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Telix Pharmaceuticals is a dynamic, fast-growing radiopharmaceutical company with offices in Australia (HQ), Belgium, Japan, Switzerland, and the United States. Our mission is to deliver on the promise of precision…
An individual-contributor project manager in Telix's Business Improvement Office who drives execution of business improvement and operational initiatives: building project plans and timelines, tracking cross-functional workstreams, and preparing analysis and decision-support materials. Requires 5+ years in analytical/PM roles with strong Excel and PowerPoint skills.
Quality Assurance CQV Lead providing QA oversight for facility construction, equipment/utility qualification, computerized systems and process validation across Telix's US radiopharmaceutical manufacturing network, ensuring cGMP compliance and GMP site readiness. Advertised as remote but requires 75%+ travel with extended stays at US manufacturing sites.
Leads global physical security and business resiliency programs for a radiopharmaceutical company, ensuring safety of people, assets, and supply chains while aligning with regulatory standards.
Leads strategic operations and process excellence for a radiopharmaceutical company, aligning business unit goals with enterprise growth while overseeing high-impact initiatives in oncology and rare diseases.
Leads global development of late-stage radiopharmaceutical therapies for oncology and rare diseases, coordinating clinical, regulatory, CMC, and commercial teams to drive regulatory approvals and commercial readiness.
Writes and manages CMC regulatory dossiers (e.g., Module 3) for radiopharmaceutical and biopharmaceutical products, ensuring compliance with global standards like ICH and FDA/EMA guidelines.
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