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Project Manager
Eingestellt von Stamford Consultants AG
Gesuchte Skills: Plm, Client
Projektbeschreibung
Our client, one of the biggest pharmaceutical companies based in Canton Solothurn in Switzerland, is now looking for a PROJECT MANAGER WITH MEDICAL DEVICE REGULATED ENVIRONMENT EXPERIENCE.
This is a contractual role between August - December 2018.
Responsibilities:
By 2020, all medical device companies must demonstrate and maintain compliance in accordance with the new EU Medical Device Regulations (EU MDR):
- Liaise with all key stakeholders when formulating and communicating the Project Plans
- Ensure continually deployment of the MDR Plan through consistent project management
- Plan, schedule and track project timelines using appropriate tools
- Facilitates project status meetings, status reporting, risk & mitigating
- Schedules and facilitates project status meetings and advises management on project status, risk and mitigation including executive reporting.
- Responsible to originate/oversee/assist in the creation & release of change orders (COs) for all label change requests through Agile PLM software.
Must Have:
- 3-5 years experience managing business or software projects
- Strong knowledge and skills in MS Office
- Strong knowledge and skills in Packaging and Labeling is required
- Experience in an Medical Device regulated environment
- Strong knowledge and skills in PLM system, Agile PLM and SAP
- Bachelor's degree in business, information systems or related discipline
This is a contractual role between August - December 2018.
Responsibilities:
By 2020, all medical device companies must demonstrate and maintain compliance in accordance with the new EU Medical Device Regulations (EU MDR):
- Liaise with all key stakeholders when formulating and communicating the Project Plans
- Ensure continually deployment of the MDR Plan through consistent project management
- Plan, schedule and track project timelines using appropriate tools
- Facilitates project status meetings, status reporting, risk & mitigating
- Schedules and facilitates project status meetings and advises management on project status, risk and mitigation including executive reporting.
- Responsible to originate/oversee/assist in the creation & release of change orders (COs) for all label change requests through Agile PLM software.
Must Have:
- 3-5 years experience managing business or software projects
- Strong knowledge and skills in MS Office
- Strong knowledge and skills in Packaging and Labeling is required
- Experience in an Medical Device regulated environment
- Strong knowledge and skills in PLM system, Agile PLM and SAP
- Bachelor's degree in business, information systems or related discipline
Projektdetails
Geforderte Qualifikationen
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Kategorie:
IT Entwicklung, Ingenieurwesen/Technik