Senior Master Data Quality Professional

Job title: Senior Master Data Quality Professional

Company: Novo Nordisk


Job description: 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!The positionThe Senior Master Data Quality Professional position is in the Quality Department for Global Patient Safety (GPS) & Regulatory Affairs (RA) based in Søborg, Denmark. Here we support the GPS and RA areas in many aspects of quality and there is now a stronger need for support within Master Data in SAP.You will become part of a diverse team consisting of 9 members who comes from several different countries. The position is very versatile, and you get the opportunity to work with stakeholders all over the world.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 Nordisk

Your tasks will be characterized by a dynamic mix of own Master Data QA approval tasks and participation in several transformational projects where your expertise within Master Data and your quality risk-based approach, will be your assets.QualificationsYour 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.About the departmentGlobal Patient Safety and Regulatory Affairs Quality (GPS & RA Quality) is one of three sister departments in Research & Development Quality Operation, which is part of R&D Quality in Novo Nordisk. We are a very diverse quality department that supports a large organization and with global stakeholder interaction.In GPS & RA Quality we offer Quality expertise for our stakeholders both in GPS, RA and Digital Supply Chain. In this position you will play a vital role in ensuring correct master data for production and supply chain, and ensuring that our products leave up to the regulatory requirements on each market.Working at Novo NordiskWe are a proud life-science company, and life is our reason to exist. We’re inspired by life in all its forms and shapes, ups and downs, opportunities and challenges. For employees at Novo Nordisk, life means many things – from the building blocks of life that form the basis of ground-breaking scientific research to our rich personal lives that motivate and energize us to perform our best at work. Ultimately, life is why we’re all here – to ensure that people can lead a life independent of chronic disease.ContactIf you want to know more about the position, please contact Lavinia Georgeta Marinescu-Pedersen on lgmp@novonordisk.comDeadline4 February 2025To ensure an efficient and fair recruitment process, please refrain from adding a photo in your CV.We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.At Novo Nordisk we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives, backgrounds and cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve and communities we operate in. Together, we’re life changing.

Expected salary:

Location: Søborg, Hovedstaden

Job date: Tue, 21 Jan 2025 23:28:24 GMT

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