Beschreibung
Duration: 6-12 monthsLocation: Canton Zurich, Switzerland.
Our Global Medical Device client is looking for an experienced Project Manager CAPA to support their compliance improvement project on site.
This role will be part of a wider quality improvement project being carried out across all QA work streams to drive regulatory compliance to an outstanding level.
Key Responsibilities:
• Create project plans
• Attend project meetings
• Lead sub-project leaders
• Tracking and reporting of projects
• Represent and report projects in Reviews and Audits
• Oversee the team working with CAPAs
Requirements
• Experience in Project Management
• Experience in dealing with CAPAs
• The position requires a sound technical background (technical degree or equivalent)
• In-depth experience within the Medical Device or Pharma industry
• Knowledge of regulatory requirements for key quality system elements (ISO 13485:2012 and 21 CFR 820)
• Experience working both independently and in a team-oriented, collaborative environment
• Ability to effectively execute tasks in a high-pressure environment is crucial
• Strong oral and written communications skills in both German and English