Jobs at Telix Pharmaceuticals Limited

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

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 Director of Marketing Strategy at Telix Pharmaceuticals leads strategic and operational marketing initiatives to drive revenue growth and brand positioning, managing cross-functional partnerships and developing data-driven marketing strategies for oncology products.

The Director of Sustainability will manage the sustainability function at Telix, ensuring compliance with regulations, developing sustainability strategies, and fostering a culture of sustainability within the organization.

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.

The Recruiter is responsible for full life-cycle recruitment for global requisitions, managing hiring processes and collaborating with hiring managers, primarily for cancer and rare disease roles.

The Senior Project Manager will oversee drug development initiatives, manage cross-functional teams, and ensure project alignment with strategic objectives, focusing on oncology and rare diseases.

The Senior Project Manager oversees the execution of therapeutic programs, ensuring alignment with strategies, managing project development plans, budgets, and cross-functional teams, while mitigating risks and facilitating communication among stakeholders.

The QA Operations Lead manages quality-related activities in manufacturing, ensuring compliance with GMP and regulatory standards, while overseeing operational quality assurance and supporting cross-functional collaborations.

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.

Senior technology leader accountable for enterprise application strategy, governance, and global IT operations. Acts as CIO delegate, leads ERP/CRM/clinical system roadmaps, manages portfolio sequencing, risk, budgets, vendors, and drives digital transformation and regulatory compliance across distributed teams.

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.

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.

The Director of Commercial Product Quality ensures compliance and quality standards in manufacturing operations, oversees quality management systems, and drives continuous improvement initiatives in pharmaceuticals.

The Director oversees product quality and regulatory compliance in commercial operations, ensuring GMP standards, leading strategic improvement initiatives, and fostering cross-functional collaboration to enhance product quality.

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.

The AI Marketing Strategy Manager drives the integration of AI in marketing, identifies AI opportunities, establishes frameworks, collaborates across functions, and ensures ethical AI implementation to enhance personalized marketing efforts.

The Quality Assurance Associate supports quality operations by ensuring GxP compliance, maintaining quality documents, supporting audits, and collaborating with cross-functional teams to ensure product quality.