POSITION SUMMARY:

Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, manufacture, and supply products that help people live better and healthier lives. Catalent is dedicated to delivering unparalleled service to pharma, biotech, and consumer health customers, supporting product development, launch, and full life-cycle supply. With time-tested experience in development sciences, delivery technologies, and multi-modality manufacturing, Catalent supports the acceleration of development programs and the launch of more than a hundred new products every year. Powered by thousands of scientists and technicians and the latest technology platforms at more than 40 global sites, Catalent supplies billions of doses of life-enhancing and life-saving treatments for patients annually.
Catalent’s Kansas City facility is home to our Oral & Specialty Drug Delivery, Biologics Analytical Services and Clinical Supply Services businesses. The site provides a range of integrated services for oral solid dosage forms, from formulation development and analytical testing to clinical and commercial-scale manufacturing. The Kansas City facility is a Center-of-Excellence for our Biologics Analytical Services business. Our talented team has over 25 years of experience providing analytical services for stand-alone and integrated biologics projects.
Catalent Pharma Solutions in Kansas City, MO is hiring an Analytics Associate Scientist II. Under general supervision, the Associate Scientist II performs work that is varied in analytical development and that may be somewhat difficult in character. Some evaluation, originality or ingenuity is required at the Associate Scientist II level. This individual follows established protocols and work plans and may be assisted by laboratory technicians/assistants.

• Execute laboratory work plans/schedules developed with input from supervisor or senior team member. Sample types include in-process, release or stability. Techniques include HPLC (High Performance Liquid Chromatography), GC (Gas Chromatography), Karl Fischer, Disintegration, Friability, Hardness, and appearance. Under direction, may perform method development, validation, or transfer activities
• May draft technical documents such as methods or certificates of analysis
• Performs parallel review of laboratory documentation and may become qualified to perform technical review of documents for accuracy, thoroughness and regulatory compliance
• Assists in the execution of efficiency improvement projects with guidance
• Maintain high quality laboratory documentation in accordance with applicable regulatory guidance and Site Standard Operating Procedures (SOPs)
• All other duties as assigned