Position: Entry level

Job type: Full-time

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Job content

About Our Client

Our client is one of the leading Engineering service providers based in Switzerland and we’re urgently looking for an experienced CQV (Commissioning, Qualification and Validation) Engineer to be based at the client’s premises in Switzerland. The final client is a large Pharmaceutical company with several locations in Switzerland. The contract will be limited until May 2022 with the option to be extended.

Tasks
  • Prepare CQV lifecycle documents (URS, FS, TS, DQ, IQ, OQ)
  • Act as a CQ system owner
  • Review vendor, supplier and construction documentation for the purposes of verifying correctness of the required documentation
  • Perform requirements according to safety and quality regulations Profile
  • Technical qualification
  • Minimum of two years in a similar role within the Pharmaceutical industry
  • Experience with project systems and in performing functional testings related to the system types (e.g. Process Systems, Utilities, Support equipment or else)
  • Ideally you’ve completed GMP-related trainings for the preparation and execution of GMP documentation
  • Experience in working in a cross-functional team to deliver qualified systems from FAT/DQ through to OQ
  • Fluency in English is required
  • Valid permit to live and work in Switzerland OR you fulfill the requirements to be eligible to work in Switzerland (relocation will be necessary) Pensum 100%
Next steps

Feel free to send us your application by following the link or give us a call to further discuss about the role.

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Deadline: 08-06-2024

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