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Support in Computer system validation (CSV) activities

VC439288 SVDL

Via Brunel

Published on 7 days ago

As part of a site wide modernization program, the resource will report and provide support to the local program lead. He/She will be responsible for the program documentation including GxP documentation of activities linked to the program. This includes automation systems, computer systems and equipment’s. All of this in accordance with our company standard processes and compliance rules. 

Support in Computer system validation (CSV) activities

Job description

He/she is responsible for: 

  • Computer System Validation; 
  • Automation System Validation and qualification; 
  • Equipment qualification; 
  • System lifecycle documentation; 
  • SOP update; 
  • Validation of Microsoft Excel workbook following GMP standards in place within our company.

 Standard meeting which he/she will participate to or organize: 

  • Weekly project meeting; 
  • Necessary meeting to succeed in the above responsibilities.


  • Pharmaceutical GxP knowledge and experience 
  • Computer System Validation experience
  • Work independently and in team
  • Speak and write in Dutch and English
  • Living in Belgium
  • Knowledge of TrackWise QMS is a plus but not mandatory 
  • Work from home is not an option
  • Working experience: 5 years or more


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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Blarenberglaan 3, 2800 Mechelen

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53 days left to apply



  • Professional bachelor (Higher Education Short Type)
  • At least 5 years experience
  • English, Dutch


  • Permanent
  • Full-time

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