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Remote Fda Internship Jobs in Illinois (NOW HIRING)

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Remote Fda Internship information

What is a remote FDA internship?

A remote FDA internship is a temporary, educational position that allows students or recent graduates to work with the U.S. Food and Drug Administration (FDA) from a remote location, rather than on-site. Interns may assist with projects related to public health, regulatory affairs, research, policy analysis, or data management. These internships are designed to provide practical experience and exposure to the FDA’s role in protecting public health, while offering flexibility for those who cannot relocate or commute. Remote FDA internships may be paid or unpaid, and requirements vary depending on the specific program or department. Applicants typically need to be enrolled in an accredited college or university and meet other eligibility criteria.

What types of projects or responsibilities can I expect as a remote FDA intern?

As a remote FDA intern, you may be involved in a variety of projects such as assisting with research and data analysis, supporting regulatory review processes, preparing reports, or helping with public health initiatives. Your exact responsibilities will depend on your assigned department, but remote interns typically collaborate with mentors and team members through virtual meetings and online platforms. This role offers exposure to federal regulatory practices, and you’ll gain valuable experience in navigating structured government workflows. Effective communication and time management are key to succeeding in this remote setting.

What are the key skills and qualifications needed to thrive as a remote FDA intern?

To thrive as a Remote FDA Intern, you generally need a background in life sciences, public health, or a related field, often supported by current enrollment in a relevant degree program. Familiarity with regulatory databases, Microsoft Office Suite, and scientific literature review tools is commonly required. Strong written communication, attention to detail, and initiative are crucial soft skills for excelling in remote collaboration and research tasks. These skills ensure interns can contribute effectively to regulatory projects, maintain compliance standards, and support the FDA’s mission in a virtual environment.

What is the difference between Remote Fda Internship vs Remote Fda Associate?

AspectRemote Fda InternshipRemote Fda Associate
Required CredentialsTypically enrolled in or recent graduate of relevant health/science programsBachelor's or Master's in life sciences, with some experience preferred
Work EnvironmentInternship program, often part-time or seasonal, supervised by professionalsFull-time remote role, more independent with ongoing responsibilities
Employer & Industry UsageUsed by FDA and biotech companies for training and entry-level talentCommon in regulatory affairs teams within pharmaceutical and biotech firms

The Remote Fda Internship is an entry-level, temporary position designed for students or recent graduates gaining industry exposure. In contrast, the Remote Fda Associate is a more advanced, full-time role requiring some experience, focusing on regulatory tasks. Both roles are vital in the FDA and biotech sectors but differ in experience level, responsibilities, and duration.

What are the most commonly searched types of Remote Fda jobs in Illinois?

The most popular types of Remote Fda jobs in Illinois are:

What cities in Illinois are hiring for Remote Fda Internship jobs?

Cities in Illinois with the most Remote Fda Internship job openings:

Remote Fda Internship jobs near you
Infographic showing various Remote Fda Internship job openings in Illinois as of August 2026, with employment types broken down into 6% Internship, 65% Full Time, 28% Part Time, and 1% Contract. Highlights an 88% Physical, 1% Hybrid, and 11% Remote job distribution.

Medical Device/Combination Product Engineer

Vernon Hills, IL • On-site, Remote

Ventura Solutions LLC
Medical Equipment and Supplies Manufacturing • 11 - 50 employees
Learn more about Ventura Solutions LLCexternal

$60K - $75K/yr

Full-time

Medical, Dental, Vision, PTO

Re-posted 12 hours ago

Job description

We are seeking passionate and driven Medical Device/Combination Product Engineers to join our medical device consulting team. This is an ideal opportunity for recent graduates or those with limited experience who are excited to apply their academic knowledge in real-world product development.

If you have a strong interest in medical devices, pharmaceuticals, and combination products, and are eager to gain hands-on experience in product development, design controls, and risk management, we want to meet you!

As a Medical Device/Combination Product Engineer, you will support the development and maintenance of medical devices and combination products by assisting with technical documentation, testing, and cross-functional collaboration. You’ll contribute to the creation of Design History Files (DHF), risk management files, and other engineering documentation in accordance with industry regulations and standards such as FDA 21 CFR 820 and ISO 14971.

Responsibilities

  • Assist in developing and maintaining Design History Files (DHF) and Risk Management Files for medical devices and combination products
  • Support product development activities, including gathering user needs, design inputs, and testing requirements
  • Participate in risk assessment activities, such as creating or supporting FMEAs
  • Help prepare and review technical documentation for design verification and validation
  • Research applicable regulations, standards, and guidance documents to support compliance efforts
  • Work closely with cross-functional teams, including Quality, Regulatory, Manufacturing, Human Factors, and Clinical
  • Contribute to design control activities and help ensure traceability from requirements through testing
  • Support documentation for inspections and regulatory submissions

Qualifications

  • Bachelor’s degree in Biomedical Engineering or related engineering discipline (e.g., Mechanical, Chemical, Electrical)
  • Strong academic foundation in engineering principles and a desire to apply them in a regulated industry
  • Understanding of or exposure to design control, risk management, and product development lifecycle through coursework, internships, or academic projects
  • Strong written and verbal communication skills
  • Detail-oriented with good documentation and organizational skills
  • Team-oriented with a willingness to learn and grow in a fast-paced environment

Preferred (Not Required) Experience

  • Internship, co-op, or project work related to medical devices, drug delivery, or combination products
  • Familiarity with standards like ISO 13485, ISO 14971, or FDA design control regulations
  • Exposure to tools such as FMEA, DHF documentation, or verification test planning
  • Experience with engineering software (CAD, Minitab, MATLAB, etc.)

Location

  • Northwest Chicago Suburbs or remote for the right candidate

Employee Type

  • W2 Employee

Compensation and Benefits

  • Salary: $60,000 - $75,000 annually, depending on experience
  • Choice of medical, dental, and vision plans
  • Paid Vacation Time
  • Competitive base salary

About Ventura Solutions

Ventura Solutions is a reputable end-to-end medical device and combination product consulting, staffing, and training firm. With our deep industry expertise spanning medical devices and combination products, coupled with an outstanding talent pool, we stand out as the preferred option for a diverse array of projects. On the consulting side, we integrate seamlessly into your team and manage small to complex Statement of Work (SOW) projects. On the staffing side, we help source, screen, and on-board reputable employees to fill temporary, temp to permanent, and permanent job openings. We accelerate product development, keep products compliant, and help build great organizations. For more information, visit us at www.ventura-solutions.com.

Equal Opportunity Employer Minorities/Women/Veterans/Disabled

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