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Junior Engineer - On site

Job in White Bear Lake, Ramsey County, Minnesota, USA
Listing for: VitaTek
Full Time position
Listed on 2026-01-01
Job specializations:
  • Engineering
    Medical Device Industry, Manufacturing Engineer
Job Description & How to Apply Below

Company Description

Vita Tek, based in Minnesota's Medical Alley, is the largest private medical device manufacturer in the state. The company offers an end‑to‑end approach for developing, manufacturing, and commercializing innovative medical devices, catering to physicians, startups, and strategic leaders. With an"Everything In‑House" model, Vita Tek provides comprehensive services, including research, prototyping, regulatory compliance, manufacturing, packaging, and market launch. Vita Tek is ISO 13485 certified and FDA registered, producing Class I‑III devices while focusing on improving lives through innovation and efficiency.

Role Description

This is a full‑time Junior Engineer role located on‑site at our facility in White Bear Lake, MN. The Junior Engineer will be responsible for supporting product development, prototyping, and manufacturing processes. Daily tasks include collaborating with cross‑functional teams, preparing technical reports, assisting with quality control, conducting testing for compliance, and ensuring adherence to regulatory standards. The role offers an opportunity to contribute to innovative medical device creation and support the launch of groundbreaking products.

Qualifications
  • Proficiency in engineering principles related to design, prototyping, and manufacturing of medical devices.
  • Skills in quality control processes, compliance testing, and regulatory adherence.
  • Excellent communication and collaboration abilities for working within multidisciplinary teams.
  • Analytical and problem‑solving capabilities to diagnose technical challenges.
  • Bachelor's degree in Mechanical Engineering, Biomedical Engineering, or a related field.
  • Knowledge of medical device industry standards, such as FDA regulations or ISO 13485, is advantageous.
  • Prior experience in medical device development or manufacturing is a plus.
  • Hands‑on experience with tools like CAD software or injection molding equipment is beneficial.
  • Adaptability and willingness to learn new technologies and methods.
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