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Document Controller
Eingestellt von Quanta Consultancy Services
Gesuchte Skills: Support, Controller
Projektbeschreibung
Role - Document Controller
Type - initially 12 month contract
Location - Co. Limerick
Profile
One of our key global Biopharmaceutical clients is heavily investing in a new facility and is in a need of a Document Controller to provide support to the Technical Operations team in relation to documentation systems and ancillary support systems.
Key Responsibilities:
Receipt, verification and archiving of project turn-over documentation
Implement and maintain document repositories and archives.
Administration of document management system
Provide guidance to Tech Ops department in proper use of document changes systems to ensure consistency of system usage.
Co-ordinate receipt, mastering, issuance, review and revision of controlled documents, eg SOPs, SWIs & forms, P&IDs, start-up protocols, maintenance & calibration records.
Maintain departmental databases.
Participate in site-wide project teams as necessary.
Prepare status reports for management.
Review documents for accuracy and completeness.
Key Experience:
Degree qualified preferred
Relevant work experience to support responsibilities of position.
Ideally experience gained within a similar Pharmaceutical/Biopharmaceutical manufacturing environments.
Type - initially 12 month contract
Location - Co. Limerick
Profile
One of our key global Biopharmaceutical clients is heavily investing in a new facility and is in a need of a Document Controller to provide support to the Technical Operations team in relation to documentation systems and ancillary support systems.
Key Responsibilities:
Receipt, verification and archiving of project turn-over documentation
Implement and maintain document repositories and archives.
Administration of document management system
Provide guidance to Tech Ops department in proper use of document changes systems to ensure consistency of system usage.
Co-ordinate receipt, mastering, issuance, review and revision of controlled documents, eg SOPs, SWIs & forms, P&IDs, start-up protocols, maintenance & calibration records.
Maintain departmental databases.
Participate in site-wide project teams as necessary.
Prepare status reports for management.
Review documents for accuracy and completeness.
Key Experience:
Degree qualified preferred
Relevant work experience to support responsibilities of position.
Ideally experience gained within a similar Pharmaceutical/Biopharmaceutical manufacturing environments.
Projektdetails
Geforderte Qualifikationen
-
Kategorie:
Organisation/Management, Sonstiges