Catalent
Pharmaceutical
PharmaceuticalDevelopmentSeniorScientistI
Neural analysis suggests this role is
optimal for Senior candidates.
“Pharmaceutical Development Senior Scientist I at Catalent. Skills: Formulation development, Process design. Serve as Technical Lead. Design experiments”
Industry & Context.
Troubleshooting
What They're Looking For.
Must Have
11+ years related work experience, 9+ years related work experience, 8+ years related work experience, Bachelor's degree in life science, Master's degree in life science, Doctorate Degree in life science, Basic/Moderate understanding of manufacturing equipment operations, Troubleshooting skills in multiple techniques
Nice to Have
Advanced knowledge of pharmaceutics principles, Knowledge of principles in other disciplines
What You'll Do.
Serve as Technical Lead
Lead clinical trial manufacturing
Ensure regulatory compliance
Ensure cGMP compliance
Ensure SOP compliance
Develop laboratory work plans
Execute laboratory work plans
Author technical documents
Review technical documents
Execute efficiency improvement projects
Identify business opportunities
Recommend business opportunities
Apply technical knowledge
Apply functional knowledge
Assist in experiment design
Assist in project design
Propose deviations from procedures
Develop manufacturing processes
Execute manufacturing processes
Lead small team projects
Recognize unmet needs
How You'll Work.
Team & Collaboration
Individual level; Team level
Full Job Description
**Pharmaceutical Development Senior Scientist I** **Position Summary** * **Work Schedule: Monday to Friday 8am-5pm** * 100% based on-site in Kansas City Catalent’s Kansas City (KCM) facility is a premier site for integrated drug development, manufacturing, and clinical supply services, supporting a wide range of pharmaceutical and biotech products. With cutting-edge technologies and a collaborative work environment, it offers exciting opportunities for professionals across all functions—from science and engineering to operations and logistics. The Kansas City **Pharmaceutical Development Senior Scientist I** serves as Technical Lead for formulation/process design and development of oral solid dosage forms. Design and execute experiments and processes necessary for developing formulations of pharmaceuticals oral solid. Lead clinical trial manufacturing endeavors and ensures that all work is carried out in compliance with regulatory requirements, good manufacturing practices (cGMP) and standard operating procedures (SOPs). **The Role** * Develop and execute laboratory work plans/schedules independently, using customer milestones and Division/site performance standards and metrics * Authors/Reviews technical documents, such as protocols, batch records, test methods, technical reports, and operating procedures * Trains, coaches or mentors’ others on technical development or business issues * Knowledge of high-shear granulation, fluid-bed technology, roller compaction, compression, encapsulation, coating technology * Executes efficiency improvement project with moderate guidance * Identify and recommend business opportunities on a project specific basis * Has advanced knowledge of the principles, theories and concepts applicable to a limited range of work in pharmaceutics and knowledge of principles and concepts in other disciplines. * Applies technical and functional knowledge to assist in experiment/project design that will enable department to meet goals. * All other
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