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Quality Engineering Technician – Cleanroom & Calibration Management

LinkedIn Cretex Medical Component and Device Technologies Minneapolis, MN
Not Applicable Posted April 17, 2026 Job link
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Requirements
  • Apply blueprint reading and GD&T knowledge to support inspection and process quality.
  • Ensure documentation and activities comply with ISO standards and regulatory requirements, maintaining an audit-ready state.
  • 2-5 years in a quality role within a regulated environment, preferably in medical device manufacturing or cleanroom operations.
  • Proficiency in cleanroom standards (ISO Class 7 and Class 8) and environmental monitoring techniques.
  • Experience with equipment calibration and maintenance, including managing calibration schedules and records.
  • Strong organizational skills with attention to detail and the ability to manage multiple tasks effectively.
  • Excellent verbal and written communication skills, with proficiency in technical writing and documentation.
  • Familiarity with applicable AAMI, ASTM, and ISO standards related to medical device sterilization and cleaning.
  • Ability to read and interpret engineering drawings and specifications, including Geometric Dimensioning and Tolerancing (GD&T).
  • Cretex Companies use cutting oils, solvents, and other chemicals in the manufacturing process.
Preferred Skills
  • “I learned that I really like the medical device industry.
Education
  • (Not required) – Associate degree in Engineering, Biology/Microbiology, or a related technical field.