Jobs at Novo Nordisk

Afdelingssekretær

Du kan lære mere om Novo Nordisk�s største produktionssite ved at bruge www.novonordisk.com/kalundborg-careers

- Administration
- Danmark - Kalundborg

Søger du nye udfordringer? Så bliv den nye afdelingssekretær hos Novo Nordisk i Diabetes Active Pharmaceutical Ingredients (DAPI) i Kalundborg

Om afdelingen
Vi søger en engageret og servicemindet afdelingssekretær til en af vores finrensningsfabrikker (PPIV) i Kalundborg. PPIV er del af Purification Plants (PP), der består af 4 finrensningsfabrikker, samt for laboratorium og support - alt i samme enhed.Afdelingen består af ca. 80 medarbejdere fordelt i 4 teams, en ledergruppe bestående af afdelingsleder, 4 teamledere, kvalitetskoordinator, cLEAN ansvarlig og ikke mindst en afdelingssekretær. Der eksisterer tillige et tværorganisatorisk samarbejde mellem sekretærerne fra alle områdets afdelinger, hvori der løses fælles opgaver.

Jobbet
Du vil i samarbejde med afdelingslederen, ledergruppen og sekretærgruppen i PP blive en nøglemedarbejder i forbindelse med løsning af opgaver i området og afdelingen. Du vil være afdelingens administrative blæksprutte, og får blandt andet ansvaret for indkøb og økonomiopfølgning på afdelingsniveau, samt at hjælpe til med møde-bookinger, forberedelse og opfølgning på forskellige aktiviteter i afdelingen. Du indgår i ledergruppen og vil her blandt andet blive inddraget i forskellige beslutningsprocesser. Ligeledes vil du blive en vigtig sparringspartner for både teamledere og afdelingslederen. Du forventes derfor at kunne håndtere fortrolige oplysninger samt at udvise udpræget grad af loyalitet.

En væsentlig del af jobbet er desuden, at du skal løse de mange praktiske ad hoc opgaver, der dukker op i en travl hverdag. Herudover benyttes der cLEAN® fremgangsmåde ved forbedring og optimering af de administrative procedurer og processer, som du vil blive en del af. Vi forventer derfor, at du er omstillingsparat og har lyst til at arbejde struktureret og samt kontinuerligt at arbejde med løbende forbedringer omkring dit eget og teamets arbejde. Endelig vil du indgå i områdets tværgående sekretærgruppe, og her også løse opgaver udenfor afdelingen. Eksempelvis vil du indgå i sekretariatet under myndighedsinspektioner, og herfra hjælpe med at der er styr på lister, papirer og personer når vi har besøg fra myndighederne.

Kvalifikationer
Vi forventer, at du har en relevant administrativ uddannelse og erfaring indenfor det administrative område. Du skal have generel god forståelse for IT samt godt kendskab til MS Office Pakken og SAP. Det vil være en fordel med en økonomisk baggrund og interesse. Du skal være selvmotiverende og selvstændigt kunne koordinere og prioritere dit arbejde. Det er en forudsætning, at du er positiv, engageret og møder dine interessenter med et smil. Det forventes ligeledes at du er holdspiller, udadvendt og initiativrig. Som person er det vigtigt, at du er omstillingsparat, har et stort overskud og trives i et turbulent miljø med mange bolde i luften. Det er vigtigt, at du kan samarbejde med interessenter på forskellige niveauer og er opmærksom på, hvad der rører sig i afdelingen og teamet.Vi kan tilbyde dig en spændende stilling i en afdeling, hvor du har rig mulighed for selv at præge din arbejdsdag.

I Novo Nordisk er det dine evner, dit engagement og dine ambitioner, der hjælper os med at forbedre mange menneskers liv. Til gengæld tilbyder vi dig muligheden for at arbejde sammen med usædvanligt talentfulde kolleger, og vi tilbyder dig en lang række muligheder for professionel og personlig udvikling.

Kontakt
Vil du vide mere om stillingen, så kontakt Troels Felding på +45 3079 4324.

