Regulatory Consultant - 's-Hertogenbosch

Vacancy information

Publication date:February 02 2021
Employment type: Permanent
Sector: Medical Devices
Function Group: Quality/RA

Function Group: Quality/RA / Quality Specialist

Organization

For a consultancy firm based in the area of ‘s-Hertogenbosch, we are looking for a Regulatory Consultant with several years of experience. Operating around in Benelux with offices in the area of ‘s-Hertogenbosch, this topnotch consultancy firm provides clients with a wide variety of global support. This consultancy firm is in the top three most promising privately owned consultancy companies in the Netherlands. With a office based in ‘s-Hertogenbosch with 30 colleagues, is serving its clients with an initial clinical study to post-approval compliance. They are working especially for medical devices and biological medicinal products and chemicals. Since they are working together with the local people, they are very successful in deeply rooted relationships with clients by providing leading industry knowledge, experience, and proven processes. This mid-size company has close to 30 clients worldwide from the top Medical Device organisations to fast growing scale-ups, 35+ colleagues, and is supporting her clients in whole Benelux.

Function

Are you interested in an independent, responsible, and consulting role in a small consultancy firm with possibilities to (further) develop yourself as a Regulatory Consultant? This could be something for you! You will work for several clients on projects with a duration between six months and three years. The work-life balance is really important for the employees of this company, everybody takes care that you will work on a project that you like and is close to home. You will be working for state of the art Medical Device companies as well as for local start-ups. You will help those companies with a very wide variety of services, such as MDR GAP analysis for a whole company, (re-)writing/reviewing several documents, prepare and update technical files, help with clinical evaluations, give support for submissions and manage interactions with notified bodies. In this role, it is important that you are able to have effective communications with clients and that you can work autonomously on projects. It goes with saying that you have over twenty-five colleagues that will have your back and support you. When you are working at a client, the client actually hires the knowledge of over a twenty-five international consultants.

Requirements

The ideal candidate has:

  • An MSc/PhD in Pharmacy, Chemistry, Life Sciences
  • Scientific and technical writing/editing skills (English)
  • Knowledge of/affinity with analytical procedures, specifications, validation methods, stability testing, process controls etc.
  • Minimum two years of experience in Regulatory Affairs (Quality experience is a plus)
  • The eagerness to learn, develop and excel
  • The ability to handle stringent deadlines
  • The ability to communicate in a convincing way
  • Able to commute to the area of ‘s-Hertogenbosch

Offer

In exchange for your talent, time and energy the organisation offers:

  • A market conform salary (depending on your experience)
  • 25 vacation days
  • Holiday allowance
  • Work in an international environment of the Medical Device industry
  • Interesting projects which will stimulate you to keep learning

Application

If you are interested in this job, or in similar ones, please feel free to contact me directly.

Quintes Hamer
Associate | Medical Devices

+31(0)6-82100758
+31(0)23-7548660
q.hamer@qtcrecruitment.com

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