Global QC Validation Lead - 75%+ Travel

Telix Pharmaceuticals Limited; United States; Presencial; USD 120.000 - 170.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Competitive salary

Bonus program

Equity incentives

Generous vacation

Wellness days

Learning & development support

Descripción de la vacante

Telix Pharmaceuticals Limited seeks a Quality Control Validation Lead to support startup, qualification, and validation of QC laboratories across the Telix Manufacturing Solution network. You will ensure compliant operations, transfer/validate analytical methods, qualify equipment, and support regulatory submissions.

You will travel >75% across US sites, collaborating with Quality Control, Manufacturing, Validation, Regulatory, and external labs to maintain inspection readiness and data

Formación

• Bachelor’s degree in chemistry or related field with GMP laboratory operations experience.
• Experience in analytical method development, validation, and transfer in pharma.
• Knowledge of FDA/ICH/USP regulatory requirements governing QC labs.
• Experience supporting regulatory inspections and quality systems.

Responsabilidades

• Lead QC lab startup, qualification, validation and readiness across the network.
• Coordinate equipment calibration, qualification, and lifecycle management.
• Establish GMP-compliant lab systems, procedures and data integrity.
• Lead analytical method development, transfer, verification and validation.
• Coordinate internal and contract laboratories for testing.
• Travel to multiple US sites to support startup and readiness.

Conocimientos

GMP knowledge

Analytical method development

Method transfer

Regulatory inspections

Travel readiness

Educación

Bachelor's degree in Chemistry, Biochemistry, Pharmaceutical Sciences or related field

Advanced degree preferred

Descripción del empleo

Telix Pharmaceuticals Limited seeks a Quality Control Validation Lead to support startup, qualification, and validation of QC laboratories across the Telix Manufacturing Solution network. You will ensure compliant operations, transfer/validate analytical methods, qualify equipment, and support regulatory submissions.

You will travel >75% across US sites, collaborating with Quality Control, Manufacturing, Validation, Regulatory, and external labs to maintain inspection readiness and data