Our Site Training Coordinator plays a vital role in ensuring the highest quality and safety standards of our pharmaceutical products. Once you complete our training, your responsibilities will include assisting the Master Compliance Training Program and supporting training initiatives for Operations and Quality business units in the manufacturing department. The site training coordinator serves as the Subject Matter Expert for the Learning management system (SME). This role involves maintaining training documentation and data, providing guidance on process-based job code curriculum, monitoring individual training progress, ensuring the availability of GxP compliance training courses, qualified trainers, and managing training documentation. Additionally, this role includes collaborating with other QuVa sites to standardize best practices and working in conjunction with the Training Specialist and Site Training Manager to meet training metrics and deliverables. Turn your passion for precision and your commitment to quality into a meaningful impact on healthcare across the US.
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Job Type
Full-time
Career Level
Entry Level
Industry
Management of Companies and Enterprises
Education Level
High school or GED