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Quality Control Lead at Telix Pharmaceuticals - ApplyBlast

Quality Control Lead

Telix Pharmaceuticals

9 days ago

3.6 on Glassdoor

Wilkes-Barre, Pennsylvania, United States

Onsite

Full Time

Senior

0 applicants

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About this role

The Quality Control Lead is a site-based role responsible for coordinating and performing Quality Control activities supporting clinical and commercial radiopharmaceutical production at the Wilkes-Barre facility. The role provides technical expertise in analytical method development and validation, specifications, stability programs, routine testing, laboratory investigations, equipment qualification, and GMP documentation. During the facility’s build and validation phase, the role supports the commissioning, qualification, validation, and operational readiness of the QC laboratory.

Responsibilities

Coordinate and perform analytical method development, validation, and routine QC testing
Support commissioning, qualification, and operational readiness of the QC laboratory
Lead or support deviations, OOS/OOT investigations, CAPAs, and change controls

Skills

Qualifications

Bachelor's degree in radiochemistry, chemistry, pharmacy, biochemistry, or a related scientific discipline

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.