Catalent

Pharmaceutical

ScientistI,BioChemicalAnalysis

$75–105k ~AI est. Kansas City, Missouri, United States FULL TIME
Market Sentiment
HIGH DEMAND

Neural analysis suggests this role is
optimal for Mid+ candidates.

The Brief

“Scientist I, BioChemical Analysis at Catalent. Skills: Method validation, cGMP, Analytical techniques. Perform method evaluation. Perform method optimization”

Industry & Context.

Pharmaceutical

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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