Quality Assurance Specialist (Hybrid)

Are you ready to join a world leader in the exciting and dynamic fields of the Pharmaceutical and Medical Device industries? We are currently seeking a dedicated and motivated Quality Control & Quality Assurance Specialist to support a major pharmaceutical project focused on quality control and quality assurance activities within a GxP-regulated environment.

The consultant will work onsite in Madrid until February, directly involved in operational and documentation-related tasks, and will then continue in hybrid mode from our headquarters or remotely.

❗ Full onsite until February 2026 for this project's duration; hybrid mode following that (remote and / or from our main office)

Execute, review, and coordinate all quality control activities related to the microbiological qualification of classified areas .

Contribute to the implementation and validation of computerized systems within the ongoing project.

Collaborate with technical and QA teams to ensure full alignment with established quality procedures.

Minimum of 2 years of experience in Quality Control, Quality Assurance, or Validation roles within the pharmaceutical or biotech industry .

Fluent Spanish and good command of technical English are required.

PQE Group gives you the opportunity to work on international projects, improve your skills and interact with colleagues from all corners of the world.