Ansøgningsfrist
30. november 2013

Procurement Coordinator

- Business Support
- Denmark - Bagsværd

Are you looking for new challenges? Now you have an exceptional opportunity. We are looking for a result-oriented Procurement Coordinator to be a part of our Purchasing team in Bagsværd for the 1st half of the year 2014

About the department
The Purchasing Service Centre (PSC) is responsible for the purchasing process for indirect spend in Novo Nordisk. We work closely together with our procurement colleagues in the Corporate Procurement organisation, Global Service Centre in Bangalore, our internal customers being the employees in Novo Nordisk, and the external suppliers.

The Job
Our internal customers are our most important stakeholders, and you will responsible for the key projects that will improve the purchasing process to the benefit of them and PSC. You will deliver best practice results in co-operation with many of the internal and external stakeholders while achieving your ambitious goals.

You will work closely together with your team colleagues in Denmark and Bangalore and stakeholders to resolve issues and improve and develop the processes in the purchasing-to-pay process.

Qualifications
You have completed a relevant master's degree (e.g. in finance, economics or supply chain) with excellent results. You have strong analytical skills, are fluent in written and spoken English and computer literate. You have 1-2 years’ experience with business analysis and project management. You are motivated by driving change and improvements involving many stakeholders at all organisational levels. You thrive in a busy environment, bring a can-do attitude, and while being a team player, it is important that you are able to work independently.

At Novo Nordisk we use our skills, dedication and ambition to help people with diabetes and change their lives. By working with us you will have the opportunity to do the same in a global business environment.

Contact
For further information, please call Nicolai Thorborg at +45 3079 5927 or Daniel Brath at +45 3079 5058.

Deadline
1 December 2013

Corporate Counsel

- Legal
- Denmark - Bagsværd

We are looking for a lawyer who can further develop our assistance in relation to strategic sourcing activities and contracts in Product Supply. The position is available as a temporary position for a 12 months term. The term might become extended.

About the department
The Pharma Law Team is located in Novo Nordisk’s headquarters and is comprised of 8 attorneys. The department is part of Novo Nordisk’s Global Legal organisation which employs more than 100 lawyers at more than 20 locations throughout the world. We provide legal advice within a broad range of areas including non-clinical development, device development, pilot production, clinical development, product registration and approval, manufacturing, marketing, distribution, sale, quality and product safety.

The Job
We are able to offer you a challenging 12 months position as Corporate Counsel in a high-performing, energetic team, servicing a dynamic and expanding group of international companies.

The primary responsibilities of the Corporate Counsel will be to provide legal assistance to the central sourcing function within our Product Supply organisation. As such, focus will be on contract law, and assignments will, among other things, include drafting and negotiating contracts in relation to sourcing of raw material, energy and components on a global scale as well as outsourcing arrangements with key suppliers. In handling the specific tasks, you will interact with key stakeholders within Novo Nordisk, as well as external counsels and partners. You will work closely together with and have independent responsibility for advising specific departments in Novo Nordisk with a large degree of empowerment. The primary work place will be in Bagsværd and Hillerød. As part of the Global Legal organisation, you would also be involved with cross-functional Global Legal projects and, in addition, various opportunities, both in Denmark and abroad, offer potential for further personal development.

Qualifications
You have a Master’s degree in law combined with 3-5 years of working experience from a law firm, a private company or public authority. You have strong experience in handling and negotiating high value contracts with multiple stakeholders. You are probably admitted to the bar in Denmark or abroad. You should have strong communication skills in English (verbal and written), be organized and detail-oriented and take a structured approach to your work. Danish language skills is an advantage, but not a prerequisite. You should be able to handle multiple tasks simultaneously, work effectively in international settings and have strong stakeholder management skills. You have familiarity with IT systems.

At Novo Nordisk, we strive for excellence. As a world leader in diabetes care and a major player in haemostasis management, growth hormone therapy and hormone replacement therapy, we offer our employees opportunities for continuous growth

Contact
For further information, please contact Corporate Counsel Henrik Beckmann at +45 3075 5207.

