Siemens Healthineers AG is seeking a Quality Specialist to strengthen QA oversight for a US site manufacturing radiopharmaceuticals. You will drive GMP investigations, CAPAs, batch release activities and audits, while mentoring staff and supporting FDA inspections.
Ideal candidates bring 3–5 years of QA experience in a regulated environment, familiarity with 21 CFR Parts 211/212, and strong problem-solving with attention to detail. Travel 10–25% is required.
#J-18808-LjbffrPet Radiopharma QA Specialist - Global Impact in cincinnati at Unknown Company
This position is listed as full time and onsite.