Plant Quality Manager
KeyStaff
Job Description
Job Description
Summary
The Quality Manager is responsible for Planning, Organizing, and Implementing all the activities
necessary to ensure the quality and compliance of our products.
Oversees and ensures that all processes in the GMP plant meet consistent results following the
appropriate regulatory standards and certifications.
Essential Functions:
Define, implement, and maintain policies, procedures, and controls necessary to meet all
regulatory requirements for dietary supplement and vitamin manufacturing facilities, including
NSF, GMP, HACCP, SQF, FDA, and related standards.
Develop and deploy procedures, programs, and practices required to achieve and maintain
certifications, customer requirements, and business objectives.
Serve as the primary liaison with regulatory agencies and certification bodies, including FDA,
FDACS, NSF, and other authorities. Lead regulatory, customer, and third-party audits and ensure
timely resolution of any observations or non-conformances.
Champion the internal audit program through continuous improvement initiatives, best practice
sharing, and cross-functional collaboration.
Lead investigations of quality non-conformances, customer complaints, deviations, and out-of-
specification results. Conduct root cause analyses, implement corrective and preventive actions
(CAPA), and ensure timely closure and documentation.
Develop, maintain, and monitor Standard Operating Procedures (SOPs) and quality system
documentation, ensuring documents are controlled, accessible, and compliant with regulatory
requirements.
Promote and enforce GMP, food safety, food defense, and quality system requirements
throughout the organization, ensuring effective communication and implementation of SQF and
related standards.
Prepare and present management reports by collecting, analyzing, interpreting, and
summarizing quality and operational data.
Establish, monitor, and drive Quality Key Performance Indicators (KPIs), leading initiatives to
improve product quality, compliance, customer satisfaction, and plant performance.
Implement and oversee methods used to inspect, test, and evaluate products, raw materials,
packaging components, manufacturing processes, and production equipment.
Review and maintain quality control testing records, evaluate analytical and microbiological
results, and make disposition decisions for raw materials, work-in-process, and finished goods to
ensure compliance with specifications.
F-SOP-0048-5 FTN USA
Support the Quality Director in the development, deployment, and continuous improvement of
quality policies, programs, and strategic initiatives.
Ensure compliance with environmental regulations, corporate standards, and applicable local,
state, and federal requirements.
Provide leadership and direction to the Sanitation Team, ensuring effective execution of the
Master Sanitation Schedule, verification activities, training programs, and continuous
improvement initiatives supporting food safety and regulatory compliance.
Serve as the primary liaison between customers and the organization for all quality-related
matters, including complaints, investigations, audits, corrective actions, specifications, quality
agreements, and performance metrics.
Ensure compliance with all City of Miramar testing ordinances and requirements, including
coordination, scheduling, review, retention, and reporting of required testing results, while
serving as the primary contact for related regulatory interactions.
Manage the procurement, inventory control, and availability of all quality-related supplies,
laboratory consumables, testing materials, sanitation verification tools, and other resources
required to support quality operations.
Develop, manage, and monitor the annual Quality and Sanitation budgets, identifying
opportunities for cost savings, operational efficiencies, and resource optimization while
maintaining compliance and product quality.
Establish and maintain supplier, material, and laboratory qualification programs, including
supplier approval, audits, requalification activities, performance monitoring, quality
agreements, and risk assessments to ensure compliance with company and regulatory
requirements.
Manage the Foreign Supplier Verification Program (FSVP), ensuring compliance with FDA
requirements through supplier qualification, hazard evaluations, verification activities,
documentation management, and ongoing supplier performance monitoring.
Act as a strategic business partner to Operations, Supply Chain, Procurement, Regulatory Affairs,
Research & Development, Sales, Customer Service, and Finance by providing quality and
regulatory expertise that supports new product development, cost reduction initiatives,
customer satisfaction, and sustainable business growth.
Serve as a member of the Crisis Management Team with primary responsibility for product
quality and food safety assessments, supporting incident response, risk evaluations,
containment decisions, corrective actions, recalls, and recovery activities.
Provide quality leadership and support to sister companies, assisting with audits, investigations,
regulatory compliance, quality systems, supplier management, customer requirements, and
continuous improvement initiatives as needed.
Perform other duties and responsibilities as assigned.
Required Experience & Skills:
Minimum 2 years of direct management experience in Quality within a manufacturing
environment.
Bilingual English / Spanish.
Well versed in GMP, SQF, or BRC type of food safety standards, HACCP Certified. Regulatory
Affairs and audit processes.
Demonstrated strategic planning experience at a management level.
F-SOP-0048-5 FTN USA
Strong communication and presentation skills
Strong analytical and problem-solving skills.
Competency in MS Office, databases, and quality-related software
Accuracy and attention to detail
Well-organized
Ability to plan and execute multiple projects/activities.
Demonstrated experience delivering results.
Qualified in Food Safety and Sanitation
Supervisory Responsibility:
The Quality Manager is responsible for direct management of all Quality Department associates and
Sanitation personnel.
Work Environment:
Frequent exposure to fumes or airborne particles, moving mechanical parts and vibration. Occasionally
exposed to a variety of extreme conditions in the plant. The noise level in the work environment can be
loud.
Physical Demands:
While performing the duties of this job, the employee is regularly required to use hands and fingers to
handle, feel, or operate objects, tools, or controls, and reach with hands and arms. The employee is
frequently required to stand, talk, and hear. The employee might regularly lift and/or move objects up
to 10 pounds. No specific vision requirements.
The physical demands described here are representative of those that must be met by an employee to
successfully perform the essential functions of this job.
Travel:
Up to 25% of the time.
Please note that this Job Description is not designed to cover or contain a comprehensive listing of
activities, duties or responsibilities that are required of the employee for this job. Duties,
responsibilities and activities may change at any time with or without notice.
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