CareerAddict

CSV Manager/Expert

Red - The Global SAP Solutions Provider

Posted on Jun 19, 2026 by Red - The Global SAP Solutions Provider
Not Specified, Germany
IT
Immediate Start
Annual Salary
Contract/Project

*CSV Expert -ASAP- Remote (EU).*

RED now has a new contract opportunity for a CSV Expert to join one of our key partners for a global pharma project. The initial contract will run until the end of the year, with a strong scope for extension.

This contract is to start ASAP and will be mostly remote, with very occasional travel to Germany (Mainz/Frankfurt).

Specific skills/experience required:

  • Strong experience in Computer System Validation (CSV)
  • Strong experience in GxP regulated environments
  • Experience with validation documentation (VSR, RVP, RTM/gRTM)
  • Experience with risk-based validation (FRA)
  • Solid knowledge of change control, deviations, and CAPA processes
  • Experience in pharma/life sciences industry
  • Excellent communication skills in English (German is a plus)
  • Able to join within short notice/ASAP

Candidates have to be located in Europe.

If you are interested, please contact Julia Dobrowolska at (see below) or apply via RED.


Reference: 3125271353

https://jobs.careeraddict.com/post/113434713
Red - The Global SAP Solutions Provider

CSV Manager/Expert

Red - The Global SAP Solutions Provider

Posted on Jun 19, 2026 by Red - The Global SAP Solutions Provider

Print
Not Specified, Germany
IT
Immediate Start
Annual Salary
Contract/Project

*CSV Expert -ASAP- Remote (EU).*

RED now has a new contract opportunity for a CSV Expert to join one of our key partners for a global pharma project. The initial contract will run until the end of the year, with a strong scope for extension.

This contract is to start ASAP and will be mostly remote, with very occasional travel to Germany (Mainz/Frankfurt).

Specific skills/experience required:

  • Strong experience in Computer System Validation (CSV)
  • Strong experience in GxP regulated environments
  • Experience with validation documentation (VSR, RVP, RTM/gRTM)
  • Experience with risk-based validation (FRA)
  • Solid knowledge of change control, deviations, and CAPA processes
  • Experience in pharma/life sciences industry
  • Excellent communication skills in English (German is a plus)
  • Able to join within short notice/ASAP

Candidates have to be located in Europe.

If you are interested, please contact Julia Dobrowolska at (see below) or apply via RED.

Print

Reference: 3125271353

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