Join to apply for the Analytical Expert role at Novartis HEOR Fellowship Program Summary Design and plan scientific experiments, report and interpret results in line with the overall TRD RLT project strategy for RLT Drug Substance(s) and Drug Product(s).
Ensure high-quality project knowledge generation and timely delivery of supplies.
Contribute to the analytical project strategy, driving scientific and operational excellence to support TRD RLT goals.
About The Role Key responsibilities: Execute and report analytical activities for RLT DS and/or DP using advanced analytical sciences following timelines and quality standards. Coordinate analytical aspects of project development for RLT, aligning strategies with APL and DPPL/FPL. Develop and share best practices within the analytical team. Create analytical documents supporting project strategies, ensuring all GMP and source documents are available. Qualify analytical methods according to ICH guidelines, especially for radiopharmaceuticals. Assist in setting specifications suitable for development stages, aligning with the project team. Support transfer of analytical procedures to manufacturing sites and radiopharmacies. Follow SOPs, GLP, GMP, and other relevant guidelines, fostering a team-oriented environment. Essential Requirements Master's degree in chemistry, pharmaceutical technology, or related field, with at least 2 years of industry experience in analytical chemistry, radiochemistry, or quality control. Proficient in English (oral and written); knowledge of site language is a plus. Understanding of GMP, regulatory, and quality standards in radiopharmaceuticals. Experience in writing CMC documents for regulatory submissions. Knowledge of safety protocols when handling hazardous materials. Detail-oriented with a commitment to quality. Strong communication skills, including technical writing and presentations. Excellent problem-solving and decision-making skills. Why Novartis? Our purpose is to reimagine medicine to improve lives.
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