On-Site QA Specialist, PET Radiopharma (Night Shift)

ADP, Inc.; Pittsburgh (Allegheny County); On-site; USD 50,000 - 60,000; Full time

Job summary

PharmaLogic is seeking an On-Site QA Specialist to ensure cGMP compliance and quality assurance across batch release, QC, and investigations at our Pittsburgh site. The role covers CAPA, SOP maintenance, environmental monitoring, and regulatory readiness.

Ideal candidates hold a BS/BA in a scientific field with 1–3 years of QA experience in pharma and are comfortable working a night shift (10:00 PM–6:00 AM) in a fast-paced radiopharmaceutical environment.

Qualifications

• BS/BA in a relevant scientific discipline with 1–3 years QA experience in pharma.
• Strong analytical, critical thinking and problem-solving skills.
• Experience with aseptic techniques and regulatory expectations is a plus.

Responsibilities

• Ensure compliance with regulatory commitments and SOPs (cGMP, radiation safety).
• Oversee batch release and record review to ensure identity, strength, quality and purity.
• Review and approve components, in-process materials, packaging, labeling and finished dosage forms.
• Perform QA oversight of production, packaging and shipping of radiopharmaceuticals.
• Support FDA inspections and maintain audit readiness.

Skills

Quality experience

cGMP knowledge

Analytical skills

Regulatory awareness

Education

BS/BA in science

Job description

PharmaLogic is seeking an On-Site QA Specialist to ensure cGMP compliance and quality assurance across batch release, QC, and investigations at our Pittsburgh site. The role covers CAPA, SOP maintenance, environmental monitoring, and regulatory readiness.

Ideal candidates hold a BS/BA in a scientific field with 1–3 years of QA experience in pharma and are comfortable working a night shift (10:00 PM–6:00 AM) in a fast-paced radiopharmaceutical environment.