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Temporary 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 ...

Sr. R&D Engineer

Vernon Hills, IL · On-site

$101.80K - $139.80K/yr

The position designs, develops and implements new products, focusing on project planning ... B.S. degree in Mechanical Engineering, Biomedical Engineering, Chemical Engineering or other ...

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Temporary Biomedical Product Development Engineer information

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

To excel as a Temporary Biomedical Product Development Engineer, you need a strong background in biomedical engineering principles, product design, and regulatory standards, typically supported by a relevant engineering degree. Familiarity with CAD software (like SolidWorks), rapid prototyping tools, and knowledge of FDA or ISO regulations are commonly required. Strong analytical thinking, collaboration, and adaptability are crucial soft skills for success in cross-functional teams and fast-paced projects. These skills and qualifications are important to ensure safe, effective, and compliant product development within tight project timelines.

What types of projects and collaboration can a Temporary Biomedical Product Development Engineer expect during their assignment?

As a Temporary Biomedical Product Development Engineer, you will likely be involved in specific phases of the product lifecycle such as prototyping, testing, or design improvements, depending on the organization's current needs. You will work closely with cross-functional teams—including R&D scientists, quality assurance, manufacturing, and regulatory affairs—to ensure that products meet both technical and compliance standards. Temporary roles often require adaptability, as project priorities can shift quickly, and you may be asked to contribute to multiple initiatives. This collaborative environment offers exposure to various aspects of biomedical engineering and can help expand your professional network.

What are Temporary Biomedical Product Development Engineers?

Temporary Biomedical Product Development Engineers are professionals who work on a contract or short-term basis to design, develop, and improve medical devices or products. They collaborate with cross-functional teams to ensure products meet regulatory standards, are safe for patients, and perform as intended. Their duties may include prototyping, testing, documentation, and supporting the transition from concept to manufacturing. These roles are often found in medical device companies during periods of increased workload or for specific projects. Temporary positions allow companies to bring in specialized expertise for a limited time.

What is the difference between Temporary Biomedical Product Development Engineer vs Temporary Biomedical Research Associate?

AspectTemporary Biomedical Product Development EngineerTemporary Biomedical Research Associate
CredentialsBachelor's or Master's in Biomedical Engineering or related fieldBachelor's or Master's in Biology, Biomedical Science, or related field
Work EnvironmentProduct design labs, R&D departments, manufacturing settingsResearch labs, clinical trial sites, academic institutions
Employer & Industry UsageMedical device companies, biotech firms, pharmaceutical companiesResearch institutions, hospitals, biotech research labs

The Temporary Biomedical Product Development Engineer focuses on designing and developing medical devices and products, often working in R&D and manufacturing environments. In contrast, the Temporary Biomedical Research Associate primarily conducts experiments and supports research projects in labs. Both roles require relevant scientific credentials but differ in their focus on product development versus research activities.

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:
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.