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Cypress HCM

Quality Engineering Technician

Cypress HCM, Minneapolis, Minnesota, United States, 55400

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Sr. Technical Recruiter | Talent Acquisition | Medical Device, Biotech, Life Sciences, Engineering, Regulated, IT Industries This role leads hands‑on quality engineering activities supporting medical device development and manufacturing in a regulated environment. The Quality Engineering Technician executes validation, testing, statistical analysis, and quality system activities to ensure products and processes meet ISO 13485 and FDA requirements.

Responsibilities

Author, review, and execute validation protocols, test methods, and technical reports

Lead verification, validation, and measurement system analysis (Gage R&R, capability studies, DOE)

Perform statistical analysis to identify trends, risks, and process improvement opportunities

Support root cause analysis and CAPA activities for product and process issues

Partner cross‑functionally with Design, Manufacturing, and Quality Engineering teams

Maintain accurate documentation and records within the electronic QMS

Support continuous improvement initiatives across development and manufacturing

Qualifications

Associate or Technical degree with 10+ years of medical device quality experience

Strong knowledge of ISO 13485, FDA QSR, validation, and design/manufacturing controls

Advanced experience with statistical tools (Minitab, SPC, Gage R&R, DOE)

Proven ability to author and approve quality protocols and reports

Background in electronics manufacturing and test methods

Strong analytical, organizational, and problem‑solving skills

Excellent written and verbal communication abilities

Pay Rate

$75‑90k

Seniority level

Associate

Employment type

Full‑time

Job function

Business Development

Industries

Staffing and Recruiting

Benefits

Medical insurance

Vision insurance

401(k)

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