Key skills required for the job are:
- PLM Domain-L3 (Mandatory)
- PLM-Product Lifecycle Management-L3 (Alternate)
As a Senior Administrator, you should be able to handle first point escalation for all technical and process issues. Provide technical subject matter expertise wherever required. Ensure proper communication and quick resolution as a crisis manager. Plan and schedule Changes, Coordinating with different stakeholders. Perform RCA for Major Incidents related to his / her tower Follow quality / security process defined for the engagement. Perform Trend analysis, identify top few incidents and work with respective teams/individual to minimize the incidents, Hardware troubleshooting & Vendor coordination Prepare Weekly and monthly status reports. Participate in business meetings with various stake holders on a need basis. Take corrective actions based on the customer satisfaction surveys. Work on the service improvement programs. Effort estimation/reviews on need basis for new projects. Training of new team members. Able to work on Knowledge acquisition and updates to related documents
Minimum work experience:3 - 5 Years
Asa CSV, you should have in-depth knowledge in FDA validation activities. As validationengineer you are expected to have knowledge handling validation of GxP, SOXrelevant systems. Understanding of FDA validation IQ, OQ, PQ, Part-11, VSE,Tracematrix, Summary reports, Deviations is must. Responsibilities includeguiding the project team in FDA validation activities and perform review ofvalidation deliverables in accordance to FDA compliance guidelines. Overall actas a liaison between SQA and project development team, business stakeholders toensure quality of validation deliverables by adhering to compliance guidelinesof company
Looking for B.e/b.tech graduates profile.