Posted 19 days ago
Description
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USA - IsoTherapeutics Group (ITG) Updated: Wednesday 30 April 2025
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 Scientist I, Radiochemistry will play a key role in the development, optimization, and production of radiopharmaceuticals, contributing to both research initiatives and clinical applications. You will collaborate with cross-functional teams to design and execute experiments, analyze complex data, and ensure compliance with stringent regulatory and quality standards. This position offers an exciting opportunity to drive innovation in radiochemistry, enhance process efficiencies, and support the advancement of next-generation radiopharmaceuticals in a dynamic and fast-paced environment.
Key Accountabilities:
- Radiochemical Synthesis & Process Optimization – Independently perform synthesis, purification, and characterization of radiopharmaceutical compounds, actively identifying opportunities for process improvement and troubleshooting synthesis challenges.
- Analytical Testing & Quality Control – Conduct and interpret complex analytical testing (e.g., HPLC, GC, TLC, spectroscopy) to assess the quality, purity, and stability of radiopharmaceutical products, ensuring compliance with regulatory and internal quality standards.
- Method & Process Development – Contribute to the design, development, and optimization of radiochemical synthesis and production processes, supporting scale-up for clinical and commercial applications.
- Experimental Design & Technical Execution – Plan, execute, and document scientific experiments with minimal supervision, ensuring adherence to research protocols, project timelines, and scientific rigor.
- Regulatory & Safety Compliance – Maintain strict adherence to radiation safety protocols, Good Laboratory Practices (GLP), Good Manufacturing Practices (GMP), and other regulatory requirements, contributing to a culture of compliance.
- Instrumentation & Laboratory Maintenance – Operate, calibrate, and maintain laboratory equipment, troubleshooting technical issues to ensure high-quality data generation and workflow efficiency.
- Data Analysis & Scientific Reporting – Analyze experimental data, draw meaningful conclusions, and prepare detailed technical reports, presentations, and regulatory documentation for internal and external stakeholders.
- Cross-Functional Collaboration – Work closely with multidisciplinary teams, including R&D, quality assurance, production, and regulatory affairs, to drive project success and ensure seamless technology transfer.
- Mentorship & Technical Guidance – Provide technical guidance and training to junior scientists and technicians, fostering knowledge sharing and skill development within the team.
Education and Experience:
- Bachelor’s degree in Chemistry, Radiochemistry, Biochemistry, or a related field required.
- 2+ years of experience in a laboratory setting, preferably in radiochemistry, radiopharmaceuticals, or a related industry.
- Knowledge of radiochemical synthesis and handling of radioactive materials is preferred.
- Proficiency in analytical techniques such as HPLC, GC, TLC, and spectroscopy.
- Strong problem-solving skills and attention to detail.
- Ability to work in a team environment and communicate effectively with diverse groups.
- Familiarity with regulatory requirements such as GMP/GLP and radiation safety practices.
- Willingness to work with radioactive materials and follow strict safety protocols.
Key Capabilities:
- Inclusive mindset: Demonstrate an understanding and appreciation for diversity, and actively work to create an inclusive environment where everyone feels valued and respected
- Creativity and innovation: Possess a willingness to think outside the box and come up with unique and creative solutions to challenges
- 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
- Ethical behavior: Act with integrity and demonstrate a commitment to ethical behavior in all interactions with colleagues and stakeholders
- Adaptability: Comfortable working in a dynamic environment, able to adjust to changing priorities, and willing to take on new 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 achieve common goals
- Resilience: Demonstrate the ability to bounce back from setbacks and persevere in the face of challenges
- Continuous learning: Show a commitment to ongoing learning and professional development, continually seeking out opportunities to expand your knowledge and skills
At Telix, we believe everyone counts, we strive to be extraordinary, and we pursue our goals with determination and integrity. You will be part of an engaged and supportive group of colleagues who all have a shared purpose: to help people with cancer and rare diseases live longer, better quality lives. Being a Telix employee means being a part of a unique, global, interdisciplinary team working to deliver what's next in precision medicine. We have hybrid and remote employees located all around the world. We offer competitive salaries, annual performance-based bonuses, an equity-based incentive program, generous vacation, paid wellness days and support for learning and development.
Telix Pharmaceuticals is an equal opportunity employer. We evaluate qualified applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, and other legally protected characteristics.
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