Jobs at Telix Pharmaceuticals Limited

Design, develop, and maintain scalable Salesforce solutions, support cross-functional collaboration, improve deployment reliability, and mentor team members.

Support development, validation, and transfer of manufacturing and QC procedures for clinical-stage radiopharmaceuticals. Manage multiple external CMOs, author CMC documentation and SOPs, ensure GMP/QMS compliance, support scale-up to commercial supply, and generate protocols, validation reports, and technical support for manufacturing and QC.

Lead Development Quality for radiopharmaceutical programs from early clinical development through registration readiness. Establish QMS elements, provide GMP and regulatory oversight (IND/CTA, CTD Module 3, NDA/BLA), manage CDMO and clinical supply quality, support inspection readiness, and hire/coach a Development Quality team while partnering cross-functionally to mitigate quality risks.

Lead development-stage quality for radiopharmaceutical programs: oversee CDMO/CMO GMP compliance, batch release, QMS processes (deviations, CAPA, change control), regulatory quality inputs, supplier audits, and mentor junior quality staff to support IND-stage programs across jurisdictions.

Leads commercial CMC programs supporting late-stage clinical and commercial radiopharmaceutical products. Oversees CMC program leads, contract manufacturers, manufacturing strategy, quality, supply chain, logistics, capacity, budgets, supplier performance, and continuous improvement. Coordinates internal and external stakeholders, manages CDMO relationships and escalations, and ensures effective execution of global manufacturing and operational plans.

Lead CMC strategies and cross-functional execution for commercial and pre-commercial radiopharmaceutical programs from Phase 3 handoff through regulatory filing, launch readiness, and lifecycle management. Coordinate internal teams and CDMO/CMO partners, manage timelines, budgets, dashboards, risks, deliverables, and vendor relationships. Ensure compliance with global regulatory requirements, facilitate development-to-commercial handoffs, provide senior leadership updates, and improve CMC processes.

The Global Product Development Lead at Telix Pharmaceuticals will oversee the development of late-stage radiopharmaceuticals, coordinating clinical, regulatory, and commercial efforts while managing risks, budgets, and stakeholder communication.

The EHS Manager is responsible for leading Environmental, Health & Safety programs across multiple sites, ensuring compliance with regulatory requirements, managing industrial hygiene programs, overseeing safety compliance, and delivering training to enhance EHS culture.

Drive territory sales and business development for radiopharmaceutical products. Manage accounts, present clinical product information, support product launches, prepare sales reports, ensure regulatory compliance, and collaborate cross-functionally to meet sales targets. Heavy domestic travel and strong healthcare reimbursement knowledge required.

Support international rollout of a prostate cancer imaging agent and late-stage pipeline. Manage project planning, budgets, schedules, risks, change control, vendor/financial tracking, and stakeholder communications across cross-functional teams using PM best practices and tools.

Drive territory sales and business development for radiopharmaceutical products, manage key hospital and academic accounts, deliver clinical presentations and training, prepare sales forecasts and reports, maintain Salesforce records, ensure regulatory compliance, and travel domestically up to 75% to support product launches and customer engagement.

Lead global development of a molecularly targeted radiopharmaceutical through Phase 2 by creating and executing the Target Product Profile and development plan. Manage cross-functional teams (manufacturing, non-clinical, clinical, quality, regulatory), oversee project managers, track progress, budgets and risks, prepare reports, and represent the program internally and externally to advance late clinical-stage oncology/rare-disease products toward registration.

The Sustainability Engineer will lead technical support for radiopharmaceutical preparation, manage tech transfer and manufacturing, and ensure regulatory compliance while engaging in continuous improvement efforts.