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WHAT
IN
Program Project Analyst
Job
Medtronic
US
-
Louisville,
Colorado
Job Code - 69295
Position - Full Time - Regular
Job First Active on: Thursday, November 05, 2009
APPLY TO THIS JOB (You will be applying directly to Medtronic for this position!)
JOB DESCRIPTION: Program Project Analyst
A Program/Project Analyst, under general supervision of either a more senior Project Manager or a Program Manager, leads and directs multiple small projects or one larger project. Works in the Office of Program Management and leads new product development projects. Performs all aspects of project management from initiating phase through commercialization phase, including assembling project teams, assigning individual responsibilities, identifying appropriate resources needed, and developing schedules and budgets to ensure timely completion of projects. Provides technical and project leadership through commercialization phase.
REQUIREMENTS - QUALIFICATIONS: Program Project Analyst
Performs all aspects of project management from initiating phase through commercialization phase, including assembling project teams, assigning individual responsibilities, identifying appropriate resources needed, and developing schedules and budgets to ensure timely completion of projects. Provides technical and project leadership through commercialization phase.
Education and experience requirements:
•B.S. in Computer or Software Engineering or related field plus 5 years post-B.S. experience.
•Formal Education in Project Management
•PMP Certified (Project Management Professional)
•Experience must include at least
•4 years experience as a Project Manager in the Medical Device industry
•3 years experience with Software Development Lifecycles, focusing on requirements engineering and management
•1 year experience working with Agile Development Teams
•1 year experience with Surgical Navigation New Product Development
Special skills:
•Knowledge of project management industry practices, techniques and standards.
•Expertise with DICOM Standard and its related standards, including direct experience working with DICOM vendors.
•Expertise in Medical Device Risk Management, including direct experience with the ISO 14971 Standard, and FDA Quality System Requirement (QSR).
Medtronics
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