FDA regulations is typically expected. Strong attention to detail, effective communication, and problem-solving skills set standout candidates apart. These abilities ensure accurate testing, regulatory compliance, and clear reporting, which are critical for patient safety and product quality.

What is an internship in medical device testing?

An internship in medical device testing is a temporary position where students or recent graduates gain hands-on experience working with medical devices to ensure their safety, effectiveness, and compliance with regulatory standards. Interns typically assist in performing laboratory tests, documenting results, and supporting engineers or quality assurance teams. This role helps interns understand industry protocols, testing methodologies, and regulatory requirements while developing practical skills for a future career in medical technology.
What cities are hiring for Internship Medical Device Testing jobs? Cities with the most Internship Medical Device Testing job openings:
What are the most commonly searched types of Medical Device Testing jobs? The most popular types of Medical Device Testing jobs are:
What states have the most Internship Medical Device Testing jobs? States with the most job openings for Internship Medical Device Testing jobs include:

Laboratory Manager - Microbiology (Pharmaceutical & Medical Device Testing)

Eurofins Scientific

San Diego, CA

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 26 days ago


Eurofins rating

7.4

Company rating: 7.4 out of 10

Based on 180 frontline employees who took The Breakroom Quiz

68th of 120 rated laboratories


Job description

Company Description

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.

The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organization services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organizations. It also has a rapidly developing presence in highly specialized and molecular clinical diagnostic testing and in-vitro diagnostic products.

In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralized and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.

2025, Eurofins generated total revenues of EUR 7.296 billion, and has been among the best performing stocks in Europe over the past 20 years.

Job Description

Position Overview

Eurofins Advantar Laboratories is seeking a Laboratory Manager - Microbiology to lead microbiology operations at our San Diego site supporting pharmaceutical and medical device clients.

This is a people leadership role responsible for overseeing laboratory operations through lab supervisors and team leads, ensuring high-quality, compliant, and timely delivery of testing services in a regulated environment.

The Laboratory Manager serves as the execution and technical leader of the department, accountable for laboratory performance across Environmental Monitoring (EM) and Microbiology testing functions. This role operates at a management level, leading leaders, and driving outcomes through effective team structure, technical oversight, and operational discipline.

Key Responsibilities

Laboratory Leadership & Organizational Management

  • Lead and manage laboratory operations through:
  • Set direction, priorities, and expectations for the laboratory organization
  • Ensure strong leadership alignment and accountability at the supervisor/lead level
  • Build and maintain a high-performing, scalable team and develop talent.

Laboratory Operations (Execution Ownership)

  •   Oversee execution of microbiology and environmental monitoring testing, including:
    • Sterility, bioburden, endotoxin, and related compendial methods
    • Environmental monitoring programs (on-site and off-site)
  •   Ensure laboratory performance consistently meets:
    • Turnaround time (TAT) commitments
    • Quality and regulatory standards
    • Client delivery expectations across timelines, scope, and output quality
  •   Own reliable and predictable delivery of laboratory services, ensuring work is executed in a manner that supports strong client outcomes
  •   Partner with Project Management to align laboratory capacity and execution with client needs and commitments
  •   Manage laboratory workflow, prioritization, and resource allocation to ensure on-time, high-quality delivery
  • Ensure laboratory operations are executed in a cost-conscious and efficient manner, optimizing labor and materials

Team Leadership & Development

  • Lead, coach, and develop supervisors and their teams
  • Oversee:
    • Hiring and onboarding
    • Performance management and development planning
    • Organizational structure and staffing alignment
  • Establish a culture of:
    • accountability
    • continuous improvement
    • technical excellence

Technical Leadership (Pharma / Medical Device Focus)

  • Serve as technical subject matter expert for microbiology operations
  • Ensure adherence to:
    • cGMP and regulated laboratory standards
    • USP microbiology methods
  • Support:
    • technical escalations
    • investigations and troubleshooting
  • Represent the laboratory in audits and client technical discussions

Quality & Compliance

  • Maintain compliance with:
    • cGMP, GDP, ISO, and USP standards
  • Lead or support:
    • Deviations / OOS investigations
    • CAPAs and change controls
  • Ensure audit readiness for:
    • FDA, ISO, and client audits

Client Technical Interface

  • Act as technical representative for clients as needed
  • Partner with Project Management to support:
    • technical discussions
    • issue resolution
    • capability alignment

Laboratory Infrastructure & Equipment

  • Ensure:
    • Qualification, maintenance, and calibration of equipment
  • Oversee:

Equipment lifecycle and implementation of new technologies

Qualifications

Minimum Requirements

  • Bachelor's degree in Microbiology, Biology, or related life science
  • 5+ years of experience in a pharmaceutical or medical device laboratory environment
  • 2+ years of leadership experience, including experience supervising laboratory staff or team leads in a regulated environment
  • Strong knowledge of:
    • cGMP and regulated lab environments
    • USP microbiology methods

Preferred Qualifications

  • Experience leading multi-team lab operations (EM + Microbiology)
  • Experience managing supervisors or functional leads
  • Experience supporting regulatory or client audits
  • Advanced degree (MS or higher) in Microbiology or related life science preferred

Skills & Competencies

  • Proven ability to lead through layered team structures
  • Strong operational leadership and execution discipline
  • Technical depth in microbiology and regulated testing
  • Ability to balance:
    • technical rigor
    • operational efficiency
    • team development
  • Excellent communication and cross-functional collaboration skills
Additional Information

Position is full-time, Monday - Friday 8:00am - 5:00pm. Candidates currently living within a commutable distance of San Diego, CA are encouraged to apply.

Pay Range: $85,000 - $115,000 per year depending on related experience

Excellent full time benefits including

  • Comprehensive medical coverage, dental, and vision options
  • Life and disability insurance
  • 401(k) with company match
  • Paid vacation and holidays

Eurofins USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.


What Eurofins employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom


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About Eurofins

Sourced by ZipRecruiter

Industry

Scientific research and development services, biotechnology research and development and environmental consulting services

Company size

10,000+ Employees

Headquarters location

Leacock, PA, US