Vacancy expired!
- Work with customer and resource managers to drive the identification of the skills, duration and effort required for successful project execution
- Develop, update and maintain detailed project plans and schedules
- Facilitate and coordinate project team meetings
- Manage the preparation and/or delegation and completion of all required project documentation while ensuring compliance with Quality System Requirements
- Create and manage Design History Files as required within the designated Product Documentation Management System (e.g., Grand Avenue)
- Develop, communicate and implement project risk/issue management plans and strategies (e.g., mitigation, avoidance, transfer, acceptance)
- Assist in the definition of project scope and objectives, involving all relevant stakeholders and ensuring technical and/or timeline feasibility risks are properly identified and actively managed
- Managing project workgroups; set deadlines, assign responsibilities and monitor and summarize progress of project
- Measure project performance and manage changes to the project scope, project schedule and project costs using appropriate tools and techniques
- Post project completion, analyze successes and opportunities for continued improvement
- Communicate pricing estimates with set frequency to customer to ensure continued alignment as project and design develops
- Bachelors/Master's degree in scientific/engineering discipline or equivalent
- Company/industry-related knowledge in medical device products, regulatory affairs, and labeling preferred
- Minimum of three to five years in project management in medical devices or similarly regulated industries required
- Engineering background, i.e. integration of suppliers, technical customer
- Team player with ability to function and influence others in a multi-cultural matrix
- Advanced project management planning and tracking skills, capable of managing multiple projects with respect to priorities
- PMP certification or equivalent preferred
Vacancy expired!