Physicochemical Analysis Chemist – HPLC/GC Specialist

Thornton Tomasetti; Ciudad de México; Presencial; MXN 420.000 - 700.000; Jornada completa

Descripción de la vacante

Abbott is seeking a Physicochemical Analysis Chemist based in Mexico City. The role focuses on evaluating physicochemical conditions for materials, process and cleaning validation, and stability studies, using methods like HPLC, GC, and AA.

The candidate will conduct method validations, transfers, and report results while developing SOPs and supporting quality initiatives within the Established Pharmaceuticals Operations Division. Fluency in technical English is required.

Formación

• Bachelor's degree in Pharmaceutical Biochemistry (QFB) or Pharmaceutical Chemistry (QFI) or Pharmaceutical Engineering; professional license required.
• Minimum 2 years of experience in analyzing pharmaceutical products (quality control, stability studies, raw materials).
• Knowledge of analytical instrumentation and software; ability to read/understand analytical methodologies.

Responsabilidades

• Perform analyses using HPLC, GC, and AA; analyze raw materials, in-process, and finished products.
• Analyze purified water, rinse water, cleaning validation, and holding time samples.
• Analyze process validation and stability program samples; prepare reports and technical documentation.
• Develop SOPs and instruction manuals; coordinate method transfers and validations.
• Coordinate shipment of samples to third-party labs; manage non-conformances and CAPA actions.

Conocimientos

Advanced English

Analytical methods knowledge

Educación

Bachelor's degree in Pharmaceutical Biochemistry (QFB) or Pharmaceutical Chemistry (QFI) or Pharmaceutical Engineering

Herramientas

HPLC

GC

AA

LIMS

Pharmacopoeias

Descripción del empleo

Abbott is seeking a Physicochemical Analysis Chemist based in Mexico City. The role focuses on evaluating physicochemical conditions for materials, process and cleaning validation, and stability studies, using methods like HPLC, GC, and AA.

The candidate will conduct method validations, transfers, and report results while developing SOPs and supporting quality initiatives within the Established Pharmaceuticals Operations Division. Fluency in technical English is required.