Freelance Regulatory Information Management professional

Den Haag Pharmaceutical Temporary/Freelance 11.02.2019

At the moment I am looking for a regulatory specialist that has good experience with labelling submissions. The job is in Leiden at a leading pharmaceutical company, they need someone from February until end of the year, with a very likely chance for extension! The position can be filled with remote work. Attending training on-site is necessary in the first two weeks.

At the moment I am looking for a regulatory specialist that has good experience with labelling submissions. The job is in Leiden at a leading pharmaceutical company, they need someone from February until end of the year, with a very likely chance for extension! The position can be filled with remote work. Attending training on-site is necessary in the first two weeks.

RESPONSIBILITIES

  • Use the tools for electronic publishing of submissions
  • Oversee the work of juniors and ensure quality of output.
  • You will be proficient in eCTD lifecycle standards
  • Representing the department on multi-functional project development teams to support regulatory aspects.

PROFILE

  • In the possession of an academic degree in computer sciences
  • You have experience in regulatory submissions
  • You have experience in EU & FDA guidelines for submissions
  • Expert in publishing tools
  • Fluent in English, dutch is a plus.

START DATE

1st of march 2018

PROJECT DURATION

1 year

INTERESTED?

If you’re interested in the above description, please apply with your CV and a letter of motivation by clicking on the ‘apply’ button below.

For further information, please contact Jordy de Vries at +31 (0)20 20 44 502 or by email at j.devries@panda-int.com.

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