- IT
- Denmark - Bagsværd
We are looking for a dedicated IT Compliance Partner with skills within IT quality management to join the Business Support team in Product Supply Biopharm. The main responsibility of the IT Compliance Partner will be to drive compliance initiatives across the organisation to secure that our IT systems meet our quality requirements. If you have a strong ability to translate high-level requirements into practical solutions, along with a wish to provide broad support within IT quality management, this may be the job for you.
About the department
Biopharm Business Support is responsible for driving processes and projects as well as providing support within logistics, strategy, finance and IT across the organisation. The organisation we support has approximately 2,300 employees across sites in Bagsværd, Gentofte, Hillerød, Kalundborg, Måløv and Værløse in Denmark and in New Hampshire in US. The IT unit within Business Support is responsible for driving strategic IT and Automation processes and initiatives across Biopharm. The responsibility includes creation and anchoring of IT strategies, governance of IT projects, and providing general IT sparring and guidance.
The Job
As IT Compliance Partner you will play a key role in ensuring IT compliance across Biopharm by driving various compliance initiatives, setting direction, and ensuring knowledge sharing. You will work closely with the Quality Assurance organisation as well as project and system managers, ensuring that the right level of IT compliance is achieved throughout the organisation.
As our new IT Compliance Partner, you will be responsible for developing the way we work with IT compliance within one of the biggest areas in Novo Nordisk. You will be responsible for developing the structures and tools needed to ensure compliance of all our IT systems and projects. Besides from this, you will be contributing to assessment of specific IT systems and initiatives.
The position is a newly established position with good possibilities to develop the role.
Being a subject matter expert within IT quality management, you will be representing Biopharm in various cross-organisational initiatives which will give you the opportunity to interact with colleagues across Novo Nordisk.
Qualifications
You have a strong background within IT & Automation and quality management, solid experience with IT in a GxP regulated industry and experience with project management. You hold a relevant academic degree, along with 5-10 years of working experience.
It is important that you have the ability to translate regulatory requirements into practical solutions and ensure that systems and documentation are in compliance.
As a person you are structured and proactive, you have a strong quality mind-set and you enjoy providing direction and support within your area of expertise. You are thorough and find it natural to work independently. Also, you have good communication skills and the ability to create a strong network.
You are fully proficient in English.
At Novo Nordisk, you will have the opportunity to build a life-changing career in a global business environment. From research and development to manufacturing, marketing and sales, we strive to improve quality of life for more than 366 million people living with diabetes.
Contact
For further information, please contact Alex Resendorf on +45 3075 8162 or Tilde Friis on +45 3075 2518.
Deadline
31 December 2015.
