QA/QC Manager - Lead Quality & Compliance in Sarasota

Phibro Animal Health SA; Sarasota (FL); On-site; USD 100,000 - 120,000; Full time

Job summary

Phibro Animal Health Corporation in Sarasota, FL is seeking a QA/QC Manager to oversee the quality program and QC lab. You will apply regulatory requirements to assess and improve product quality and ensure compliance across audits and documentation.

You will supervise lab personnel, drive continuous improvement, and coordinate with management and external audits to uphold cGMP standards and partner with site teams for quality initiatives.

Qualifications

• Bachelor’s degree in a technical field and 3–5 years of quality experience.
• Minimum 1 year of supervisory experience.
• Understanding of cGMP, HACCP, FSMA, and related regulations.

Responsibilities

• Develop and maintain internal quality system.
• Address nonconformities from audits.
• Administrative: follow-up on and close pending preventive/corrective actions.
• Analyze customer and regulatory requirements to assess impact on the internal quality system.
• Support customer and agency audits.
• Quality assurance record retention and documentation controls.
• Determine overall plant product quality by evaluating tests and ingredients/packaging.
• Educate plant personnel in quality control testing, equipment, sanitation and housekeeping.
• Discuss plant evaluations with management and set improvement timetables.
• Manage internal cGMP audit function to verify regulatory and PAHC requirements.
• Lead the process toward regulatory compliance to applicable local and international requirements.
• Review Quality Agreements with third parties.

Skills

Team collaboration

Attention to detail

Problem solving

Time management

Quality systems knowledge

Regulatory compliance

Education

Bachelor’s Degree in Chemistry, Food Science, Food Safety, Engineering or related technical field

Job description

Phibro Animal Health Corporation in Sarasota, FL is seeking a QA/QC Manager to oversee the quality program and QC lab. You will apply regulatory requirements to assess and improve product quality and ensure compliance across audits and documentation.

You will supervise lab personnel, drive continuous improvement, and coordinate with management and external audits to uphold cGMP standards and partner with site teams for quality initiatives.