• Engineering Technician

    Actalent (Minneapolis, MN)


    Job Title: Engineering Technician IIJob Description

     

    The Engineering Technician II will collaborate with Manufacturing Engineers to support technical operations within a high-volume medical device contract manufacturing facility. The role involves assembling prototypes, executing test protocols, documenting results, evaluating new manufacturing process instructions, and providing feedback to both engineering and manufacturing teams. Additionally, the position includes assisting in the development and maintenance of tooling and fixtures with a focus on catheter process development and manufacturing processes.

    Responsibilities

    + Monitor, inspect, set up, calibrate, and maintain manufacturing process equipment.

    + Research and identify manufacturing or engineering solutions.

    + Diagnose and troubleshoot technical issues, including machining, injection molding, laser processing, stamping, and packaging.

    + Assist engineers in creating, modifying, and testing products and processes.

    + Inspect products and processes for flaws and identify areas of improvement.

    + Conduct tests and collect data to support validation activities.

    + Utilize computer-aided design and drafting software.

    + Develop production drawings for manufacturing.

    + Read and comply with work instructions, set up sheets, and checklists.

    + Enter production information into the ERP system in a timely manner.

    + Generate ECO/DCO and process documentation changes related to manufacturing changes.

    + Perform equipment set-ups as required.

    + Support and comply with the company Quality System, ISO, and medical device requirements.

    Essential Skills

    + At least 3 years of experience working as an engineering technician.

    + Hands-on experience building medical catheters using typical assembly techniques and equipment is strongly preferred.

    + Experience with catheter assembly.

    + Experience facilitating, executing, and documenting process characterization and validation studies.

    + Demonstrated ability to execute process improvement.

    + Knowledge of Good Manufacturing Practices & Quality Systems Regulations.

    + Experience in medical product manufacturing.

    + Good communication and documentation skills.

    + Problem-solving and critical thinking skills.

    Additional Skills & Qualifications

    + Working knowledge of CAD software platforms such as AutoCAD, SolidWorks, or Pro-E is desired.

    Work Environment

    The role is based in a brand new, state-of-the-art facility located in Brooklyn Park. The facility combines three operational companies into a single building equipped with highly updated technology necessary for success in the medical device space. It includes some clean room spaces, as well as general production lines throughout the building.

     

    Job Type & Location

     

    This is a Permanent position based out of Minneapolis, MN.

    Pay and Benefits

    The pay range for this position is $72000.00 - $83000.00/yr.

     

    Supportlinc - No-cost resource (separate from your health plan)Health Partners - Medical, dental, and flexible spending account (FSA)Principal - Retirement and 401KLincoln Financial - Long-term disability, life and AD&D insurance, critical illness, and accident insurance programsEyeMed - VisionOptum - Health savings account (HSA)Wishbone - Pet insurance

     

    Workplace Type

     

    This is a fully onsite position in Minneapolis,MN.

     

    Application Deadline

     

    This position is anticipated to close on Nov 7, 2025.

    About Actalent

    Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.

     

    The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

     

    If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email [email protected] (%[email protected]) for other accommodation options.