CQV Project Manager at PQE Group

Descripción del Puesto:

Última información laboral de PQE Group para la posición de CQV Project Manager. If the CQV Project Manager vacante en España coincide con tus calificaciones, envía tu solicitud o currículum directamente a través del portal actualizado de Jobkos.

Ten en cuenta que aplicar a un trabajo puede no ser siempre fácil, ya que los candidatos deben cumplir con ciertos requisitos establecidos por la empresa. Esperamos que esta oportunidad en PQE Group para la posición de CQV Project Manager se ajuste a tu perfil profesional.

Are you ready to join a world leader in the exciting and dynamic fields of the Pharmaceutical and Medical Device industries? PQE Group has been at the forefront of these industries since 1998 , with 40 subsidiaries and more than 2000 employees in Europe, Asia and the Americas.

We are currently seeking an experienced Commissioning, Qualification & Validation (CQV) Project Manager in León, España . This role will focus on the qualification and validation of equipment and systems in biotechnological production facilities .

Responsibilities include, but are not limited to:

• 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 .
• Review technical documentation , P&IDs , FAT/SAT protocols , and vendor manuals .
• Identify, troubleshoot , and document deviations , ensuring timely resolution .
• Ensure all activities meet GMP , FDA , EMA , and ICH requirements .
• Provide project updates and progress reports to stakeholders .

Required Qualifications:

• Bachelor’s degree in Engineering, Life Sciences , or related field.
• Proven experience in CQV for pharmaceutical/biotech facilities , including construction of production plants .
• Strong knowledge of GMP , FDA , and EU regulations .
• Experience in IQ/OQ/PQ protocol development and execution .
• Excellent analytical , problem-solving , and communication skills .
• Ability to work independently and collaboratively in a project environment .
• Fluent in English and Spanish (written and spoken ).

Sig Steps

Upon receiving your application, if a match is found, the Recruiting department will contact you for an initial HR interview.

If there's a positive match, a technical interview with the Hiring Manager will be arranged.

In the case of a positive outcome coming from Hiring Manager interview, recruiter will contact you for further steps or to discuss our proposal.

Alternatively, if the outcome is negative, we will contact you to halt the recruitment process.

Working at PQE Group

As a member of the PQE team, you will be part of a challenging, multicultural Empresa that values collaboration and innovation . PQE Group gives you the opportunity to work on international projects, improve your skills and interact with colleagues from all corners of the world.

If you are looking for a rewarding and exciting career, PQE Group is the perfect place for you.

Apply now and take the Primero step towards an amazing future with us.

Información de la Vacante:

• Empresa: PQE Group
• Puesto: CQV Project Manager
• Lugar de Trabajo: España
• País: ES

Cómo Enviar tu Postulación:

Después de leer y comprender los criterios y requisitos mínimos explicados en la información del trabajo CQV Project Manager at the office España anterior, completa de inmediato tus archivos de solicitud, como carta de presentación, CV (Hoja de Vida), copia de diploma y otros suplementos. Envía a través del enlace Siguiente Página abajo.