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Internship Medical Device Testing Jobs in Indiana

Brooksource

Software Quality Engineer

Indianapolis, IN · On-site

$55 - $64/hr

Support the design, development, and testing of medical device software, including Software as a Medical Device (SaMD) products * Provide leadership, guidance, and expertise on software development ...

OrthoPediatrics

Post Market Quality Engineer

Warsaw, IN · On-site

$69K - $89K/yr

The Post Market Quality Engineer is responsible for medical device complaint investigations and ... Knowledge on non-destructive testing and measuring techniques. * Must have excellent verbal and ...

Red Star

Sterile Packaging Manager

IN · On-site

... for the medical device industry. From concept through high-volume production, our teams work ... transit testing, aging studies, and ongoing process monitoring. * Ensure effective monitoring ...

Red Star

Senior Sterile Packaging Engineer

IN · On-site

Design, evaluate, and approve packaging components and sterile packaging systems for medical device ... testing, aging studies, and ongoing process monitoring. * Monitor, evaluate, and improve sterile ...

Red Star

Senior Sterile Packaging Engineer

Larwill, IN · On-site

Design, evaluate, and approve packaging components and sterile packaging systems for medical device ... testing, aging studies, and ongoing process monitoring. Monitor, evaluate, and improve sterile ...

Red Star

Sterile Packaging Manager

Larwill, IN · On-site

... for the medical device industry. From concept through high-volume production, our teams work ... testing, aging studies, and ongoing process monitoring.Ensure effective monitoring, control, and ...

Collabera

Software Validation Engineer III

Warsaw, IN · On-site

... testing protocols. Verify the design and participate actively in validation activities ... Medical device experiences a plus. Other regulated environment experience is a plus. Additional ...

Levisonics Inc

Engineering Project Manager

Fishers, IN · On-site

We are a dynamic and innovative medical device startup developing a point-of-care portable blood coagulation testing device. Job Summary: We are looking for an experienced Engineering Project Manager ...

Sotera Health

Operator

Columbia City, IN · On-site

$16 - $21/hr

Nelson Labs is a global leader in outsourced microbiological and analytical chemistry testing and advisory services for the medical device and pharmaceutical industries.

Sotera Health

Operator

Columbia City, IN · On-site

$16 - $21/hr

Nelson Labs is a global leader in outsourced microbiological and analytical chemistry testing and advisory services for the medical device and pharmaceutical industries.

Zimmer, Inc.

Development Engineer II

Warsaw, IN

... ups, benchtop testing and executing simulated operating room cadaveric product evaluations ... FDA QSR and EU MDR medical device regulatory requirements, and industry/ regulatory body recognized ...

Sotera Health

Operator

Columbia City, IN · On-site

$16 - $21/hr

Nelson Labs is a global leader in outsourced microbiological and analytical chemistry testing and advisory services for the medical device and pharmaceutical industries.

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All JobsMedical Device Testing JobsInternship Medical Device Testing JobsInternship Medical Device Testing Jobs in Indiana

Internship Medical Device Testing information

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 are the most commonly searched types of Medical Device Testing jobs in Indiana? The most popular types of Medical Device Testing jobs in Indiana are:
What cities in Indiana are hiring for Internship Medical Device Testing jobs? Cities in Indiana with the most Internship Medical Device Testing job openings:
Internship Medical Device Testing jobs near you