Deadline
2 December 2013

Technical Trial Manager

- Research & Development
- Denmark - Søborg

Clinical Pharmacology is looking for a Technical Trial Manager, starting 01-Feb-2014. In this job you will be offered exciting opportunities to increase your experience within clinical pharmacology trials and to develop your competencies within a trial life cycle ranging from trial preparation through implementation to trial finalisation.

About the department
Clinical Pharmacology is part of Global Development and our main responsibility is planning, execution, and reporting of clinical pharmacology trials within the area of diabetes. The position is located in Søborg, Denmark.

The job
As Technical Trial Manager, you will play a key role in coordinating the trial activities in close collaboration with the trial responsible Clinical Pharmacologist, and you will be responsible for dedicated operational and administrative trial tasks. On a day to day basis you will be collaborating with a wide range of internal and external stakeholders worldwide, and have the opportunity to enhance your drug development skills.

Qualifications
You are experienced in the planning and execution of clinical trials. As a minimum you have a bachelor degree within relevant scientific area. You are reliable, loyal and service-minded, and act with a strong sense of responsibility. You have a can-do attitude, enjoy working under tight deadlines and master good coordination skills. You have solid IT skills and work in a structured manner with a sense for the details. It is essential that you can act independently, but also as a team player who thrives on contributing to any team you are a part of. You have the ability and willingness to adjust quickly to new situations in a continuously developing environment. Fluency in written and spoken English is essential.

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 Karin Kramer Nielsen at +45 3075 4843.

Deadline
29 November 2013.

Laborant til analyse laboratorium

- Kvalitetssikring
- Danmark - Bagsværd

Er du laborant og kunne du tænke dig at arbejde med support opgaver til vores analyselaboratorium.Så vil et laborantjob i et af analyseteamene i QC Raw Materials i Bagsværd utvivlsomt være noget for dig.

Om afdelingen
QC Raw Materials er en afdeling med 51 medarbejdere. Afdelingen er opdelt i 4 teams, 2 teams i Kalundborg og 2 teams i Bagsværd, hvor denne stilling opslås.De to teams i Bagsværd er ansvarlige for kemisk kontrol af råvarer til både API, færdigvarer og primær pak samt til basis varer. Teamet forestår og behersker en bred vifte af analytiske teknikker og skal sammen med indkøbs- lager- og QA-funktionerne sikre, at produktionsflowet til enhver tid kan opretholdes gennem frigivne råvarer.

Jobbet
Du vil komme til at indgå i et team bestående af en god blanding af laboranter og kemikere.Som laborant vil du blive oplært til en række forskellige af teamets rutinemæssige opgaver og du vil efterfølgende få ansvar for selv og i samarbejde med teamet at planlægge i den takt, der er aftalt. Der vil ske en løbende koordinering med andre funktioner i Novo Nordisk, hvilket kan føre til nye prioriteringer med kort varsel for at sikre, at en produktion ikke står stille.Vi har en åben kultur hvor vi dagligt giver hinanden anerkendende og udviklende feedback.Vi arbejder meget med LEAN, så vores hverdag og aftaler er struktureret omkring daglige tavlemøder, hvor opgaverne fordeles og vi er sikre på, at vi er på rette vej i forhold til vores mål.

Kvalifikationer
På den faglige side skal du være uddannet laborant/tekniker og skal gerne have erfaring med at arbejde i et GMP-reguleret miljø.Du skal have lyst til en afvekslende hverdag, hvor prioriteterne kan skifte med kort varsel.Du skal føle en ansvarlighed for og stolthed ved at nå dit arbejde til aftalt tid, så laboratoriet kan holde en høj troværdighed udadtil.Erfaring med almindelig laborant færdigheder som reagensfremstilling opmærkning af reagenser og kemikalier er et krav.Endelig prøver vi løbende at forbedre vores arbejdsgange via vores LEAN-program. Du forventes derfor at være engageret i arbejdet med problemløsning og optimeringer sammen med dine kolleger, så vi opererer så effektivt som muligt som team og afdeling.

