Medline Industries, LP is seeking a quality-focused professional to independently set basic in-process quality standards and lead efforts to develop testing methods, sampling plans, and training programs. You will evaluate production processes, qualify vendors, and maintain DMRs and device master records to support CE and regulatory requirements.
The role requires at least 4 years in Quality or Engineering with strong knowledge of 21 CFR 820, ISO13485, and related standards.
#J-18808-LjbffrSenior Quality Engineer: Process Control & CAPA in northfield township at Unknown Company
This position is listed as full time and onsite.