The Senior Scientist at PPD Development, L.P. is responsible for independently performing method validations, method transfers, and analytical testing of pharmaceutical and biopharmaceutical compounds in various formulations and delivery systems. The role requires a strong understanding of methods and protocols applicable to assigned tasks, as well as the ability to design and execute experiments with minimal supervision. The Senior Scientist will prepare study protocols, project status reports, final study reports, and other project-related technical documents. Effective communication of data and technical issues to clients is essential, along with mentoring and training other team members. The position also involves assisting with quality systems, new equipment, and designing method validation or transfer protocols while establishing project timelines. The Senior Scientist will review, interpret, and analyze data for technical quality and compliance with protocols, methods, SOPs, client criteria, and Good Manufacturing Practices (GMP) or Good Laboratory Practices (GLP). Self and peer review of data for accuracy and compliance with reporting requirements prior to submission to QA and issuance to customers is also a key responsibility.
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