Responsibilities:
·Author ECOs
· Obtain inputs from all stakeholders
· Work closely with Configuration Control Specialist & Doc Control Specialist
· Control the Change Release Process
· Coordinate Change Timeline & Activities for Seamless Execution
· Master the PDM database & Changes in it.
Required Qualification:
Strong Technical Orientation/Background
Excellent communication skills in English (Read/Write/Speak)Experience interfacing with QA
Required Experience:
Min. 3-years’ experience in Medical Device Industry
Min. 5-years’ Relevant experience (product engineering).