Tasks

- Provide leadership of CQV activities in assigned Projects
- Responsible for ensuring that CAPEX projects are compliant with global CQV guidelines
- Act as expert on internal CQV standards
- Keep oversight on CQV -standards, -timelines
- Address immediate time/quality constraints and act adequately
- Consider EHS requirements
- Development and delivery of CQV Documents as well as Commissioning Documents and QV-Documents

Qualifications

- Technical degree Bachelor’s or higher in engineering or applied science
- Profound experience in CQV, preferably (strong) CSV experience
- Familiarity with biologic as well as chemical manufacturing technologies
- Significant experience in qualification of biotech manufacturing lines
- Significant experience in regulated pharmaceutical industry
- Experience in leading leading large senior reports and great knowldedge of KPIs.
- Fluent English, German is an advantage