I Novo Nordisk er det dine evner, dit engagement og dine ambitioner, der hjælper os med at forbedre mange menneskers liv. Til gengæld tilbyder vi dig muligheden for at arbejde sammen med usædvanligt talentfulde kolleger, og vi tilbyder dig en lang række muligheder for professionel og personlig udvikling.

Kontakt
Hvis du vil vide mere om jobbet, kan du kontakte Britta Johansen på +45 3075 7463.

Ansøgningsfrist
30. november 2013

Laborant

Du kan lære mere om Novo Nordisk�s største produktionssite ved at bruge www.novonordisk.com/kalundborg-careers

- Produktion
- Danmark - Kalundborg

Søger du nye udfordringer? Vil du være en del af et team i udvikling, hvor vores fokus er kvalitet, faglighed og et positivt mindset omkring at vil være det bedste team inden for vores felt? Er svaret ja kan din nye arbejdsplads være vores kemiske detemir 1 team i Purification Plants laboratoriet i Kalundborg.

Om afdelingen
Vi har en udfordrende og varierende arbejdsdag og supporterer flere forskellige fabrikker i Kalundborg. Vi arbejder med forskellige analysemetoder i teamet, bl.a. HPLC, GC, UV samt TOC og vandkemiske analyser. Du kan forvente en varierende hverdag, hvor du får indflydelse på hvordan vi bedst muligt strukturerer vores opgaver, således at vi bliver endnu bedre til at levere analyser af rette kvalitet og til den aftalte tid.

Analyser, vedligehold og optimeringer.

I teamet søger vi en energisk laborant med drive og initiativ, som har viljen og lysten til at gå forrest med hensyn til at optimere og udvikle på vores arbejdsrutiner, således at vi altid sikrer størst mulig reduktion af omkørselsprocenter på vores analyser. Din primære opgave i teamet vil blive TOC og sprit 7120 metoden vi er det eneste sted i DAPI den bliver kørt. Så det vil være fordel at kende til HPLC og analysen men ikke et krav. Der vil således også være mulighed for at din hverdag kan indeholde projektorienterede opgaver, som du er med til at drive både i afdelingen og på tværs i Diabetes API.

Jobbet
Du bliver medansvarlig for den daglige drift i laboratoriet og vil indgå i teamet bestående af 12 laboranter og 3 kemikere. Dine arbejdsopgaver vil primært være udførsel af analyser, samt deltagelse i systematisk problemløsning i forbindelse med udfordringer på analyserne. Derudover kan du, som vores nye laborant forvente på sigt, at komme til at arbejde med udarbejdelse og revision af dokumenter, vedligeholdelse, optimering og kvalificering af udstyr samt godkendelse af analyseresultater.

Kvalifikationer
Du er uddannet laborant, laboratorietekniker eller har en anden relevant uddannelse indenfor analytisk kemi. Fra tidligere job har du måske fået erfaring fra farmaceutisk industri underlagt GMP-krav. Men ellers vil oplæring finde sted for den rette person.

Som person er du optimistisk, robust og åben i din daglige dialog med kolleger og besidder et supportmindset i forhold til vores kunder. Du er struktureret, systematisk og kvalitetsbevidst. Du har fra tidligere ansættelser vist, at du kan arbejde selvstændigt og er god til at samarbejde og kommunikere. Du bevarer overblikket og et godt humør i et til tider meget travlt arbejdsmiljø.

I Novo Nordisk er det dine evner, dit engagement og dine ambitioner, der hjælper os med at forbedre mange menneskers liv. Til gengæld tilbyder vi dig muligheden for at arbejde sammen med usædvanligt talentfulde kolleger, og vi tilbyder dig en lang række muligheder for professionel og personlig udvikling.

Kontakt
Vil du vide mere om stillingen så kontakt Rune Olsen på +45 3075 1026.

Ansøgningsfrist
29.november 2013

Industrial PhD fellow

- Research & Development
- Denmark - Måløv

In this PhD project you will have the chance to start your scientific career in haemophilia research and thereby in the longer term positively impact the lives of people with haemophilia.

