You are responsible for
· Create and clarify clear project charter in good project agreement with system project manager
· Mainly responsible for general project management including, time scheduling, activities and resources planning, quality planning, risk and communication management.
· Set up the formal and informal communication mechanism, organize the project steering meeting, make decision, assign and follow up tasks.
· Plan the necessary activities, resources and durations; define the constraints and identify the conflict resources and risks.
· Budget for project phases.
· Manage the subsystem cost including prototype costing and volume delivery product cost.
· Coordinate with stakeholders to identify the project risk, severity and probability, manage the mitigation and report to management.
· Involved into product quality planning and monitoring.
· Ensure the project compliance to the process quality and related regulation.
· Build up the breakdown procedure and guideline to ensure cross functional teamwork and cooperation.
· Report regularly to management and stakeholders about project status.
You are a part of
A progressive and energetic team that contributes directly to the growth of the business. You have a direct reporting line to the PMO leader, with Cross functional team as your key stakeholders.
To succeed in this role, you should have the following skills and experience
· 10+ years working experience in manufacture industry, development field or comprehensive working background. Better in medical device industry.
· Familiar with product development procedure.
· Skilled in MS office including Powerpoint, excel, word, project, visio.
· English can be taken as working language.
· Better to know IS
Better to have below competency:
· Empathy communicator
· Skilled presenter
· Action promoter
· Network builder
· Logical planner
· Process smoother
· Comprehensive thinker
· Quick learner
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