Quality Projects Associates Ref: 1876

Overview

SPGL is a dynamic and well established professional technical services group, operating in a range of market sectors including Bio-Pharmaceuticals, Medical Devices & Diagnostics, Healthcare, Regulated Consumer Products, Chemicals & Mission Critical. We are a responsible, diverse and inclusive organisation, driven by our vision of ‘making quality a way of life’ and a strong desire to achieve more for our customers. We are proud to have a great team of highly skilled, smart professionals who help, care and support both our clients and each other.

Role

  • Quality Review of Validation Documentation, Change Records and procedures.
  • Performance of Regulatory Impact assessments.
  • Coordination of Regulatory Submissions and Responses.
  • Support in Quality Management Systems (Validation, QRM, Change Management, Regulatory Systems…).

Requirements

  • Master degree in the relevant field.
  • At least 1 year experience in the pharma industry (in validation, registration, quality) is a must.
  • Dutch as native language.
  • Must be able to commit to a year.

What SPGL can offer you

We are a people centric company where our staff are the heart and soul of our organisation. If you’re looking for a forward-thinking workplace and see yourself as a dynamic professional, come and join our team and you can expect:

  • Competitive starting salary
  • Excellent private healthcare
  • Pension and life insurance
  • A variety of challenging projects, with blue-chip customers
  • International project assignments
  • Continuous training and personal development
  • Strong career pathway
  • A mix of young and experienced professionals
  • Multi-cultural and caring organisation
  • An equal opportunity employer
  • Regular team building events and social gatherings

For further information on this role please e-mail careers@spgl.eu

Apply