Technician I (Tissue)

4 C Medical Technologies•Maple Grove, MN
•$25 - $29

About The Position

The Tissue Technician I performs technical manufacturing activities in support of transcatheter mitral valve replacement (TMVR) product development and manufacturing operations. The role builds delivery systems, supports nitinol processing activities, and executes manufacturing procedures in a controlled environment. Work is performed under close supervision while the technician develops proficiency across multiple manufacturing and technical processes. The position primarily works in a Controlled Environment Room (CER)/cleanroom, with regular interaction with Manufacturing, Quality, Engineering, and Supply Chain personnel. It involves frequent rotation among technical workstations and manufacturing processes and may support engineering builds and development activities outside standard production schedules. Overtime and schedule flexibility may be required.

Requirements

  • High School Diploma or equivalent required.
  • 0–2 years of medical device manufacturing or process development experience required.
  • Proficient with inspection equipment.
  • Basic understanding of engineering drawings and dimensional inspection.
  • Strong troubleshooting capabilities.
  • Working knowledge of manufacturing documentation systems.
  • Ability to sit or stand for extended periods.
  • Ability to perform repetitive hand and wrist movements.
  • Ability to use microscopes and precision tools for extended periods.
  • Ability to maintain fine motor dexterity and hand-eye coordination.
  • Ability to lift and move materials up to 25 pounds occasionally.
  • Ability to wear required cleanroom attire and personal protective equipment (PPE).
  • Ability to visually inspect small components with or without corrective lenses.
  • Ability to work under magnification for extended periods while maintaining precision and quality standards.
  • Ability to safely operate manufacturing and inspection equipment.

Responsibilities

  • Assemble TMVR delivery systems following approved manufacturing procedures and work instructions.
  • Perform basic nitinol processing, material reflow, and electropolishing activities following established procedures.
  • Support production and engineering builds while maintaining compliance with quality requirements.
  • Accurately document build activities and maintain production records.
  • Rotate among multiple technical workstations as needed.
  • Identify and escalate process, equipment, or material issues.
  • Communicate component and consumable shortages.
  • Participate in process improvement activities and provide feedback regarding manufacturability.
  • Work effectively with Manufacturing, Quality, and R&D personnel.
  • Maintain cleanroom standards and safety requirements.
  • Perform additional duties as assigned.
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