Document Specialist
- Research & Development
- Denmark - Måløv
Is your IT mind set on structure and quality, then join Novo Nordisk, Non-Clinical Development department in Måløv and help us meet the internal and regulatory demands for non-clinical documentation.
About the Department
You will have 6 dedicated and focused colleagues in Submission & Study Support, who supports more than 60 scientists in different departments in Research & Development. Look forward to a job where you will juggle with several IT programmes and have a central role in a key function of Novo Nordisk. All pharmaceutical companies are committed to live up to the very strict rules and regulations for documentation, and Novo Nordisk is furthest advanced in this process.
The job
The prime objective for you and your colleagues will be to support fulfilment of internal and regulatory demands for non-clinical documentation. You make sure that the documents are in the right format and in compliance with international requirements for electronic submission (e-CTD). Moreover, you support internal and external partners in document and template handling and train and support your colleagues in the use of our electronic document management system. You will be handling large amounts of reports in several IT systems, and this challenging and interesting job is all about making these systems collaborate and work together.
Qualifications
There are many entries into this interesting job, however an academic degree will be an advantage i.e. within information science or similar. The all-important and indispensable requirement is that you have the right mindset, are curious and take pride in solving highly critical issues and tricky challenges. Besides, it is important that you are an experienced IT system user, have technical flair and knowledge of electronic document management systems. You are an advanced user of MS Word (preferably with VBA knowledge) and Adobe Writer, and you easily switch between various IT programmes in order to find the best suitable programme for the given task. This calls for an excellent eye for details and a quality mindset above average, and if you are already familiar with Good Laboratory Practice regulations, it is a great plus. You thrive in a hectic environment and do not lose your general view even when priorities change and you are compelled to readjust. You are a dedicated team player but you also take on individual responsibility and see disseminating information as a challenge. Lastly, you have a good sense of humour, proficiency in spoken and written English and good communication skills.
At Novo Nordisk, your skills, dedication and ambition help us change lives for the better. In exchange, we offer you an opportunity to work with extraordinary talent and benefit from a range of possibilities for professional and personal development.
Contact
For further information, please contact Sandie Philipsen +45 3075 3713.
Deadline
25 November 2013.
- Research & Development
- Denmark - Måløv
Is your IT mind set on structure and quality, then join Novo Nordisk, Non-Clinical Development department in Måløv and help us meet the internal and regulatory demands for non-clinical documentation.
About the Department
You will have 6 dedicated and focused colleagues in Submission & Study Support, who supports more than 60 scientists in different departments in Research & Development. Look forward to a job where you will juggle with several IT programmes and have a central role in a key function of Novo Nordisk. All pharmaceutical companies are committed to live up to the very strict rules and regulations for documentation, and Novo Nordisk is furthest advanced in this process.
The job
The prime objective for you and your colleagues will be to support fulfilment of internal and regulatory demands for non-clinical documentation. You make sure that the documents are in the right format and in compliance with international requirements for electronic submission (e-CTD). Moreover, you support internal and external partners in document and template handling and train and support your colleagues in the use of our electronic document management system. You will be handling large amounts of reports in several IT systems, and this challenging and interesting job is all about making these systems collaborate and work together.
Qualifications
There are many entries into this interesting job, however an academic degree will be an advantage i.e. within information science or similar. The all-important and indispensable requirement is that you have the right mindset, are curious and take pride in solving highly critical issues and tricky challenges. Besides, it is important that you are an experienced IT system user, have technical flair and knowledge of electronic document management systems. You are an advanced user of MS Word (preferably with VBA knowledge) and Adobe Writer, and you easily switch between various IT programmes in order to find the best suitable programme for the given task. This calls for an excellent eye for details and a quality mindset above average, and if you are already familiar with Good Laboratory Practice regulations, it is a great plus. You thrive in a hectic environment and do not lose your general view even when priorities change and you are compelled to readjust. You are a dedicated team player but you also take on individual responsibility and see disseminating information as a challenge. Lastly, you have a good sense of humour, proficiency in spoken and written English and good communication skills.
At Novo Nordisk, your skills, dedication and ambition help us change lives for the better. In exchange, we offer you an opportunity to work with extraordinary talent and benefit from a range of possibilities for professional and personal development.
Contact
For further information, please contact Sandie Philipsen +45 3075 3713.
Deadline
25 November 2013.
