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Orano Med:

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.

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Orano Med is seeking a GMP Quality Control Analyst/Chemist to support the analysis and testing work performed as part of it's drug product development processes.

The QC Analyst will perform a variety of analytical tasks including but not limited to:

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

Our Full-Time Benefits

• Des postes évolutifs et de réelles perspectives de parcours professionnels
• Des parcours d’intégration individualisés
• Des packages de rémunération complets selon la nature de votre contrat de travail : primes, intéressement, participation, santé prévoyance, compte épargne temps, plan d'épargne retraite collectif, primes de cooptation, activités sociales CSE...

• Des accords de télétravail avantageux
• France Avantage 6
• Une entreprise apprenante : Ecole des métiers, Ecole du management, Plateformes digitales en libre accès, Co-développement…

All candidates should 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.

• Must have a comprehensive understanding of cGMPs, proper documentation, and data integrity.
• Must be able to work independently in a team-based setting and function in a rapidly changing environment while balancing multiple priorities simultaneously.
• Must have a Bachelor’s degree in a scientific discipline with a zero (0) to three (3) years of pharmaceutical QC experience.
• Must have excellent analytical and writing skills.
• Must have experience with a variety of HPLC, MS and CE methods.

Orano is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.