Jobs at Telix Pharmaceuticals Limited

Provides transactional and operational logistics support for domestic and international radiopharmaceutical shipments. Prepares shipping, customs, and hazardous materials documentation; tracks shipments; coordinates with carriers, couriers, freight forwarders, customs brokers, vendors, and distribution partners; reconciles invoices; maintains records; monitors delays and exceptions; and escalates critical delivery issues. Coordinates schedules with manufacturing, packaging, and customer requirements while supporting audits and accurate, timely product delivery.

Coordinates pricing, contracting, and commercial requests across Sales, Finance, Legal, Distribution, and Contracting teams. Manages intake, triage, workflow tracking, Pricing Committee preparation, data validation, approvals, system updates, reporting, and process improvement. Ensures submissions are complete, decisions are documented, downstream execution is accurate, and bottlenecks are resolved. Supports scalable commercial operations within a pharmaceutical environment.

Supports field adoption and utilization of radiopharmaceutical products across Northeast imaging sites. Leads site onboarding, PET/CT protocol optimization, training, HCP education, product launch activities, stakeholder engagement, competitive intelligence, and cross-functional projects while ensuring pharmaceutical compliance and contributing to sales objectives.

Lead onboarding and optimization of imaging sites using Telix radiopharmaceuticals, standardize PET/CT protocols, support product launches and healthcare professional education, and collaborate with account managers and cross-functional teams. Manage site engagement, training, competitive intelligence, market insights, compliance, and strategic projects while supporting product adoption and patient access. The role requires advanced oncologic PET/CT experience, radiopharmaceutical expertise, professional certification, and up to 50% travel.

Leads Telix’s national Theranostics Specialist team and scales field-based technical support for radiopharmaceutical adoption. Responsibilities include team strategy, site onboarding, PET/CT workflow optimization, scanner and protocol support, customer education, training, launch execution, compliance, competitive intelligence, and cross-functional collaboration with commercial, medical, marketing, market access, operations, and compliance teams.

Leads legal operations transformation and enablement, including legal technology architecture, AI-enabled workflows, contract lifecycle management, process optimization, metrics, vendor management, change management, and budgeting. Builds scalable contracting infrastructure, improves self-service and legal intake, reduces outside counsel reliance, partners with IT and enterprise teams on technology delivery, and manages legal operations staff while supporting commercial and procurement contracting.

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.

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.

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.

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.

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.