Scientist II, Scientist II (pharmaceutical 3D printing & Compounding Formulations)

About the Company The U.S. Pharmacopeial Convention (USP) is an independent scientific organization that collaborates with the world’s leading health and science experts to develop rigorous quality standards for medicines, dietary supplements, and food ingredients. We believe in scientific excellence driven by fairness, integrity, and collaboration, reflected in our core value of Passion for Quality. USP employs over 1,300 professionals across twenty global locations to strengthen the supply of safe, high‑quality medicines worldwide. USP is an equal‑employment‑opportunity employer. We provide reasonable accommodations for individuals with disabilities and support an inclusive and collaborative work environment. Job Overview As a Scientist II, Additive Manufacturing, you will design and execute laboratory‑based research to advance USP’s work in emerging pharmaceutical manufacturing technologies. The role supports development and evaluation of pharmaceutical additive manufacturing processes, formulation and analytical method development, and generation of high‑quality scientific data to assess feasibility, performance, and quality. Responsibilities Conduct additive manufacturing lab research: design, execute, and analyze experiments for emerging additive manufacturing technologies for pharmaceutical applications. Develop, optimize, validate, and apply analytical methods to characterize 3D‑printed pharmaceutical (re)formulations. Use established and novel analytical and manufacturing approaches to investigate performance, quality, and feasibility of additive manufacturing processes. Apply scientific judgment, academic training, and prior experience to troubleshoot technical challenges and generate data‑driven solutions. Collect, curate, analyze, and manage high‑quality scientific data to support interpretation, reporting, and technology assessment. Maintain complete and traceable lab records in accordance with research and quality expectations. Review and evaluate scientific literature and emerging technology trends to inform experimental design, method development, and research direction. Manage research studies and technical projects from study design and protocol development through data analysis and final reporting. Develop, validate, and document analytical methods and research outcomes through technical reports, protocols, and SOPs aligned with USP R&D and laboratory standards. Collaborate with internal and external stakeholders to advance research objectives and deliver high‑quality, publishable scientific outcomes. Demonstrate commitment to continuous learning and proactively expand technical and scientific capabilities. Collaborate effectively within multidisciplinary, cross‑functional teams to support innovation. Work independently while contributing positively as a collaborative, adaptable team member. Participate in and, as appropriate, present at internal and external scientific meetings. Recommend, evaluate, and implement innovative approaches, workflows, or tools to enhance research efficiency and impact. Perform other duties and projects as assigned. Qualifications Advanced degree in pharmacy, pharmaceutical science, chemistry, chemical engineering, or a related field. 3–5 years of experience in 3D printing of pharmaceuticals (alternate combinations of experience and education may be considered). Strong skills and hands‑on experience in formulation development in any dosage form. Experience designing and optimizing formulations suitable for pharmaceutical 3D printing. Knowledge and hands‑on experience in developing test methods using HPLC, Raman, or NIR. Skilled in anticipating, troubleshooting, and solving technical problems. Strong documentation and SOP skills. Desired Preferences Experience with pharmaceutical compounding in 503(a) settings. Familiarity with compendial testing or USP standards. Experience with pediatric or individualized dosage forms. Experience using Design of Experiments (DoE) and Quality‑by‑Design (QbD) concepts. Supervisory Responsibilities None – this is an individual contributor role. Benefits USP offers benefits to protect you and your family, including company‑paid time off, comprehensive healthcare options, and retirement savings. Compensation Base Salary Range: USD $75,500.00 – $93,300.00 annually. Target Annual Bonus: variable based on level of role. Individual compensation packages depend on skill set, experience, qualifications, equity, and other relevant factors. Equal Opportunity Statement USP is an equal‑employment‑opportunity employer, committed to fair, merit‑based selection processes that welcome diverse expertise. We uphold policies that create an inclusive and collaborative work environment. Legal Requirements This employer must provide notice to all applicants of their rights under federal employment laws. For more information, please review the Know Your Rights notice from the Department of Labor. #J-18808-Ljbffr BioSpace