Physicochemical Analyst Chemist - 12-Month Project

Abbott; Soledad Atzompa; On-site; MXN 180,000 - 300,000; Full time

Job summary

Abbott in Mexico City seeks a Physicochemical Analyst Chemist to evaluate samples across raw materials, in-process and finished products, and stability studies using HPLC, GC, AA, and related equipment.

You will validate methods, develop SOPs, and support process validation and change controls. A Bachelor’s degree in Pharmaceutical Biochemistry or related field with 2+ years in pharma QA/analytical is required; rotating shifts and a 12-month assignment.

Qualifications

• 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 pharma or contract labs; QC, analytical development, and method validation.
• Experience with analytical lab instrumentation and software such as HPLC.
• Advanced English: technical level for reading methodologies.
• Knowledge of LC, GC, AA, LIMS, pharmacopoeias and their applications.
• Schedule includes rotating morning/evening shifts and a 12-month assignment.

Responsibilities

• Perform analyses using HPLC, GC, AA; analyze raw materials, in-process and finished products.
• Analyze purified water, rinse water, cleaning validation, and holding time samples.
• Analyze process validation, stability program samples, and holding time samples.
• Prepare statistical reports, calculations, and review results.
• Develop SOPs, method verifications, transfers, and change controls.
• Operate physicochemical control equipment and maintain documentation.

Skills

HPLC

Analytical chemistry

English - technical

Pharma QA/analytical

Education

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

Tools

HPLC

GC

AA (Atomic Absorption)

LIMS

Job description

Abbott in Mexico City seeks a Physicochemical Analyst Chemist to evaluate samples across raw materials, in-process and finished products, and stability studies using HPLC, GC, AA, and related equipment.

You will validate methods, develop SOPs, and support process validation and change controls. A Bachelor’s degree in Pharmaceutical Biochemistry or related field with 2+ years in pharma QA/analytical is required; rotating shifts and a 12-month assignment.