Head of Analytical Quality Control

Placements24; Monterrey; On-site; MXN 700,000 - 1,000,000; Full time

Benefits offered by this job

Health, dental, and vision insurance

Retirement savings plans

On-site position in Monterrey

Training and development opportunities

Job summary

Placements24 seeks a Jefe de Control de Calidad Analítica to lead the analytical laboratory in Monterrey, ensuring rigorous testing for raw materials, in-process samples, and finished products. The role demands expertise in HPLC, GC, MS, spectroscopy, method development, and validation, with a strong GMP focus.

The successful candidate will supervise and train analysts, oversee CAPA processes, and ensure data integrity for regulatory compliance and product release in a fast-paced pharmaceutical

Qualifications

• Bachelor's or Master's degree in Chemistry, Pharmaceutical Sciences, or a related analytical science field.
• 6+ years in pharmaceutical analytical testing and quality control with at least 2 years in leadership.
• Expertise in HPLC, GC, UV-Vis, IR spectroscopy, and Mass Spectrometry.

Responsibilities

• Lead and manage the analytical quality control laboratory, ensuring efficient and compliant operations.
• Develop, validate, and implement analytical methods for raw materials, intermediates, and finished products.
• Oversee routine testing, stability studies, and release testing of pharmaceutical products.
• Ensure GMP, ICH guidelines, and other regulatory requirements.
• Manage laboratory equipment, including calibration, maintenance, and qualification.
• Supervise and mentor laboratory analysts to foster a high-performance team.

Skills

Laboratory leadership

Analytical testing

Regulatory compliance

Quality management

CAPA

Education

Bachelor's or Master's in Chemistry

Tools

HPLC

GC

Mass Spectrometry

Spectroscopy

Job description

Placements24 seeks a Jefe de Control de Calidad Analítica to lead the analytical laboratory in Monterrey, ensuring rigorous testing for raw materials, in-process samples, and finished products. The role demands expertise in HPLC, GC, MS, spectroscopy, method development, and validation, with a strong GMP focus.

The successful candidate will supervise and train analysts, oversee CAPA processes, and ensure data integrity for regulatory compliance and product release in a fast-paced pharmaceutical