CONSULTANT SENIOR F/H

Jordan martorell s.l.; Madrid, Barcelona; Presencial; EUR 40.000 - 60.000; Jornada completa

Descripción de la vacante

A leading company in pharmaceutical projects in Madrid is seeking a Commissioning & Qualification Engineer. This role includes supporting crucial qualification activities in pharmaceutical projects, ensuring compliance with GMP standards, and collaborating with diverse teams. The ideal candidate will hold a relevant bachelor's degree and have at least three years of experience in the field, being fluent in both English and Spanish.

Formación

• Three or more years of experience in Commissioning & Qualification within the pharmaceutical or biotech industry.

Responsabilidades

• Support commissioning and qualification activities for pharmaceutical facilities, utilities, and process equipment.
• Prepare and execute C&Q documentation.
• Collaborate with cross-functional teams to ensure compliance with project timelines.
• Participate in project meetings and provide updates on progress.

Conocimientos

Fluent in English and Spanish

Team collaboration

Educación

Bachelor’s degree in Engineering, Life Sciences, or a related field

Descripción del empleo

Overview

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 Commissioning & Qualification (C&Q) Engineer to support facility, utility, equipment, and system qualification activities in Barcelona and Madrid. The role involves ensuring compliance with GMP requirements, company standards, and regulatory guidelines while contributing to the successful delivery of pharmaceutical projects.

Responsibilities

• Support commissioning and qualification activities for pharmaceutical facilities, utilities, and process equipment.
• Prepare and execute C&Q documentation (URS, DQ, IQ, OQ, PQ protocols, test scripts, and summary reports).
• Collaborate with cross‑functional teams (Engineering, QA, Validation, Manufacturing) to ensure compliance with project timelines and regulatory requirements.
• Participate in project meetings and provide updates on progress, risks, and mitigations.

Qualifications

• Bachelor’s degree in Engineering, Life Sciences, or a related field.
• Three or more years of experience in Commissioning & Qualification within the pharmaceutical or biotech industry.
• Fluent in English and Spanish (written and spoken).

About PQE Group

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