Plan, schedule, manage, and coordinate all aspects of the project life cycle. This includes engineering design, procurement, production, assembly, testing, and project closure.
Sync project stakeholders - generate, monitor, and control schedules
Prioritize project tasks based on capacity, due dates & critical path.
Create and maintain Risk Management files, DHF, product tree, assembly instructions, product specs.
Perform FMEA along with the R&D and Engineering teams.
Plan and execute Design Reviews.
Follow up and execute the movement of materials closely managing external vendors.
Manage V&V tests.
QA and Regulation support.
Requirements:
Bachelors degree in Engineering (Mechanical/Biomedical) a must!
5+ years of work experience in project management and execution in the medical device field - a must!
Experience in the life cycle of medical device product including V&V, regulation, QA, production, purchasing a must!
Ability to understand technical documents, disseminate information, and write technically in English.
Ability to work independently in a dynamic and rapidly changing environment.
Team player and cross collaborator with excellent written and oral communication skills.
Microsoft Project scheduling experience.
Solidworks experience an advantage.