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GMP Packaging Documentation Writer

  • Location:


  • Contact:

    Pascal Lagendijk

  • Job type:


  • Contact phone:

    +31 (0)20 406 97 50

  • Industry:

    Pharmaceutical , Life Sciences

  • Contact email:

If you can easily structure workflow and write eloquent and clear instructions and enjoy making Standard Operating Procedures, this could be a very interesting position for you!

Job Description
In this position of GMP Documentation Writer you write SOPs, templates and assist with data extraction of GMP data. A versatile administrative position at a global pharmaceutical company.


  • Write User Requirement Specifications, qualification protocols
  • Update documentation systems
  • Extract data (e.g. SAP data) when required
  • Support projects (e.g. qualification, etc)


  • Minimally finished HBO or MSc education, eg in Life sciences or process engineering
  • Work experience in pharma and GMP
  • Experience writing documents such as SOP's is required
  • Experience with scientific writing is a plus
  • Very good skills with MS Word. Templates and layout settings have no secrets for you
  • You have very good understanding of English, both written and spoken
  • You can work independent and have no problem working remote (during covid) and partially on site (after covid)


  • Employment: Temporary for a period of 7 months with Oxford Global Resources Solutions. Project duration is minimal 1 year
  • Salary indication: From approximately € 3000 to € 4500 gross per month
  • Working hours: full time
  • Location: Region Nijmegen

Vacancy number: 16403