Verified Job
IT / Software / Data Analyst
Pharmaceutical Development Senior Scientist I
IT / Software / Data Analyst
#813336
Remote / WFH
Catalent
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).
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).
