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Project Management CAPA
Eingestellt von Quanta Consultancy Services
Gesuchte Skills: Support, Client
Projektbeschreibung
Duration: 6-12 months
Location: 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
Location: 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
Projektdetails
Geforderte Qualifikationen
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Kategorie:
IT Entwicklung, Sonstiges