QA Specialist-2

UPS; Santiago; Presencial; CLP 6.000.000 - 8.000.000; Jornada completa

Descripción de la vacante

UPS is seeking a QA professional to monitor the distribution center's Quality System status, ensure compliance with drug and medical device regulations, and lead procedures, training, and inspections. The role includes QPIC duties and collaboration with auditors and clients.

The candidate will oversee NCRs, change controls, and continuous improvement of Quality Systems, participating in regulatory audits and ensuring regulatory compliance across processes.

Formación

• Pharmaceutical, mandatory.
• Bachelor’s Degree in Science related field (or internationally comparable degree) required - Preferred.

Responsabilidades

• Ensure staff are trained in GMP and Quality procedures.
• Write and revise Standard Operating Procedures (SOPs).
• Conduct facility inspections and recordkeeping; coordinate corrective actions.
• Communicate with clients during external audits and regulatory audits with Health Canada involvement.
• Provide QA support and respond to questions and concerns.

Conocimientos

GMP knowledge

Quality systems

Regulatory compliance

Auditing

Educación

Bachelor's degree in Science

Descripción del empleo

Explore your next opportunity at a Fortune Global 500 organization. Envision innovative possibilities, experience our rewarding culture, and work with talented teams that help you become better every day. We know what it takes to lead UPS into tomorrow—people with a unique combination of skill + passion. If you have the qualities and drive to lead yourself or teams, there are roles ready to cultivate your skills and take you to the next level.

Job Description

Job Summary

This position monitors the overall Quality System status of the distribution center. This position acts in compliance to drug, medical device, and local regulations. Ensures quality processes are maintained through the implementation of procedures, training, and regular inspections.

Responsibilities

• Ensures all staff is trained in their respective job functions, including GMP.
• Writes and revises Standard Operating Procedures as required.
• Conducts regular inspections of the facility and recordkeeping, including summarization and 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 Customer/Client QA related questions and concerns.
• Monitors the processes and systems within the Department to ensure regulatory compliance and effective operation.
• Investigates discrepancies and problems, and advise the appropriate individuals of the findings.
• Assists in development of pro‑active strategies as a preemptive measure against potential future problems with systems or processes.
• Completes NCR reports and change control requests and provide necessary follow-up.
• Performs maintenance, support, and continuous improvements of Quality Systems.
• QPIC designation duties.

Qualifications

Pharmaceutical, mandatory

Quality Assurance Experience - Preferred

Bachelor’s Degree in Science related field (or internationally comparable degree) required - Preferred

Employee Type

• QPIC/AQPIC designation - Preferred
• Fixed Term (duración determinada)

UPS is committed to providing a workplace free of discrimination, harassment, and retaliation.