Pharmaceutical Analytical Project Analyst

Design and guide analytical strategies to support manufacturing process development.Lead the planning, development, execution, and data interpretation performed by other scientists in a collaborative, matrixed environment.Oversee and review the development, validation, and transfer of analytical methods to ensure robust and reliable data generation.Manage stability studies to assess degradation pathways and establish shelf-life parameters.Develop impurity control strategies to ensure product quality and regulatory compliance.Experience with a wide range of analytical testing including dissolution, HPLC/UPLC, SFC, disintegration, compendial testing (e.g., excipients / packaging release testing), generic testing (e.g., solvents, water, ash, titrations, heavy metals, ICP/MS, UV) and compound specific methodsCollaborate with cross-functional teams to identify and apply the most effective analytical techniques, including the use of computational modeling, predictive tools, and data visualization platforms.Evaluate scientific data to draw clear conclusions, guide future work, and communicate findings through presentations, technical reports, and other media.Contribute to regulatory submissions by authoring relevant sections of the quality modules, ensuring alignment with global standards and expectations.Maintain compliance with GLP/GMP standard and safety protocols