Join us in pioneering breakthroughs in healthcare. For everyone. Everywhere. Sustainably. Our inspiring and caring environment forms a global community that celebrates diversity and individuality. We encourage you to step beyond your comfort zone, offering resources and flexibility to foster your professional and personal growth, all while valuing your unique contributions.ResponsibilitiesProviding quality oversight of a US based site that manufactures and distributes radioactive sterile injectables (PET) per 21 CFR Part 212 and USP 825 for Siemens Healthineers – Radiopharma.Focusing on GMP investigations and CAPA's, change management, batch release and batch record reviews, site quality audits and data integrity audits to support Radiopharma's quality oversight functions.Provide on‑site support for the purposes of training and mentoring, performing internal and third‑party quality audits and supporting FDA inspections.Serve as the subject matter expert on assigned topics, providing input on policies, procedures and decisions related to those topics.Participate in continuous improvement projects.Manage quality metrics at the site, including focus on reduction of batch record corrections, investigations, failed batches due to operator error and other quality metrics as assigned.Perform internal form review, inventory management, observations of staff qualifications and facility inspection.QualificationsExperience in the pharmaceutical industry (preferably sterile drug manufacturing) and/or PET radiopharmaceuticals per 21 CFR Part 212 and Part 11 and/or USP 825.Experience interpreting regulatory policies and guidance documents and applying them appropriately.Expertise in the quality assurance disciplines of problem‑solving, root cause analysis, investigation writing and management of corrective and preventive actions.Ability to identify procedural gaps and product risk and recommend contingency plans and strategies to mitigate compliance issues.Completed studies in microbiology and/or analytical chemistry.Experience with MS Office software (Word, PowerPoint, Excel and Outlook).Flexibility to travel.Required SkillsBachelor's degree in a scientific field (biology, chemistry, microbiology, pharmacy, etc.) preferred or equivalent experience required.Excellent attention to detail.Creative problem solver capable of reprioritizing multiple times per day while working at the speed of business and delivering results on time.Willingness to travel 10% – 25%.Relevant QA experience for 3–5 years in a 21 CFR Part 211 or 212 regulated industry.Pay Range$80,300 – $110,407BenefitsMedical insurance, dental insurance, vision insurance, 401(k) retirement plan, life insurance, long‑term and short‑term disability insurance, paid parking/public transportation, paid time off, paid sick and safe time.Equal Employment Opportunity Statement: Siemens Healthineers is an Equal Opportunity and Affimissive Action Employer encouraging diversity in the workplace. All qualified applicants will receive consideration for employment without regard to their race, color, creed, religion, national origin, citizenship status, ancestry, sex, age, physical or mental disability unrelated to ability, marital status, family responsibilities, pregnancy, genetic information, sexual orientation, gender expression, gender identity, transgender, sex stereotyping, order of protection status, protected veteran or military status, or an unfavorable discharge from military service, and other categories protected by federal, state or local law.#J-18808-Ljbffr