Associate Scientist II, Commercial testing

Catalent•Kansas City, MO

1d•Onsite

About The Position

Catalent’s Kansas City facility is a leading center for integrated development, manufacturing, and packaging services for oral solid dosage forms. The site combines advanced technologies with a collaborative environment to support pharmaceutical development from early-stage formulation through commercial supply. With a strong focus on quality and innovation, the campus offers modern laboratories, state-of-the-art manufacturing suites, and specialized capabilities to meet diverse client needs. This location fosters teamwork and continuous learning, making it an excellent setting for professionals who want to contribute to delivering life-changing therapies while working in a dynamic and supportive environment. Catalent Pharma Solutions in Kansas City, MO is hiring an Associate Scientist II, Commercial testing. The Associate Scientist II in Commercial Testing is primarily responsible for testing samples and reporting data under cGMP regulatory guidance for Large Molecules/Biologics product development, release and related stability studies.

Requirements

Bachelor’s Degree in Life Sciences or Physical Science field.
No work experience required.
Has basic knowledge of the principles and concepts of a discipline (e.g., Biology, Chemistry, Biochemistry).
Excellent written and verbal communications skills with internal customers, colleagues, and supervisor.
Well organized with ability to multitask and be flexible with daily work schedule.
Ability to work effectively under pressure to meet deadlines.
Ability to pay attention to detail and exhibit critical thinking.

Responsibilities

In support of Large Molecules/Biologics Therapeutics, will execute laboratory testing using the following techniques as required: Compendial assays (i.e. appearance, pH, moisture, Osmolality, HIAC, CCI, etc), Capillary and Gel Electrophoresis (i.e. CE-SDS, SDS-PAGE, icIEF, IEF, western blot, etc.), HPLC/UPLC (i.e. SEC, IEX, RP, HIC, peptide map, glycan analysis, etc.), UV-VIS, In vitro cell based potency methods, ELISA assays, quantitative and potency (i.e. fluorescence, luminescence, colorimetric, MSD), Flow cytometry.
Reads and follows Standard Operating procedures with attention to details.
Successfully trains on 1-2 methods and/or techniques mentioned above and performs adhoc sample testing activities under cGMP as required.
Applies basic scientific and laboratory concepts and theories related to specific testing in the group.
Follow cGMP requirements for legible, accurate and thorough documentation to meet regulatory compliance.
Supports drafting of simple methods, method forms and result reports.