Catalent
Pharmaceutical
ScientistI,BioChemicalAnalysis
Neural analysis suggests this role is
optimal for Mid+ candidates.
“Scientist I, BioChemical Analysis at Catalent. Skills: Method validation, cGMP, Analytical techniques. Perform method evaluation. Perform method optimization”
Industry & Context.
What They're Looking For.
Must Have
6+ years relevant experience, 4+ years relevant experience, Doctorate degree in Life Sciences, Bachelor's Degree in Life Sciences, Bachelor's Degree in Physical Science, Master's degree in Life Sciences, Master's degree in Physical Science, Applied knowledge of scientific principles, Experience with analytical techniques, Experience in cGMP-regulated environment, Experience with method development, Experience with method transfer, Experience with method validation, Experience with method optimization, Experience drafting technical documents, Experience reviewing technical documents
Nice to Have
Method lifecycle activities support
What You'll Do.
Perform method evaluation
Perform method optimization
Perform method transfer
Perform method validation
Execute analytical testing
Draft technical documents
Review technical documents
Perform ad hoc sample testing
Support method lifecycle activities
Follow standard operating procedures
Ensure compliant documentation
Train peers on methods
Train peers on instrumentation
Train peers on laboratory practices
How You'll Work.
Team & Collaboration
Collaborative environment; Teamwork
Full Job Description
Scientist I, BioChemical Analysis **Position Summary** * **Shift:** Monday-Friday 8am-5pm * 100% on-site 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. The **Scientist I** is primarily responsible for method evaluation, optimization, transfer and validation activities under cGMP regulatory guidance for Large Molecules/Biologics product development and related stability studies. Also responsible for drafting technical documents such as methods, method forms, validation protocols and reports. **The role:** * Perform method evaluation, optimization, transfer, and validation activities under cGMP guidance * Execute analytical testing for biologics using techniques such as HPLC/UPLC, electrophoresis, spectroscopy, and compendial assays * Draft and review technical documents including methods, validation protocols, and reports * Perform ad hoc sample testing and support method lifecycle activities * Follow standard operating procedures with strong attention to detail * Ensure accurate, legible, and compliant documentation in accordance with cGMP requirements * Perform peer review of laboratory notebooks, logbooks, and technical documentation * Train and coach peers on methods, instrumentation, and laboratory practices **The candidate:** * Bachelor’s Degree in Life Sciences or Physical Science with 6+ years of rel
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