The role requires maintaining company compliance with FDA Quality System Regulations and ISO 13485 standards while actively participating in internal audits
Job Summary
The role requires maintaining company compliance with FDA Quality System Regulations and ISO 13485 standards while actively participating in internal audits.
Candidates will lead continuous improvement projects and act as a subject matter expert for SPC, FMEA, DOE, and process validation.
The position involves providing direction to product development teams to successfully launch new products into active production in a timely manner.
Matching Summary
The role requires maintaining company compliance with FDA Quality System Regulations and ISO 13485 standards while actively participating in internal audits.
Skills & Requirements
Must-have
FDA Quality System Regulations compliance
ISO 13485 standards knowledge
SPC FMEA DOE process validation expertise
Bachelor's degree in engineering
3 years manufacturing experience
Nice-to-have
Excellent verbal and written communication skills
Strong data analysis in statistical packages
ERP system familiarity
Geometric tolerance and mechanical drawing knowledge
Project management support capabilities
Key Requirements
Minimum Bachelor's degree in engineering
3 years working experience in manufacturing environment