Pfizer Tecnico garantia de Calidad (Temp hasta noviembre) in Algete, Spain

Reporting to the Quality Assurance responsible, the incumbent will work with internal stakeholders managing all or part of the following Quality Systems: Change control, Quality agreements; Annual Product Quality review; Cold Chain; Documentation, Validation, Investigations; Quality Risk Management. An important part of the position is continuous improvement of the Quality Systems and the processes associated using OpEX methodologies.


Manage routine Quality systems: Change Control, APQR, Quality Agreement, Documentation and Investigations (laboratory and manufacturing). Review and approve equipment, process and utilities validation documentation. Review and participate in Quality Risk Management process Develop internal procedures and implement process improvements Ensure compliant site Quality Systems. Assist during regulatory inspection as requested by Management. Apply Lean Tools to the daily operations


  • University degree in pharmaceutical science, biology, chemistry, or related science.

  • 1 year in a Quality role in the pharmaceutical industry, preferably with different functions including Quality, Manufacturing, Regulatory and laboratory is desired

  • Working knowledge of English is required (fluent)

  • Familiarity with computer systems QTS, PDOCS, SAP

Other requirements

  • Problem solving ability (ability to recognize symptoms of problems or situations that require further evaluation, analyze symptoms to determine potential causes, suggest possible corrective actions)

  • Ability to work independently

  • Ability to collaborate with cross-functional groups

  • Knowledge in process and equipment validation will be well valued.

Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.