IT Compliance Consultant

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Bagsværd

Are you passionate about how IT, digitalisation and data can create business value? Do you have a consulting mindset and experience working with IT Compliance and regulated industries? As IT Compliance Consultant you will engage in DD&IT (Digital, Data & IT) projects and agile setups acting as Subject Matter Expert within Compliance and Quality. You will work with different parts of the organisation and take on various roles and assignments depending on your interests, experience and development wishes. You will join a team of highly engaged colleagues with whom you will do sparring as basis for continuously increasing your knowledge about compliance and the complex pharma industry. Curios? Then continue reading and send us your application. About the position In the role as IT Compliance Consultant you will lead and/or participate in compliance work streams across projects as responsible for end-to-end quality and compliance activities. You will define the quality- and compliance strategy for the projects and scope the documentation, validation and testing of the IT systems and platforms. You will work closely with the project/product manager, QA, business areas and external vendors and leverage your experience for how to work with IT processes and Quality Management Systems. You will be responsible for the development and delivery of complete validation packages, incl. IT Risk Assessment, Requirement Specifications, Validation Plan/Report (VPL/VR), Installation/Operational/Performance Qualification and validation activities including test execution, documentation review and approval. You will promote best practices and take active part in defining and driving continuous improvement and simplification of existing processes. As consultant you can expect to be assigned to one or more projects for a period of 6-18 months, depending on the development and complexity. You will get to work with different areas of the value chain, from early research & development to manufacturing and sales. In any role, you will be given plenty of responsibility and be a key player in some of the largest initiatives within IT, data and digitalisation in Novo Nordisk. You will have the opportunity to learn from highly experienced colleagues and be given the freedom to impact and shape your own development and career. Qualifications You hold an academic degree within an IT Quality and/or Computer Science or alternatively accumulated similar level of insight and experience over an extended period of professional work life.
  • You have a relevant educational background and minimum 2-5 years of Quality Management and GxP system validation experience. Your experience preferably comes pharma (GxP) or from either automotive, aerospace, energy or other industries where quality and regulatory compliance is vital to succeed.
  • You have good knowledge about the GAMP framework, ITIL and DGPR foundation.
  • Having a basic understanding of Agile (SAFe, Scrum, Kanban) is a benefit.
  • Fluency in both written and spoken English is a pre-requisite.
    • To succeed, it is crucial that you thrive with working in teams where you can inspire and motivate your stakeholders to take informed decisions. You have good communication skills, and you easily navigate complex stakeholder landscapes. You can train, guide, and coach colleagues and external collaboration partners in compliance processes and best practices. About the department You will join an ambitious team of experienced IT Compliance Consultants and Project Managers working on large scale projects and initiates across the organisation. Organisationally, the team is anchored in Cross DD&IT responsible for developing and managing solutions that benefits users across the whole organisation (modern integrations, intelligent automations, data liberalisation etc). Your colleagues all work on different projects but meet on a regular basis to share experiences as a basis for continued development and best practice implementations. The team is based in Bagsværd, Denmark, but the scope of our projects is global. Business travel is limited but may be expected. Working at Novo Nordisk At Novo Nordisk, your skills, dedication and ambition will support our ambition of improving quality of life for more than 366 million people living with diabetes. You will have the opportunity to build a life-changing career in a global business environment. We offer you an opportunity to work with talented colleagues in an engaged and people focused culture. Contact For further information, please contact department manager Katrine Bisgaard Høy at [email protected] or Senior IT Compliance Consultant Nicolai Krog Andersen at [email protected] Deadline February 26th, 2023 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. Please refrain from adding a photo to your CV to ensure an efficient and fair recruitment process. 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 Bagsværd.

    Jobbet er oprettet på vores service den 19.1.2023, men kan have været deaktiveret og genaktiveret igen.

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