Quality Manager (Pharmaceutical)

DHL Supply Chain; Cuautitlán Izcalli; Presencial; MXN 50,000 - 200,000; Jornada completa

Descripción de la vacante

A leading logistics company in Cuautitlán Izcalli is seeking a Quality Assurance Specialist to ensure compliance with regulatory standards in the pharmaceutical industry. Candidates should possess an education in a relevant field and demonstrate leadership and project management capabilities. Advanced English is essential. This role offers a dynamic work environment in a recognized Great Place to Work.

Formación

• Advanced English is essential.
• Familiarity with local and regional regulatory requirements applicable to medicines.
• Desirable: Experience in warehouses for medicines and medical devices.

Responsabilidades

• Maintain the Quality Management System (QMS).
• Implement work plans for regulatory compliance.
• Manage and administer projects effectively.
• Monitor environmental conditions and ensure instrument calibration.
• Execute and receive QMS audits from clients.

Conocimientos

Leadership capability

Project management

Customer service focus

Advanced English

Educación

Pharmaceutical Chemist

Biologist

Pharmacist

Industrial Pharmaceutical Chemist

Industrial Chemical Engineer

Descripción del empleo

Overview

As the world’s largest contract logistics specialist, we create a competitive advantage for our customers by giving them logistics solutions based on our globally standardized warehousing, transportation, and integrated services.

Our people is our biggest asset. We are certified as a Great Place to Work Company. In DHL you will find a culture that embraces diversity, collaboration; boost your strengths and generate confidence.

A world driven by logistic. A company driven by people!

Job Purpose

To ensure that all storage and distribution operations comply with quality standards and applicable regulations in the pharmaceutical industry, guaranteeing the safety and efficacy of products.

Key Responsibilities

• Maintain the Quality Management System (QMS), including CAPA’s, change controls, risk analysis, and document control.
• Implement work plans that clearly identify priorities and ensure regulatory compliance.
• Master problem-solving methodologies and process mapping.
• Effectively manage and administer projects.
• Review and approve quality agreements in compliance with regulations.
• Follow up on complaints and deviations, ensuring systemic corrective actions and timely effectiveness checks.
• Monitor environmental conditions (temperature/relative humidity) and ensure instrument calibration, as well as maintenance of validated status.
• Execute and receive QMS audits from clients and global organizations.
• Attend verification visits from the authority (COFEPRIS).

Who We Are Looking For

• Education: Pharmaceutical Chemist, Biologist, Industrial Pharmaceutical Chemist, Industrial Chemical Engineer, Pharmacist, or related field.
• Advanced English is essential.
• Familiarity with local and regional regulatory requirements applicable to medicines and medical devices (NOM 059, NOM 241, United Mexican States Pharmacopoeia, LGS, etc.) and ISO 9001
• Leadership capability, project management, development of high-performance teams, and a customer service focus.
• Desirable: Experience in warehouses for medicines and medical devices.