Description
Job Description
EDUCATION and/or EXPERIENCE
Bachelor’s degree in engineering (industrial, chemical, manufacturing, or any other related).
And/or 3 years on QA/QC engineering work experience on QA/QC in medical device manufacturing processes such device assembly, injection molding or extrusion, preferable.
Preferable ISO 13485 certified internal auditor.
JOB DESCRIPTION
CPF-815 (11/23)
Knowledge by school or work experience in risk Management analysis, FMEA – Control Plans management, statistical data analysis on Minitab, preferable, Test Method validation and GR&R execution, root cause analysis technics management, CAPA – Complaint - NCMR execution and management.
Experience in Lean and Kaizen participation and execution is preferred.
Negotiation and leadership skills.
Advanced Computer skills (Minitab, Office, Word, Excel, Power Point, and/or Application Programs, Statistical Software, Databases. Etc.).
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