Abbott seeks a Quality Engineer for 2nd Shift in the Vascular division to support manufacturing and product development operations. The role involves process optimization, defect control, quality planning, and leading improvement initiatives within a regulated medical device environment.
Responsibilities
- Identify and control manufacturing process defects through root cause analysis and corrective/preventive actions
- Develop product quality plans, specifications, and documentation with cross-functional teams
- Establish process monitoring systems and reduce process variation to eliminate defects
- Lead process improvement initiatives by analyzing quality metrics and supporting product development
- Provide technical guidance and mentorship to less experienced staff
Requirements
- Bachelor's degree plus 2-5 years related work experience, or Master's degree with 0-2 years experience
- CAPA (Corrective and Preventive Action) experience
- Data analysis skills
- Risk management experience
- Quality systems knowledge and application
- CQE certification preferred
- Medical device industry experience preferred
Quality Engineer - 2nd Shift in temecula at Unknown Company
This position is listed as full time and onsite.