Design and manage analytical approaches to support process development, with a focus on chromatographic and dissolution-based methods.Oversee and review the planning, development, execution, and interpretation of analytical studies performed by other scientists in a collaborative, matrixed environment.Lead the development, validation, and transfer of robust analytical methods, ensuring high-quality data generation and reproducibility.Manage stability studies to assess degradation pathways and establish shelf-life parameters.Develop impurity control strategies to ensure product quality and regulatory compliance.Collaborate cross-functionally to identify and apply optimal analytical techniques, including 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.Maintain compliance with GLP/GMP standard and safety protocolsTechnical Expertise:Extensive hands-on experience with HPLC/UPLC, dissolution testing, and data review in a pharmaceutical R&D setting.Familiarity with a broad range of analytical techniques, including SFC, disintegrations, compendial testing (e.g., excipients, packaging release testing), generic testing (e.g., UV, ICP-MS, titrations)Proficiency in analytical instrumentation and troubleshooting
