Analytical Sciences Specialist

Sumitomo Pharma Co., Ltd. is a prominent global pharmaceutical company headquartered in Japan, dedicated to meeting patient needs in oncology, urology, women's health, rare diseases, cell & gene therapies, and CNS. With a robust portfolio of marketed products and a diverse pipeline of investigational assets at various stages, we strive to expedite the discovery and development of novel therapies to improve patient outcomes. We are looking for a motivated and innovative Analytical Sciences Specialist to join our team. In this vital role, you will support analytical operations and enhance decision-making through data-driven insights across Technical and Quality Operations. Your responsibilities will include maintaining product static data in our Laboratory Information Management Systems (LIMS) and working alongside IT and Quality teams to improve system functionalities. You will use advanced statistical techniques to develop real-time monitoring dashboards and support continuous improvement initiatives. Additionally, you will play a key part in investigations, process assessments, and regulatory documentation using data mining, statistical analysis, and visualization techniques. Your success in this role will rely on a solid foundation in statistical analysis, data visualization, and data management, along with experience in analytical tools and knowledge of data architecture principles. We are seeking a well-organized strategic thinker capable of executing detailed tasks while maintaining a broad vision. Strong communication skills and the ability to work collaboratively across teams are essential for this role. Key Responsibilities: Oversee product static data management in Laboratory Information Management Systems (LIMS) while collaborating with IT to enhance system capabilities. Utilize statistical techniques such as multivariate analysis and statistical process control for continuous improvement initiatives. Create real-time monitoring tools for batch release and stability data using platforms like JMP, R, Python, and MATLAB. Develop predictive models and perform large-scale data analysis to support informed decision-making. Drive innovation by integrating data and technology from the data science field to uncover new opportunities and boost operational excellence. Assist in analytical release and stability testing of drug materials at contract laboratories and contribute to compiling and reviewing quality documents for regulatory compliance. Support regulatory submissions by preparing and reviewing analytical data summaries and associated documentation. Core Competencies: Strong background in statistical analysis, data visualization, and data management for analytical and operational decision-making. Experience with tools like JMP, MATLAB, Minitab, R, or Python for predictive modeling and multivariate analysis. Knowledge of data architecture principles. Excellent communication skills to convey complex analytical results clearly to various stakeholders. Ability to collaborate across diverse teams, manage multiple projects, and maintain meticulous attention to detail. Skilled in identifying opportunities and implementing detail-oriented solutions for significant outcomes. Organized and strategic with the capacity to balance detailed execution and overarching objectives. Education and Experience: Bachelor's or higher degree in Data Science, Statistics, or related fields. 0 to 3 years of relevant experience in the biotech or pharmaceutical industry. Experience in analytical sciences is preferred. The base salary range for this position is $77,300 to $96,000. In addition to base salary, our total rewards package includes opportunities for merit-based salary increases, short incentive plan participation, eligibility for a 401(k) plan, and comprehensive medical, dental, vision, life, and disability insurance. We offer a robust time-off policy with flexible paid time off, 11 paid holidays, additional leave during the last week of December, and 80 hours of paid sick time available upon hire and annually thereafter. Total compensation offered will depend on individual candidate experiences, skills, education, and other legally permitted factors. Confidential Information: All information encountered (written, verbal, electronic, etc.) is considered confidential. Compliance: Ensure compliance with all applicable regulations and operational procedures, adhering to industry best practices and ethical standards. This role may involve working in a fast-paced environment while managing multiple demands. High levels of initiative, independence, and excellent communication skills are essential. Candidates must be able to use a personal computer for extended periods. Sumitomo Pharma America is an Equal Employment Opportunity employer. Qualified applicants will be considered without regard to race, color, creed, religion, national origin, age, ancestry, nationality, marital status, sex, gender, sexual orientation, disability, veteran status, or any other legally protected characteristic. For reasonable accommodations related to the application process, please contact us directly.

Created: 2026-03-09