Cypress HCM
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)
#J-18808-Ljbffr
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)
#J-18808-Ljbffr