Catalent

pharmaceutical and biotech

AnalyticsSeniorAssociateScientistII

Kansas City, Missouri, United States FULL TIME
The Brief

“Analytics Senior Associate Scientist II at Catalent. Skills: HPLC, Karl Fischer, data analysis, method development, method validation. Execute laboratory work plans/schedules. Sample types include in-process, release or stability”

What You'll Achieve.

advancing new medicines from early development to clinical trials and to the market

Industry & Context.

pharmaceutical and biotech
Problems you'll solve

Proactively identify and address work-related issues; Ability to process, maintain, interpret, and analyze data; basic understanding of instrument operation and troubleshooting

Eligibility Requirements

100% on-site, standing constantly, walking and sitting frequently, lifting, pushing, and pulling up to 40, occasional kneeling, frequent reaching, Work is performed in a manufacturing environment with exposure to noise and vibration, constant exposure to potential hazards, occasional exposure to temperature changes, humidity, wet conditions, and extreme heat or cold

What They're Looking For.

Must Have

Bachelor's degree in related life science or physical science field with a minimum of 2 years of related work experience, Hands-on experience operating HPLC, Hands-on experience operating Karl Fischer (KF), Ability to process, maintain, interpret, and analyze data, basic understanding of instrument operation and troubleshooting across multiple techniques, written and verbal communication skills, excellent organization, time-management, and multitasking abilities

Nice to Have

4+ years of related work experience, Master's degree in related life science or physical science field with a minimum of 1 year of related work experience, 2+ years of related work experience (with Master's degree), GC experience, LC-MS experience, disintegration testing experience, friability testing experience, TGA testing experience

What You'll Do.

Execute laboratory work plans/schedules

Sample types include in-process

Maintain accurate and high-quality laboratory documentation in accordance with regulatory guidance and Site SOPs

Draft technical documents such as methods or certificate of analysis

Performs parallel review of laboratory documentation

Perform technical review of documents for accuracy

thoroughness and regulatory compliance

Assists in execution of efficiency improvement projects

Trains others on laboratory techniques

How You'll Work.

Team & Collaboration

work plans/schedules developed with input from a supervisor or senior team member; Proactively identify and address work-related issues at both the individual and team level; internal and external customers

Communication Scope

written and verbal communication skills with internal and external customers

Process & Methodology

efficiency improvement projects

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