Medical Device Project Manager (QS)
Medical Device Project/Program Manager (QS/MDR Complaint)
Our client is a large medical device manufacturer. They manufacturing a number of class 2 and 3 medical devices. The client is currently in need of a Project Manager to work out of the PMO on a variety of programs for quality/compliance initiatives.
Principle Duties and Responsibilities:
This consultant will be joining the PMO and working with executive management on a variety of quality and compliance programs. The consultant must have extensive experience as a project/program manager for quality and compliance initiatives. They ideally will have worked in a global medical device manufacturing company to drive projects to successful completion. The focus of this project will be around MDR/Complaint system harmonization. If the consultant has experience with a roll out/initiative like this, that would be a huge plus.
The consultant must be comfortable sitting in meetings with top level management. They must be comfortable presenting on data they are tracking, and provide updates to upper management on the status’ of various projects. They must have excellent written and verbal communication skills and have expert knowledge of the MS suite.
- Project Manager/Program Manager
- 7-10+ years of experience
- MDR/Complaint Roll Out/Harmonization
- Expert in MS Suite
- Medical Device quality/compliance background
Job Type: Contract