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Quality Management System Supervisor - Old Fort, OH 44836
A collective energy and ambition. A place where you can make a real difference.
United by the belief that when we strive for growth, anything is possible. While we might not be the largest company in our industry, we believe we can have the biggest impact because: Together We Have the Power to Win.
We have an excellent opportunity at our Old Fort, Ohio facility for a Quality Management System Supervisor. The core hours for this position are Monday-Friday 7:30am-4:00pm.
Reporting to the site Quality Manager and interfacing with cross-functional plant and corporate personnel, a supervisory role of the Quality Management System to ensure all areas of the program are effectively managed and maintained at the Old Fort manufacturing plant.
Maintain and monitor the effectiveness of the site document control program to ensure overall personnel, process, and regulatory compliance.
Maintain and monitor the effectiveness of the site change control program to ensure overall personnel, process, and regulatory compliance.
Responsible for batch record review, approval, and historical control of records.
Responsible for finished goods release and issue escalation.
In partnership with Corporate Quality, lead the site supplier quality oversight program in the handling of all issues with materials and contracted services, as well as metrics reporting in support of the Suppler Performance System (SPS).
As needed, perform regional supplier audits and trouble-shooting visits/hosting in support of projects Lead the site with developing, implementing and communicating overall plant Quality KPI and related performance metrics.
Support and supervise personnel in the materials, finished goods, and distribution center areas to ensure continued compliance to process, procedures, and overall regulatory requirements.
Maintain and monitor the effectiveness of the site training program, including personnel qualification requirements and GMP support.
Manage the site internal audit program to ensure continued compliance to nonconformance CAPA time line closure and overall metrics reporting.
Provide direct support to the C&D global CAPA program as part of the P-QMS system.
Responsible for site-related specification team review and approval to ensure all critical to quality areas are effectively identified for manufacturability success, as well as meeting customer and consumer requirements General interface with plant leadership, Corporate Quality, Operations and R&D in the communication and support of all key areas noted above.
Experience and Skillsets:
Church & Dwight is proud to be an Equal Opportunity Employer/Veterans/Individuals with Disabilities.
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