A minimum of 3 years' experience and a proven track record in:
o Applying project management tools to manage Product Development Projects
o Applying project management tools to manage Engineering Projects
o Building, managing, and maintaining business partnerships.
o Applying knowledge of ISO standards and FDA Design Control regulations
Experience in development of complex sophisticated software controlled electromechanical medical devices with verification & validation activities is a plus.
Experience in outsourced medical device manufacturing, manufacturing technologies and process development is a plus.
BS in engineering or technical field with 3+ years of product development (medical device engineering) and 3+ years of applicable project management experience in medical devices, healthcare, or pharma development environment.
Possesses interpersonal skills to negotiate and reconcile differences, while optimising overall business goals.
Excellent written and verbal communications skills with strong competency in MS Office tools and Project management applications.
Certification in Process Excellence (Green Belt or Black Belt) or project management certification PMP is a plus.