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Senior Quality Professional I

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Job Specifications
Employment Type Full time jobs
Job Description

Department: Novo Nordisk Quality GBS
Are you passionate about ensuring quality standards and compliance? Do you have experience in approval of Master data in SAP? We are looking for a Senior Quality Professional to join our team at Novo Nordisk. If you are ready for a new challenge and want to make a difference in the pharmaceutical industry, read on and apply today for a life:changing career.
The position
As a Senior Quality Professional at Novo Nordisk, you will have the following responsibilities:
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Key role in approval of Master Data, ECO (Engineering Change Order) for NN products
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Key role in approval of SAP Master Data for Printed Packaging Materials, on plant level for Danish sites.
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Planning, coordinating and executing the Master Data QA tasks as required
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Quality Assurance service for PS and other relevant areas in Sourcing QA dept
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Review and give input to deviations related to area of responsibility, including timely follow up and providing enough documentation.
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Plan, coordinate, and execute Master Data QA tasks involves ensuring accurate and timely approvals on the first attempt, particularly for launch and pre:approval activities.
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Ensure excellent collaboration within the QA dept and other stakeholders globally
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Be able to communicate business understanding and be able to explain the reason behind request, to ensure compliance with the newest requirements and demands
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Suggest improvements and approach stakeholders to seek for quality improvements during projects and workshops
Qualifications
We are looking for quality mindset professionals with the following qualifications/expertise:
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Graduate or postgraduate degree in science or equivalent professional experience.
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8:10 years of overall work experience, with 4:6 years in the SAP system.
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Proficient in PC:tools, extensive MS Office knowledge, and excellent presentation skills.
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Advanced MS Office skills, including data analysis and advanced Excel.
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Familiarity with Quality processes and tools (Deviation, CR, QAP, QMR, SOPs, etc.).
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Experience managing cross:functional project groups across borders and cultures.
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Professional proficiency in spoken and written English.
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Strong communication skills, initiative:taking ability, and flexible attitude for teamwork.
About the department
NN Quality GBS Unit: Our purpose is to make "Quality " simple, easy and understandable Novo Nordisk Quality works across our value chain, partnering with our business to ensure highest quality from laboratory to patient. As a member of our unit, you will be part of an ambitious and dynamic group of over 100 quality professionals who ensures "highest quality to patients ".
The unit has strong competencies in the area of IT Quality Assurance, GCP and PV Audits, Quality Management Systems operations, SOP operations, Digital Learning Services, Records Management and Translation Services. We have teams who are experts in CR, Deviation and Validation Processes who collaborate with the global organization to ensure high quality deliverables.
Working at Novo Nordisk
At Novo Nordisk, we are driving change to defeat diabetes and other serious chronic conditions. Our treatments today are benefiting millions of people living with diabetes, obesity, and rare blood and endocrine diseases. From our labs to our factory floors, we are discovering and developing innovative biological medicines and making them accessible to patients throughout the world. Since the company was founded in Denmark more than 100 years ago, we have been translating the unmet medical needs of people living with serious chronic diseases into innovative medicines and delivery. Our focus is on these diseases, which affect hundreds of millions of people and are among the most urgent global health challenges. By combining our innovation and commercial excellence, we draw upon insights from patients and part
Job Type: Permanent
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