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CSV Engineer



Our client, one of the world’s largest pharmaceutical organisations is responsible for developing and manufacturing medicines, consumer products and vaccines for a wide range of medical disciplines. They have been responsible for the development of a number of key and revolutionary products and have a presence in the USA, EU and Asia-Pacific.

  • With continued organisational growth and a considerable amount of investment across the portfolio and capital programme.

  • They are seeking the expertise of a CSV Engineer to join their North East office on an initial 6 month contract.

  • The successful candidate will be responsible for the global implementation of the Serialisation systems across their sites. As the CSV Engineer you will have experience with Installation, Qualification and Testing of Serialisation/MES systems.

  • Key Duties:

  • Support the validation of the automated Serialisation/MES systems to ensure the systems are operational and remain validated.

  • Ensure that all qualification activities associated with the automated control systems that are used in manufacturing are performed in accordance with all relevant quality and safety standards

  • To act as the Subject Matter Expert to all the external regulatory bodies and suppliers for validation of automation systems

  • Training and mentoring technical staff on the validation aspect of Automation Control Systems

  • Authoring and Executing of test packs with serialisation systems

Key Skills:

  • Strong experience in validation of either MES, EDMS, Data Collection or Serialisation systems
  • Previous experience of working within Pharmaceuticals in a cGMP or regulated industry
  • Good working knowledge of authoring and executing test packs
  • Experience with automation validation project implementation taking a risk based approach

 If this position matches your experience, then please do not hesitate to contact me.

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Posted 6 days ago

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