Analytical Development Chemist at AtomVie

Elevate your career as an Analytical Development Chemist with AtomVie Global Radiopharma in a GMP environment. This role emphasizes method development, validation, and quality testing of radiopharmaceuticals. As part of AtomVie, you will support the expansion of our portfolio by conducting analytical method development, validation, and stability testing.

Your technical expertise will be essential for testing drug products and ensuring compliance with regulatory guidelines such as ICH and USP. Join a community committed to transforming lives through innovative healthcare solutions. Key Responsibilities: • Conduct analytical method development, transfer, and validation • Perform microbiological testing on development products • Write test reports and technical documents • Conduct validation activities and write reports • Manage quality control and testing of drug products Requirements: • University Degree in relevant science, M.Sc. or Ph.D. preferred • 3-4 years in analytical chemistry within cGMP • Experience with HPLC, GC, and microbiology tests • Familiarity with sterile products and BSL2 • Ability to lift 23 kilograms Bring your analytical skills, method development expertise, and commitment to quality to AtomVie and shape the future of radiopharmaceuticals. #J-18808-Ljbffr