QA Document Control Specialist
- Radiopharma CDMO
- Indianapolis - Onsite
RBW are collaborating with a pioneering leader in the field of nuclear medicine, dedicated to developing innovative therapies for cancer treatment. With a rich history rooted in scientific excellence and a commitment to improving patient outcomes, they consistently push the boundaries of medical research and technology.
Establishing their networks across the US and Europe, they are looking to build their QA teams in Indianapolis. As the Quality Assurance Document Control Specialist, they are looking for a candidate with attention to detail to maintain the integrity and accuracy of the documentation processes and the eQMS.
The team are passionate about unlocking the capabilities that the system has to offer and committing to reaching the Gold Standard within Quality.
If you could be interested in exploring new opportunities and learning more about this position, please apply or reach out directly.
I look forward to hearing from you!
