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Project Manager (French-speaking)

PQE Group

Madrid

Presencial

EUR 50.000 - 70.000

Jornada completa

Hace 2 días
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Descripción de la vacante

A multinational pharmaceutical company is seeking an experienced Commissioning, Qualification & Validation Project Manager in León, Spain. This role involves leading CQV activities for pharmaceutical equipment, preparing validation documentation, and collaborating with cross-functional teams to ensure compliance with GMP guidelines. Candidates should hold a Bachelor's degree in Engineering or Life Sciences and be fluent in English and Spanish. This position offers the opportunity to work on international projects and enhance skills in a dynamic environment.

Formación

  • Experience in commissioning, qualification, and validation of pharmaceutical equipment.
  • Ability to prepare and execute validation documentation.
  • Strong collaboration skills in a project environment.

Responsabilidades

  • Lead commissioning, qualification, and validation activities.
  • Prepare and review C&Q and validation documentation.
  • Collaborate with cross-functional teams for compliance.
  • Provide project updates to stakeholders.

Conocimientos

Leadership in commissioning and qualification
GMP compliance knowledge
Collaboration with cross-functional teams
Fluent in English
Fluent in Spanish

Educación

Bachelor’s degree in Engineering or Life Sciences
Descripción del empleo

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 an experienced Commissioning, Qualification & Validation (CQV) Project Manager in León, Spain.

Responsibilities
  • Lead and execute commissioning, qualification, and validation activities for pharmaceutical/biotech equipment and systems.
  • Prepare, review, and execute C&Q and validation 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 GMP regulatory guidelines, and project timelines.
  • Provide project updates and progress reports to stakeholders.
Qualifications
  • Bachelor’s degree in Engineering, Life Sciences, or related field.
  • Ability to work independently and collaboratively in a project environment.
  • Fluent in English and Spanish (written and spoken).

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

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