Description
Our world leading Biopharmaceutical client has a contract requirement for an experienced Senior Documentation Specialist, to work on the creation and development of a new document management system for 3 major business areas.Following on from organisational change within the business, we require a good Senior Documentation Specialist with previous cGMP Pharmaceutical experience, to carry out a review of all the existing documents and work closely with Directors, manufacturing and users to set up a paperless system.
This will involve looking at the manufacturing, client and system documenation and oversee the development of process, executing the document organisation and implement a new system across various site locations within Europe.
Based in the North West of England and interfacing with 4 international locations, this role will involve travel to client sites across Europe.
Interfacing with other web based documentation management project’s, this is an excellent opportunity to take project ownership and retain ‘hands on’ involvement.
Requirements
• Previous documentation management experience- within a biotech/ biopharmaceutical environment
• Experience working with large volumes of documentation.
• Extensive GMP/GXP exposure.
• Knowledge of systems such as LIMS/ Labware/ Trackwise are advantageous.
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