We are currently seeking an experienced CQ Manager for a contract position based in Visp, Switzerland. This role is crucial within the pharmaceutical manufacturing sector and involves developing global standard operating procedures across all facilities.
Key Responsibilities:
- Develop Level 2 and 3 C&Q (Commissioning & Qualification) Schedule
- Execution Readiness
- Document Preparation management and coordination
- C&Q execution management and coordination
- Resource management including C&Q Doc Prep and C&Q Exec
- Oversight of FATs (Factory Acceptance Tests) and SATs (Site Acceptance Tests)
- Execution of onsite C&Q test cases
- Maintain C&Q input to level 4 schedule and cost report
- Coordinate with Ops regarding PQ (Performance Qualification) and engineering runs
- Adherence to safety, compliance and quality procedures
- Progress tracking and monthly report
- System CFR (Commissioning Final Report) / QFR (Qualification Final Report)
- Complete System Handover
- Technical support for Clean Utilities PQ 1 and EM (Environmental Monitoring) PQ 1
- C&Q Close Out (QFR) Participation as SME during Authority Inspection and audits
- Control Training status of C&Q team
Necessary Skills:
- Minimum 10 years of experience in C&Q and project management
- Similar previous positions in a growth project environment (>50mCHF)
- Fluent in English, German is an advantage
For further information about this position, please apply with your CV
*Please note, only those with the right to work in Switzerland or EU passport holders can apply!*
