Jobs at Telix Pharmaceuticals Limited

Serve as primary finance contact for an assigned business area, owning budgeting, forecasting, reporting and analysis. Advise leaders on financial performance, support strategic evaluations, ensure SOX-compliant controls, drive process improvements, and partner with Finance Systems on automation.

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.

Lead and coordinate CMC strategies and deliverables for radiopharmaceutical programs across development through regulatory submission. Manage cross-functional teams, CDMO/CMO selection and relationships, project dashboards, budgets, risks, and regulatory compliance (GxP). Provide status updates to senior management and enable global hand-offs to commercial lifecycle management.

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.

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 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.

Manage planning, execution, and closure of pharmaceutical product development projects. Maintain project tools (SmartSheet), schedules, RAID logs, budgets, vendor/contracts, risk/change management, cross-functional stakeholder communication, and regular reporting to ensure on-time, within-budget delivery.

The Principal Scientist will lead radiochemistry projects, contribute to technology development, provide scientific expertise, and ensure compliance with regulatory standards.

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.

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.

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.