Senior Director of Quality & Compliance

Avet Pharmaceuticals Inc.; Brunswick (GA); On-site; USD 170,000 - 200,000; Full time

Benefits offered by this job

401(k) matching

Medical, Dental and Vision

Flexible Spending Account

Job summary

Avet Pharmaceuticals Inc. is seeking a Director of Quality Assurance in Brunswick, GA. This role requires strategic leadership for ensuring compliance with Good Manufacturing Practices (cGMP) and regulatory standards. The Director will oversee quality systems, inspections, supplier qualification, and continuous improvement initiatives.

Qualified candidates should have at least 10 years of experience in a cGMP-regulated environment and a solid background in pharmaceutical quality assurance. Competitive salary ranges from $170,000 to $200,000 annually, plus benefits.

Qualifications

• Minimum of ten (10) years of progressive Quality Assurance leadership experience.
• Extensive knowledge of current Good Manufacturing Practices (cGMP) and FDA regulations.
• Demonstrated experience leading regulatory inspections.

Responsibilities

• Oversee Quality Assurance department to ensure compliance with cGMP regulations.
• Serve as primary coordinator for regulatory inspections including FDA and DEA.
• Lead and oversee Corrective and Preventive Action (CAPA) activities.

Skills

Regulatory Compliance & Quality Systems Leadership

Strategic Leadership & Cross-Functional Collaboration

Analytical skills

Problem-solving skills

Leadership skills

Organizational skills

Communication skills

Education

Bachelor's degree in Biology, Chemistry, Biochemistry, Pharmacy, or a related scientific discipline

Tools

Electronic Quality Management Systems (eQMS)

Microsoft Office Suite

Job description

Avet Pharmaceuticals Inc. is seeking a Director of Quality Assurance in Brunswick, GA. This role requires strategic leadership for ensuring compliance with Good Manufacturing Practices (cGMP) and regulatory standards. The Director will oversee quality systems, inspections, supplier qualification, and continuous improvement initiatives.

Qualified candidates should have at least 10 years of experience in a cGMP-regulated environment and a solid background in pharmaceutical quality assurance. Competitive salary ranges from $170,000 to $200,000 annually, plus benefits.