Your new company

Your new role

• Reviewing and releasing batch documentation on time. This verifies that the product meets the requirements of GMP, internal quality standards and registration.
• Resolving problems/issues following the review of the batch documentation.
• Archiving batch documentation is one of the tasks.
• Participate in (daily) tier meetings and team/departmental consultations
• Participate in improvement projects

What you'll need to succeed

Completed MBO4 and/or HBO education, preferably pharmacology or MLO/HLO. Experience in QC or production within a GMP environment is required. Command of the Dutch language and good communication skills in English. You are accurate, able to work independently within a team, and a good communicator. You are proactive, work well under time pressure and flexible.

What you'll get in return

Hays Detachering | This is a project that will start with a contract for 12 months through Hays. Extension to stay within the department is anticipated. In this position, you will get a competitive salary and your travel expenses are covered.

What you need to do now

If you are interested in this role as QA Associate, click ‘Apply now’ to send an up-to-date CV, or give us a call! Is this job isn’t quite right for you, but are you still looking for a new position? Please contact us for a confidential discussion about your career.