Essential Functions of the job: Select appropriate methods and techniques and perform phase appropriate analytical method development and validation to support drug substance and drug product development. Recommend alternatives, research new methods/techniques, and proactively seek out senior personnel to discuss potential solutions to problems. Design and oversee execution of stability studies, summarize data and justify specifications, contribute to analytical strategies. Author technical reports, protocols, and participate in the authoring of CMC sections of the clinical trial applications (IND/IMPD/CTA) and/or marketing applications (NDA/MAA) with manager’s guidance. May work as analytical workstream lead (WSL) or acting analytical team lead (acting ATL) under the supervision of analytical team lead (ATL), and collaborate with cross functional CMC team to deliver overall project goal. Support platform establishment as needed by providing scientific input. Publish and/or present in conferences with manager’s supervision, build scientific connections in the analytical science community. Education Required: Ph.D. in pharmaceutical science, chemistry, biology, engineering or other relevant subjects with or without postdoc/industry experience. Other Qualifications: Demonstrate technical expertise on state-of-the-art analytical technologies (e.g.: chromatography, mass spectrometry, solid state characterization) Good track record of publication and/or conference presentation Excellent learning agility, strong passion for science Must think critically and creatively and be able to work independently, determine appropriate resources for resolution of problems and have reasonable organizational and planning skills Good scientific communication skills (both verbal and technical) and interpersonal skills Capable of using English as working language (both in verbal and in writing)