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Support in document reviewing and approving

VC442053 SVDL

Via Brunel

Published on 14 days ago

As part of a project, one of our clients is currently looking for support in reviewing and approving documents. 

This project involves that various local platforms will be transferred to a single global platform. In this context, different SOP's must be reviewed from a QA perspective.

Support in document reviewing and approving

Job description

  • Perform review and approval of documents from a QA perspective
  • Work in electronic documentation system (MIDAS) 
  • Attend daily communication (TIER process) 
  • Work according to applicable safety guidelines 


  • Master's or bachelor degree in chemistry/sciences/pharmaceutics or equivalent by experience
  • Experience with SOP-writing, review and approval
  • Working knowledge of cGMP and GDP requirements
  • Quality Assurance knowledge
  • (Q-) knowledge of SAP/LIMS/MES is a plus
  • Good verbal and written communication skills
  • Ability to work precisely and accurately
  • Team player with ability to work independently and to work in global cross-functional project teams
  • Strong computer skills, including experience using Microsoft Word, Excel
  • Good knowledge of Dutch and English language


  • We are always looking for new talents who fit in our Brunel team and who match with our clients need for specialized support
  • We offer an interesting salary package and job opportunities in dynamic high-tech life sciences environments
  • Become a member of our Brunel Crew and we will help you fulfill your career ambitions
Mechelen - Lier

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46 days left to apply



  • Professional bachelor (Higher Education Short Type)
  • At least 2 years experience
  • English, Dutch


  • Permanent
  • Full-time

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