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Project Manager Document Management (Clarity, PMM, CSV) 50%
Eingestellt von ITech Consult
Gesuchte Skills: Support
Projektbeschreibung
PROJECT MANAGER DOCUMENT MANAGEMENT (CLARITY, PMM, CSV) 50%
REFERENCE: 915865KS
INDUSTRY: Pharma
ORT: Basel and Region
DURATION: July 2016. (latest start date: 11.07.2016)
WORK LOAD: 50%
ROLE: Project Management of a complex project with key stakeholders in San Francisco. Three systems in California will be replaced: DocLink, CEDM and BRES at Platform GMPLiveLink (a validated environment).
- We are looking for a senior project manager with profound experience of document management in a validated environment
- End date: 31.07.2017. Extension: no extension planned. Work location: Basel. Remote: 1 day per week possible (prior to agreement). Travelling: no travelling required. Team: Project team of 8 seniors. Working days: Part time 50%, candidate should work every day 4 hours in the afternoon as there are a lot of interactions with US.
TASK AND RESPONSIBILITIES:
- Leading one or more high-level, complex technical projects within the constraints of scope, quality, time, and cost, to deliver specified requirements. Manage Stream leaders and be accountable for budget, resource and timelines. Provide plan and support to stream leads. Interacting with management, coordinating and directing activities of project team members. Ensuring all project requirements and/or objectives are documented. Manage and oversee documentation
REQUIREMENTS:
- 8 years of experience as Project Manager. Recognized expert-level knowledge of relevant methodologies (PMM), technologies (Clarity), standards (CSV) and processes, preferably with broad industry exposure. Roche experience. Profound communication skills in English and German. Excellent ability to communicate to others not only what is being done and how, but also why, ability to engage and motivate. Excellent understanding of complex landscapes and relationships (business, systems, policies, etc.).
- Capability to think strategically
- Manage Project and meetings in a lean and efficient manner.
Next steps: Interviews should take place on 27.06. und 28.06.2016
REFERENCE: 915865KS
INDUSTRY: Pharma
ORT: Basel and Region
DURATION: July 2016. (latest start date: 11.07.2016)
WORK LOAD: 50%
ROLE: Project Management of a complex project with key stakeholders in San Francisco. Three systems in California will be replaced: DocLink, CEDM and BRES at Platform GMPLiveLink (a validated environment).
- We are looking for a senior project manager with profound experience of document management in a validated environment
- End date: 31.07.2017. Extension: no extension planned. Work location: Basel. Remote: 1 day per week possible (prior to agreement). Travelling: no travelling required. Team: Project team of 8 seniors. Working days: Part time 50%, candidate should work every day 4 hours in the afternoon as there are a lot of interactions with US.
TASK AND RESPONSIBILITIES:
- Leading one or more high-level, complex technical projects within the constraints of scope, quality, time, and cost, to deliver specified requirements. Manage Stream leaders and be accountable for budget, resource and timelines. Provide plan and support to stream leads. Interacting with management, coordinating and directing activities of project team members. Ensuring all project requirements and/or objectives are documented. Manage and oversee documentation
REQUIREMENTS:
- 8 years of experience as Project Manager. Recognized expert-level knowledge of relevant methodologies (PMM), technologies (Clarity), standards (CSV) and processes, preferably with broad industry exposure. Roche experience. Profound communication skills in English and German. Excellent ability to communicate to others not only what is being done and how, but also why, ability to engage and motivate. Excellent understanding of complex landscapes and relationships (business, systems, policies, etc.).
- Capability to think strategically
- Manage Project and meetings in a lean and efficient manner.
Next steps: Interviews should take place on 27.06. und 28.06.2016
Projektdetails
Geforderte Qualifikationen
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Kategorie:
Sonstiges