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Internship Biomedical Product Development Engineer Jobs in Illinois

Product Development Engineer

Lisle, IL · Hybrid

$80K - $115K/yr

Product Development Engineer The Product Development Engineer will design and develop high-speed connector and cable systems that support rapidly growing data storage, telecommunications, and ...

Product development and modification of Suction and Oxygen Therapy products to established design control processes and good engineering practices. * Lead product development from concept through ...

Product development and modification of Suction and Oxygen Therapy products to established design control processes and good engineering practices. * Lead product development from concept through ...

Senior Product Development Engineer Location: 1222 Hamilton Parkway, Itasca, IL, 60143 Job Duties : Design, develop, and manage activities for a specific product or group of products from product ...

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Internship Biomedical Product Development Engineer information

What are the key skills and qualifications needed to thrive as an Internship Biomedical Product Development Engineer, and why are they important?

To thrive as an Internship Biomedical Product Development Engineer, you need a strong background in biomedical engineering principles, problem-solving, and familiarity with product development processes, typically gained through coursework or related internships. Experience with CAD software, lab equipment, and knowledge of regulatory standards such as FDA or ISO is highly valuable. Strong teamwork, communication skills, and a detail-oriented mindset help interns collaborate effectively and contribute to innovative solutions. These competencies are essential to ensure the safe, effective, and compliant development of biomedical products within multidisciplinary teams.

What types of projects and responsibilities can I expect as an Internship Biomedical Product Development Engineer?

As an Internship Biomedical Product Development Engineer, you will typically support product design and prototyping, conduct laboratory testing, and assist with documentation for regulatory compliance. You'll often collaborate closely with cross-functional teams, including engineers, quality assurance, and clinical specialists, to bring innovative medical devices or products from concept to early development stages. Common challenges include balancing creative problem-solving with strict regulatory requirements and managing multiple tasks to meet project deadlines. This role offers hands-on experience that can lead to full-time opportunities and valuable exposure to the entire product development lifecycle.

What does an Internship Biomedical Product Development Engineer do?

An Internship Biomedical Product Development Engineer assists in designing, developing, and testing medical devices and healthcare products under the supervision of experienced engineers. Interns may participate in research, prototyping, data analysis, and documentation to support product development from concept to prototype. They often collaborate with cross-functional teams, learn industry regulations, and gain hands-on experience with tools and technologies used in biomedical engineering. This role offers valuable exposure to real-world challenges in healthcare innovation and product design.

What is the difference between Internship Biomedical Product Development Engineer vs Biomedical Research Assistant?

AspectInternship Biomedical Product Development EngineerBiomedical Research Assistant
Required CredentialsEnrolled in or recent graduate of biomedical engineering, bioengineering, or related fieldsTypically pursuing or holding a degree in biology, biomedical sciences, or related areas
Work EnvironmentProduct development labs, engineering teams, R&D departmentsResearch labs, academic institutions, clinical research settings
Employer & Industry UsageMedical device companies, biotech firms, healthcare product developersUniversities, research institutes, hospitals

While both roles involve biomedical sciences, the Internship Biomedical Product Development Engineer focuses on designing and developing medical devices and products, often in a corporate setting. In contrast, a Biomedical Research Assistant primarily conducts scientific research, experiments, and data analysis in academic or clinical research environments. The former emphasizes engineering and product innovation, whereas the latter centers on scientific investigation and data collection.

What are the most commonly searched types of Biomedical Product Development Engineer jobs in Illinois? The most popular types of Biomedical Product Development Engineer jobs in Illinois are:
What are popular job titles related to Internship Biomedical Product Development Engineer jobs in Illinois? For Internship Biomedical Product Development Engineer jobs in Illinois, the most frequently searched job titles are:
What job categories do people searching Internship Biomedical Product Development Engineer jobs in Illinois look for? The top searched job categories for Internship Biomedical Product Development Engineer jobs in Illinois are:
What cities in Illinois are hiring for Internship Biomedical Product Development Engineer jobs? Cities in Illinois with the most Internship Biomedical Product Development Engineer job openings:
Product Development Engineer

