Quality Control Analyst

Orano Med Theranostics

Orano Med has developed new processes for producing high-purity lead-212, a rare radioactive isotope. Lead-212 is currently at the heart of promising research projects in nuclear medicine to develop new treatments against cancer. The innovative approach, known as targeted alpha therapy (TAT), recognizes and destroys cancer cells while limiting the impact on nearby healthy cells.

We are seeking a QC Analyst that conducts cGMP testing of final products, in-process materials, raw materials and stability samples. This person maintains laboratories, assists in writing and optimizing methods, performs method validation and qualification of lab equipment on an as needed basis.

Key Responsibilities:

• Perform testing on final products, in-process materials, raw materials and stability samples
• Test samples with a variety of methods including chromatography, spectroscopy, wet chemistry and radionuclide assays
• Complete test records and review data; report any quality anomalies
• Perform deviation and laboratory investigations, as needed
• Draft data summaries (i.e. CofA or stability summary table)
• Write / update SOPs, technical reports, investigations and trend reports
• Maintain laboratory supplies and chemicals
• Prepare testing reagents
• Assist in validation and/or development of analytical methods and techniques
• Participate in the qualification of QC laboratory equipment
• Package and send samples to contract laboratories
• Other duties as assigned

All candidates must meet the following minimum requirements in order to be considered for this opportunity. Candidates who exceed minimum qualifications may be considered for a higher-level position.

Minimum Qualifications

• Bachelor's degree in a scientific discipline
• 0+ years experience in Pharmaceuticals or related industry