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Open nowPosted 23 days ago

CQV Manager

Hays (Schweiz) AG

Where
Visp, VS, Switzerland
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Your applicationOpen nowCQV ManagerHays (Schweiz) AG · Visp, VS, Switzerland

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  4. 21.8%14 days
  5. 36.6%30 days
  6. 58.9%60 days
This job: posted 23 days ago

The posting

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

Posting text belongs to the employer. Removal requests: contact us.

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