Quality Compliance Specialist – FDA-Regulated, WV Site

PHIBRO ANIMAL HEALTH CORP; West Virginia; On-site; USD 75,000 - 114,000; Full time

Job summary

Phibro Animal Health Corporation in Willow Island, WV is seeking a dedicated Quality Compliance Specialist to support quality compliance systems and drive continuous improvement across manufacturing and warehouse activities.

You will collaborate with Quality Control, Production, and Regulatory Affairs to ensure adherence to cGMP and CFR standards, assist in audits, CAPA, and training, and lead documentation control and SOP development.

Qualifications

• BS degree in a scientific field; preferred.
• Minimum of 2 years of related experience, preferably in an FDA-regulated industry.
• Fundamental understanding of cGMP regulations and global regulatory standards.
• Willingness to travel (~10% domestic).
• Ability to work independently.

Responsibilities

• Provide quality and compliance oversight for manufacturing and warehouse activities, including on-the-floor support to assess deviations and incidents.
• Support the release of finished goods documentation, including COA, labeling, and batch records reviews.
• Facilitate CAPA plans and investigations; coordinate and investigate customer complaints.
• Maintain compliance tracking systems and archive records; assist SOP development.
• Prepare the site for FDA, USDA, and other audits and assist in remediation plans.
• Educate and mentor employees on quality system requirements and cGMP standards.

Skills

Written and oral communication

Attention to detail

Time management

Problem solving

Interpersonal skills

Travel willingness

Education

BS degree in a scientific field

Tools

Microsoft Office

Job description

Phibro Animal Health Corporation in Willow Island, WV is seeking a dedicated Quality Compliance Specialist to support quality compliance systems and drive continuous improvement across manufacturing and warehouse activities.

You will collaborate with Quality Control, Production, and Regulatory Affairs to ensure adherence to cGMP and CFR standards, assist in audits, CAPA, and training, and lead documentation control and SOP development.