GMP Partner and Associate Manager for Compliance Improvement Team in DFP Bagsværd
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Bagsværd
- Quality
- Bagsværd
Do you have a strong GMP and quality background combined with leadership experience? Are you able to set direction in a high complexity environment while driving simplicity and improvements proactively? Then you might be the right person for this special position as GMP partner for site management and manager for our Compliance Improvement Team.
About the department
Compliance Improvement Team (CIT) is an important part of the strategy to continuously improve our processes ensuring timely delivery of our products without compromising on quality. CIT is a part of Business Support and supports all processes in the factory which means that our stakeholders range from all departments at the site to external stakeholders in QA and other areas. Our main tasks are to support and drive proactive improvement projects, but the team is also responsible for preparing the site to inspections and audits. Lastly, the team support major critical issues in daily operations across the entire site.
The team consist of highly experienced supporters that are individually chosen for their expertise and experience from several years in production and quality areas. They are ambitious and high-performing with a strong team spirit. They strive to support each other, simplify by always being curious and empower by trusting each other in every task.
We offer you an exciting position where you will contribute with your relevant experience and where you are guaranteed to learn and develop your skills in this highly complex aseptic production facility. You will have a wide contact interface and be empowered to run important and strategic projects for the site. You will also be part of a team that is high performing every day and have fun at the same time!
The position
As GMP Partner your primary task is to ensure that a GMP and quality mindset is applied in daily management decisions and operation. Our production site is an aseptic insulin factory that produce insulin and GLP-1 to most countries in the world. You will have close contact with site management and is expected to advice and support in quality related activities.
The job will be adjusted in accordance to your relevant experience, but it is important to have a general strong GMP and quality mindset and experience. You could be asked to take lead in coordinating major critical cases, high stake inspections and other critical projects for the site. In those situations, it is important you are to keep calm, be strategic and apply your strong communication skills. In general, it is important as GMP partner to have a holistic view of a situation.
As Associate Manager you will be daily manager for four highly skilled, motivated and independent supporters. The tasks are mainly run as projects and ‘on and off’ support to the site on critical cases. 2-3 times a year, the team prepares the site for inspections from health authorities where it will be important to prioritise projects and communicate with stakeholders. The job requires a strong ability to multitask with a high degree of stakeholder management. You must be structured, ensure delivery and communicate clearly.
Qualifications
We are looking for a person with hands on experience of the quality system in a similar pharmaceutical industry area. Maybe you have been a specialist and now you are looking for some leadership experience as a next step in your career development. You are keen on working with optimisation and is known to be curious, creative, solution-oriented and communication comes natural to you.
As a minimum, you have an academic degree such as M.Sc or equivalent with minimum of 4 years of experience in a pharmaceutical production. Preferably you have some experience as manager or similar in for instance senior project management.
Contact
If you want to hear more about the position, please contact: Mads Wørmer phone no. 3079 4131.
Deadline
13 April 2020
Millions rely on us
To work for Novo Nordisk you will need the skills, dedication and ambition to change lives for the better for millions of patients living with diabetes and other chronical diseases. In exchange, we offer the chance to be part of a truly global workplace, where passion and engagement are met with opportunities for professional and personal development.
Information og data
Denne ledige stilling har jobtypen "Softwareudvikler", og befinder sig i kategorien "Informationsteknologi".
Arbejdsstedet er beliggende i Bagsværd.
Jobbet er oprettet på vores service den 18.3.2020, 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.
- Softwareudvikler
- Bagsværd
- Mandag den 13. april 2020
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