Sr Radiochemist / Center for Advance Biomedical Imaging
Full-time
MD Anderson
The University of Texas MD Anderson Cancer Center is a leading institution focused on cancer care, research, education, and prevention. As part of its commitment to advancing medical science, UT MD Anderson integrates patient care with innovative research and comprehensive educational programs to eliminate cancer in Texas, the nation, and the world. The Senior Radiochemist plays a key role within the Center for Advance Biomedical Imaging , supporting clinical and preclinical research through the safe manufacturing and quality control of radiopharmaceuticals. The Senior Radiochemist is responsible for ensuring compliance with regulatory requirements and guiding technical staff. The Senior Radiochemist position contributes directly to UT MD Anderson's mission by supporting high-quality diagnostic imaging and advancing research capabilities. The ideal candidate will have a strong foundation in radiochemistry, pharmaceutical manufacturing, or a related scientific discipline, combined with experience in Good Manufacturing Practice environments and analytical methods. The candidate should demonstrate the ability to lead technical teams, troubleshoot complex production and analytical challenges, and contribute to research and regulatory processes. Licenses and certifications are not specified but familiarity with compliance standards and radiation safety is essential. Why Us? Working as a Senior Radiochemist at UT MD Anderson offers the opportunity to contribute to groundbreaking cancer research and patient care while working in a highly collaborative and mission-driven environment. This role supports professional growth through advanced research exposure, regulatory experience, and leadership opportunities, while maintaining a structured and supportive work setting focused on safety and innovation. • Employer-paid medical coverage starting day one for employees working 30+ hours/week, plus optional group dental, vision, life, AD&D, and disability insurance.
• Accruals for PTO and Extended Illness Bank, plus paid holidays, wellness, childcare, and other leave options.
• Tuition Assistance Program after six months of service and access to extensive wellness, fitness, and employee resource groups.
• Defined-benefit pension through the Teachers Retirement System, voluntary retirement plans, and employer-paid life and reduced salary protection programs. Responsibilities Manufacturing Operations
• Produce radiopharmaceuticals that are safe and of the highest quality for clinical use
• Operate, maintain, and calibrate automated and semi-automated manufacturing and quality control equipment
• Perform all duties associated with manufacturing and quality control of PET diagnostic imaging agents
• Provide technical assistance and resolve production-related issues
• Guide and supervise radiochemists and quality control personnel
• Collaborate with staff to prepare Chemical Manufacturing and Control documentation for IND submissions to the FDA Quality Control Operations
• Perform quality control procedures in accordance with Standard Operating Procedures
• Conduct analytical testing using techniques such as radio-HPLC, gas chromatography, and thin-layer chromatography
• Validate and implement analytical methods independently or collaboratively
• Troubleshoot analytical method issues and resolve discrepancies
• Interpret data and maintain accurate analytical records and backup documentation
• Report equipment malfunctions and perform minor repairs when applicable
• Maintain service logs and calibration records Research and Development
• Develop and optimize radiolabeling procedures independently as assigned
• Contribute to the planning and development of new radiopharmaceuticals and analytical processes
• Provide input and recommendations on research approaches and methodologies
• Collaborate with Lab Manager or Director on innovation and experimental design Regulatory Responsibilities
• Follow Standard Operating Procedures to maintain compliance with current Good Manufacturing Practice
• Review, evaluate, and contribute to the development of SOPs
• Ensure data is accurately recorded and accessible for review
• Adhere to radiation safety protocols aligned with the ALARA principle
• Provide training to staff on regulatory and safety requirements Additional Duties
• Perform other duties as assigned EDUCATION
• Accruals for PTO and Extended Illness Bank, plus paid holidays, wellness, childcare, and other leave options.
• Tuition Assistance Program after six months of service and access to extensive wellness, fitness, and employee resource groups.
• Defined-benefit pension through the Teachers Retirement System, voluntary retirement plans, and employer-paid life and reduced salary protection programs. Responsibilities Manufacturing Operations
• Produce radiopharmaceuticals that are safe and of the highest quality for clinical use
• Operate, maintain, and calibrate automated and semi-automated manufacturing and quality control equipment
• Perform all duties associated with manufacturing and quality control of PET diagnostic imaging agents
• Provide technical assistance and resolve production-related issues
• Guide and supervise radiochemists and quality control personnel
• Collaborate with staff to prepare Chemical Manufacturing and Control documentation for IND submissions to the FDA Quality Control Operations
• Perform quality control procedures in accordance with Standard Operating Procedures
• Conduct analytical testing using techniques such as radio-HPLC, gas chromatography, and thin-layer chromatography
• Validate and implement analytical methods independently or collaboratively
• Troubleshoot analytical method issues and resolve discrepancies
• Interpret data and maintain accurate analytical records and backup documentation
• Report equipment malfunctions and perform minor repairs when applicable
• Maintain service logs and calibration records Research and Development
• Develop and optimize radiolabeling procedures independently as assigned
• Contribute to the planning and development of new radiopharmaceuticals and analytical processes
• Provide input and recommendations on research approaches and methodologies
• Collaborate with Lab Manager or Director on innovation and experimental design Regulatory Responsibilities
• Follow Standard Operating Procedures to maintain compliance with current Good Manufacturing Practice
• Review, evaluate, and contribute to the development of SOPs
• Ensure data is accurately recorded and accessible for review
• Adhere to radiation safety protocols aligned with the ALARA principle
• Provide training to staff on regulatory and safety requirements Additional Duties
• Perform other duties as assigned EDUCATION
- Required: Bachelor's Degree Chemistry, Biochemistry or related field.
- Preferred: Master's Degree Chemistry, Biochemistry or related field.
- Required: 5 years Experience in manufacturing and or quality control of PET radiopharmaceuticals.
- Preferred: Authorized user listed in Radioactive Materials (RAM) License as per Nuclear Regulatory Commission (NRC). Upon Hire
- Requisition ID: 181708
- Employment Status: Full-Time
- Employee Status: Regular
- Work Week: Days
- Minimum Salary: US Dollar (USD) 89,000
- Midpoint Salary: US Dollar (USD) 111,000
- Maximum Salary : US Dollar (USD) 133,000
- FLSA: exempt and not eligible for overtime pay
- Fund Type: Hard
- Work Location: Hybrid Onsite/Remote
- Pivotal Position: Yes
- Referral Bonus Available?: No
- Relocation Assistance Available?: Yes
Vacancy posted 2 days ago
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