Scientist II, Analytical Chemistry
Telix Pharmaceuticals Limited
June 25, 2026
On-site
Angleton, TX
Clinical Research and Development
Scientist II, Analytical Chemistry supports IsoTherapeutics Group’s radiochemistry laboratory by contributing to the development, validation, and technical transfer of analytical methods used in radiopharmaceutical manufacturing. Executes and validates non‑microbiological quality control assays, including HPLC, Radio‑TLC, immunoreactivity testing, and related analytical techniques. Routine handling of radioactive materials in a GMP‑regulated environment; focus on data integrity, compliance, and method robustness.
Key Accountabilities
- Quality Control: Conduct analytical testing (e.g., HPLC, TLC, spectroscopy) to evaluate quality and purity of radiopharmaceutical products.
- Analytical Method Transfer: Assist or lead technical transfer of analytical methods from external vendors into GMP use.
- Experimental Design and Execution: Plan, execute, and document experiments; adhere to project timelines.
- Regulatory Compliance: Follow safety protocols, radiation safety guidelines, GLP, and other regulatory requirements.
- Instrumentation Maintenance: Operate, calibrate, and maintain laboratory equipment and instruments.
- Data Analysis and Reporting: Analyze data, interpret results, and prepare technical reports/presentations.
- Collaboration: Work with QA, production, and R&D to achieve project goals.
Education and Experience
- Education: Minimum BS + 5 years, MS + 3 years, or PhD + 2 years.
- Experience in handling radioactive material (desired).
- Proficient with Open Lab (preferred) or similar analytical chemistry software (required).
- Experience writing/reviewing SOPs and reports (required).
- Experience maintaining routine analytical equipment (HPLC, ICP, etc) (desired).
- GMP environment experience (preferred).
- Hosting/supporting external audits (preferred).
Key Accountabilities
- Quality Control: Conduct analytical testing (e.g., HPLC, TLC, spectroscopy) to evaluate quality and purity of radiopharmaceutical products.
- Analytical Method Transfer: Assist or lead technical transfer of analytical methods from external vendors into GMP use.
- Experimental Design and Execution: Plan, execute, and document experiments; adhere to project timelines.
- Regulatory Compliance: Follow safety protocols, radiation safety guidelines, GLP, and other regulatory requirements.
- Instrumentation Maintenance: Operate, calibrate, and maintain laboratory equipment and instruments.
- Data Analysis and Reporting: Analyze data, interpret results, and prepare technical reports/presentations.
- Collaboration: Work with QA, production, and R&D to achieve project goals.
Education and Experience
- Education: Minimum BS + 5 years, MS + 3 years, or PhD + 2 years.
- Experience in handling radioactive material (desired).
- Proficient with Open Lab (preferred) or similar analytical chemistry software (required).
- Experience writing/reviewing SOPs and reports (required).
- Experience maintaining routine analytical equipment (HPLC, ICP, etc) (desired).
- GMP environment experience (preferred).
- Hosting/supporting external audits (preferred).