System Process Expert
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Søborg
Are you ready to take responsibility as an expert in our regulatory core system. Do you want to participate in a digitalization journey where you act as a system expert, knowing all details, challenges, and opportunities?
If you want to join us on our digitalization journey, and become part of an organization, with a key responsibility regarding ensuring fast regulatory approvals, efficient manufacturing setup and robust processes – then please continue reading. We are searching for an experienced and data driven system expert to take up a role with a very broad stakeholder landscape and responsibility.
It means that you need to be able to both dive into details while also being able to understand processes and systems in a bigger context. Solving day-to-day support issues, while also being able to provide ideas and run process optimizations for how to use our core IT systems.
Our core regulatory system is based on the Veeva platform – in the Vault RIM suite. It will be viewed as an advanced if you have previous experience with the platform, however it is not a requirement, as we are certain, that the right profile will be able to self-explore and get to know the system in a fast and efficient manner.
The role will develop over time along with the department and area as a general, you will be part of ongoing projects and support in our day-to-day life.
Your key responsibilities will include:
• Support colleagues across the organization with key process and IT insight into how we work with our core regulatory systems
• Participate in business process development projects
• Proactively suggest process optimization and investigate how to mature both our processes, usage of IT systems and increasing our data awareness and quality
• Work with cross organizational teams to improve both data structures and processes and participate in projects Qualifications
The ideal candidate has M.Sc. in a relevant field, business, economics, supply chain or similar. Furthermore:
• At least 5 years of experience from a similar position.
• Ability to understand a broad range of different core IT system and capable of fast understanding new systems and processes.
• A strong cross value chain business understanding, good stakeholder management capabilities and communication skills.
• Fluency in English both written and spoken. About the department
Novo Nordisk Regulatory Affairs makes medicine available to patients all over the world by ensuring fast regulatory submissions and approvals in all our global markets.
You will be part of a relatively new department responsible for project management, scientific and regulatory strategic input to capacity and manufacturing project.
We are also responsible for enabling fast approvals for world-wide roll-out and return on investment for the growing manufacturing network – and not least creating overview of regulatory activities across the value chain, where data and data quality plays a key role.
The department consist of colleagues with very diverging backgrounds, nationalities – but also roles, reaching from very specialised RA experts to more generic business roles, etc. heading up transformation projects with a big digital element.
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 to manufacturing, marketing, and sales – we’re all working to move the needle on patient care.
Contact
For more information, please contact Malene Østergaard Jørgensen at +45 3079 5844.
Deadline: 18 June 2023. Applications will be evaluated continuously when received and candidates may be called for interview before the deadline.
We are looking for several Regulatory Affairs profiles at Novo Nordisk now. Therefore, hiring managers from different teams might also look at your application.
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 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.
If you want to join us on our digitalization journey, and become part of an organization, with a key responsibility regarding ensuring fast regulatory approvals, efficient manufacturing setup and robust processes – then please continue reading. We are searching for an experienced and data driven system expert to take up a role with a very broad stakeholder landscape and responsibility.
It means that you need to be able to both dive into details while also being able to understand processes and systems in a bigger context. Solving day-to-day support issues, while also being able to provide ideas and run process optimizations for how to use our core IT systems.
Our core regulatory system is based on the Veeva platform – in the Vault RIM suite. It will be viewed as an advanced if you have previous experience with the platform, however it is not a requirement, as we are certain, that the right profile will be able to self-explore and get to know the system in a fast and efficient manner.
The role will develop over time along with the department and area as a general, you will be part of ongoing projects and support in our day-to-day life.
Your key responsibilities will include:
• Support colleagues across the organization with key process and IT insight into how we work with our core regulatory systems
• Participate in business process development projects
• Proactively suggest process optimization and investigate how to mature both our processes, usage of IT systems and increasing our data awareness and quality
• Work with cross organizational teams to improve both data structures and processes and participate in projects Qualifications
The ideal candidate has M.Sc. in a relevant field, business, economics, supply chain or similar. Furthermore:
• At least 5 years of experience from a similar position.
• Ability to understand a broad range of different core IT system and capable of fast understanding new systems and processes.
• A strong cross value chain business understanding, good stakeholder management capabilities and communication skills.
• Fluency in English both written and spoken. About the department
Novo Nordisk Regulatory Affairs makes medicine available to patients all over the world by ensuring fast regulatory submissions and approvals in all our global markets.
You will be part of a relatively new department responsible for project management, scientific and regulatory strategic input to capacity and manufacturing project.
We are also responsible for enabling fast approvals for world-wide roll-out and return on investment for the growing manufacturing network – and not least creating overview of regulatory activities across the value chain, where data and data quality plays a key role.
The department consist of colleagues with very diverging backgrounds, nationalities – but also roles, reaching from very specialised RA experts to more generic business roles, etc. heading up transformation projects with a big digital element.
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 to manufacturing, marketing, and sales – we’re all working to move the needle on patient care.
Contact
For more information, please contact Malene Østergaard Jørgensen at +45 3079 5844.
Deadline: 18 June 2023. Applications will be evaluated continuously when received and candidates may be called for interview before the deadline.
We are looking for several Regulatory Affairs profiles at Novo Nordisk now. Therefore, hiring managers from different teams might also look at your application.
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 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 Søborg.
Jobbet er oprettet på vores service den 8.6.2023, 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.
- Øvrige
- Søborg
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