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 Theranostics
Are you passionate about ensuring the highest standards in pharmaceutical manufacturing? Do you thrive in a fast-paced, detail-oriented environment where your work directly impacts clinical trial success? Join our Quality Assurance team as a QA Specialist II and play a vital role in safeguarding the integrity of raw materials and sterile drug products. Whether you're beginning your QA journey or seeking your next challenge, this is your chance to grow within a dynamic, mission-driven organization that’s transforming oncology from the inside out.
The QA Specialist II supports GMP manufacturing operations by reviewing documentation, inspecting materials, and ensuring compliance with SOPs and regulatory standards. This role plays a key part in maintaining quality systems, supporting sterile manufacturing, and driving continuous improvement across QA processes.
Key Responsibilities
- Review and inspect documentation for incoming raw materials and packaging components
- Release/disposition GMP products for Macrocyclics and OM
- Conduct thorough reviews of production batch records, logbooks, and associated documentation
- Perform area release for manufacturing operations
- Oversee sterile manufacturing processes and provide instruction on sterile gowning and aseptic techniques
- Review equipment and instrumentation documentation supporting GMP operations
- Scan and archive manufacturing documentation (e.g., batch records, audits, investigations, CAPAs, change controls)
- Follow up on investigations, CAPAs, and change controls to ensure timely and compliant resolution
- Participate in internal audits of GMP labs and non-GMP processes
- Assist in updating Quality SOPs and perform secondary documentation reviews
- Support documentation review related to technology transfer from R&D
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
Education & Experience
- Education: Bachelor’s Degree in a scientific or technical discipline
- Experience: 2–5 years in the pharmaceutical or related industry, including 2–3 years in sterile manufacturing is preferred
Required Skills & Competencies
- Experience writing and revising SOPs
- Strong understanding of GMP and sterile manufacturing practices
- Experience reviewing batch records and quality documentation
- Proficient in Microsoft Office (Word, Excel, PowerPoint)
- Excellent written and verbal communication skills
- Highly organized and detail-oriented
- Ability to manage multiple priorities and adapt to changing demands
Preferred Skills & Competencies
- Familiarity with CAPA, change control, and internal audit processes
- Knowledge of technology transfer documentation from R&D
- Prior experience with sterile gowning and aseptic technique instruction
- Experience with document archiving systems and electronic quality management tools
Orano Med Theranostics is an Equal Opportunity Employer. We welcome all qualified applicants regardless of race, gender, identity, background, or ability.
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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