CQV Manager (m/f/d)

Our many years of recruitment experience and our expert knowledge of the engineering job market make us a strong partner for engineers and technicians. We maintain close relationships with customers across all industries and therefore can provide engineering specialists with exciting projects and attractive job opportunities, drawing on your personal interests and experience. As your professional companion, we support you throughout the entire process, from the first contact to the first day on your new job – all this completely free of charge. Register now and look forward to many interesting and suitable positions and projects.

• 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

• 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

Ihr Kontakt

Referenznummer
897996/1

Kontakt aufnehmen
Telefon:+41 44 225 50 00
E-Mail: positionen@hays.ch

Anstellungsart
Freiberuflich für ein Projekt