IT Validation Lead for Integrations
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Are you passionate about data and quality and do you want to play a key role working with integration of data from acquired companies? Would you like to cooperate with colleagues with different backgrounds and interact with stakeholders across the organization? If so, there is a unique job opportunity waiting for you, read more and apply now! The Position In this role, you will be responsible for validation activities related to data migration from acquired companies. You will be part of a newly established Quality System Integration Office working closely together with the team in different integration projects. Besides developing and optimizing our approach to validation, your main tasks will include: • Plan and drive validation activities related to data migration from acquired companies into
• Ensure that related validation documentation is prepared and approved accordingly
• Coordinate with suppliers of migration services, on activities related to data migration and related validation
• Collaborate with data/system owners and process managers, to achieve a compliant and effective data migration
• Collaborate with QMS Integration Project Manager, committing to overall plans, following up on execution and reporting status Overall, in collaboration with QMS Specialists and Professionals, you will facilitate compliance with data integrity and IT principles. Qualifications We are looking for someone who is familiar with complex projects based on business needs, GXP compliance, providing integrated IT solutions and you are quality-minded with good ability to execute within deadlines. To succeed in this role, you: • Hold an academic degree in a relevant subject
• Have several years of experience with IT Validation
• Have gained said experience within the pharmaceutical or other highly regulated industry
• Are fluent in English As a person, you are well-organized and have focus on collaboration by engaging your colleagues, showcasing a great ability to communicate clearly and collaborate. About the Department
Quality Processes, a part of Quality, is responsible for maintaining and continuously developing the core quality processes and their supporting IT systems at Novo Nordisk. We ensure that our processes comply with regulatory requirements and operate as smoothly as possible. The department covers Deviations, Change Control, CAPA, process management, Quality Management Review, Quality Risk Management, Metrology, and reference materials. Further, we support the Quality System area in integration of Quality Processes. Our ambition is to build a robust and simple quality management system that can support in maintaining world-class quality in the future. The position is based in Bagsværd, and you will report to the Senior Manager of QMS Operations.
Working at
As a proud life-science company, life is our reason to exist. We draw inspiration from life in all its forms and shapes, embracing its opportunities and challenges. For employees at , life encompasses many aspects – 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 are all here – to ensure that people can lead a life independent of chronic disease. Contact
For further information, please contact Senior Manager Stine Akselsen at +. Referral (for internal)
Do you know someone who might be a great fit for this position and is it someone who you would like to have as a colleague? All you need to do is select “'Refer a candidate” on the specific job and your friend will receive an email allowing them to send their official application and be registered as referral. Deadline
19 April 2024 You do not need to attach a cover letter to your application, but please include a few sentences about why you are applying in your resume or CV. To 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 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.
• Ensure that related validation documentation is prepared and approved accordingly
• Coordinate with suppliers of migration services, on activities related to data migration and related validation
• Collaborate with data/system owners and process managers, to achieve a compliant and effective data migration
• Collaborate with QMS Integration Project Manager, committing to overall plans, following up on execution and reporting status Overall, in collaboration with QMS Specialists and Professionals, you will facilitate compliance with data integrity and IT principles. Qualifications We are looking for someone who is familiar with complex projects based on business needs, GXP compliance, providing integrated IT solutions and you are quality-minded with good ability to execute within deadlines. To succeed in this role, you: • Hold an academic degree in a relevant subject
• Have several years of experience with IT Validation
• Have gained said experience within the pharmaceutical or other highly regulated industry
• Are fluent in English As a person, you are well-organized and have focus on collaboration by engaging your colleagues, showcasing a great ability to communicate clearly and collaborate. About the Department
Quality Processes, a part of Quality, is responsible for maintaining and continuously developing the core quality processes and their supporting IT systems at Novo Nordisk. We ensure that our processes comply with regulatory requirements and operate as smoothly as possible. The department covers Deviations, Change Control, CAPA, process management, Quality Management Review, Quality Risk Management, Metrology, and reference materials. Further, we support the Quality System area in integration of Quality Processes. Our ambition is to build a robust and simple quality management system that can support in maintaining world-class quality in the future. The position is based in Bagsværd, and you will report to the Senior Manager of QMS Operations.
Working at
As a proud life-science company, life is our reason to exist. We draw inspiration from life in all its forms and shapes, embracing its opportunities and challenges. For employees at , life encompasses many aspects – 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 are all here – to ensure that people can lead a life independent of chronic disease. Contact
For further information, please contact Senior Manager Stine Akselsen at +. Referral (for internal)
Do you know someone who might be a great fit for this position and is it someone who you would like to have as a colleague? All you need to do is select “'Refer a candidate” on the specific job and your friend will receive an email allowing them to send their official application and be registered as referral. Deadline
19 April 2024 You do not need to attach a cover letter to your application, but please include a few sentences about why you are applying in your resume or CV. To 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 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.
Information og data
Denne ledige stilling har jobtypen "Øvrige", og befinder sig i kategorien "Øvrige stillinger".
Arbejdsstedet er beliggende i Bagsværd.
Jobbet er oprettet på vores service den 5.4.2024, men kan have været deaktiveret og genaktiveret igen.
Dagligt opdateret: Dette job opdateres dagligt ud fra jobudbyderens hjemmeside via vores søgemaskineteknologi og er aktivt lige nu.
- 05.04.2024
- Øvrige
- Bagsværd
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