Jobs at Telix Pharmaceuticals Limited

Leads onboarding and optimization of imaging sites using Telix radiopharmaceuticals. Supports product launches, healthcare professional education, site engagement, competitive intelligence, cross-functional initiatives, and compliance. The role requires nuclear medicine expertise, advanced oncologic PET/CT experience, radiopharmaceutical knowledge, strong communication, and the ability to travel up to 50% within an assigned Southeast geography.

Develops, validates, transfers, and executes radiochemistry processes for radiopharmaceutical products in a GMP environment. Authors and reviews SOPs, batch records, protocols, reports, deviations, change controls, and validation documentation. Performs radiochemical synthesis and analytical testing using HPLC, GC, TLC, mass spectrometry, and gamma spectroscopy. Supports manufacturing, QC, QA, regulatory submissions, root-cause investigations, radiation safety, and compliance with USP <823> and applicable GMP standards.

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 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.

Owns Salesforce governance, platform operations, data quality, request prioritization, user support, training, UAT, release management, and continuous improvement for commercial teams. Partners with IT, developers, reporting teams, and stakeholders to translate business requirements into scalable CRM solutions, enforce standards, improve adoption, and align Salesforce with commercial workflows and analytics needs.

Leads onboarding and optimization of imaging sites using Telix radiopharmaceuticals, including protocol standardization, scanner settings, workflow improvements, product launch support, and healthcare professional education. Collaborates with account managers and cross-functional teams, presents business reviews, manages site engagement and strategic projects, gathers competitive intelligence, represents the company at conferences, and ensures pharmaceutical regulatory and ethical compliance.

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 CMC programs for commercial and pre-commercial radiopharmaceuticals from late-stage development through regulatory filing, launch readiness, and lifecycle management. Coordinates cross-functional teams, CDMO/CMO partners, timelines, budgets, dashboards, risks, deliverables, and regulatory requirements. Supports manufacturing strategy, vendor selection, project handoffs, senior-management reporting, and process improvements across global programs.

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.

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.

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.

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.

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.