QA Controlled Documents Lead- Maywood NJ
Extensive experience working with controlled document for each department: QA, HR and Safety.
Needs someone who will be able to stream line the documentation process for easy access during an audit.
At least 5 years of experience in QA preferably working with Pharmaceutical or Food industries.
Must have previous background handling FDA audit.
BS Degree in Science or Engineering.
Constantly interface with cross functional teams and specifically work with the Quality Assurance, Safety and HR group.
Previous experience working with Catalyst software, tool used for complex discovery, regulatory investigations and compliance.
Skilled in Policy Tech software for procedure management
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