Telix Pharmaceuticals Limited

www.telixpharma.com

1 Job

608 Employees

About the Company

Telix is a biopharmaceutical company focused on the development and commercialisation of therapeutic and diagnostic ('theranostic') radiopharmaceuticals. Telix is headquartered in Melbourne, Australia with commercial operations in the United States, Europe (Belgium and Switzerland) and Japan. Telix is developing a portfolio of radiopharmaceutical products that aims to address significant unmet medical need in oncology and rare diseases. Telix is listed on the Australian Securities Exchange (ASX: TLX).

Listed Jobs

Company Name: Telix Pharmaceuticals Limited
Job Title: Senior Scientist, Radiochemistry
Job Description: Job title: Senior Scientist, Radiochemistry Role Summary: Lead the development, validation, and scale‑up of manufacturing and QC procedures for clinical‑stage radiopharmaceuticals, ensuring GMP compliance and readiness for regulatory submissions and commercial production. Expectations: Deliver robust, GMP‑compliant manufacturing and QC processes, manage multiple CMOs with minimal oversight, author CMC documentation for regulatory filings, and support method transfers and optimization to meet clinical and commercial needs. Key Responsibilities: - Interface with external CMOs to coordinate manufacturing and QC procedure development. - Manage development, validation, and scale‑up of manual or automated manufacturing and non‑compendial QC methods. - Generate protocols, SOPs, reports, and CMC sections for INDs, NDAs, BLAs. - Provide technical support for manufacturing and QC across all products. - Ensure documentation aligns with QMS and GMP standards. - Facilitate method transfers to external manufacturers and optimize procedures for commercial supply. Required Skills: - Practical radiochemistry, radiolabeling, and conjugation of biologics. - Development of HPLC, TLC, or GC QC methods for radiopharmaceuticals. - GMP‑compliant manufacturing experience. - Strong written and verbal communication. - Ability to manage CMOs and multi‑project environments. - Experience with regulatory filing method development (preferred). Required Education & Certifications: - Bachelor’s degree + 8+ years experience, or Master’s degree + 6+ years, or Doctorate + 5+ years. - Demonstrated practical radiochemistry expertise and GMP manufacturing background.