Compliance Project Manager
- Quality
- Denmark - Søborg
Are you a competent change agent? Can you win acceptance for enhanced business processes from stakeholders in a complex production environment? Then we could have the vacancy for you as Compliance Project Manager in Diabetes Finished Products (DFP).
About the department
You will join our brand new Compliance team of 3 skilled colleagues specialised in quality compliance and business optimisation in DFP Compliance Support. We provide support to all DFP sites to secure that our processes to ensure compliance are as efficient as possible. As we support sites from Denmark, China, France, Brazil and the USA, you will be working across national borders and different working cultures.
The Job
Your job will be to optimise complex business processes across business areas such as quality, manufacturing development and production in DFP and Product Supply. Specifically, you will drive various projects that seek to continuously optimise our compliance level, e.g. by improving the processes we use to implement new requirements in our quality management system and on the shop floor. An important part of your job will be to track compliance and report the status to the senior management on a regular basis. You will also communicate the findings from audits and inspections to the sites and follow up on the implementation accordingly. In all your work you secure alignment with your stakeholders at all levels – from Operators to Vice Presidents.
Qualifications
You hold an MSc within a business-related, pharmaceutical or engineering discipline. Your educational background is supplemented with solid experience from a job as Business Analyst or similar. This has provided you with competences to drive projects from a-z – preferably in an international setting. In other words, you know how to facilitate change management in a complex business environment, and if you have insight into a quality management system, it will be appreciated. You have excellent analytical skills, and you can easily comprehend larger piles of data, extract the essences, and interpret and present these in a clear way. It is important you thrive in a job where you work with documentation on a daily basis. Coordinating many simultaneous tasks, you will need a structured approach, and you thrive performing independently relying on your high level of drive to create sustainable results. As you will interact with an array of different stakeholders, you need an open mind and outstanding 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 Ida Bøkman at +45 3075 1282.
Deadline
9 June 2013
- Quality
- Denmark - Søborg
Are you a competent change agent? Can you win acceptance for enhanced business processes from stakeholders in a complex production environment? Then we could have the vacancy for you as Compliance Project Manager in Diabetes Finished Products (DFP).
About the department
You will join our brand new Compliance team of 3 skilled colleagues specialised in quality compliance and business optimisation in DFP Compliance Support. We provide support to all DFP sites to secure that our processes to ensure compliance are as efficient as possible. As we support sites from Denmark, China, France, Brazil and the USA, you will be working across national borders and different working cultures.
The Job
Your job will be to optimise complex business processes across business areas such as quality, manufacturing development and production in DFP and Product Supply. Specifically, you will drive various projects that seek to continuously optimise our compliance level, e.g. by improving the processes we use to implement new requirements in our quality management system and on the shop floor. An important part of your job will be to track compliance and report the status to the senior management on a regular basis. You will also communicate the findings from audits and inspections to the sites and follow up on the implementation accordingly. In all your work you secure alignment with your stakeholders at all levels – from Operators to Vice Presidents.
Qualifications
You hold an MSc within a business-related, pharmaceutical or engineering discipline. Your educational background is supplemented with solid experience from a job as Business Analyst or similar. This has provided you with competences to drive projects from a-z – preferably in an international setting. In other words, you know how to facilitate change management in a complex business environment, and if you have insight into a quality management system, it will be appreciated. You have excellent analytical skills, and you can easily comprehend larger piles of data, extract the essences, and interpret and present these in a clear way. It is important you thrive in a job where you work with documentation on a daily basis. Coordinating many simultaneous tasks, you will need a structured approach, and you thrive performing independently relying on your high level of drive to create sustainable results. As you will interact with an array of different stakeholders, you need an open mind and outstanding 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 Ida Bøkman at +45 3075 1282.
Deadline
9 June 2013
