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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 This role provides technical support and training for radiopharmaceutical preparation as well as participating in validation activities, CDMO (Contract Development/Manufacturing Organization) qualification initiatives, technical transfers, troubleshooting, and continuous improvement endeavors.  Role will provide leadership and technical expertise - both internally and externally - to cross-functional teams as well as support field execution with focus on compliance with industry regulations, quality standards, and regulatory frameworks.  This role also provides first line technical support for ongoing batch manufacturing. Key Accountabilities: Technical lead of tech transfer and manufacturing activities related to drug substance and drug product formulation, radiolabeling, and fill/finish of small molecule and biologic based radiopharmaceuticals Analyze production processes and report results. Identify and communicate gaps, risks, and inefficiencies. Drive implementation of process improvements and risk mitigations. Lead manufacturing investigations and root cause analyses Support implementation of cold and hot analytical methods under the guidance of internal QC SMEs, ensuring alignment with approved methods, validation requirements, and quality standard. Provide support to Regulatory Affairs for product IND and new NDA submissions, support inspection readiness, participate in regulatory agency inspections, and provide audit support, as required Manage technical collaborations with multiple CDMOs to provide technical support and achieve key project milestones Author and review documents such as SOPs, batch records, protocols, and reports to produce clinical and/or commercial products Ensure appropriate compliance through document creation/review/approval, quality investigations, corrective actions, and change control within a Quality system Follows procedures to support intellectual property protection Provide first line technical support for ongoing batch manufacturing as the first point of contact for technical questions, concerns, and/or escalations Work closely and collaboratively with Quality Assurance to provide ongoing support to manufacturing partners Education and Experience: Bachelor’s or Master’s degree in science or engineering with > 7 years of experience in the radiopharmaceutical industry, including GMP; or PhD in science or engineering with >5 years of experience in radio-pharmaceutical or biopharmaceutical industry, including GMP. PET manufacturing, handling of automated synthesis modules, and analytical experience is desirable Hands‑on experience with multiple isotopes like F-18, Lu-177 and I-131 etc. are a plus for this position Demonstrated leadership and managerial skills Experience working cross-functionally with a team of internal scientists and engineers, managing external CDMOs to ensure compliance with project timelines/cGMPs, and on-going manufacturing operations Experience working in radiopharmaceutical manufacturing environments, including knowledge of radiation safety principles, ALARA, and applicable regulatory requirement Experience in MS Office suite applications (e.g., Excel, Word, Project) Experience in authoring challenging technical documents, including but no