CQV Manager (m/f/d)

Project overview

CQV Manager (m/f/d)

Reference: 95160bc5-bb4b-48ef-9457-c300bd2d8544

Responsibilities

• Lead and manage CQV (Commissioning, Qualification & Validation) activities across large-scale CAPEX projects in a GMP-regulated pharmaceutical environment
• Develop and implement CQV strategies to ensure successful project delivery and regulatory compliance
• Oversee project planning, resource allocation, budgets, timelines and execution of CQV workstreams
• Manage internal and external CQV teams, contractors and project stakeholders
• Collaborate with Engineering, Manufacturing, Quality and Regulatory teams throughout the project lifecycle
• Identify, assess and mitigate project risks affecting CQV deliverables
• Drive execution of qualification and validation activities in line with corporate and industry standards
• Provide technical leadership and guidance on CQV best practices
• Support continuous improvement of CQV processes, methodologies and standards
• Ensure projects are delivered on time, within budget and in full compliance with GMP requirements

Requirements

Main advantages:

• Master's degree in Engineering, Pharmaceutical Sciences, Life Sciences or a related field
• Well-founded experience within Pharmaceutical, Biotech or Life Sciences environments
• Proven experience leading CQV activities on large CAPEX projects
• Strong background in Project Management, Commissioning, Qualification and Validation
• Demonstrated experience managing resources, budgets, schedules and project risks
• Experience leading cross-functional teams and complex stakeholder environments
• Strong understanding of GMP, cGMP and pharmaceutical manufacturing processes
• Fill & Finish experience is highly desirable
• NEAT experience required, DeltaV knowledge is an advantage
• Fluent English required, German is a strong advantage
• Opportunity to lead strategic pharmaceutical CAPEX investments with global impact
• High-visibility role within a complex and challenging project environment
• Leadership responsibility across international and multidisciplinary teams
• Exposure to large-scale GMP manufacturing and infrastructure projects
• Long-term planned project perspective with extension potential
• Opportunity to influence CQV strategy, standards and execution excellence
• Collaborative environment with global stakeholders
• Involvement in cutting-edge pharmaceutical manufacturing initiatives
• Professional growth within a highly regulated and innovative industry

Project details

asap

12 MM++

• Start: ab sofort
• Duration: 12 Monate
• Remote: onsite
• Location: Visp, Schweiz, CH
• Languages: English, German

Source notes

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