Welcome to Orano
Helping to meet current and future challenges to preserve our world and build the world of tomorrow while taking care of everyone's health is stimulating for you. For us too. By joining the Orano Group, a leading international player in the nuclear industry, you are in the right place.
Every day we work to produce efficient low-carbon energy, to fight global warming, to find solutions that save natural resources, and to contribute to progress in health.
Our strengths? Across the entire fuel cycle, we have extensive expertise in cutting-edge technologies, safe, high value-added products and services, and a strong capacity for innovation. All of these factors reflect the strong skills of our 17,000 employees, whom we are constantly striving to develop. With their different backgrounds and experience, they are proof of our openness to all talents. They share the same ambition: to give nuclear energy its full value.
Every day we work to produce efficient low-carbon energy, to fight global warming, to find solutions that save natural resources, and to contribute to progress in health.
Our strengths? Across the entire fuel cycle, we have extensive expertise in cutting-edge technologies, safe, high value-added products and services, and a strong capacity for innovation. All of these factors reflect the strong skills of our 17,000 employees, whom we are constantly striving to develop. With their different backgrounds and experience, they are proof of our openness to all talents. They share the same ambition: to give nuclear energy its full value.
Job description
Orano Med is seeking a detail-oriented QC Analyst to join our Quality Control team. In this role, you will conduct cGMP testing of final products, in-process materials, raw materials, and stability samples. You will maintain laboratories, assist in writing and optimizing methods, perform method validation, and qualify lab equipment as needed.
Key Responsibilities
- Perform comprehensive testing on final products, in-process materials, raw materials, and stability samples
- Execute a variety of testing methods including chromatography, spectroscopy, wet chemistry, and radionuclide assays
- Complete and review test records with accuracy and attention to detail
Report any quality anomalies according to established protocols - Perform deviation and laboratory investigations as needed
- Draft data summaries including Certificates of Analysis (CofA) and stability summary tables
- Update methods, technical reports, and investigations documentation
- Prepare testing reagents and maintain laboratory supplies and chemicals
- Conduct environmental monitoring (EM) sampling, incubation, and testing
- 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
- Additional responsibilities as assigned
Our Full-Time Benefits
- Competitive compensation
- Health, Dental, and Vision insurance – with generous employer contributions
- 401(k) with employer matching and contribution amounts
- Life insurance and Short- and Long-Term Disability insurance provided by the company
- Generous Paid Time Off and holiday schedules
- Numerous Training and Development opportunities
- and more…
Ideal qualifications
Requirements
- Bachelor's degree in Chemistry, Biochemistry, Pharmaceutical Sciences, or related field
- Experience in a regulated laboratory environment, preferably in pharmaceuticals or biotechnology
- Proficiency with a variety of HPLC, MS, and CE (Capillary Electrophoresis) methods
- Comprehensive understanding of cGMPs, proper documentation, and data integrity
- Strong analytical and organizational skills
- Excellent written and verbal communication abilities
- Demonstrated ability to work independently in a team-based setting
- Capability to function effectively in a rapidly changing environment
- Skill in balancing multiple priorities simultaneously
- Flexibility to easily switch between multiple ongoing projects and adjust priorities based on business needs
What We Offer
- Collaborative and innovative work environment
- Opportunities for professional growth and development
- Competitive compensation and benefits package
Orano Med is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.
Orano is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, national origin, age, disability, citizenship, veteran status, marital status, sexual orientation, gender identity, genetic predisposition or carrier status or any other characteristic protected by law.
Orano Med
Orano Med is at the forefront of research in nuclear medicine and is developing new therapies against cancer. Based on its unique expertise in the production of lead-212 (Pb-212) and radiolabeling technologies, Orano Med is developing innovative radioligand therapies which consist of selectively destroying cancer cells while limiting the impact on surrounding healthy cells. With a solid portfolio of molecules in development capable of targeting various forms of cancer, and a reliable supply chain for Pb-212, Orano Med aims to become a leader in targeted alpha therapies, in particular for patients with currently unmet medical needs.
Find out more about Orano Med
Find out more about Orano Med
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