GMP Chemist, HPLC/UPLC Method Support (Foundry)

100 Eli Lilly and Company; Lebanon (IN); Presencial; USD 66.000 - 172.000; Jornada completa

Descripción de la vacante

Initial location in Carmel, IN with permanent placement at the Lilly Medicines Foundry in Lebanon, Indiana. The role is onsite only in a GMP laboratory and focuses on routine testing, method development, qualification, and validation for multiple modalities.

Qualified candidates will have HPLC/UPLC experience, strong data integrity awareness, and the ability to collaborate with Manufacturing and Quality teams to ensure timely equipment release and compliant documentation.

Formación

• B.S. in Analytical Chemistry or a closely related STEM field with 2+ years of lab experience, or M.S. with 1+ year of lab experience.
• Hands‑on experience with HPLC/UPLC with UV detection, including sample prep, instrument operation, and data processing.
• GMP laboratory environment experience, with knowledge of cGMP, data integrity principles, and good documentation practices.

Responsabilidades

• Perform routine GMP testing of swab and rinse samples using HPLC/UPLC with UV detection to support timely equipment release.
• Support development, qualification, and validation of analytical methods for residue analysis across multiple modalities.
• Execute swab and rinse recovery studies and evaluate method performance (sensitivity, linearity, accuracy, precision, specificity).
• Operate, maintain, and troubleshoot HPLC/UPLC instrumentation and chromatographic methods.
• Document work accurately in compliance with cGMP and data integrity and assist with procedures, protocols, and reports.

Conocimientos

HPLC/UPLC operation

GMP laboratory practices

Data review & reporting

Educación

B.S. in Analytical Chemistry or related STEM

M.S. in Analytical Chemistry or related STEM

Herramientas

Empower CDS

LC-MS

SOP documentation

Descripción del empleo

Initial location in Carmel, IN with permanent placement at the Lilly Medicines Foundry in Lebanon, Indiana. The role is onsite only in a GMP laboratory and focuses on routine testing, method development, qualification, and validation for multiple modalities.

Qualified candidates will have HPLC/UPLC experience, strong data integrity awareness, and the ability to collaborate with Manufacturing and Quality teams to ensure timely equipment release and compliant documentation.