Regulatory Affairs Coordinator

  • The Randstad, The Netherlands
  • 5000.00 - 6000.00
  • 32-40 hours
  • Bachelor degree


Our client is a consultancy in the food and pharmaceutical industry.


Our client is a consultancy in the food and pharmaceutical industry. They participate in very attractive projects for experienced engineers in the pharmaceutical industry. They offer challenging, varied projects with ample opportunities for personal contributions and development.


  • Bachelor’s degree in scientific discipline required; advanced degree preferred.
  • At least 5-8 years previous experience with regulatory affairs in the pharmaceutical industry, preferably with International Markets.
  • Strong organizational skills with the ability to manage large projects and provide regulatory guidance/training to internal stakeholders and others in the department as needed. Project leader experience.
  • Excellent communication and writing skills (advise, convince, negotiate, listen, present and edit).
  • Ability to communicate effectively with cultural awareness and sensitivity and maintain effective working relationships.
  • Experience in working in multidisciplinary teams.
  • High integrity with respect to maintenance of proprietary, confidential information.
  • Fluent in English, both spoken and written.

What do you get?

  • Pension entitlement as from day one
  • Collective WGA / WIA insurance
  • NBBU / ABU collective labor agreement
  • 25 holidays days
  • 8,33% holiday allowance
  • 100% payment in case of illness after one waiting day
  • Travel allowance


Your main tasks:
  • Develop the regulatory strategy and planning to support the commercial strategy;
  • Coordinate its execution in collaboration with other functions (incl. Commercial, Supply Chain, QA, PV, Medical Affairs, Legal);


Peter Debrichy


Send your resume to referring to job id (890)

More information?

Please contact Peter Debrichy working at our office in Zoetermeer, phone number +31 6-10191580