Junior Validation Engineer
Provided cGMP validation consulting services to the medical manufacturing sector. This included developing and executing Engineering Change Orders, writing and updating specifications throughout the document lifecycle including, but not limited to, URS, FDS, DS, traceability matrices, risk assessments, IOQ validation protocols, and standard operating procedures. In addition to the management of engineering change order execution and documentation, I also provided 3D modeling and prototyping services, providing cost-savings in terms of down time, part lead time, and part machining costs while maintaining an average turnaround time of ≤ 1 week.