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Senior Project Coordinator (Scientific & Manufacturing)
Eingestellt von ITech Consult
Gesuchte Skills: Support
Projektbeschreibung
SENIOR PROJECT COORDINATOR/LABORATORY EXPERIENCE/QUALITY CONTROL/IT QUALITY/CSV/PHARMA
About us:
ITech Consult AG is a certified ISO 9001/2008 Swiss company with offices also located in Germany, Great Britain and Ireland. ITech Consult is specialised in delivering ICT candidates for contract work. We were founded in 1997 by IT professionals; hence we well understand what it means to be professionally supported in your search for a new project and being employed.
REFERENCE NO: 916169NC
ROLE: Senior Project Coordinator (Scientific & Manufacturing)
INDUSTRY: Pharmaceutical
LOCATION: Basel Region
WORKLOAD: 100%
START DATE: 01.02.2017
DURATION: 31.12.2017 (An extension is currently not planned, but would be possible (depending on business demands).
TRAVEL %: Some travel (up to 40%, especially to Germany) may be required.
REMOTE OPTION: Remote/Home Office (up to 20%) is an option, prior approval required.
Role Description:
- We are looking for a Senior Project Coordinator (with CSV background) who will also have the role as a Business Analyst.
- The contractor will work closely with the global and the local PM (project manager), the BAs (business analysts), the SMEs (subject matter experts) and the BPO (business process owner).
- The main responsibility of the contractor will be the responsibility to support local project scheduling and to manage implementation documentation.
Tasks:
- Responsible to support local project scheduling (global timelines)
- Manage implementation documentation (plan/checklist/report), including prioritization.
- Coordinate and support site-team activities, involving subject matter experts (SMEs), the global and the local IT teams as appropriate.
- Coordinate and support the QC/LES method/template development activities
- Coordinate escalation of challenges and questions
Must Haves:
- Background in QC/analytical labs (+7 years of experience)
- Strong IT affinity/experience as a member of (global) IT project team in Pharma
- Knowledge in configuring/administration of commercial LIMS, LES or ELN systems is an advantage (LIMS and ELN systems are equal to LES)
- Great customer focus skills and attention to details (proactive, communicative and a "thinker")
- Proactive investigation of issues and functionalities that may be required.
- Great communication skills (excellent German AND English language skills)
- Great team player
- Strong leadership skills and proven track record of decision taking and escalations handling
- CSV background and experience in working with IT Quality
- Okay to travel/be partially onsite (specifically to Germany, Mannheim)
- There is no specific education background required. More importantly, you would be required to have laboratory working experience of 7+ years.
Nice to Haves:
- International pharma experience is a big plus.
- Experience in multi-site deployment projects.
- Experience in leading teams.
- Former pharma experience (ideally having worked together with one or more business functions and IT in the past)
About us:
ITech Consult AG is a certified ISO 9001/2008 Swiss company with offices also located in Germany, Great Britain and Ireland. ITech Consult is specialised in delivering ICT candidates for contract work. We were founded in 1997 by IT professionals; hence we well understand what it means to be professionally supported in your search for a new project and being employed.
REFERENCE NO: 916169NC
ROLE: Senior Project Coordinator (Scientific & Manufacturing)
INDUSTRY: Pharmaceutical
LOCATION: Basel Region
WORKLOAD: 100%
START DATE: 01.02.2017
DURATION: 31.12.2017 (An extension is currently not planned, but would be possible (depending on business demands).
TRAVEL %: Some travel (up to 40%, especially to Germany) may be required.
REMOTE OPTION: Remote/Home Office (up to 20%) is an option, prior approval required.
Role Description:
- We are looking for a Senior Project Coordinator (with CSV background) who will also have the role as a Business Analyst.
- The contractor will work closely with the global and the local PM (project manager), the BAs (business analysts), the SMEs (subject matter experts) and the BPO (business process owner).
- The main responsibility of the contractor will be the responsibility to support local project scheduling and to manage implementation documentation.
Tasks:
- Responsible to support local project scheduling (global timelines)
- Manage implementation documentation (plan/checklist/report), including prioritization.
- Coordinate and support site-team activities, involving subject matter experts (SMEs), the global and the local IT teams as appropriate.
- Coordinate and support the QC/LES method/template development activities
- Coordinate escalation of challenges and questions
Must Haves:
- Background in QC/analytical labs (+7 years of experience)
- Strong IT affinity/experience as a member of (global) IT project team in Pharma
- Knowledge in configuring/administration of commercial LIMS, LES or ELN systems is an advantage (LIMS and ELN systems are equal to LES)
- Great customer focus skills and attention to details (proactive, communicative and a "thinker")
- Proactive investigation of issues and functionalities that may be required.
- Great communication skills (excellent German AND English language skills)
- Great team player
- Strong leadership skills and proven track record of decision taking and escalations handling
- CSV background and experience in working with IT Quality
- Okay to travel/be partially onsite (specifically to Germany, Mannheim)
- There is no specific education background required. More importantly, you would be required to have laboratory working experience of 7+ years.
Nice to Haves:
- International pharma experience is a big plus.
- Experience in multi-site deployment projects.
- Experience in leading teams.
- Former pharma experience (ideally having worked together with one or more business functions and IT in the past)
Projektdetails
Geforderte Qualifikationen
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Kategorie:
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