About the department
You will be located in the department of In Vivo Haemophilia Pharmacology at Novo Nordisk. Our main focus is state of the art in vivo effect models of haemophilia. We support the Novo Nordisk haemophilia portfolio as well as the global haemophilia society with basic and advanced pharmacology data and disease understanding. The department comprises four PhD’s with backgrounds in biology, human biology, pharmacy and veterinary medicine, six in vivo laboratory technicians, and a trainee.

The Job
Haemophilia A is a bleeding disorder caused lack of coagulation factor VIII (FVIII) in the blood. In haemophilia A, much research has gone into replacing the lacking FVIII. However, there may potentially also be a therapeutic benefit of pharmacologically inhibiting fibrinolysis, i.e. the process leading to clot resolution. There is still a significant lack of knowledge within this field and in this regard several relevant scientific questions can only be appropriately addressed in vivo. The PhD project will try to answer such questions in mouse and rat models of haemophilia.

In support of the project, a research collaboration between the University of Copenhagen, Children's Hospital Research Foundation at the University of Cincinnati College of Medicine, The University of North Carolina at Chapel Hill, and Novo Nordisk A/S is set up. Thus, you will have access to support from world-leading experts in the field.

As an industrial PhD fellow in In Vivo Haemophilia Pharmacology your key responsibility will be to drive the project forward. This primarily means planning and executing in vivo experiments. Additionally, the curriculum includes attending courses (30 ECTS) and giving scientific presentations internally as well as externally.

Qualifications
You hold an academic degree (MSc level) in veterinary medicine, medicine, human biology or similar with outstanding marks. Preferably, you have knowledge on haemostasis and hands on experience with in vivo research in rodents. You are a dedicated self-motivating team player with a high degree of flexibility and a strong personal drive. Fluency in written and spoken English is essential. The project includes a three month stay in the US for which you must be able to temporarily relocate.

At Novo Nordisk, we strive for excellence. As a world leader in diabetes care and a major player in haemostasis management, growth hormone therapy and hormone replacement therapy, we offer our employees opportunities for continuous growth.

Contact
For further information regarding the position, please contact Tom Knudsen at +45 3075 1869.

Deadline
7 December 2013

QA tekniker

- Kvalitetssikring
- Danmark - Gentofte

Kunne du tænke dig at være med til at kvalitetssikre Novo Nordisk A/S hæmofili og væksthormon portefølje? Trives du i situationer hvor der kræves personligt ansvar og evne til at tage beslutninger med kvaliteten i fokus?

I Biopharm QA sikrer vi kvalitet ved at være tæt på processen. Vi søger derfor engagerede medarbejdere der vil være med til at tage ansvar for denne QA rolle.

Om afdelingen
Biopharm QA AP varetager kvalitetssikring af 3 fyldefabrikker samt forsyninger til hele Site Ge. Den her beskrevne udvidelse vil være til team 545.06 QA-Visuel Inspektion, som QA supporter for afd. 111 i Gentofte. Afd. 111 producerer markedsførte hæmofili- og væksthormonpræparater samt flere produkter til klinikproduktion. Den alsidige produktion i vores kundeafdeling bidrager med en kompleksitet der stiller krav til vores medarbejderes faglige kompetencer. Vi kan tilbyde et job blandt dygtige kollegaer i et område, hvor du vil få et enestående overblik over myndighedsforventninger og krav i den farmaceutiske industri.

Jobbet
Som QA supporter vil din hverdag primært være inde i produktionsområdet. Her vil du være ansvarlig for at udføre inspektion af stikprøver på færdigt produkt, udtage analyseprøver til analyselaboratorier, udføre QA review af logbøger og varetage stempling og udlevering af batchdokumentation til produktionen. Du skal via dit arbejde bidrage til at forebygge fejl og sikre det rette quality mindset og GMP-niveau i produktionen.

Kvalifikationer
Du har en uddannelse som farmakonom, laborant eller tilsvarende. Erfaring fra medicinalindustrien er at foretrække, men er ikke en forudsætning for at komme i betragtning. Du skal besidde evnen til at foretage selvstændige vurderinger, men også evnen til at spørge efter hjælp når du er i tvivl. Du skal have et quality mindset, som sikrer at du altid sætter kvalitet først.

