Document Control Specialist
On-siteTempe, Arizona, United States
Job Summary
Originate, edit, and revise technical documentation while creating controlled documents and managing change request packets in the Electronic Document Management System. Track associated paperwork for New Product Development and product transfers, ensuring all project team documentation is owned and updated. Develop operating procedures, process flow charts, and manufacturing procedures, and assist cross-functional teams with cross-training on existing processes. Monitor project progress and adjust workflows to ensure successful completion, while performing necessary clerical duties such as database maintenance and correspondence preparation.
Required Qualifications
- Excellent oral and written communication skills in English
- Previous experience in the medical device industry
- Proven experience in working in a cross-functional team environment
- Ability to function independently
- Ability to define and create solutions to challenges or opportunities
- Ability to communicate with all levels of technical and operations personnel
- Ability to complete position responsibilities with limited direct supervision
- Good attention to detail
- Ability to work in a team environment
- Ability to communicate clearly and effectively
- Ability to multi-task and prioritize workload
- Positive and professional attitude
- Must be able to work onsite
- US Citizens Or GC Holders Only
Desired Qualifications
- Master's degree preferred
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