QC Lab Supervisor

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About Phibro Animal Health Corporation

Phibro Animal Health Corporation is a publicly traded, global organization with a rich history in animal health and nutrition as a manufacturer and marketer of medicated feed additives, vaccines, nutritional specialty products, and mineral nutrition. We strive to be a trusted partner with livestock producers, farmers, veterinarians, and consumers who raise or care for farm and companion animals by providing solutions to help them maintain and enhance the health of their animals.

Phibro is a diversified company in manufacturing and marketing products for ethanol performance, microbials for plants, home and industrial applications, and specialty chemicals for various industrial markets. In addition to, Phibro’s revenues are in excess of $1 billion and are supported by over 2,400 employees worldwide.

At Phibro, people are our greatest asset. We strive to develop a diverse workforce that fosters an environment where people feel supported in openly sharing their creativity and skills that allows them to be the most successful that they can be.

If you are interested in working for Phibro and feel that you do not meet all qualifications, we encourage you to apply as you might be the right candidate for this role or other positions.

TheQC Lab Supervisor is an integral part of our Quality team based out of our US - Willow Island, WV site.

The Finished Product Quality Control Laboratory Supervisor leads daily QC operations in an FDA-regulated manufacturing environment. This role oversees staff, resources, analytical testing, data integrity, inspection readiness, continuous improvement, and regulatory support to ensure accurate, timely results and compliance with cGMP, FDA, and Phibro quality systems.

• Plan and direct laboratory testing, studies, and projects supporting production, product release, stability, validation, and regulatory submissions.
• Set priorities, assign work, manage resources and timelines, and ensure effective use of personnel and equipment.
• Review data, reports, protocols, and product-disposition recommendations for scientific accuracy, completeness, and compliance.
• Provide basic HR support. Lead, coach, train, and evaluate laboratory personnel; maintain staff competency, development, and safe working practices.
• Provide technical oversight for laboratory methods and equipment, including HPLC, GC, UV/VIS, FTIR, balances, pH meters, titrations, sieves, and ovens.
• Ensure testing and documentation comply with FDA cGMP, GMP/GLP/GDP principles, SOPs, specifications, and data-integrity requirements.
• Maintain inspection readiness and oversee deviations, OOS or atypical results, nonconformances, CAPAs, and effectiveness checks.
• Oversee method validation, verification, transfer, lifecycle management, and continuous improvement.
• Ensure instruments are suitable, qualified, calibrated, maintained, and used in accordance with approved procedures.
• Evaluate SOPs, protocols, studies, and regulatory documentation with appropriate functions to support compliant, efficient operations and required changes.
• Support preparation and review of regulatory documents, including Annual Product Reviews, VMFs and NADAs.
• Communicate laboratory status, risks, findings, and recommendations clearly to management, staff, customers, vendors, and external partners.
• Prepare audit-ready technical reports and presentations, present data-based recommendations, and participate in internal and external audits.
  
  Monitor scientific, industry, and regulatory developments and implement appropriate changes.
• Partner with Manufacturing, Quality Assurance, Engineering, Product Development, Regulatory, Supply Chain, and external laboratories…