Scientist II, Radiochemistry - Analytical

See Yourself at Telix

The Scientist II, Radiochemistry - Analytical is responsible for supporting the development, validation, and transfer of analytical methods used in radiopharmaceutical manufacturing. This includes performing and validating assays such as HPLC, Radio-TLC, and Immunoreactivity, as well as other non-microbiological quality control tests. The role involves routine handling of radioactive materials and requires strict compliance with GMP standards. The position is suited to an analytical chemist who can operate effectively in a fast-paced environment and contribute to the development of clinical-grade radiopharmaceutical products.

Key Accountabilities:

• Quality Control: Conduct analytical testing (e.g., HPLC, TLC, spectroscopy) to evaluate the quality and purity of radiopharmaceutical products.
• Analytical Method Transfer: Assist or lead the technical transfer of analytical methods from external vendors into GMP use at IsoTherapeutics Group
• Experimental Design and Execution: Plan, execute, and document experiments to support research objectives, ensuring adherence to project timelines.
• Regulatory Compliance: Maintain compliance with safety protocols, radiation safety guidelines, Good Laboratory Practices (GLP), and other regulatory requirements.
• Instrumentation Maintenance: Operate, calibrate, and maintain laboratory equipment and instruments to ensure reliable and accurate results.
• Data Analysis and Reporting: Analyze experimental data, interpret results, and prepare technical reports and presentations for internal and external stakeholders.
• Collaboration: Work closely with cross-functional teams, including quality assurance, production, and R&D, to achieve project goals.

Education and Experience:

• Education: Bachelor's degree with 5 years, Masters with 3 years, PhD with 2 years of relevant experience.
• Experience in handling radioactive material is required.
• Experience in hosting or supporting external audits.
• Proficient use with Open Lab (preferred) or similar analytical chemistry software.
• Experience in writing and reviewing SOPs and reports.
• Experience in coordinating or performing maintenance on routine analytical equipment (HPLC, ICP, etc).

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
• Indirect influence: impact project outcomes and team performance without direct control, through relationship building, collaboration, communication and motivation
• 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