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SOP Writer

  1. France
Toulouse
  1. Contract
Competitive
  1. Commissioning, Qualification and Validation
31009

This vacancy has now expired

SOP Writer – Pharmaceuticals – Contract – Toulouse

Our client, a global biotechnology organisation, is recruiting for a SOP Writer to join their capital project in the South of France. This new build facility will house a therapeutic protein production plant, and we are looking for a SOP Writer to help expand our client's biotech operations throughout Europe. As the SOP Writer you will be responsible for the implementing all safety requirements for a new build facility, estimated at approximately 14,900m2.

SOP Writer Responsibilities:
  • Work together with the Documentation Coordinator, MSAT, Training, Compliance and QA to prepare Site SOPs, Work Instructions, OJT documentation, Forms, Lists and other work process documentation as required for site validation and qualification purposes.
  • Discuss, review, challenge and support definition and documentation.
  • Align with IT and key users and document way of working and best practices for Work Instructions.
  • Write site specific SOPs.
  • Write site specific documentation required for validation and qualification purposes from a pharmaceutical regulatory perspective
About you:
  • Bachelor’s degree in systems engineering or related field
  • 10+ years of experience in the pharmaceutical, biotechnology or medical devices industry in business process delivery including writing process documentation
  • Strong English writing skills and experience writing SOPs
  • Understanding of general supply chain processes and terminology
Does this SOP Writer position sound like a good fit for you? Apply today!

The candidate must have the rights to work in the location stated in the job advert.

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