Senior Master Data Quality Professional

at  Novo Nordisk

Senior Master Data Quality Professional
Category: Quality
Location:Søborg, Capital Region of Denmark, DK
Do you enjoy making an impact by driving data quality, process improvements and automation? Do you want to work closely with colleagues from all over the world in a company that is growing?
Then you may be our Senior Master Data Quality Professional colleague that we are looking for, apply and join us!

QUALIFICATIONS

Your background covers a Bachelors or master’s degree within life sciences.

To be successful in this role, you should have:

• At least 5 years of experience within Master Data, material master, Bill of material in SAP, preferably from pharmaceutical or similar highly regulated industry
• Working experience within quality, quality processes, or GxP regulated areas
• Experience with working with labellings and labelling process is an advantage
• Experience with driving improvements and contributing to projects, project management or cLEAN (continuous improvement)
• A strong command of written and spoken English

You are proactive, detail-oriented, and adaptable, with strong communication and interpersonal skills. You excel at communicating complex information in simple ways, take initiative, and thrive on continuous improvement. Your ability to balance detail with the big picture ensures high-quality work and a positive attitude.

Your core responsibilities will be to:

• Quality Assurance - QA review and approve the client Master Data (MD) critical fields for all purchased, semi-finished, and all finished products in SAP
• Quality Assurance for global Labelling, for all Novo Nordisk products
• Ensure implementation of new Master Data requirements and setups in SAP
• Quality partner and advisor within Master Data and Labelling processes
• Ensure built-in quality from the start by contributing to relevant Master Data projects where you will ensure a robust link between regulatory requirements and production Master Data
• Participate in and contribute to audit and inspections as Quality advisor
• Contribute with solutions for integrating new systems, new technology, new products within the SAP system in Novo Nordis

To be successful in this role, you should have:

• At least 5 years of experience within Master Data, material master, Bill of material in SAP, preferably from pharmaceutical or similar highly regulated industry
• Working experience within quality, quality processes, or GxP regulated areas
• Experience with working with labellings and labelling process is an advantage
• Experience with driving improvements and contributing to projects, project management or cLEAN (continuous improvement)
• A strong command of written and spoken Englis