Biomarker Production Specialist (Charlottesville, VA)

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. Join the global leader shaping the future of PET imaging. At Siemens Healthineers , we operate the world's largest PET radiopharmaceutical network - delivering over 1 million doses annually with a >99% fulfillment rate and supporting more than 2,800 imaging centers worldwide. Important: This is a primarily overnight role. Candidates must be willing to work overnight and have the flexibility to rotate into alternative shifts as business needs evolve. Why You'll Love Working Here Industry‑leading 5‑week paid training program (in‑person + virtual). Competitive benefits: medical/dental/vision, 5% bonus , 100% 401(k) match. 20 days PTO + 5 floating holidays. Meaningful work that supports patient care and advanced medical imaging. Essential Job Functions and Responsibilities You are responsible for the synthesis, quality control, packaging, logistics, and strict regulatory compliance of radiopharmaceuticals used in diagnostic imaging and treatment of diseases. Your role supports manufacturing through regular preventive maintenance, calibration, and troubleshooting of analytical equipment used in operations. You also communicate regularly with couriers and customers to ensure the accurate and timely delivery of biomarkers. In addition, you assist with facility housekeeping, maintenance of laboratory inventory levels, creation of quality control documentation as needed, and adherence to strict safety protocols and regulations related to the production and transport of radioactive materials. Operate chemistry instruments (HPLC, GC, TLC, and chemistry modules) and advanced systems (cyclotron) for the routine manufacturing and quality control of radiopharmaceuticals. Author and maintain precise documentation for manufacturing, quality control, preventive maintenance, customer support, laboratory investigations, deviations, and out‑of‑specification events. Perform preventive maintenance, inspections, and troubleshooting of critical equipment. Prepare products for shipment, coordinate courier logistics, and provide customer support. Maintain aseptic environments (cleanroom) to create sterile consumables and prevent contamination during the production of injectable materials. Conduct environmental monitoring on a regular and defined basis. Maintain compliance with strict safety, sterile environment, and regulatory standards. Minimum Qualifications High school diploma or equivalent required. Specialized skill training or certification may be required. Physical Demands: Applicants should be comfortable working in a fast‑paced laboratory environment and able to lift up to 100 lbs. Willingness to work overtime as needed. Detail‑oriented with strong critical thinking skills. Ability to work independently. Basic computer skills such as spreadsheet, word processing, and email. Effective verbal and written communication skills. Preferred Qualifications An associate's degree in chemistry, Biochemistry, Biology, Medical Technology, or a related Life Science field. Understanding of current Good Manufacturing Practices and Good Documentation Practices. Previous work experience in a laboratory environment or related role. Previous experience with analytical laboratory equipment and laboratory software systems. Familiarity with radiation safety or ALARA principles. Knowledge, Skills, and Abilities Excellent communication and interpersonal skills. Strong command of Good Documentation Practices (GDP) to ensure data integrity and audit readiness. Excellent problem‑solving and analytical skills, as well as critical thinking ability. Excellent organizational skills and attention to detail. Ability to treat confidential information with sensitivity. Ability to meet deadlines and work in a fast‑paced, multi‑priority environment. Ability to plan and organize job responsibilities and priorities. Ability to apply standard operating procedures (SOPs) in a production environment. Demonstrated ability to maintain a sterile environment. Ability to understand, prioritize, and implement laboratory safety protocols. Who we are We are a team of more than 72,000 highly dedicated Healthineers in more than 70 countries. As a leader in medical technology, we constantly push the boundaries to create better outcomes and experiences for patients, no matter where they live or what health issues they are facing. Our portfolio is crucial for clinical decision‑making and treatment pathways. How we work: When you join Siemens Healthineers, you become one in a global team of scientists, clinicians, developers, researchers, professionals, and skil #J-18808-Ljbffr onehealthineers