CQV Project Lead – Pharma/Biotech GMP & Validation

PQE Group; Madrid; Presencial; EUR 50.000 - 70.000; Jornada completa

Descripción de la vacante

A leading pharmaceutical company in León, Spain, seeks an experienced CQV Project Manager to lead commissioning, qualification, and validation activities for pharmaceutical and biotech systems. The ideal candidate will possess a relevant Bachelor's degree and proven experience in CQV. Strong knowledge of GMP and FDA regulations is essential, as is fluency in English and Spanish. Join to work on international projects and develop your skills in a rewarding environment.

Servicios

International project opportunities

Skill development

Formación

• Bachelor's degree in Engineering, Life Sciences, or a related field.
• Proven experience in CQV for pharmaceutical / biotech facilities.
• Strong knowledge of GMP, FDA, and EU regulations.

Responsabilidades

• Lead commissioning and validation activities for pharmaceutical equipment.
• Prepare and review C&Q documentation like URS, DQ, IQ, OQ, PQ.
• Collaborate with teams to ensure compliance with regulatory guidelines.

Conocimientos

Fluent in English and Spanish

Analytical skills

Problem-solving

Communication skills

Educación

Bachelor’s degree in Engineering or Life Sciences

Descripción del empleo

A leading pharmaceutical company in León, Spain, seeks an experienced CQV Project Manager to lead commissioning, qualification, and validation activities for pharmaceutical and biotech systems. The ideal candidate will possess a relevant Bachelor's degree and proven experience in CQV. Strong knowledge of GMP and FDA regulations is essential, as is fluency in English and Spanish. Join to work on international projects and develop your skills in a rewarding environment.