Site Quality Lead — Radiopharma GMP & Compliance

Jubilant Pharma Limited; Chicago (IL); Presencial; USD 110.000 - 160.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Annual performance bonus

Generous vacation

401K matching

Descripción de la vacante

Jubilant Radiopharmacies is seeking a Site Quality Lead to ensure radiopharmaceutical manufacturing meets FDA, cGMP, and internal quality standards. You will oversee quality systems, support sterile manufacturing operations, and partner with operations, QC, and corporate quality teams.

The role appeals to detail-oriented professionals with strong quality compliance knowledge and a drive to improve processes impacting patient safety.

Formación

• Bachelor's degree in a scientific discipline.
• 3+ years of experience in pharmaceutical quality assurance or quality compliance, preferably in sterile or radiopharmaceutical manufacturing.
• Strong knowledge of FDA regulations, cGMP, and quality systems.
• In-depth understanding of GxP regulations, FDA 21 CFR Part 11, 21 CFR Part 211, 21 CFR Part 212, USP, and global data integrity standards.

Responsabilidades

• Maintain and improve quality systems, including CAPA, change control, deviations, complaints, and document control.

Conocimientos

Quality assurance

Regulatory compliance

Documentation

Cross-functional collaboration

Analytical thinking

Technical writing

Independent work

Educación

Bachelor's degree in science

Herramientas

LIMS

MES

ERP

CDS

Descripción del empleo

Jubilant Radiopharmacies is seeking a Site Quality Lead to ensure radiopharmaceutical manufacturing meets FDA, cGMP, and internal quality standards. You will oversee quality systems, support sterile manufacturing operations, and partner with operations, QC, and corporate quality teams.

The role appeals to detail-oriented professionals with strong quality compliance knowledge and a drive to improve processes impacting patient safety.