Join a major pharmaceutical manufacturing expansion project in Switzerland as a CQV Manager . Lead Commissioning, Qualification & Validation (CQV) activities for a large-scale CAPEX program in a highly regulated environment.
Key Responsibilities:
- Develop and execute CQV strategies aligned with GMP/cGMP standards.
- Oversee multidisciplinary teams , contractors, and stakeholders to ensure project success.
- Manage planning, resources, timelines, and risk mitigation for validation deliverables.
- Collaborate with Engineering, Manufacturing, Quality, and Project Management teams.
- Drive continuous improvement and best practices in CQV.
Your Profile:
- MSc/Bachelor’s in Engineering, Pharmaceutical Sciences , or related field.
- Extensive experience (5+ years) in CQV, Validation, Engineering, or Project Management (pharma/biotech).
- Strong GMP/cGMP knowledge, CAPEX project experience, and leadership in CQV/Validation roles .
- Fluent English (required); German (advantage).
- Knowledge on sterile manufacturing, Fill & Finish, DeltaV, or NEAT environments are a plus.
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CQV Manager in Wallis Arbeitgeber: Alten
ALTEN ist ein hervorragender Arbeitgeber, der dir als Werkstudent im Projektmanagement am Standort Berlin die Möglichkeit bietet, praktische Erfahrungen in einem dynamischen Umfeld zu sammeln. Unsere offene und inklusive Unternehmenskultur fördert die persönliche und berufliche Entwicklung, während du an innovativen Projekten in der Luftfahrtbranche mitarbeitest. Zudem profitierst du von flexiblen Arbeitszeiten und der Chance, mit internationalen Teams zusammenzuarbeiten, was deine Karrierechancen erheblich steigert.
