Finished Product & Stability Chemist (9-Month)

Abbott Laboratories; Ciudad de México; Híbrido; MXN 280.000 - 420.000; Jornada completa

Descripción de la vacante

Abbott Laboratories in Mexico City is seeking a Finished Product & Stability Analyst Chemist for a 9-month project. The role focuses on evaluating finished product and stability samples using validated analytical methods, including HPLC and dissolution testing, within a GLP/GMP framework.

You will prepare and transfer test methods, generate reports, and support method validation activities. The ideal candidate has 3+ years of QC/analytical chemistry experience, advanced technical English, and

Formación

• Bachelor's degree in pharmaceutical sciences or related field with professional license preferred.
• Minimum 3 years as an Analyst Chemist in physicochemical QC, finished product testing, and stability studies.
• Experience with HPLC and dissolution testing required; strong English skills.

Responsabilidades

• Receive and analyze in-process products, finished products, stability samples, and special analyses.
• Prepare solutions and execute method validations, verifications, and transfers.
• Report results per procedures and GMP requirements; issue validation/verification reports.
• Conduct self-training on SOP updates; prepare LIRs and ERs as needed.

Conocimientos

Analytical method validation

Analytical method verification

Test Method Transfer (TMT)

HPLC analysis

Dissolution testing

Quality control

Analytical instrumentation

Laboratory software

Advanced English

Educación

Bachelor’s degree in Pharmaceutical Chemistry (QFB)

Industrial Pharmaceutical Chemist (QFI)

Biology or related disciplines

Professional license preferred

Herramientas

Laboratory equipment

Analytical software

Descripción del empleo

Abbott Laboratories in Mexico City is seeking a Finished Product & Stability Analyst Chemist for a 9-month project. The role focuses on evaluating finished product and stability samples using validated analytical methods, including HPLC and dissolution testing, within a GLP/GMP framework.

You will prepare and transfer test methods, generate reports, and support method validation activities. The ideal candidate has 3+ years of QC/analytical chemistry experience, advanced technical English, and