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Quality Assurance Commissioning, Qualification, and Validation (CQV) Lead at Telix Pharmaceuticals - ApplyBlast

Quality Assurance Commissioning, Qualification, and Validation (CQV) Lead

Telix Pharmaceuticals

18 days ago

3.6 on Glassdoor

Remote

Full Time

Senior

4 applicants

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About this role

The Quality Assurance Commissioning, Qualification, and Validation (CQV) Lead provides quality oversight and support for facility construction, equipment qualification, and process validation across the Telix Manufacturing Solution network in the United States. This highly mobile role requires extensive travel to ensure CQV activities meet cGMP requirements and support the transition of sites to routine GMP operations. The position partners with cross-functional teams to drive project readiness, compliance, and inspection readiness for clinical and commercial manufacturing.

Responsibilities

Provide Quality Assurance oversight for CQV and operational readiness activities
Review and approve validation lifecycle documentation including protocols and reports
Ensure facility startup and expansion activities comply with cGMP requirements

Skills

About Telix Pharmaceuticals

telixpharma.com

Headquarters

North Melbourne, Victoria, Australia

Company Size

201-500 employees

Founded

2015

View Profile

Telix Pharmaceuticals is a global, commercial‑stage biopharmaceutical company developing diagnostic and therapeutic “theranostic” products that use targeted radiation to detect and treat cancer. It advances radiopharmaceuticals through clinical development, regulatory approval, manufacturing and commercialisation to bring imaging agents and targeted therapies to patients. Telix works with the nuclear medicine community and international partners to scale access and improve outcomes. Its stated mission is to help patients with cancer live longer with better quality lives.