I Novo Nordisk er det dine evner, dit engagement og dine ambitioner, der hjælper os med at forbedre mange menneskers liv. Til gengæld tilbyder vi dig muligheden for at arbejde sammen med usædvanligt talentfulde kolleger, og vi tilbyder dig en lang række muligheder for professionel og personlig udvikling.

Kontakt
Vil du vide mere om stillingen, så kontakt Rasmus Madelung Nielsen på +45 3075 6071.

Ansøgningsfrist
25.november.2013

Requisition ID 18170BR
Title Pharma Field Sales-Diabetes Care Specialist (DCS)-Marine Park, NY
Job Category Field Sales
Job Description Pharma Field Sales - Diabetes Care Specialist (DCS) - Marine Park, NY

Novo Nordisk is a focused healthcare company and a world leader in diabetes care. We are actively working to change the course of the diabetes pandemic, improve the daily lives of people with diabetes, and to expand the possibilities for people with hemophilia.

This position represents Novo Nordisk within an assigned territory with the goal of maximizing sales and positioning Novo Nordisk as the leading company in diabetes care. The DCS must assume responsibility for achieving sales goals by implementing marketing and sales strategies aimed at effectively selling and promoting Novo Nordisk’s portfolio of diabetes products to physicians, pharmacists, nurses, and other paramedical customers and current co-promotion partners who make or are involved in purchasing and prescribing decisions. This position also determines and recommends the most appropriate Novo Nordisk product and approved usage for the needs of the customers.

The DCS reports to the District Business Manager of the specific sales territory and interacts regularly with territory partners. The DCS sells and promotes Novo Nordisk’s portfolio of diabetes products with a focus on targeted and non-targeted primary care physicians, pharmacists, nurses, and other members of patients’ primary care team.

KEY SUCCESS FACTORS: EDUCATION, EXPERIENCE, KNOWLEDGE AND SKILLS
•At least one year pharmaceutical sales experience OR at least one year business-to-business (B2B) sales required.
•Bachelor’s Degree from college or university accredited by an organization recognized by the US Department of Education required. Advanced degree preferred.
•Top 20% sales ranking for 1 out of last 2 years in a sales role, documented (regionally or nationally) or equivalent documentation for B2B candidates
•Proven leadership and decision-making ability.
•Solid understanding of diabetes disease state and Novo Nordisk’s products, coupled with aptitude for learning and ability to communicate technical and scientific product and disease management information.
•Must have a consistent proven track record of winning sales results
•Must be a self-starter and be able to evaluate options and make decisions with minimal supervision.
•Intermediate computer skills required (Windows, Word, Excel)
•Prior computer experience using sales data/call reporting software ideal
•Must maintain a valid driver’s license and obey all applicable traffic laws.
•Approximately 10% overnight travel

A winning attitude and passion for making a real difference in the lives of our patients ensures the right fit for you and the team at Novo Nordisk. Our passion for helping people live better lives and our award-winning product pipeline can only be as effective as our ability to provide life-changing information to physicians and customers. Our Sales professionals ensure that the latest therapies and products reach the people who need them most, by listening to their needs and advocating for even greater enhancements.
Department SALES - SOUTH BROOKLYN NY
Position Location US - Field Based - Across US
City MARINE PARK
State/Provinces US - NY
Degree Required Bachelor's Degree Required
Percent Travel 0 - 10%

Training Partner

- Production
- Denmark - Hjørring

Are you ready for a key role in developing a new training organisation in Novo Nordisk Devices & Supply Chain Management (D&S)? Then apply for this newly established position where you will have an impact on the organising and structuring of training across our production site in Hjørring.

About the department
You will join a team of 5 highly skilled colleagues in the Business Support of Needle Manufacturing and Sourcing (NMS). It is our main responsibility to deliver support of highest possible quality to the management by ensuring effectiveness and efficiency in business processes and providing project portfolio management and training. The production site has a total of 225 colleagues who work dedicatedly to secure the global supply of pen needles.

