Interim Quality/Regulatory Consultant

Interim Quality/Regulatory Consultant in the Medical Devices industry in Utrecht, The Netherlands

  • Interim Quality/Regulatory Consultant
  • Medical Devices
  • Utrecht, The Netherlands

Morgan Green is looking for an Interim Quality/Regulatory Consultant in the MD industry for an organisation located in Utrecht. It is a senior role within the Medical Device Regulations project team of the organization. Are you experienced in the MD industry? Then continue reading!

Company description

The role is in an organization in the Medical Devices industry, located in Utrecht, The Netherlands.

Job description


As senior Interim Quality/Regulatory Consultant, your responsibilities are:

  • Implementing the current readiness plan.
  • Communication with the internal stakeholders, about renewed laws and regulations, and the progress of the readiness plan.
  • Updating of the workstreams, procedures, technical files and documentation.

Requirements

  • Relevant Bachelor's Degree
  • Minimum of 5 years experience within the MD industry
  • Experience with MDR compliance is a plus
  • Excellent oral and written command of English

What we offer

Length of the job: minimum of 6 months , 32-40 hours per week

In case you're not a freelancer, but you are interested in this interim project, Morgan Green can arrange a payroll construction (where we take care of your payment and you will keep your social rights). For more information, please contact Marloes Bartels via 020 7979825 .

Uren:
32

Vaardigheden

  • Voor deze functie is er geen minimale werkervaring vereist

Opleiding

HBO

Wat wij bieden

tijdelijk
Solliciteer
direct via Jobbird
Of solliciteer later

Morgan Green

Sanne Burgering
Morgan Green

Telefoon 0207979825