QA Intern: GMP & Regulatory Quality Systems

Ups; Málaga; Presencial; EUR 6700 - 10.000; A tiempo parcial

Descripción de la vacante

UPS in Málaga is seeking an Intern to monitor the overall Quality System status of the distribution center, ensuring compliance with GMP, drug and local regulations, and maintaining quality processes through procedures, training and inspections.

You will support SOP development, conduct inspections, assist with NCRs, change controls, and participate in audits with clients and regulators, gaining hands-on QA experience in a Fortune Global 500 environment.

Formación

• GMP familiarity with quality systems and procedures.
• Quality Assurance experience in relevant industries is preferred.
• Knowledge of regulatory requirements for pharmaceuticals/healthcare/food is a plus.
• QPIC/AQPIC designation is preferred.

Responsabilidades

• Ensures staff is trained in GMP and related procedures.
• Writes and revises Standard Operating Procedures as required.
• Conducts regular inspections and maintains records including findings and actions.
• Coordinates with clients and assists during external audits.
• Liaises with regulatory officials during audits where applicable.
• Supports QA questions and provides timely feedback to stakeholders.
• Monitors processes to ensure regulatory compliance and effective operation.
• Investigates discrepancies and initiates corrective actions as needed.
• Contributes to proactive quality improvement initiatives and change control processes.
• Completes NCR and change control documentation and follow-up.

Conocimientos

GMP training

Quality Assurance

Regulatory compliance

Auditing

Educación

Bachelor's degree in Science

Descripción del empleo

UPS in Málaga is seeking an Intern to monitor the overall Quality System status of the distribution center, ensuring compliance with GMP, drug and local regulations, and maintaining quality processes through procedures, training and inspections.

You will support SOP development, conduct inspections, assist with NCRs, change controls, and participate in audits with clients and regulators, gaining hands-on QA experience in a Fortune Global 500 environment.