Your new company

Your new role

• Provide QA guidance and support in the production area at ABR.
• Perform batch record review of batches assembled, packaged and labelled at ABR.
• Establish effective working relationships with Production, Warehouse, Maintenance and Engineering, QA Management and the Qualified Person.
• Act as a first point of contact in case of production queries (quality related) during packaging and labelling operations.
• Review and approve batch production record data entries before production activities take place.
• Perform finished product checks during (commercial) production run. Act as author for operational SOP’s and Work Instructions, as needed.
• Review of operational SOP’s and Work Instructions, as needed.
• Assist in development and delivery of GMP training activities for QA and production staff.
• Participate in QA production related projects, as needed.

• MBO or BSc in Pharmaceutical Sciences, Life Sciences, or a related discipline, or equivalent experience.
• Minimum 3 years of Quality Assurance or manufacturing experience in the pharmaceutical or medical device industry.
• Experience in batch record review and investigations.
• Strong understanding of GMP, GDP, and/or GCP principles.
• Experience with manufacturing or quality analytical processes.
• Fluent in English (written and spoken).

What you'll get in return

Hays Detachering | This is a project that will start with a 12-month contract via Hays. An extension to stay within the department is anticipated. In this position, you will get a competitive salary starting at €4400 bruto per month and your travel expenses are covered. Please note sponsorship cannot be provided.

What you need to do now

If you are interested in this role, 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 on your career.