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Document Control Manager
Eingestellt von Quanta Consultancy Services
Gesuchte Skills: Design, Controller
Projektbeschreibung
DOCUMENT CONTROLLER
Our global pharmaceutical client, based in central Switzerland, is currently undertaking a new-build project of a high-spec, automated facility of the future. They are building the project team and need experienced and confident individuals to support.
LOCATION: Switzerland.
DURATION: 12 months.
ROLE:
- Receipt, review and verification for all project documentation from design through to validation.
- Review documents for accuracy and completeness.
- Work with internal and external stakeholders to request comments, expedite review of comments and ensure completion of all documentation to required industry standards.
- Co-ordinate receipt, mastering, issuance, review and revision of controlled documents, eg design documents, URS, FDS, C&Q, Validation etc.
- Work closely with senior project management to set strategy for document management for the project.
- Set up and implements a document storage and filing systems - ensure processes are put in place and maintain integrity of document storage.
- Ongoing administration of document management system.
- Work closely with EPCM companies to ensure document sharing and availability.
- Set up Sharepoint sites for sharing of project documentation with EPCMs and vendors.
- Prepares status reports for management.
KEY SKILLS/EXPERIENCE:
- Extensive and broad experience working as a document controller in the pharmaceutical industry is essential.
- Previous experience of working as part of a CapEx project team required, ideally large value investments.
- Knowledge of how to set up a document filing system for a CapEx project.
- Confident dealing with internal and external stakeholders.
- Excellent communication skills, confident and highly organised.
- Solution orientated approach.
- Comfortable working as part of a team, as well as inpendently and highly self-motivated.
- Open minded and flexible individual who enjoys working with new technologies and strategies.
- Fluent German language skills essential, some English language knowledge required.
Our global pharmaceutical client, based in central Switzerland, is currently undertaking a new-build project of a high-spec, automated facility of the future. They are building the project team and need experienced and confident individuals to support.
LOCATION: Switzerland.
DURATION: 12 months.
ROLE:
- Receipt, review and verification for all project documentation from design through to validation.
- Review documents for accuracy and completeness.
- Work with internal and external stakeholders to request comments, expedite review of comments and ensure completion of all documentation to required industry standards.
- Co-ordinate receipt, mastering, issuance, review and revision of controlled documents, eg design documents, URS, FDS, C&Q, Validation etc.
- Work closely with senior project management to set strategy for document management for the project.
- Set up and implements a document storage and filing systems - ensure processes are put in place and maintain integrity of document storage.
- Ongoing administration of document management system.
- Work closely with EPCM companies to ensure document sharing and availability.
- Set up Sharepoint sites for sharing of project documentation with EPCMs and vendors.
- Prepares status reports for management.
KEY SKILLS/EXPERIENCE:
- Extensive and broad experience working as a document controller in the pharmaceutical industry is essential.
- Previous experience of working as part of a CapEx project team required, ideally large value investments.
- Knowledge of how to set up a document filing system for a CapEx project.
- Confident dealing with internal and external stakeholders.
- Excellent communication skills, confident and highly organised.
- Solution orientated approach.
- Comfortable working as part of a team, as well as inpendently and highly self-motivated.
- Open minded and flexible individual who enjoys working with new technologies and strategies.
- Fluent German language skills essential, some English language knowledge required.
Projektdetails
Geforderte Qualifikationen
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Kategorie:
Medien/Design, Organisation/Management