Location: Plymouth, Minnesota, United States
Job Summary:
Job Duties:
- Support CAPA Portfolio; mentorship and project management
- Communicate timelines for CAPA projects
- Process QA requests and manage responses
- Lead QA system meetings and communications
- Ensure database integrity for QA systems
- Facilitate CAPA training and continual improvement
- Analyze and report CAPA data metrics
- Comply with FDA regulations and company policies
Required Skills (Keywords):
- Quality assurance
- FDA, GMP, ISO 13485
- Communication
- Data analysis
- Project management
- Organizational skills
- Teamwork
Required Experiences (Topics):
- Bachelor’s degree in Engineering or Technical Field
- 2-4+ years technical experience
- Previous Quality assurance experience
- Medical Device Experience (preferred)
Job URLs: