iMPact Business Group
Product Development Engineer (Medical Device)
iMPact Business Group, Cary, Illinois, United States, 60013
Job Description
Our client, a
Global Medical Device Manufacture
has an immediate opening for a
Product Development Engineer
for a
12 Month + Contract . Our client offers results-driven people a place where they can make a difference - every day! You will also have the opportunity to work with other like-minded, self-directed and detail oriented Top Talents in an extremely collaborative and professional environment.
Position Description (Principle Duties and Responsibilities)
Designing and developing new products that meet functional, safety, and cost requirements. Specifying and documenting precise product functional requirements. Testing and integrating components to deliver optimized final product designs. Evaluating product effectiveness, safety, reliability, and cost to ensure compliance with standards. Developing and executing product specifications, fitness-for-use testing, and process validation plans. Creating and reviewing material part specifications and bills of materials (BOMs). Collaborating with internal manufacturing partners, contract manufacturers, designers, and product specialists to ensure manufacturability and quality. Utilizing CAD/CAE systems to model designs, produce engineering drawings, and validate design solutions. Supporting continuous improvement initiatives to enhance product development processes. Job Requirements
What you need
Bachelor's degree in Mechanical Engineering, Biomedical Engineering, or related technical discipline required. Minimum of 2+ years of engineering experience in product design, validation, or development. Strong proficiency in CAD/CAE software (e.g., SolidWorks, Creo, CATIA, or equivalent). Strong problem-solving and analytical skills. Experience with testing, validation, and process development. Excellent communication and collaboration skills. Experience in the medical device, life sciences, or highly regulated industry. Knowledge of design controls, FDA regulations, or ISO standards. Familiarity with GD&T (Geometric Dimensioning and Tolerancing). Experience with manufacturing processes (e.g., machining, molding, assembly). APQP, DFMEA, PFMEA, or Six Sigma certification a plus.
Our client, a
Global Medical Device Manufacture
has an immediate opening for a
Product Development Engineer
for a
12 Month + Contract . Our client offers results-driven people a place where they can make a difference - every day! You will also have the opportunity to work with other like-minded, self-directed and detail oriented Top Talents in an extremely collaborative and professional environment.
Position Description (Principle Duties and Responsibilities)
Designing and developing new products that meet functional, safety, and cost requirements. Specifying and documenting precise product functional requirements. Testing and integrating components to deliver optimized final product designs. Evaluating product effectiveness, safety, reliability, and cost to ensure compliance with standards. Developing and executing product specifications, fitness-for-use testing, and process validation plans. Creating and reviewing material part specifications and bills of materials (BOMs). Collaborating with internal manufacturing partners, contract manufacturers, designers, and product specialists to ensure manufacturability and quality. Utilizing CAD/CAE systems to model designs, produce engineering drawings, and validate design solutions. Supporting continuous improvement initiatives to enhance product development processes. Job Requirements
What you need
Bachelor's degree in Mechanical Engineering, Biomedical Engineering, or related technical discipline required. Minimum of 2+ years of engineering experience in product design, validation, or development. Strong proficiency in CAD/CAE software (e.g., SolidWorks, Creo, CATIA, or equivalent). Strong problem-solving and analytical skills. Experience with testing, validation, and process development. Excellent communication and collaboration skills. Experience in the medical device, life sciences, or highly regulated industry. Knowledge of design controls, FDA regulations, or ISO standards. Familiarity with GD&T (Geometric Dimensioning and Tolerancing). Experience with manufacturing processes (e.g., machining, molding, assembly). APQP, DFMEA, PFMEA, or Six Sigma certification a plus.