Manufacturing Quality Engineer

Primary responsibilities include ensuring the quality of all products. You will also be required to review/maintain quality system documents and records; be involved in new mold/product validation, cross qualifications, and continuous improvement activities; and be assigned daily 5S and/or process audits.

 

·         Participate in product design reviews.

·         Resolve internal product quality issues to reduce defects/scrap.

·         Be on the CAPA team. 

·         Participate in resolving customer on-site quality issues and/or quality reviews.

·         Perform part specific quality training.

·         Perform daily 5S and process audits.

·         Verify and validate reports after mold repair, including capability studies, gauge R & R’s, first article reports, etc.

·         Develop and maintain statistical process control database for new medical components.

·         Perform daily inspection of product on the production floor.

·         Support Internal Audits, Customer Audits, and ISO/QS Audits

·         Assist in procedure development and/or maintenance.

·         Responsible for MRB disposition of nonconforming products in the absence of the Quality Manager

 

·         Degree in engineering or related discipline.

·         Plastics experience.

·         Manufacturing experience with excellent problem-solving skills and the ability to perform root cause analyses.

·         Must have experience in CMM, GD&T, Vision Systems and Minitab.

·         Demonstrated teaching skills, with a desire and the ability to train and mentor others.

·         Previous quality control experience to include data collection and quality analytics.

·         Knowledge of data collection and some Statistical Quality/Process Control. 

·         Excellent written/verbal communications and organizational skills.

·         Flexibility to work additional hours when necessary.

·         Must be able to lift to 50 lbs.