Job Description
The ideal candidate will be energetic and focused, with a can-do attitude and strong problem- solving and data analytics skills. You will join a highly collaborative international team supporting various projects across different development lifecycles. Responsibilities: Manages own work to ensure that agreed targets are met in a timely manner and to agreed quality standards and communicating progress appropriately. Performs relevant experiments and interprets results based on a standard methodology in collaboration with formulation and/or device teams. Able to identify aberrant data and effectively communicate with project teams. Play a key role in supporting development work for automation to manual methods for inhalation products such as Delivered Dose Uniformity (DDU), aerodynamic particle size. Support technical and scientific review of data generated by peers. Identify and lead continuous improvement efforts to streamline laboratory operations and eliminate waste, ensuring compliance with GMP/GxP expectations. Demonstrate an active interest in leveraging AI /ML and other data science tools to enhance analytical results interpretation and workflow performance. Minimum Qualifications: Bachelor’s (3+ years), or Master’s (1+ years), in Chemistry, Pharmaceutical Sciences, or closely related field. Strong background in analytical methodologies for inhalation as well as oral dosage forms Hands-on experience working with HPLC/UPLC, moisture analyzer, and mass spectrometry is required. Proficiency with analytical software such as Empower and ELN is required. Hands-on proficiency with workflow optimization. Experience with statistical tools such as JMP is preferable. Excellent organizational, problem-solving, and collaborative communication skills. Experience working in a GMP/GxP regulated environment. Stron