CQV Manager

Stellenbeschreibung

# CQV Manager # (m/f/d) Freelance/temporary employment for a project Visp Start date: asap Reference number: 897996/1 ### 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 ### Profile ### * 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 ### Benefits ### * 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