Validation & Regulatory Quality Associate - Antwerpen

Function Group: Quality/RA / Validation Manager

Organization

A world renowned pharmaceutical company with the highest quality of internal training programs is looking for a Validation & Regulatory Quality Associate to support the BIO team. The team consists of around eight people and focus on the development of biologicals and vaccins. This international magnate and leader within the pharmaceutical development highlights themselves by their ability to offer an above average salary, high end internal training and room for people to keep growing. This image is well supported by employees who have been working there over the last ten years.

The BIO team has set their eyes on a Validation & Regulatory Quality Associate with a highly critical mind who is not afraid to challenge the teams’ thoughts.

Function

The position of Validation & Regulatory Quality Associate is to be fulfilled by someone with a highly critical mind that is able to ask the right questions and switch gears within different phases of multiple projects. This is because you will be working with different departments and disciplines concerning the correct registration and validation of registration activities. During the processes you will perform quality reviews and support regulatory submissions by instructing coworkers on site. You will also have a direct line with global HQ by providing project details and validation data. In case of approval by the appointed council you will coordinate the implementation of change per individual market.

Requirements

The ideal candidate has:

  • Either a junior with a PhD or a medior with a MSc and work experience
  • Fluency in Dutch and English
  • The ability to think critically and to communicate your vision
  • No fear to ask questions
  • A quality mindset
  • The ability to prioritise and switch gears when necessary
  • Advantage when: experience with GMP, WA and FDA/EM

Offer

When joining this elite organisation you will get the following benefits:

  • Working within an international family of pharmaceutical excellence
  • Access to their top notch internal training programs
  • Room to grow and advance within the company
  • For freelancers the rate is between €425.- and €500.- per day depending on your experience
  • Starting date: 2/12/2019 till 31/07/2020 with the possibility to extend
  • For non-freelancers there is room to talk about different kinds of contracting

Application

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

Yvo Selderbeek
Associate

+31(0)6-12576648
+31(0)23-7548660
y.selderbeek@qtcrecruitment.com

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