Quality Systems Specialist - Documentation Control

Join our dynamic team at DEKA and be part of creating innovative medical solutions!

As our Quality Documentation Control Specialist, you'll play a vital role in supporting the QMS through document control processes in our medical device R&D environment.

You'll work collaboratively with cross-functional teams to ensure documentation accuracy and accessibility.

Key responsibilities as a QA Documentation Specialist:

• Process and manage Engineering Change Orders (ECOs), Temporary Change Orders (TCOs), and Reprocessing Orders (ROs) through to completion Maintain and utilize Engineering Resource Planning (ERP) database and Electronic Quality Management Systems (eQMS) for effective document control Coordinate training activities, managing review of training database, oversight of onboarding activities, and providing company-wide support for eQMS training processes Modify and format technical documents according to established SOPs and r...