Interim QA Advisor

Project overview

As an Interim QA Advisor, you will work within a pharmaceutical logistics environment on the quality system.

Profile of the suited interim professional:

• Setting up and managing the quality system according to GMP and GDP guidelines
• Reviewing and independently handling deviation, CAPA, and change control processes, including follow-up
• Conducting internal audits and supplier audits and monitoring compliance with quality guidelines
• Drafting and updating procedures and quality documentation
• Providing training in the field of quality and compliance
• Supporting projects related to storage locations, equipment validation, and supplier qualification
• Minimum of 5 years of experience as a QA Advisor
• Minimum of 3 years of experience in the pharmaceutical industry
• Extensive knowledge of GMP and GDP regulations and their application
• Several years of experience in setting up and managing quality systems
• Good command of the Dutch and English languages
• Bachelor's degree level of working and thinking

Project details

• Start: flexible
• Duration: 6 months
• Location: Utrecht, Utrecht, Flevoland, NL
• Languages: Dutch