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Project Manager
Eingestellt von Harvey Nash IT Recruitment Switzerland
Projektbeschreibung
Harvey Nash is looking for a Project Manager with experience in pharmaceutical regulatory authoring for a 7 + month project (80 to 100% to be agreed with candidate) with possible renewal for 2015 in Switzerland.
The role is about managing programs and projects; ensuring performance in terms of costs, quality and deadlines.
You are responsible for
- Workshop preparation and facilitation, solution assessments, stakeholder management, organizational change management
- Project documentation according to the clients' internal Project Management Methodology (PMM), especially Validation Plan, Validation Report, Project Charter, System Risk Assessment, Roles and Responsibilities, Project Schedule, Project Requirements, Organizational Impact, Analysis, Functional Risk Assessment, Organizational Change Plan, Deployment Plan, Training Material, Communication Material etc.
Requirements
- At least 5-10 years in IT Project Management
- Experience in pharmaceutical regulatory authoring, publishing and/or submission tracking/planning is mandatory
- Track record in managing global projects working with multinational teams that are geographically distributed is mandatory
- Experience with project status reporting and project management documentation tools would be of great advantage
- Experience in managing solution delivery by third party vendors would be of great advantage
- 2-3 trips to Germany and/or San Francisco possibly required
- Working language: English
Are you available immediately, have experience working within a Life Science company? Please send your complete CV (Word documents preferred)
The role is about managing programs and projects; ensuring performance in terms of costs, quality and deadlines.
You are responsible for
- Workshop preparation and facilitation, solution assessments, stakeholder management, organizational change management
- Project documentation according to the clients' internal Project Management Methodology (PMM), especially Validation Plan, Validation Report, Project Charter, System Risk Assessment, Roles and Responsibilities, Project Schedule, Project Requirements, Organizational Impact, Analysis, Functional Risk Assessment, Organizational Change Plan, Deployment Plan, Training Material, Communication Material etc.
Requirements
- At least 5-10 years in IT Project Management
- Experience in pharmaceutical regulatory authoring, publishing and/or submission tracking/planning is mandatory
- Track record in managing global projects working with multinational teams that are geographically distributed is mandatory
- Experience with project status reporting and project management documentation tools would be of great advantage
- Experience in managing solution delivery by third party vendors would be of great advantage
- 2-3 trips to Germany and/or San Francisco possibly required
- Working language: English
Are you available immediately, have experience working within a Life Science company? Please send your complete CV (Word documents preferred)
Projektdetails
Geforderte Qualifikationen
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Kategorie:
Sonstiges