Finished Product & Stability Analyst Chemist (Temporary Project)- CDMX Site

Abbott; Ciudad de México; Híbrido; MXN 180.000 - 240.000; Jornada completa

Descripción de la vacante

Abbott is seeking a Finished Product & Stability Analyst Chemist for a 9-month temporary project in Mexico City. You will perform analyses on in-process products, finished products, and stability samples, and support method validation and transfers.

The role requires a chemistry degree, hands-on experience with HPLC, and strong English skills. You will work with Quality teams to ensure GMP compliance and timely reporting, with shift options in the afternoon/evening.

Formación

• Bachelor's degree in Pharmaceutical Chemistry or related field; license preferred.
• Minimum 3 years as an Analyst Chemist in QC, finished product testing, or stability studies.
• Experience with HPLC and dissolution testing.
• Advanced English required (written and spoken).
• Strong teamwork and collaboration skills.

Responsabilidades

• Receive and perform analyses of in-process products, finished products, and stability samples.
• Prepare solutions, validate methods, and support transfers.
• Document results per GMP procedures and generate reports.

Conocimientos

Advanced technical English

Strong teamwork

Shift availability

Educación

Bachelor's degree in Pharmaceutical/ related

Professional license preferred

Related scientific disciplines

Herramientas

HPLC

Dissolution testing

Laboratory software

Descripción del empleo

Finished Product & Stability Analyst Chemist (TEMPORARY PROJECT: 9-MONTH ASSIGNMENT)

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 meaningful work, grow and learn, care for yourself and your family, be your authentic self, and live a full life. You will have access to:

• Professional development with an international company where you can grow the career you aspire to.
• Benefits above those required by law.
• A company recognized as a great place to work in dozens of countries worldwide and named one of Fortune's Most Admired Companies.
• A company recognized as one of the best large employers, as well as a top workplace for diversity, working mothers, women leaders, and scientists.

The Opportunity

This position is located in Tlalpan, Mexico City , within the Established Pharmaceuticals Division (EPD). We are committed to bringing the benefits of our trusted medicines to more people in some of the world's fastest-growing markets. 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.

What You'll Do

• Receive and perform analyses of in-process products, locally manufactured and imported finished products, long-term stability samples, accelerated stability samples, and special analyses.
• Prepare analytical solutions used for testing and execute analytical method validations, co-validations, verifications, and transfers.
• Report analytical results obtained from testing activities in accordance with established procedures and current GMP requirements.
• Prepare and/or issue protocols and reports related to method validation, method verification, and analytical method transfers (Test Method Transfer).
• Complete self-training on updates to operating procedures and manuals.
• Conduct laboratory investigations and prepare Laboratory Investigation Reports (LIRs) and Exception Reports (ERs).

Required Qualifications

• Bachelor's Degree in: Pharmaceutical Chemist Biologist (QFB)
• Industrial Pharmaceutical Chemist (QFI)
• Related scientific disciplines
• Degree completed and professional license preferred.
• Minimum 3 years of recent experience as an Analyst Chemist in:
• Physicochemical Quality Control
• Finished Product Testing
• Stability Studies
• HPLC Analysis
• Dissolution Testing
• Advanced technical English, both written and spoken. MUST
• Experience in Quality Control, including finished product and stability testing.
• Strong knowledge and hands‑on experience with analytical instrumentation, laboratory equipment, and analytical laboratory software.
• Strong teamwork and collaboration skills.
• Availability to work: Tuesday through Saturday (1:30 PM - 9:30 PM), or Wednesday through Sunday (1:30 PM - 9:30 PM)

Preferred Qualifications

• Analytical method development.
• Analytical method validation.
• Knowledge and use of national and international medical and pharmaceutical literature.
• Strong analytical and problem‑solving skills.

Abbott is an Equal Opportunity Employer, committed to employee diversity.

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 : Remote

WORK SHIFT: Standard

TRAVEL: Not specified

MEDICAL SURVEILLANCE: Not Applicable

SIGNIFICANT WORK ACTIVITIES: Not Applicable