Job Details
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Job Description
- Work cross functionally to manage and schedule change activities to ensure consistency of supply.
- Developing knowledge of the format of documentation and software for our quality system and to promote standardization and usage.
- Ensuring Quality System procedures are defined and followed.
- Assisting with the Management of Device Master Records, Device History Files including Engineering Change Orders, review minutes and validation protocol and reports.
- Support QA staff to assist engineers ensuring the correct templates or documents and procedures are used.
- Management of an accurate and structured filing system within Document and Change Control including historical data ensuring all items are logged and scanned where applicable and readily retrievable.
- Ensuring Device Master Record traceability is available and audit able through Change Plans and Engineering Change Orders.
Job Requirements
- 3-5 years in same position
- Hard worker
- High analytical skills
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