Quality Engineering Technician: Cleanroom & Calibration

Cretex Companies, Inc.; Brooklyn Park (MN); On-site; USD 31,795 - 46,094; Full time

Benefits offered by this job

401k retirement savings plan with company match

Comprehensive medical insurance

Discretionary holiday bonus program

Wellness program with incentives

Job summary

Cretex Companies, Inc. is seeking a Quality Engineering Technician in Brooklyn Park, Minnesota. This pivotal role involves overseeing cleanroom operations, ensuring compliance with standards, and maintaining equipment calibration to uphold product quality. Responsibilities include conducting environmental monitoring, managing equipment calibration, performing inspections, and supporting continuous quality improvement initiatives.

The successful candidate will have an associate degree in a relevant field, along with 2-5 years of experience in a regulated quality role, preferably in medical device manufacturing.

Qualifications

• 2-5 years in a quality role within a regulated environment, preferably in medical device manufacturing.
• Proficiency in cleanroom standards (ISO Class 7 and Class 8) and environmental monitoring techniques.
• Strong organizational skills with attention to detail and ability to manage multiple tasks.

Responsibilities

• Conduct monthly environmental monitoring in Class 7 and Class 8 cleanrooms.
• Assist engineers in validation and verification activities.
• Conduct process audits to verify adherence to quality protocols.

Skills

Environmental monitoring

Equipment calibration

Documentation

ISO standards compliance

Communication skills

Organizational skills

Education

Associate degree in Engineering, Biology/Microbiology, or a related technical field

Job description

Cretex Companies, Inc. is seeking a Quality Engineering Technician in Brooklyn Park, Minnesota. This pivotal role involves overseeing cleanroom operations, ensuring compliance with standards, and maintaining equipment calibration to uphold product quality. Responsibilities include conducting environmental monitoring, managing equipment calibration, performing inspections, and supporting continuous quality improvement initiatives.

The successful candidate will have an associate degree in a relevant field, along with 2-5 years of experience in a regulated quality role, preferably in medical device manufacturing.