Physicochemical Analysis Chemist (Temporary Project) - Cdmx Site

Abbott

Soledad Atzompa

Presencial

MXN 420.000 - 660.000

Jornada completa

14 días+

Una candidatura completa en un minuto

Currículum y carta de presentación personalizados, listos para enviar.

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Descripción de la vacante

Abbott is seeking a Physicochemical Analyst Chemist in Mexico City for a 12-month assignment within Established Pharmaceuticals Operations Division. You will perform analyses on raw materials, intermediates, and finished products using HPLC, GC, and AA, and support method transfers and validation.

You will work with analytical instrumentation, develop SOPs, and coordinate external testing while handling non-conformances and CAPA. Strong English and pharmaceutical knowledge are required.

Formación

  • Bachelor’s degree in Pharmaceutical Biochemistry (QFB), Pharmaceutical Chemistry (QFI), Pharmaceutical Engineering, or related field.
  • Minimum 2 years of recent experience in pharma companies or contract laboratories analyzing pharmaceutical products.
  • Experience with analytical lab instrumentation such as HPLC, GC, AA among others.
  • Technical English to read analytical methodologies.
  • Knowledge of analytical lab instrumentation, chromatography, LIMS, pharmacopoeias.
  • Schedule with rotating morning/evening shifts.
  • Temporary project: 12-month assignment.

Responsabilidades

  • Perform analyses using HPLC, GC, AA on raw materials, in-process and finished products.
  • Analyze purified water, rinse water, cleaning validation samples, and holding time samples.
  • Analyze process validation, stability program, and holding time samples.
  • Prepare statistical reports and technical reports of results.
  • Develop SOPs and method verifications, transfers, and change controls.
  • Coordinate shipment of samples to third-party labs for analysis.
  • Manage non-conformances, LIRs and CAPA action plans.

Conocimientos

Advanced English

Educación

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

Herramientas

HPLC
Gas Chromatography (GC)
Atomic Absorption Spectroscopy (AA)
LIMS

Descripción del empleo

JOB DESCRIPTION:

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: Technical level with the ability to read and understand analytical methodologies.
  • 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
  • TEMPORARY PROJECT: 12-MONTH ASSIGNMENT

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.

Pursue your career aspirations with Abbott and explore diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer committed to employee diversity.

Connect with us at www.abbott.com, on Facebook at www.facebook.com/Abbott, and on Twitter/X at @AbbottNews and @AbbottGlobal.

The base pay for this position is

N/A

In specific locations, the pay range may vary from the range posted.

JOB FAMILY:

Operations Quality

DIVISION:

EPD Established Pharma

LOCATION:

Mexico > Mexico City : Tlalpan

ADDITIONAL LOCATIONS:
WORK SHIFT:

Standard

TRAVEL:

Yes, 10 % of the Time

MEDICAL SURVEILLANCE:

Not Applicable

SIGNIFICANT WORK ACTIVITIES:

Not Applicable

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