Job Description

We are seeking for a highly motivated individual with experience on document management to join our QA Team!

Your responsibilities, among others, will be:

• Responsible for timely controlled issuance of batch document and label packages including Final product labels per cGMP, as requested by operational departments.
• Responsible for timely controlled issuance of logbooks.
• Responsible from timely consumption of consumables/GMP materials used or informing the responsible person.
• Ensure accuracy and completeness of QA issued documents.
• Identify and escalate compliance gaps across the controlled issuance process.
• Support/ invetigate deviations on controlled issuance process and develop effective corrective action plans.
• Additional duties as assigned.

Your profile

• 2+ years of experience on document management in a regulated environment
• Advanced level of English.

We will accept applications only for people located in the Netherlands.