Jobs at Telix Pharmaceuticals Limited

Senior leader responsible for defining and executing operational strategy and portfolio management for the TMS Business Unit. Leads governance, prioritization, cross-functional alignment, and value realization of strategic initiatives, advises executive leadership, drives continuous improvement, and builds organizational capability.

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-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.

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 global development of PSMA diagnostic products through Phase 3 by creating and executing development and commercialization plans, managing cross-functional teams (clinical, manufacturing, quality, regulatory), overseeing budgets and timelines, tracking risks and documentation, and reporting to senior management to secure product approvals and successful international roll-out.

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

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.

The EHS Manager provides strategic leadership and technical expertise for Environmental, Health & Safety programs across multiple manufacturing, R&D, and distribution sites, ensuring compliance and continuous improvement.

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.

Lead enterprise AI strategy, operating model, governance, platform enablement, and CoE to deploy safe, compliant, and scalable AI across R&D, Clinical, Manufacturing, Quality, Commercial, and Corporate functions in a regulated pharmaceutical environment.

Provide operational People & Culture support for HRIS, integrations, data integrity, and employee lifecycle transactions. Troubleshoot systems, perform data reconciliation, support audits (including SOX), maintain SOPs, enable continuous improvement, and serve as a primary service desk contact for employees and managers.

The Senior Scientist in Radiochemistry will independently lead experimental workstreams, contribute to scientific strategy, and mentor junior scientists within radiopharmaceutical development for oncology and rare diseases.

As a QC Specialist at Telix Pharmaceuticals, you will execute analytical testing, ensure GMP compliance, and manage QC materials and lab equipment while supporting regulatory interactions and lab investigations.

Support Supplier Quality by developing consolidated Supplier Quality Agreement (QAA) templates, defining sustainable processes, identifying stakeholders, creating work instructions, coordinating with supplier quality, supply chain, legal, and stakeholders to gain buy-in, and developing a schedule and process for periodic QAA reviews and updates. Use Windows-based tools, Microsoft Word styles, and SmartSheet to document and manage templates and schedules.

Support Corporate Quality with document control and quality records: establish Policy/SOP/WI template styles, support document owners through MasterControl workflows, assist with e-workflows and change control, and contribute to smaller quality projects.

The R&D Project Manager oversees research activities, builds project plans, tracks progress, manages budgets, and coordinates stakeholders to advance clinical projects in oncology and rare diseases.

The Director leads the upstream commercial strategy for Telix's PSMA imaging portfolio, focusing on market evolution and lifecycle management. They oversee cross-functional alignment, competitive intelligence, and the execution of high-impact initiatives while ensuring that commercial strategies support product development and market access needs.

Build and operate a global trade compliance program for radiopharmaceutical products. Lead HTS classification, IOR/Exporter of Record processes, duty optimization/drawback, country-specific permits and radioactive material licensing. Partner cross-functionally to ensure compliant international movement of regulated materials, train stakeholders, support audits, and advise leadership on trade risk and regulatory changes.

Lead enterprise budgeting, forecasting, long-range planning and FP&A for a business unit. Drive financial strategy, capital allocation, modeling, M&A support, reporting, KPI definition, systems improvements, and lead a high-performing FP&A team to enable cross-functional decision-making.