Your new company

Your new role

In this role, you will be responsible for ensuring the quality and compliance of SAP Master Data and pharmaceutical artwork through thorough QA review and approval. You will manage and improve QA systems, contribute to SOP-development and reviews, and support investigations and quality-related projects. Working closely with cross-functional teams such as Regulatory Affairs, Global Artwork, and Master Data, you will play a key role in maintaining data integrity, ensuring regulatory compliance, and supporting continuous improvement within a GMP-regulated environment.

• Review and approve of Master Data related activities (such as critical value verification and Bill of Materials).
• Perform approval of artwork for medicinal products.
• Participate in operational life cycle management
• Act as author for operational SOP’s and Work Instructions
• QA Review of operational SOP’s and Work Instructions
• Participate in QA related projects as needed
• Assist in various investigations as needed
• Ensure compliance
• Develop solutions to technical problems of moderate complexity
• Screens, categorises, evaluates, reconciles reports and resolves data integrity issues.

What you'll need to succeed

• Masters or Bachelor’s degree in Life Sciences or related field, or the equivalent combination of education and/or experience.
• Previous experience in GMP/pharma.
• 3 years of related Quality Assurance or manufacturing experience in the pharmaceutical or medical device industry
• Good Manufacturing Practice (GMP), Good Distribution Practice (GDP) and/ or Good Clinical Practice (GCP) knowledge with the ability to interpret and apply in mainly routine cases.
• Fluent in English.
• Accurate mindset

What you'll get in return

What you need to do now

If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV.