Senior IT Quality Professional
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Do you have a passion for working in a team of motivated skilled QA professionals/specialists to reach ambitious goals? Do you have the desire to strive for the best quality in IT? Do you wish to be at the forefront of working with new digital technologies? Then you might be our next Senior IT QA Specialist, apply now to join our company! The position At Novo Nordisk the IT QA is responsible for defining, implementing, and verifying quality activities for regulated (GxP) applications/solutions. Together with the IT specialists, analysts, and managers, you will be a key contributor in setting the direction for the global application and implementation of regulatory requirements, based on pharmaceutical industry standards and best practices.
Key responsibilities include:
• Provide IT QA subject matter expertise (SME) in the GMP domain to projects/systems/services with focus on key quality activities and deliverables. Activities will range from advising on risk management, quality planning, approving quality related deliverables, to preparations for internal audits and external inspections by authorities
• Provide coaching and set direction for IT colleagues in quality and compliance tasks/issues or stakeholder matters.
• Work closely with the agile project management teams and stakeholders in Line of Business (LoB). You are expected to leverage quality assurance, IT and business process knowledge (GMP), including IT technical expertise to ensure both efficient and effective quality assurance and compliance in an Agile setting.
The position offers a unique possibility to work with IT Quality Management globally in Novo Nordisk and to develop you professionally through challenging opportunities on the job as well as formal training.
Qualifications The position requires significant insight into quality processes like audit, deviation handling, validation, CAPA, change control, records management, data integrity, as well as insights into Good Manufacturing Practice (GMP), including solid working knowledge from within manufacturing and or working with infrastructure services for intended use Key IT processes, like Incident and Problem management, Configuration and Change management, Release and Deployment management, Testing and Validation (CSV), Operations management, Security and Risk management, etc. are implied. We are especially looking for a candidate who can tick off most of the following:
• BSc degree in Computer Science, Engineering, or another relevant field, preferably with a strong IT substance.
• 5+ years of work experience, as an IT QA in the pharmaceutical industry, preferably in the GMP domain.
• You can easily take full ownership for your work and have a strong sense for meeting objectives and delivering high quality.
• You thrive with stakeholder interaction, and you can present complex matters in a clear and precise way.
• You are fluent in written and spoken English.
• It is an advantage if you possess solid IT technical knowledge and if you are familiar with agile methodology and have experience in working with Azure DevOps. We have two open positions to fill, one candidate for large and complex IT systems within production and the second one for IT infrastructure for intended use.
The department IT QA Office is a part of IT Quality which employs 55 highly skilled and ambitious quality professionals in Denmark and India. We are responsible for ensuring that external and internal requirements are reflected in Novo Nordisk IT processes, and the department serves as competence centre for IT quality assurance throughout Novo Nordisk. Our responsibilities also include quality assurance of IT projects and IT systems, services and infrastructure used globally.
In IT QA Office we have highly motivated, engaged, and independent colleagues, an international environment where we share knowledge, experience, and where we help each other when needed.
Working at Novo Nordisk Founded in Denmark in 1923, Novo Nordisk has become one of the world’s leading healthcare companies. At Novo Nordisk, we are committed to driving change to defeat diabetes and other serious chronic diseases. To fulfil this purpose, we pioneer scientific breakthroughs, expand access to our medicines, and work to prevent and ultimately cure disease. That said, we are anything but linear. With us, your skills, commitment, and ambition help us change patients’ lives worldwide. In exchange, we offer you a rewarding and purpose-driven culture with talented and diverse co-workers. Therefore, your professional and personal development is essential for us, and in Novo Nordisk, the sky is the limit for career opportunities.
Contact For further information, please contact department manager Lars Voigt at [email protected]
Deadline 21 st of January 2024. To ensure a fair and equal recruitment process, please refrain from adding a photo to your CV, but please include a few sentences about your motivation for applying in your resume or 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.
Key responsibilities include:
• Provide IT QA subject matter expertise (SME) in the GMP domain to projects/systems/services with focus on key quality activities and deliverables. Activities will range from advising on risk management, quality planning, approving quality related deliverables, to preparations for internal audits and external inspections by authorities
• Provide coaching and set direction for IT colleagues in quality and compliance tasks/issues or stakeholder matters.
• Work closely with the agile project management teams and stakeholders in Line of Business (LoB). You are expected to leverage quality assurance, IT and business process knowledge (GMP), including IT technical expertise to ensure both efficient and effective quality assurance and compliance in an Agile setting.
The position offers a unique possibility to work with IT Quality Management globally in Novo Nordisk and to develop you professionally through challenging opportunities on the job as well as formal training.
Qualifications The position requires significant insight into quality processes like audit, deviation handling, validation, CAPA, change control, records management, data integrity, as well as insights into Good Manufacturing Practice (GMP), including solid working knowledge from within manufacturing and or working with infrastructure services for intended use Key IT processes, like Incident and Problem management, Configuration and Change management, Release and Deployment management, Testing and Validation (CSV), Operations management, Security and Risk management, etc. are implied. We are especially looking for a candidate who can tick off most of the following:
• BSc degree in Computer Science, Engineering, or another relevant field, preferably with a strong IT substance.
• 5+ years of work experience, as an IT QA in the pharmaceutical industry, preferably in the GMP domain.
• You can easily take full ownership for your work and have a strong sense for meeting objectives and delivering high quality.
• You thrive with stakeholder interaction, and you can present complex matters in a clear and precise way.
• You are fluent in written and spoken English.
• It is an advantage if you possess solid IT technical knowledge and if you are familiar with agile methodology and have experience in working with Azure DevOps. We have two open positions to fill, one candidate for large and complex IT systems within production and the second one for IT infrastructure for intended use.
The department IT QA Office is a part of IT Quality which employs 55 highly skilled and ambitious quality professionals in Denmark and India. We are responsible for ensuring that external and internal requirements are reflected in Novo Nordisk IT processes, and the department serves as competence centre for IT quality assurance throughout Novo Nordisk. Our responsibilities also include quality assurance of IT projects and IT systems, services and infrastructure used globally.
In IT QA Office we have highly motivated, engaged, and independent colleagues, an international environment where we share knowledge, experience, and where we help each other when needed.
Working at Novo Nordisk Founded in Denmark in 1923, Novo Nordisk has become one of the world’s leading healthcare companies. At Novo Nordisk, we are committed to driving change to defeat diabetes and other serious chronic diseases. To fulfil this purpose, we pioneer scientific breakthroughs, expand access to our medicines, and work to prevent and ultimately cure disease. That said, we are anything but linear. With us, your skills, commitment, and ambition help us change patients’ lives worldwide. In exchange, we offer you a rewarding and purpose-driven culture with talented and diverse co-workers. Therefore, your professional and personal development is essential for us, and in Novo Nordisk, the sky is the limit for career opportunities.
Contact For further information, please contact department manager Lars Voigt at [email protected]
Deadline 21 st of January 2024. To ensure a fair and equal recruitment process, please refrain from adding a photo to your CV, but please include a few sentences about your motivation for applying in your resume or 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.
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Denne ledige stilling har jobtypen "Øvrige", og befinder sig i kategorien "Øvrige stillinger".
Arbejdsstedet er beliggende i Ballerup.
Jobbet er oprettet på vores service den 12.12.2023, 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.
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