SIRE Life Sciences®

Document Controller

Location: Netherlands

SIRE Life Sciences® is the market leader in life science recruitment. We believe the recruitment market needs to gear up in technology and continues innovation. We like technology, in a life science market driven on science, we couldn’t stay behind; we drive Recruitment Science. Investing a majority of our turnover in technology enables us to use unique Resource Technologies. By using highly advanced algorithms, we enable our team of Resource & Data Strategists© to maintain the most advanced, detailed and complete Life Sciences network in Europe. This big data enables us to work Reverse Recruitment©: we first analyze the market in-depth before we go out to the market. Because we analyze the whole market, we can compare facts and data. This enables us to do Facts & Big Data Recruitment©, making sure we, or better yet, you find the right career!

THE COMPANY

Our client is a professional Biotechnology and Pharmaceutical organization, based in Noord-Brabant Netherlands.

The company you will be working for in this position is one of the biggest Biopharmaceutical companies in the world, located in multiple countries around the globe. Their mission is to expand human life expectancy by researching, developing and creating new ways for treating patients.

ROLE DESCRIPTION

As a document controller you will be responsible for maintenance, version control, issue and recall of all master documents. You will be transferring master documents to the electronic document management system. Control users access and issue of master documents. Removal of superseded documents from the system, both electronic and hard copies. Load electronic profiles, masters and permissions in the electronic systems such as EDM Quality or Sharepoint. Control and maintain user access to electronic documents according to defined profiles. Manage reconciliation, scanning and filing of all controlled company documents. Control and issue documents required by operations staff for study work. Format and proof reading of master documents for staff( SOP's, protocols etc.)

RESPONSIBILITIES

-RFI log maintenance and follow up
-Submittal log maintenance and follow up
-Job Folder Administration
-Quality document coordination
-Open new project numbers (Financial)
-Maintain spreadsheets
-Coordinate and attend project meetings, transcribe and distribute meeting notes
-Assist in preparing design presentations
-Assist in maintaining project schedules
-Assist in the coordination of vendor presentations
-Maintaining complete and thorough project documentation and records

REQUIREMENTS

-3 to 5 years of project coordination or administrative professional experience in an architecture or design firm
-Proficient in Microsoft office including Word, Excel and Powerpoint
-Experience with document management systems
-Extreme attention to detail and the ability to multi-task and prioritize required
-Must be organized, efficient and enjoy working with a team
-Able to work independently with minimal guidance, and a motivated self-starter
-Excellent verbal and written communication in Dutch and English is essential

Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact .

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SIRE Life Sciences®

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