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QUALITY ASSURANCE TRAINEE

Novartis

Zaragoza

Presencial

EUR 30.000 - 50.000

Jornada completa

Hace 30+ días

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Descripción de la vacante

A multinational pharmaceutical company in Zaragoza is seeking a Quality Assurance trainee to provide support in various quality assurance functions. The role includes receiving training in multiple departments, assisting in documentation preparation, and contributing to quality management processes. The ideal candidate will gain insight into GMP practices and quality systems while working collaboratively with the QA team. This is a full-time internship position ideal for recent graduates or individuals entering the field.

Formación

  • Intern position with exposure to various quality assurance activities and processes.
  • Responsible for assisting in the review of batch manufacturing records.
  • Must understand GMP Good Aseptic practices and data integrity principles.

Responsabilidades

  • Receive training in the QA department and understand departmental interactions.
  • Support documentation preparation, issuance, and archiving.
  • Assist in managing events and deviations while supporting quality systems.

Conocimientos

Digital Electronics
Account Management
Corporate Risk Management
Law
Courier Delivery
Descripción del empleo
Job Description Summary

The Quality Assurance trainee will receive training in the QA department as well as in other departments to capture the overview of the organization. The learning process will not be limited to individual departments but will extend to understand how these various departments interact and function collaboratively. The Quality Assurance trainee will learn how a Quality team from a manufacturing site operates and will support Standard Operating Procedures (SOPs) Documents Batch Record APQR review among other activities and contribute actively to team activities and projects.

Job Description
  • Internal / external training in GMP Good Aseptic practices and Data integrity.
  • Support the preparation, issuance and archiving of controlled documents (SOPs, work instructions, forms). Ensure documentation is accurate, complete and compliant with data integrity principles (ALCOA).
  • Assist in review of batch manufacturing records issuance and review (and supporting documents under supervision).
  • Events management training including deviations, CAPAs and change controls.
  • Support the implementation and maintenance of quality management systems in line with internal and regulatory requirements.
  • Support the Material / supplier qualification process.
Skills Desired

Required Experience: Intern

Key Skills
  • Digital Electronics
  • Account Management
  • Corporate Risk Management
  • Law
  • Courier Delivery
Employment Details
  • Employment Type: Full-Time
  • Experience: 0 years
  • Vacancy: 1
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