Development Engineer-III

US Tech Solutions; Lake Forest (IL); On-site; USD 70,000 - 90,000; Full time

Job summary

A global staff augmentation firm is seeking an experienced professional to join their Consumables R&D team in Lake Forest, Illinois. The role focuses on Design Verification for Consumables products and requires a B.S. in Engineering and 2-5 years of relevant experience, particularly in Medical Device Development. Key responsibilities include defining testing procedures and creating detailed protocols and reports. Excellent communication, analytical, and technical writing skills are essential for success in this position.

Qualifications

• 2 to 5 years of related experience in Medical Device Development.
• Familiarity with ISO standard test methods and related test instrumentation is preferred.
• Experience in creating protocols and reports.

Responsibilities

• Responsible for Design Verification of assigned Consumables products.
• Define testing to verify product design meets design requirements.

Skills

Analytical skills

Communication skills

Technical writing

Team collaboration

Education

B.S. in Engineering or science discipline

Job description

US Tech Solutions is a global staff augmentation firm providing a wide-range of talent on-demand and total workforce solutions. To know more about US Tech Solutions, please visit our website www.ustechsolutions.com.

We are constantly on the lookout for professionals to fulfill the staffing needs of our clients, sets the correct expectation and thus becomes an accelerator in the mutual growth of the individual and the organization as well.

Keeping the same intent in mind, we would like you to consider the job opening with US Tech Solutions that fits your expertise and skillset.

Job Description

• As a key contributor to the Consumables R&D team this position is responsible for Design Verification of assigned Consumables products.
• Following Design Control procedures, this position will define testing to verify product design meets design requirements. Engineering protocols, data analysis, and reports are authored by this position.

Requirements

• B.S. in Engineering or science discipline and 2 to 5 years related experience.
• Familiarity with ISO standard test methods and related test instrumentation preferred.
• Excellent analytical and communication skills required.
• Ability to work and solve problems in team environment.
• Technical writing skills are required for protocol and report writing.
• 3-5 years of experience in Medical Device Development. Must know Design Controls, Product Development and CAPA investigations.
• Must be able to create protocols and reports. Strong communication skills required.