IT CSV Validation Consultant

Masento

Posted on Sep 30, 2024 by Masento
Brussel (Stad), Brussel, Belgium
IT
Immediate Start
Annual Salary
Contract/Project

Masentó Group are seeking an experienced IT CSV (Computer System Validation) Consultant with a background in life sciences to support a key client in Brussels, Belgium. The ideal candidate will have 7-12 years of experience in IT system validation, be native/fluent French proficient, and comfortable delivering projects in English & French.

This is a 12-month initial freelance contract with the project lasting at least 3-years.

You will be required to help set-up new managed services for validation activities to ensure all IT systems are running in a compliant manner.

Skills Criteria:

  • 7-12 years of experience in IT CSV within the life sciences industry.
  • Validate IT systems & define and manage the Project Documentation List.
  • Author key validation documents (Validation Plan, Validation Report) and review deliverables such as URS, FS, CS/DS, IQ, OQ, PQ, FRA, Test Strategy Plan/Report.
  • Proficiency in native French; project delivery in English.
  • Strong understanding of validation processes, including system deliverables and operational activities.
  • Availability to work 3-4 days per week from the client's office in Brussels.

Please apply with your latest CV for immediate consideration.


Reference: 2829848475

https://jobs.careeraddict.com/post/95659949

This Job Vacancy has Expired!

Masento

IT CSV Validation Consultant

Masento

Posted on Sep 30, 2024 by Masento

Brussel (Stad), Brussel, Belgium
IT
Immediate Start
Annual Salary
Contract/Project

Masentó Group are seeking an experienced IT CSV (Computer System Validation) Consultant with a background in life sciences to support a key client in Brussels, Belgium. The ideal candidate will have 7-12 years of experience in IT system validation, be native/fluent French proficient, and comfortable delivering projects in English & French.

This is a 12-month initial freelance contract with the project lasting at least 3-years.

You will be required to help set-up new managed services for validation activities to ensure all IT systems are running in a compliant manner.

Skills Criteria:

  • 7-12 years of experience in IT CSV within the life sciences industry.
  • Validate IT systems & define and manage the Project Documentation List.
  • Author key validation documents (Validation Plan, Validation Report) and review deliverables such as URS, FS, CS/DS, IQ, OQ, PQ, FRA, Test Strategy Plan/Report.
  • Proficiency in native French; project delivery in English.
  • Strong understanding of validation processes, including system deliverables and operational activities.
  • Availability to work 3-4 days per week from the client's office in Brussels.

Please apply with your latest CV for immediate consideration.

Reference: 2829848475

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