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Telix Pharmaceuticals is a dynamic, fast-growing radiopharmaceutical company with offices in Australia (HQ), Belgium, Japan, Switzerland, and the United States. Our mission is to deliver on the promise of precision medicine through targeted radiation. At our core, we exist to create products that seek to improve the quality of life for people living with cancer and rare diseases. You will be supporting the international roll-out of our approved prostate cancer imaging agent and helping us to advance our portfolio of late clinical-stage products that address significant unmet need in oncology and rare diseases. See Yourself at Telix The Radiopharmaceutical Manufacturing Associate supports daily manufacturing operations by performing routine production support tasks, preparing materials and work areas, completing documentation, and following established procedures under supervision. This role operates in compliance with applicable GMP requirements, site safety procedures, and radiation safety practices. Key Accountabilities: Performs routine production support activities (e.g., staging materials, preparing kits/consumables, cleaning and stocking work areas). Executes basic manufacturing steps per approved SOPs and batch records under direct supervision. Completes GMP documentation accurately and in real time (logbooks, cleaning records, inventory transactions, batch record entries as assigned). Performs equipment and room cleaning/ sanitization per procedures; supports environmental monitoring activities as trained. Assists with receipt, labeling, and movement of raw materials/components following GMP and site controls. Follows radiation safety practices (ALARA), wears dosimetry/PPE as required , and immediately escalates safety concerns. Supports investigations by providing timely information and documentation; participates in training and qualification activities. Contributes to a culture of safety, quality, and continuous improvement. Education and Experience: High school diploma with relevant manufacturing or laboratory exposure; Associate degree or certificate preferred Internship, co-op, or lab coursework Ability to follow written procedures and perform detailed documentation. Basic math skills and comfort working in regulated environments. Experience in GMP, pharmaceutical, biotech, hospital nuclear medicine, or cleanroom environments preferred. Familiarity with basic lab/manufacturing equipment and controlled documentation practices preferred. Key Competencies Attention to detail Reliability Learning agility Safety and compliance mindset Team collaboration Working Conditions & Physical Requirements Work in controlled manufacturing areas (e.g., cleanroom/controlled environments) requiring gowning and PPE. May work around radioactive materials with appropriate controls and monitoring. Ability to stand for extended periods, perform repetitive tasks, and lift/move materials (e.g., up to 25–50 lbs as required by site). Shift work, weekends, holidays, and on-call support may be required based on production schedule. Key Capabilities: Commitment to excellence: Take pride in your work and consistently strive for excellence in everything you do Results-oriented: Driven to achieve goals and objectives, with a strong focus on delivering measurable results Creativity and innovation: Possess a willingness to think outside the box and come up with unique and creative solutions to challenges Strong communication skills: Able to communicate effectively with colleagues and stakeholders at all levels, using clear and concise language Collaboration: Work effectively as part of a team, actively sharing knowledge and expertise to