Software Quality Engineer

Brooksource

Indianapolis, IN • On-site

$55 - $64/hr

Contractor

Medical, Dental, Vision, Retirement, PTO

Posted 6 days ago

Job description

Software Quality Engineer
Warsaw, IN
Hybrid role (3 days in office)
$55 - $64 per hour
ABOUT THE ROLE
Join a Fortune 50 Life Sciences company as a Software Quality Engineer, providing quality leadership for a new product project team focused on the development of medical device software systems. In this hybrid role based in Warsaw, IN, you will serve as the subject matter expert in requirements gathering, software risk assessments, test strategy definition, and guiding the team on design controls and defect analysis. You will partner closely with R&D throughout the full development lifecycle-from upstream requirements and risk through mid-stream verification to ongoing compliance and audit readiness. This is a high-visibility opportunity to own quality end-to-end, gain exposure to a full medical device software toolchain, and collaborate cross-functionally with business partners and mentors.
WHAT YOU'LL DO
  • Support the design, development, and testing of medical device software, including Software as a Medical Device (SaMD) products
  • Provide leadership, guidance, and expertise on software development processes, procedures, and practices
  • Serve as a subject matter expert in requirements gathering, test strategy definition, and design controls
  • Facilitate documentation and tracking of verification activities, including code review findings
  • Review test case execution results and manage software defects
  • Facilitate software risk assessment sessions and own the development of risk documentation
  • Support regulatory filings and registrations, including 510(k) submissions and Design History File (DHF) creation
  • Provide technical support for audits of software suppliers and consultants, including cybersecurity and threat modeling topics
  • Conduct training on medical device software development processes and quality systems; develop associated work instructions
  • Provide expertise in applicable industry standards and regulations (e.g., IEC 62304, FDA guidance, FDA Part 11, ISO 13485, EU MDR, ISO 14971, IEC 62366, ISO 27001, HIPAA)
  • Collaborate closely with R&D and cross-functional teams to ensure compliance with industry standards and regulatory requirements

WHAT YOU BRING
  • Bachelor's degree or university degree in Engineering, Computer Science, Information Systems, or Biomedical/Bio-engineering (required)
  • Minimum 4 years of regulated industry experience in quality, new product development, or manufacturing engineering
  • Experience in the medical device industry
  • Proficiency with quality tools, systems, and processes (e.g., Windchill, Polarion, ETQ)
  • Strong interpersonal, organizational, and verbal/written communication skills
  • Ability to work collaboratively in a team environment and demonstrate leadership
  • Ability to perform duties in accordance with company policies, procedures, and civil rights requirements
  • ASQ Certification as a Software Quality Engineer or equivalent (preferred)
  • Expertise in applicable industry standards and regulations (e.g., IEC 62304, FDA guidance, FDA Part 11, ISO 13485, EU MDR, ISO 14971, IEC 62366, ISO 27001, HIPAA)
  • Experience supporting regulatory filings and registrations (e.g., 510(k) submissions, DHF creation)
  • Ability to facilitate software risk assessments and develop risk documentation

WHAT'S IN IT FOR YOU
  • Opportunity to own quality end-to-end on a high-visibility project for a Fortune 50 Life Sciences company
  • Exposure to a full medical device software toolchain (Windchill, Polarion, ETQ) and hands-on involvement
  • Meaningful mentorship scope and cross-collaborative team and business partners
  • Hybrid work environment (3 days in office)

Disclaimer: Brooksource, Medasource, and Calculated Hire are part of the Eight Eleven Group family of companies and operate under Eight Eleven Group, LLC. All employees receive the same benefits, policies, and terms of employment.
EEO:
We are committed to creating an inclusive environment for all employees and applicants. We do not discriminate on the basis of race, color, religion, creed, sex, sexual orientation, gender identity or expression, national origin, ancestry, age, disability, genetic information, marital status, military or veteran status, citizenship, pregnancy (including childbirth, lactation, and related conditions), or any other protected status in accordance with applicable federal, state, and local laws.
Benefits & Perks:
Brooksource offers competitive medical, dental, vision, Health Savings Account, Dependent Care FSA, and supplemental coverage with plans that can fit each employee's needs. We offer a 401k plan that includes a company match and is fully vested after you become eligible, paid time off, sick time, and paid company holidays. We also offer an Employee Assistance Program (EAP) that provides services like virtual counseling, financial services, legal services, life coaching, etc.
Pay Disclaimer:
The pay range for this job level is a general guideline only and not a guarantee of compensation or salary. Additional factors considered in extending an offer include (but are not limited to) responsibilities of the job, education, experience, knowledge, skills, and abilities, as well as internal equity, alignment with market data, applicable bargaining agreement (if any), or other law.

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