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Project Manager Medical Devices

iTech US Inc
San Francisco, California, United States
February 15, 2018

iTech US a leading global workforce management provides end-to-end solutions for customized Software Development Solutions and staffing solutions provider to Fortune 1000 firms .

Globally who trust us to design, execute and manage sophisticated workforce management solutions, large scale staffing engagements and strategic Business Process and consulting engagements.

We have Project Manager Medical Devices Job in San Francisco, CA

If you are seeking to apply please do share your updated resume, contact detail and best time to reach you.

Job Title: Project Manager Medical Devices

Location: San Francisco, CA

Duration: 6 Months Contract

Note: Required In Person Interview


• Responsible for project management of medical devices capital equipment product development projects which involves working with R&D and other cross-functional teams

• Lead Cross Functional teams to manage NPD R&D projects through planning, execution and implementation (product development, design transfer and product launch/commercialization)

• Responsible for change management, project communication, managing product traceability, and product requirements; design review and risk management activities

• Facilitate and lead effective project meetings, manage change and conflict, and develop resource planning estimates to manage project workload and productivity.

• Responsible for activities such as project reviews, monthly status updates and project status communication to stakeholders in the organization

• Define project scope, schedule and objectives; define and monitor tasks, milestones and risks throughout the project

Desired Experience:

• Bachelors in Engineering is required; Masters in Engineering preferred

• 7+ years of experience in product development (medical devices)

• 10+ years of experience in leading the teams for product development projects

• Strong project mgt. background in Medical Device (Class II and Class III)

• Medical device knowledge of CE, FDA and GMP experience, experience in ISO 13485

• PMP is preferred

• Working knowledge of standard Project Management tools (MS Project, Excel, Visio, SharePoint) and templates

Thanks & Regards