Catalent

Pharmaceutical

AnalyticalChemistI

$0–0k Greenville, North Carolina, United States FULL TIME
The Brief

“Analytical Chemist I at Catalent. Skills: chromatography, data review, troubleshooting, technical understanding. Perform routine analytical testing in support of pharmaceutical products following all applicable safety, quality, and regulation requirements.. Maintain data integrity and employ good documentation practices when performing experiments.”

Industry & Context.

Pharmaceutical
Problems you'll solve

troubleshooting

Eligibility Requirements

Ability to lift 10-50lbs, unassisted., Majority of the work day is performed while standing, walking, lifting, pulling, and pushing., Requires bending, squatting, crawling, climbing, and reaching., Some exposure to hazardous chemicals and other active chemical ingredients.

What They're Looking For.

Must Have

Bachelor’s degree a science-related discipline (e.g. Biology, Chemistry, Pharmaceutical Sciences), Associate degree in Biotechnology, Chemistry or equivalent science degree with one year of professional experience in pharmaceutical analytical chemistry., Ability to lift 10-50lbs, unassisted., Majority of the work day is performed while standing, walking, lifting, pulling, and pushing., Requires bending, squatting, crawling, climbing, and reaching., Some exposure to hazardous chemicals and other active chemical ingredients.

Nice to Have

Experience in a Catalent analytical laboratory in a role that is independent and proficient in chromatography and data review as well as troubleshooting and technical understanding may be substituted for two years of professional experience.

What You'll Do.

Perform routine analytical testing in support of pharmaceutical products following all applicable safety

and regulation requirements.

Maintain data integrity and employ good documentation practices when performing experiments.

Compare laboratory data against specifications and trend data where applicable to determine if results meet requirements.

and return of calibration standards including

Ensure accuracy of testing by following method/standard instructions and adhering to internal SOPs to eliminate the potential for repeat testing

Under general supervision

perform primarily routine testing for chromatographic and spectrophotometric methods of analysis in support of pharmaceutical excipients

API and/or drug product.

Testing can include but is not limited to assays (potencies

rate of release (dissolution)

and other various wet chemistry-based HPLC and/or GC based methods are commonly employed along with titrations

Enter data into established reports/templates or software-based systems.

Free ATS check

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