Latitude Inc
Manufacturing Quality Manager (Relocation Assistance)
Latitude Inc, Mayfield, Kentucky, United States, 42066
Overview
Position Overview:
We are seeking a highly experienced
Manufacturing Quality Manager
with extensive
Good Manufacturing Practices (GMP)
expertise to lead our quality operations within a regulated manufacturing environment. This role is responsible for ensuring that all products are manufactured in compliance with GMP standards, regulatory requirements, and internal quality systems. The ideal candidate will have a strong background in managing quality assurance and quality control teams, implementing continuous improvement initiatives, and supporting regulatory audits. Responsibilities
Oversee all aspects of quality management systems (QMS) within the manufacturing environment. Ensure compliance with GMP regulations, ISO standards, and company quality policies. Develop, implement, and maintain quality procedures, policies, and documentation. Lead internal and external audits, including FDA, ISO, and customer audits. Manage CAPA (Corrective and Preventive Action) and deviation systems to ensure timely resolution and preventive actions. Review and approve manufacturing batch records, validation protocols, and change control documentation. Partner with production, engineering, and supply chain teams to identify quality risks and drive continuous improvement. Provide quality oversight of suppliers, contractors, and raw materials. Lead root cause analysis and implement long-term quality improvement strategies. Train and mentor quality staff on GMP and compliance requirements. Salary: $90,000 - $110,000 a year
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Position Overview:
We are seeking a highly experienced
Manufacturing Quality Manager
with extensive
Good Manufacturing Practices (GMP)
expertise to lead our quality operations within a regulated manufacturing environment. This role is responsible for ensuring that all products are manufactured in compliance with GMP standards, regulatory requirements, and internal quality systems. The ideal candidate will have a strong background in managing quality assurance and quality control teams, implementing continuous improvement initiatives, and supporting regulatory audits. Responsibilities
Oversee all aspects of quality management systems (QMS) within the manufacturing environment. Ensure compliance with GMP regulations, ISO standards, and company quality policies. Develop, implement, and maintain quality procedures, policies, and documentation. Lead internal and external audits, including FDA, ISO, and customer audits. Manage CAPA (Corrective and Preventive Action) and deviation systems to ensure timely resolution and preventive actions. Review and approve manufacturing batch records, validation protocols, and change control documentation. Partner with production, engineering, and supply chain teams to identify quality risks and drive continuous improvement. Provide quality oversight of suppliers, contractors, and raw materials. Lead root cause analysis and implement long-term quality improvement strategies. Train and mentor quality staff on GMP and compliance requirements. Salary: $90,000 - $110,000 a year
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