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Sr. Quality Engineer
Baldwin Park, CA
Job Description
Working at Freudenberg: "We will wow your world!" This is our promise. As a global technology group, we not only make the world cleaner, healthier and more comfortable, but also offer our 51,000 employees a networked and diverse environment where everyone can thrive individually. Be surprised and experience your own wow moments.
At Freudenberg Medical, we make products that save and improve the lives of people every day, all around the world. We are a global provider for medical device design and manufacturing with more than 2,500 employees. Innovation is at the core of our company, and we are proud of our industry-leading quality, lean manufacturing, and focus on innovation in products and processing technologies. Freudenberg Medical is an exciting place to work with lots of opportunity to learn, develop, and grow your career. Come join us and together we can make a difference in the future of healthcare. You support our team as Sr. Quality Engineer
At Freudenberg Medical, we make products that save and improve the lives of people every day, all around the world. We are a global provider for medical device design and manufacturing with more than 2,500 employees. Innovation is at the core of our company, and we are proud of our industry-leading quality, lean manufacturing, and focus on innovation in products and processing technologies. Freudenberg Medical is an exciting place to work with lots of opportunity to learn, develop, and grow your career. Come join us and together we can make a difference in the future of healthcare. You support our team as Sr. Quality Engineer
Responsibilities
- Provides expertise in statistical analysis for Quality Engineering projects.
- Handles multiple projects and tasks, from product inception through product launch and maintenance.
- Leads plant activities in process validation, process capability improvement, and resolving customer issues by initiating corrective and preventive action, with an eye to increased capability and customer satisfaction that support the site Quality System.
- Drives with the investigation of root cause and determination of corrective and preventive actions relating to NCMRs, CARs, and QANs. Responsible for corrective action effectiveness verification after implementation of corrective actions.
- Works continuous improvement projects from beginning to end. Characterizes the problem, identifies key process inputs, determines optimal operating window, implements controls to maintain output at desired level, and quantifies the improvement in savings, avoidance, or value.
- Works on complex issues where analysis of situations or data requires an in-depth evaluation of variable factors. Exercises judgment in selecting methods, techniques and evaluation criteria for obtaining results Internal and external contacts often pertain to company plans and objectives.
Qualifications
- Bachelor's degree in engineering or related field.
- Medical Devices experience
- 5+ years' experience in injection molding manufacturing operations or equivalent.
- 5+ years quality engineering experience in the medical device industry
- Preferred: Project Management experience and Lean/Six Sigma certification
- Demonstrated knowledge in Quality System/Good Manufacturing Practices.
- Demonstrated competency in data analysis, continuous process improvement, including lean, six sigma, and validations
- Demonstrated competency in interpersonal skills.
Job Summary
Start Date
As soon as possible
Employment Term and Type
Regular, Full Time
Required Education
Bachelor's Degree
Required Experience
5+ years
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