Job description
Job Description
· Engineering support for medical devices manufacturing
· Support with program/project documentation
· Adhere to design and development program documentation
· Participate in Core and Extended Team meetings to identify and flag risks
· Schedule, organize and lead meetings, maintain agenda, record, and publish minutes.
· Work with program/project core team members on essential data verification in Business Systems.
· Keep partners informed on the status of work completion relative to schedule deadlines.
· Responsible for coordinating Engineering Control Requests (ECR/O) and Quality Notification (QN) for Reagents PMO
· Identify critical issues and work with multi-functional departments for resolution, and actively participate in Continuous Improvement projects.
· Participates in activities that review processes to recommend changes and process improvements where justifiable.
· Ensure compliance with the company’s design control requirements, Document business, and system processes.
· Stays ahead of requirements for compliance for each project to maintain compliance.
Job Type: Contract
Schedule:
- 8 hour shift
Ability to commute/relocate:
- Covington, GA: Reliably commute or planning to relocate before starting work (Required)
Work Location: One location
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