Product Development Engineer

TIDI PRODUCTS LLC

Lincolnshire, IL • On-site, Remote

$85K - $95K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 12 days ago


Job description

Description
We are hiring Product Development Engineer!!
This position can work remotely, but must be within 3 hours of Neenah, WI AND Lincolnshire, IL.
The Product Development Engineer is responsible for product development within TIDI Products. Working closely with cross-functional team members, the individual will lead projects to deliver new products, line extensions, and product improvements.
ESSENTIAL RESPONSIBILITIES:
• Serves as project leader, technical leader, or team member for projects including new product development, line extensions, and product improvements.
• Collaborates with product development and cross-functional team to develop timelines and project plans.
• Interfaces with customers (marketing, end user customers and OEM customers) to translate user needs into design requirements and validate designs.
• Uses engineering, analytical, and technical skills to design products to meet requirements.
• Develops and utilizes test methods and plans to evaluate product characteristics and performance.
• Creates, revises, and collaborates on project documents, protocols, drawings, and documentation to applicable internal and external standards.
• Collaborates with manufacturing team to transfer designs, develop manufacturing processes and documentation, and begin production.
• Engages outside design firms, testing labs and technical consultants to apply specialized expertise to projects.
• Leads engineering change controls to create and configure products within the TIDI Quality Management System.
• Identify and create standard work for new processes.
• Balance multiple projects, check and adjust on priorities, and adjust work appropriately.
• Uses basic knowledge of FDA and ISO Design Controls, Risk Management, and Design Transfer to follow TIDI procedures in accordance with regulations and complete all necessary documentation.
• Performs other tasks, as required or directed.
CORE VALUES & GUIDING PRINCIPLES:
• Understands internal and external customers
• Assure a safe work environment
• Encourage individual development
• Demonstrates teamwork and flexibility/adaptability
• Demonstrates honesty
• Keep our commitments
• Think systemically and ensure constancy of purpose
• Lead with humility and respect every individual
• Focus on process, embrace scientific thinking, flow and pull value, assure quality at the source and seek perfection
QUALIFICATIONS:
• BS Engineering Degree (Mechanical, Biomedical, Material-Science, or Manufacturing preferred).
• At least 3 years experience as an engineer in a medical device company.
• Experience in medical device under FDA 21 CFR 820.30 Design Controls, ISO 13485 and ISO 14971 Risk Management.
• Demonstrated engineering, analytical, problem solving, and technical skills.
• Effective written and oral communication in English language.
• Successful team player; demonstrated successful interpersonal and influence management skills.
• Track record of successfully collaborating with multiple functions and teams to drive successful project outcomes.
• Strong project management skills.
• Energetic, self-motivated and can work independently; strong work ethic.
• Working knowledge of U.S. and international standards as applicable to medical device development.
• Proficient with Microsoft Outlook, Word, Excel, PowerPoint, and Teams.
• Proficient with CAD software such as AutoCAD, Pro/E or SolidWorks.
• Able to travel to visit customers, manufacturing plants, and vendors (up to 10% time).
At TIDI Products we are committed to offering a comprehensive employee benefits program than help our employees stay healthy, feel secure and maintain a work/life balance.
About TIDI Products...
TIDI Products is a market leading manufacturing of disposable infection prevention products and patient safety products, headquartered in Neenah, WI. We have manufacturing and distribution facilities in Neenah, WI and Tijuana, MX. And office spae in Lincolnshire, IL TIDI provides best in class products and service to major healthcare products distributors and users worldwide.
We Support Care Givers and Protect Patients!!
Disability Accommodation
For individuals with disabilities that need additional assistance at any point in the application and interview process, please email WIHR@tidiproducts.com or call 920-751-4300 x 4044.
Equal Opportunity Employer
TIDI Products is proud to be an equal opportunity employer and is committed to maintaining a diverse and inclusive work environment. All qualified applicants will receive considerations for employment without regard to race, color, religion, sex, age, disability, marital status, family.
Estimated starting annual base salary pay ranges is $80,000.00 - $95,000.00 less applicable withholdings and deductions, paid on a bi-weekly basis. Please note that the actual compensation offered may vary based on relevant factors as determined by the Company, which may include, but is not limited to, location, experience, qualifications, education, skillset, and market conditions. The target base compensation for this role is in the low to middle of the range, with the top of the range reserved for only exceptional circumstances. TIDI Products offers a competitive benefits package to eligible full-time employees, which currently includes medical, dental, and vision plans, 401(k) with employer matching contributions, life insurance, paid time off, tuition reimbursement, and more, as well as paid sick leave in accordance with applicable law. Each benefit is subject to eligibility requirements as specified in plan documents, and the Company reserves the right to modify the benefits it offers from time to time.