What are the responsibilities and job description for the Quality Engineering Technician position at Freudenberg Medical?
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 52,000 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.
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.
Some of your Benefits
Safe Environment
401K Match
Diversity & Inclusion
Sustainability & Social Commitment
Corporate Events
Jeffersonville, IN
On-Site
Freudenberg Medical LLC
You support our team as
QUALITY ENGINEERING TECHNICIAN
Responsibilities
- Investigation of product complaints
- Troubleshooting manufacturing processes
- Product inspection / testing, data collection and basic analysis
- Review device history records for accuracy and lot traceability
- Review of documentation for correctness & accuracy
- Assist ongoing product development and manufacturing
- Provide support to quality instrumentation and calibration system
- Assist in generating required documentation for Product Development deliverables.
- Assist in writing technical report.
- Data entry
Qualifications
- Quality experience, preferable in medical device or similar industry that has similar requirements for lot history control (regulated industry).
- MS Word/Excel
- Blueprint reading
- Good math skills
- Instrumentation and calibration experience
- Willingness and eager to learn
The Freudenberg Group is an equal opportunity employer that is committed to diversity and inclusion. Employment opportunities are available to all applicants and associates without regard to race, color, religion, creed, gender (including pregnancy, childbirth, breastfeeding, or related medical conditions), gender identity or expression, national origin, ancestry, age, mental or physical disability, genetic information, marital status, familial status, sexual orientation, protected military or veteran status, or any other characteristic protected by applicable law.
Additional Information
Teresa Smallwood
