Catalent
Pharmaceutical
SeniorAssociateScientistI,BiochemicalAnalysis
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“Senior Associate Scientist I, Biochemical Analysis at Catalent. Skills: Biochemical Analysis, cGMP, HPLC/UPLC. Perform sample testing for biologics. Participate in method transfer”
Industry & Context.
100% on-site
What They're Looking For.
Must Have
2+ years of relevant experience, Bachelor's Degree in Life Sciences or Physical Science, Knowledge of scientific principles, Experience working in a laboratory environment, Experience with analytical techniques, Experience with cGMP regulations
Nice to Have
Master's degree, Experience with HPLC/UPLC, Experience with electrophoresis, Experience with spectroscopy
What You'll Do.
Perform sample testing for biologics
Participate in method transfer
Participate in validation activities
Draft analytical reports
Execute laboratory testing
Follow standard operating procedures
Ensure accurate documentation
Ensure legible documentation
Ensure compliant documentation
Perform peer review of notebooks
Perform peer review of logbooks
Perform peer review of method documentation
Operate laboratory equipment safely
Operate laboratory equipment in compliance
How You'll Work.
Team & Collaboration
Collaborative environment; Teamwork
Communication Scope
Written communication; Verbal communication
Full Job Description
Senior Associate 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 **Senior Associate Scientist I** is primarily responsible for testing samples, participate in method transfer and validation activities, draft methods, and report data under cGMP regulatory guidance for Large Molecules/Biologics product development and related stability studies. **The role:** * Perform sample testing for biologics under cGMP regulatory guidance * Participate in method transfer and validation activities * Draft methods, method forms, and analytical reports * Execute laboratory testing using techniques such as HPLC/UPLC, electrophoresis, spectroscopy, and compendial assays * Follow standard operating procedures with strong attention to detail * Ensure accurate, legible, and compliant documentation in accordance with cGMP * Perform peer review of laboratory notebooks, logbooks, and method documentation * Operate laboratory equipment safely and in compliance with procedures **The candidate:** * Bachelor’s Degree in Life Sciences or Physical Science with 2+ years of relevant experience, OR * Master’s degree in Life Sciences or Physical Science (no experience required) * Knowledge of scientific principles in disciplines such
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