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Company | Johnson & Johnson |
Address | Jacksonville, FL, United States |
Employment type | FULL_TIME |
Salary | |
Category | Hospitals and Health Care |
Expires | 2023-07-07 |
Posted at | 11 months ago |
- A minimum of a Bachelor's degree is required.
- Support on FDA/BSI/Corporate audit assessments
- Performs monthly metrics for QUMAS and Global360 applications for management review
- Performs validation activities for system upgrades
- Monitors/maintains performance of QUMAS and Global 360 applications
- Performs content/context/format review of all QUMAS submissions
- Represents Document Control for new product/process teams
- Project management experience
- A minimum of 2 years of related work experience
- Knowledge of FDA, ISO and GMP requirements
- Knowledge of manufacturing processes and business processes
- Experience in QA, R&D or RA environment
- Extensive experience with Microsoft Office applications, such as Word, Excel, and Visio
- Adobe Application Experience
- Excellent written and verbal communication and interpersonal skills; strong negotiation skills, ability to team empower and create a collaborative environment with exceptional service orientation is required.
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