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Process & cleaning validation consultant

Manresa
PQE Group
Publicada el Publicado hace 12 hr horas
Descripción

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.

Experiencia, cualificaciones y habilidades interpersonales, ¿tiene todo lo necesario para triunfar en esta oportunidad? Descúbralo a continuación.

We are currently looking for a Process & Cleaning Validation Specialist with solid experience in pharmaceutical validation activities. The selected consultant will be involved in validation lifecycle management, supporting both routine operations and project-related activities within a GMP-regulated environment.

!! Please note: for the first year, the role requires 100% on-site presence in El Masnou .

Responsibilities include, but are not limited to:

* Execute and coordinate process validation and cleaning validation activities in compliance with GMP requirements
* Draft, review, and approve validation documentation, including validation protocols, risk assessments, reports, SOPs, and related supporting documents
* Support validation lifecycle activities from planning through execution and final closure
* Collaborate with Production, QA, QC, and Engineering teams to ensure timely project execution
* Support investigations related to deviations, non-conformities, and change controls
* Ensure compliance with internal quality standards and applicable international regulatory requirements
* Participate in continuous improvement initiatives related to manufacturing and validation processes

Required Qualifications:

* At least 2 years of proven experience in Process Validation and Cleaning Validation within the pharmaceutical or biotechnology industry
* Experience in thermal sterilization processes will be considered a strong advantage
* Good knowledge of GMP regulations and validation requirements
* Experience working in manufacturing environments under strict quality standards
* Strong technical writing and documentation skills
* Ability to work autonomously and manage priorities in a dynamic environment
* Fluent in English and Spanish
* Salary starting from €32,000 gross per year

Next Steps

After receiving your application, if a match is identified, our Recruitment team will contact you for an initial HR interview.

If successful, a technical interview with the Hiring Manager will be scheduled.

In the event of a positive outcome, the recruiter will contact you to discuss the next steps or our offer.

If the outcome is negative, we will inform you accordingly and conclude the recruitment process.

Working at PQE Group

As part of the PQE team, you will join a challenging and multicultural company that values collaboration and innovation. xqysrnh PQE Group offers the opportunity to work on international projects, develop your skills, and collaborate with colleagues from all over the world.

If you are looking for a rewarding and exciting career, PQE Group could be the right place for you.

Apply now and take the first step toward an exciting future with us.

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