GMP Quality Specialist – Regulatory & Systems

United Parcel Service, Inc.; Ciudad de México; On-site; MXN 450,000 - 750,000; Full time

Job summary

United Parcel Service, Inc. is seeking a Permanent Quality Assurance Professional in Mexico City to monitor the distribution center's Quality System status and ensure compliance with drug, medical device, and local regulations.

You will train staff, write SOPs, perform inspections, and lead corrective actions to uphold GMP and regulatory standards in a fast-paced logistics environment.

Qualifications

• Bachelor’s Degree in Science related field (or internationally comparable degree) required.
• QPIC/AQPIC designation - Preferred.
• Quality Assurance experience - Preferred.

Responsibilities

• Monitors the overall Quality System status of the distribution center.
• Ensures quality processes are maintained through procedures, training, and inspections.
• Writes and revises Standard Operating Procedures as required.
• Conducts regular inspections and maintains records including reporting of findings.
• Coordinate or assist with corrective actions and preventative measures.
• Communicates with clients and provides information during external audits; liaises with Health Canada officials during regulatory audits.
• Provides feedback and assistance to QA-related questions and concerns.
• Monitors processes and systems to ensure regulatory compliance and effective operation.
• Investigates discrepancies and advises on findings.
• Assists in developing proactive strategies against potential future problems.
• Completes NCR reports and change control requests and follow-ups.
• Performs maintenance, support, and continuous improvements of Quality Systems.
• QPIC designation duties.

Skills

Quality Assurance

GMP

Regulatory compliance

Education

Bachelor's Degree in Science

QPIC/AQPIC designation

Job description

United Parcel Service, Inc. is seeking a Permanent Quality Assurance Professional in Mexico City to monitor the distribution center's Quality System status and ensure compliance with drug, medical device, and local regulations.

You will train staff, write SOPs, perform inspections, and lead corrective actions to uphold GMP and regulatory standards in a fast-paced logistics environment.