QA Manager – PET Radiopharmaceuticals (cGMP)

Automatic Data Processing, Inc.; Austin (TX); On-site; USD 110,000 - 165,000; Full time

Job summary

PharmaLogic seeks a QA Manager to lead the site quality program ensuring cGMP compliance for radiopharmaceutical manufacturing. The role oversees QA activities from materials to batch release, with responsibilities spanning CAPA, investigations, and inspection readiness.

The position requires hands-on leadership and cross-functional collaboration to sustain regulatory quality standards. The candidate will manage regulatory expectations, drive continuous improvement, and support FDA inspections

Qualifications

• BS/BA degree in a scientific discipline.
• 3–5 years QA experience in pharma.
• Experience with radiation safety a plus.

Responsibilities

• Ensure regulatory commitments with cGMP and SOPs.
• Oversee batch release and record review.
• Lead FDA and agency audits; maintain inspection readiness.

Skills

Quality Assurance

cGMP

Regulatory Compliance

FDA Inspections

Analytical Thinking

Education

BS/BA in Scientific Field

Job description

PharmaLogic seeks a QA Manager to lead the site quality program ensuring cGMP compliance for radiopharmaceutical manufacturing. The role oversees QA activities from materials to batch release, with responsibilities spanning CAPA, investigations, and inspection readiness.

The position requires hands-on leadership and cross-functional collaboration to sustain regulatory quality standards. The candidate will manage regulatory expectations, drive continuous improvement, and support FDA inspections