Company seeks a manufacturing engineer with experience with plastic processing equipment and materials. Prefferably, cadidates will have experience in the medical device profession.
The Manufacturing Engineer will report directly to the Manufactu...
Overview: This position is focused on processing domestic and export shipments accurately and timely, in compliance with U.S. export regulations and in conjunction with the expectations of the customers.
Responsibilities:
Manages th...
The Medical writer will need to be able to write scientific and regulatory documents of different types. The primary focus will be on writing and updating Clinical Evaluation Reports and the supporting documents. Other writing will focus on regulato...
As Sr. Specialist, Quality Assurance, he/she will perform task that will uphold and improve the product quality of medical devices manufactured and meet regulatory requirement to stay in compliance.
Executes day to day activities based on quality...
This position supports the SVP, Quality, Regulatory, & Clinical Affairs in all department related activities
Tracks and updates Quality Assurance, Regulatory, and Clinical metrics
Maintains and updates Quality Assurance, Regulatory, and Cli...
Complete in-process, final inspection of medical devices and review DHR and record QC Chemistry and Microbiology results.
Read work instructions to complete in-process and final inspections.
Use a wide assortment of QC inspection instruments t...
