• Designs and executes formulation, compatibility, and process studies to support phase appropriate development of NBPI’s drug product portfolio.
o Duties will include, but not limited to design of programs, evaluation of data, recommendations on strategy, and authoring reports.
• Prepares technical reports and makes recommendations to senior management based on research outcomes.
• Manages and authors appropriate development reports and other documents for internal use and support of regulatory filings.
• Supports project activities and collaborates with colleagues in performing formulation, compatibility, and analytical studies as needed.
• Supports the organization in maintaining a safe working environment focused on quality and that fosters learning, respect, open communication, collaboration, integration, and teamwork.
• Sustains expertise and proficiency in parenteral drug product development.
• Sustains knowledge of formulation, process development.
• Sustains written and verbal communication skills to effectively interface across functional teams and present technical concepts and results.
• Sustains ability to identify and resolves critical issues, implement technical and operational plans.
• Sustains problem-solving skills and demonstrate good judgment and decision-making experience.