Senior IT QA Professional
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Do you have a passion for working in a team of initiative-taking and QA professionals/specialists with ambitious goals? Do you have the desire to strive for the highest 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 Quality Professional, apply now to join our company! The position At Novo Nordisk, the IT Quality Assurance (QA) role is crucial for defining, implementing, and verifying quality activities for regulated (GxP) applications and solutions. Collaborating with IT specialists, analysts, and validation managers, you will play a key role in setting the direction for implementing global solutions that meet stringent regulatory requirements based on pharmaceutical industry standards and best practices. Key responsibilities include: Providing IT QA subject matter expertise (SME) in the GMP domain, focusing on quality activities and deliverables such as risk management, quality planning, and IT quality oversight. Advising and guiding on quality-related deliverables, including preparing for internal audits and external inspections by authorities. Collaborating closely with QA colleagues and Line of Business (LoB) stakeholders, leveraging knowledge of quality assurance, IT, and business processes (GMP) to ensure compliance in an Agile setting. Applying IT technical expertise to implement efficient and effective quality assurance measures. Engaging in global IT Quality Management initiatives, offering opportunities for professional development through challenging projects and 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. Further, sound knowledge of 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 particularly seeking a candidate who can meet the following qualifications: Bachelor’s degree in Computer Science, Engineering, or a related field, preferably with a substantial IT focus Extensive experience as an IT Quality Assurance professional within the pharmaceutical industry, with a preference for experience in the GMP domain Proven ability to take full ownership of tasks, demonstrating a strong commitment to meeting objectives and delivering high-quality results Excellent interpersonal skills, with the ability to clearly and precisely communicate complex matters to stakeholders Fluency in both written and spoken English About the department Sourcing QA is responsible for Quality Assurance of Raw Materials and Packaging Materials going into all of Novo Nordisk A/S marketed products. We are responsible for Quality Assurance of our suppliers who are located all over the world. A combination of ensuring a high standard of incoming materials, and involvement in investigations into quality issues by the use of LEAN tools is part of our daily work. In total, we are 65 dedicated employees divided into 5 teams working closely together. We collaborate with stakeholders across the organization and all over the world. You can expect to have a large degree of independence within your work and at the same time, have the chance to collaborate with highly skilled colleagues across the organization. Working at Novo Nordisk At Novo Nordisk, we don’t wait for change. We drive it. We’re a dynamic company in an even more dynamic industry, and we know that what got us to where we are today is not necessarily what will make us successful in the future. We embrace the spirit of experimentation, striving for excellence without fixating on perfection. We never shy away from opportunities to develop, we seize them. From research and development, through to manufacturing, marketing and sales – we’re all working to move the needle on patient care. Contact For further information, please contact manager Oktay Eminovski at +4530795408 Deadline 28 July 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.
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 25.6.2024, 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.
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