Analista Químico - Validación Analítica GMP

Pfizer Inc; Toluca; On-site; MXN 420,000 - 550,000; Full time

Job summary

Pfizer is seeking a method validation specialist to support analytical method validation, verification, and transfer in a GMP environment. You will prepare samples, calibrations, and documentation while ensuring data integrity and compliant records.

Responsibilities include instrument readiness checks, data review, and supporting investigations, deviations, and change controls across cross‑functional teams. A chemistry background and strong communication are required for success.

Qualifications

• Bachelor's degree in Chemistry or related scientific discipline with GMP‑regulated lab experience.
• Experience supporting analytical method validation, verification, transfer, or lifecycle activities.
• Ability to interpret validation/protocols, compendial procedures, and regulatory expectations.
• Working knowledge of GMP, GLP, data integrity, and lab documentation requirements.
• Ability to organize validation activities, manage multiple priorities, and maintain inspection‑ready records.
• Strong written and verbal communication skills for technical results and cross‑functional reporting.
• Proficiency with laboratory instruments and systems used for method validation/verification.

Responsibilities

• Plan and execute analytical method validation activities for chemical/physicochemical methods.
• Prepare samples, standards, reagents, and documentation for validation studies.
• Verify instrument readiness, calibration, and system suitability before testing.
• Document and report validation results in computerized systems; support approvals and audits.
• Support investigations, deviations, change controls, and lifecycle management of analytical methods.

Skills

Analytical validation

GMP knowledge

Data integrity

Documentation skills

Cross-functional communication

Instrument proficiency

Education

Bachelor's degree in Chemistry or related science

Relevant GMP laboratory experience

Tools

Chromatography data systems

gLIMS

Electronic lab notebooks

Document management systems

Quality management systems

Job description

Pfizer is seeking a method validation specialist to support analytical method validation, verification, and transfer in a GMP environment. You will prepare samples, calibrations, and documentation while ensuring data integrity and compliant records.

Responsibilities include instrument readiness checks, data review, and supporting investigations, deviations, and change controls across cross‑functional teams. A chemistry background and strong communication are required for success.