As the Quality Systems Manager, you will act as the internal Subject Matter Expert (SME) for the QMS and assist in implementation projects.
Responsibilities:
Be the site Subject Matter Expert (SME) for the systems. Be responsible for the implementation of new systems. Ensure business-wide compliance with MHRA/EMA/FDA regulatory standards. Perform continuous improvement on the Quality Management Systems (QMS).
Qualifications:
Significant experience with an Electronic Quality Management System (eQMS). GxP knowledge gained within the pharmaceutical industry.
Desirable Criteria:
Previous experience implementing eQMS systems.
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