Michael Page
Medical Device - Catheter Process Engineer - Hudson, MA
Michael Page, Hudson, Massachusetts, us, 01749
Lead process development and optimization for advanced catheter systems.
Play a key role in bringing new cardiac devices from concept through production.
About Our Client
My client is an innovative medical device company focused on advancing catheter-based therapies for cardiac care. With a track record of developing novel technologies and bringing new products to market, the organization provides engineers with the opportunity to work on meaningful projects that directly impact patient outcomes.
Job Description
Responsibilities:
Develop, validate, and scale catheter manufacturing and assembly processes. Support design transfer from R&D to manufacturing. Create and execute test methods, protocols, validations, and reports. Design fixtures, components, and subsystems for complex catheters. Conduct statistical analysis of process and product data. Build prototypes, manage DOE studies, and optimize designs for manufacturability. Collaborate with vendors to source materials, components, and subassemblies. MPI does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity or expression, national origin, age, disability, veteran status, marital status, or based on an individual's status in any group or class protected by applicable federal, state or local law. MPI encourages applications from minorities, women, the disabled, protected veterans and all other qualified applicants.
The Successful Applicant
Ideal Candidate:
Bachelor's degree in Mechanical, Biomedical, or related engineering discipline (Master's preferred). 3+ years of experience in catheter/disposable medical device development and commercialization. 2+ years developing catheter assembly processes. Knowledge of materials such as Pebax, nylon, PTFE, FEP, PEEK, and metals like nitinol and steel. Skilled in SolidWorks 3D CAD and familiar with shop/fabrication tools. Strong communication skills and working knowledge of medical device regulatory requirements. What's on Offer
What's To Offer:
Direct involvement in developing life-saving cardiac technologies. Collaborative environment with cross-functional exposure (R&D, Quality, Clinical, Manufacturing). Opportunities for innovation and hands-on engineering across the full development cycle. Competitive compensation with growth potential based on experience and contributions.
Contact
Josephine Belcher
Quote job ref
JN-092025-6835938
My client is an innovative medical device company focused on advancing catheter-based therapies for cardiac care. With a track record of developing novel technologies and bringing new products to market, the organization provides engineers with the opportunity to work on meaningful projects that directly impact patient outcomes.
Job Description
Responsibilities:
Develop, validate, and scale catheter manufacturing and assembly processes. Support design transfer from R&D to manufacturing. Create and execute test methods, protocols, validations, and reports. Design fixtures, components, and subsystems for complex catheters. Conduct statistical analysis of process and product data. Build prototypes, manage DOE studies, and optimize designs for manufacturability. Collaborate with vendors to source materials, components, and subassemblies. MPI does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity or expression, national origin, age, disability, veteran status, marital status, or based on an individual's status in any group or class protected by applicable federal, state or local law. MPI encourages applications from minorities, women, the disabled, protected veterans and all other qualified applicants.
The Successful Applicant
Ideal Candidate:
Bachelor's degree in Mechanical, Biomedical, or related engineering discipline (Master's preferred). 3+ years of experience in catheter/disposable medical device development and commercialization. 2+ years developing catheter assembly processes. Knowledge of materials such as Pebax, nylon, PTFE, FEP, PEEK, and metals like nitinol and steel. Skilled in SolidWorks 3D CAD and familiar with shop/fabrication tools. Strong communication skills and working knowledge of medical device regulatory requirements. What's on Offer
What's To Offer:
Direct involvement in developing life-saving cardiac technologies. Collaborative environment with cross-functional exposure (R&D, Quality, Clinical, Manufacturing). Opportunities for innovation and hands-on engineering across the full development cycle. Competitive compensation with growth potential based on experience and contributions.
Contact
Josephine Belcher
Quote job ref
JN-092025-6835938