Physicochemical Analysis Chemist (Temporary Project) - CDMX Site

Abbott; Ciudad de México; Presencial; MXN 360.000 - 480.000; Jornada completa

Descripción de la vacante

Abbott seeks a Physicochemical Analyst Chemist in Mexico City for a 12‑month temporary project. You will evaluate samples (raw materials, in-process, finished products) via HPLC, GC, and AA, conduct validation activities, and support stability studies.

You will prepare reports, develop SOPs, and coordinate external lab testing while ensuring compliance with pharmacopoeias and quality standards.

Formación

• Bachelor's degree in Pharmaceutical Biochemistry (QFB), Pharmaceutical Chemistry (QFI), Pharmaceutical Engineering, or related field.
• Professional license required.
• Minimum 2 years of recent experience in pharmaceutical QA/QC analysis.
• Experience with analytical methods validation, verification, and transfers.
• Advanced English is mandatory.

Responsabilidades

• Perform analyses using HPLC, GC, AA to evaluate samples (raw materials, in-process, finished products).
• Analyze purified water, rinse water, and cleaning validation samples.
• Assess stability program samples and holding time samples.
• Prepare statistical reports and calculations; review results.
• Develop method verifications, transfers, and SOPs; update specs.
• Coordinate shipment of samples to third‑party labs; manage non-conformances.

Conocimientos

Advanced English

Educación

Pharma degree

Herramientas

HPLC

GC

AA

LIMS

Descripción del empleo

Physicochemical Analysis Chemist

About Abbott

Abbott is a global healthcare leader that creates breakthrough science to improve people's health. We are always looking toward the future, anticipating changes in medical science and technology.

Working at Abbott

At Abbott, you can do work that matters, grow and learn, care for yourself and your family, be your true self, and live a full life. You will have access to:

• Career development with an international company where you can grow the career of your dreams.

• A company recognized as one of the best large companies to work for, as well as a great workplace for diversity, working mothers, female executives, and scientists.

The Opportunity

This position is based in Mexico City within our Established Pharmaceuticals Operations Division , where we are committed to bringing the benefits of our trusted medicines to more people in some of the world's fastest-growing countries. Our broad portfolio of high-quality, differentiated branded generic medicines spans multiple therapeutic areas, including gastroenterology, women's health, cardiometabolic care, pain management/central nervous system, and respiratory health.

As a Physicochemical Analyst Chemist , you will perform activities such as evaluating the physicochemical conditions of samples including raw materials, process validation, cleaning validation, finished products, and stability studies. You will also execute analytical method validations, verifications, and transfers.

Required Qualifications

• Education: Bachelor's degree in Pharmaceutical Biochemistry (QFB), Pharmaceutical Chemistry (QFI), Pharmaceutical Engineering, or related field. Professional license required.

• Minimum 2 years of recent experience in pharmaceutical companies or contract laboratories analyzing pharmaceutical products, including:

• Quality Control (finished products, stability studies, and raw materials)

• Analytical Development

• Analytical Method Validation

• Experience with analytical laboratory instrumentation, equipment, and software such as HPLC , among others.

• Advanced English: MUST

• Knowledge of:

• Analytical laboratory instrumentation, equipment, and software

• Liquid and Gas Chromatography

• Atomic Absorption Spectroscopy

• LIMS

• Pharmacopoeias and their application

• Schedule: Availability to work rotating morning and evening shifts:

• Tuesday to Saturday: Morning and evening shifts

• Sunday to Thursday: Morning and evening shifts

• Saturday to Sunday: Morning shift

• 12-MONTH TEMPORARY PROJECT

What You'll Do

• Perform analyses using Liquid Chromatography (HPLC), Gas Chromatography (GC), Atomic Absorption Spectroscopy (AA) , and analyze raw materials, in-process products, and finished products.

• Conduct analyses of purified water, rinse water, cleaning validation samples, and holding time samples.

• Analyze process validation samples, stability program samples, and holding time samples.

• Prepare statistical reports, perform mathematical calculations, and review results.

• Develop stability protocols, method verifications, method transfers, and execute the respective analyses, including results reporting and technical reports.

• Prepare change controls for updating and implementing methods and specifications for raw materials and finished products.

• Demonstrate extensive experience in operating physicochemical control equipment such as HPLC, GC, spectrophotometers (including AA), and related laboratory instruments.

• Develop Standard Operating Procedures (SOPs) and equipment operation manuals.

• Coordinate the shipment of imported product samples, stability samples, and raw materials to authorized third-party laboratories for analysis.

• Manage non-conformances, LIRs, and CAPA action plans.

An Equal Opportunity Employer

Abbot welcomes and encourages diversity in our workforce.

We provide reasonable accommodation to qualified individuals with disabilities.

To request accommodation, please call 224-667-4913 or email [e-mail]