hirly

Abbott

Physicochemical Analysis Chemist (Temporary Project) - CDMX Site

Mexico - Cuidad de Mexico - Cuidad de Mexico

See how you match this job — and similar ones. Free.

Upload your resume and hirly scores it against this role at Abbott first, then against similar open jobs, and shows where you fit and why.

PDF or DOCX, up to 12MB. No sign-up to see your matches.

Get past the screening software and onto a recruiter's desk

hirly rewrites your resume for this job — matching the keywords and skills in the posting, moving your most relevant experience to the top, and writing a cover letter to fit. About 30 seconds.

  • Keywords matched to this posting
  • Fit score before you apply
  • Cover letter included

Matched against 2.3M live jobs from 200,000+ employers in 200+ countries.

Tailor my resume for this job →

hirly's read of this role

Seniority
Mid level
Country
MX
Work mode
On-site / unstated
First seen by hirly
27 Sept 2026

Derived automatically from the posting. Upload your resume above to see how the role scores against it.

the posting

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.

Apply Now

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

Original posting on Abbott's site ↗

Want this one?

Upload your resume and hirly rewrites it for this job and writes the cover letter — in about thirty seconds, before you sign up.

Tailor my resume for this job