Project Engineer Product Support Biologicals

What are your responsibilities?

This role will require process validation and filing activities for internal projects (filling line transfers / batch size increase).
Expected Activities:.
  • The position will require the application of process and product knowledge to ensure a successful validation of process changes on drug product manufacturing. It will require extensive team work and interaction with groups across the site and in the network.
Job Responsibilities:
  • Perform risk based process validation.
  • Author of regulatory sections for authorities.
  • Provide technical input for material, in-process, release, and testing-related evaluations.
  • Author and contribute to technical documentation.
  • This role will require process validation and filing activities for a new product into the site.

Who are we looking for?

  • University degree in scientific field: Industrial engineer, Industrial pharmacist, Civil engineer, Bio-engineer
  • At least 2-3 years of relevant experience in projects in the pharmaceutical, chemical or other industry. Experience with (sterile) drug product is an asset as well as knowledge of Quality Systems, product testing/qualification
  • Teamplayer
  • Dynamic and enthusiastic
  • Respect for agreed timing and decisions
  • Respect for procedures and Good documentation practices
  • Good communicator, convincing
  • 'On the field' mentality
  • Flexibile and agile
  • Dutch mothertongue and good English is required

What does QbD offer you?

  • A young and dynamic company with a feel good culture, and a great openness and a no-nonsense approach
  • Real investment in people through education and fun events
  • A competence development model focused on your personal ambitions
  • An attractive salary package
Interested? Apply now by sending us your CV and motivation.