The Job
As training partner you will take on different roles such as project manager, facilitator and teacher at workshops and developer of training roles and organisation. You will be responsible for developing and implementing an effective learning set-up and training plan for the site. As such, you will drive the development, implementation and follow up on learning activities. At workshops and on the production floor you will train employees, mainly operators, in using the standard training tools and methods, while ensuring that the standard is translated into the employee’s everyday context. As an advocate for the training standard you will play a major role in promoting and implementing the agenda and related learning processes. At the same time, you keep developing the training setup to be an effective provider of clearly defined roles and responsibilities. Furthermore, you will be part of a training community with other training partners in D&S.

Qualifications
You hold a Master’s degree, e.g. within Psychology, Communication or Education. Your background covers experience from a position as HR Consultant or similar role providing you with coaching and training experience. You know exactly how to utilise your strong social and communication skills to become an excellent go-to person who can lead the way by engaging and motivating colleagues. You are a natural when it comes to building strong relations, and you are able to drive processes proactively in complex environments of many different stakeholders. Moreover, you have a pragmatic and positive mindset allowing you to create solutions that make a positive difference on the production floor. To be a success, you must have experience with change management processes and project management. We look forward to receiving your application in Danish or in English whichever you prefer.

At Novo Nordisk, you will join a patient-centred culture of talented professionals. We respect individuality and empower you to make the most of your potential.

Contact
For further information, please contact Maja Hjorth Just at +45 3979 2850.

Deadline
1 December 2013

Administrativ assistent med ambitioner

- Administration
- Danmark - Gentofte

Vores administrative kollega har fået nye udfordringer og vi søger derfor en ambitiøs administrativ assistent med reference til afdelingslederen i Biopharm QA API.

Om afdelingen
Du skal have lyst til at arbejde i en QA afdeling, hvor trivsel og høje ambitioner går hånd i hånd. Vi er hovedsageligt placeret i Gentofte, men har også teams på andre sites.Afdelingen beskæftiger sig med kvalitetssikring af FVII, Glucagon og hGH API under hensyntagen til cGMP og gældende myndighedskrav.

Jobbet
Du er ledelsens højre hånd og yder højt kvalificeret support og sikrer en velfungerende infrastruktur i afdelingen. Du skal kunne lide at arbejde selvstændigt og synes om at løse praktiske opgaver, der letter hverdagen for andre. Du ser ofte selv, hvor du kan gøre en forskel og tager initiativet til dette.Stillingen består overordnet i at udføre administrative opgaver. Udfordringen er at sikre, at alle afdelingernes administrative processer altid er ”up to date”. Dette omfatter dels en række faste administrative opgaver såsom vedligehold af afdelingsmappe og GlobeShare, afregning i Concur/ICE og budgetopfølgning. Endvidere vil der være praktiske opgaver såsom indkøb, opfølgning på afdelingsmål, planlægning af møder samt f.eks. opgaver i forbindelse med personaleansættelser og fratrædelser. Desuden vil du deltage i planlægning og afvikling af den praktiske side af myndighedsinspektioner i Biopharm.

Du er med til at sikre gode samarbejdsrelationer. Bl.a. er samarbejdet med de øvrige QA afdelinger vigtig og der vil også være opgaver på tværs i Biopharm QA området. Du skal derfor have lyst og evne til at kommunikere, være fleksibel og initiativrig. Du vil være en aktiv deltager i netværket for de administrative i Biopharm QA.Arbejdet foregår i et afslappet og uformelt miljø, hvor vi lægger vægt på trivsel, vilje til at gøre en forskel, humor og engagement.

Kvalifikationer
Du har en relevant administrativ uddannelse og gerne flere års erfaring. Du har allerede demonstreret overbevisende resultater og en ambitiøs tilgang til dit arbejde. Du er rutineret bruger af diverse IT systemer. Dine opgaver kræver både selvstændighed og evne til at kommunikere, og du skal have gode formuleringsevner i både skrift og tale. Som person er du engageret og struktureret med et positivt livssyn og trives med mange store udfordringer.

I Novo Nordisk er det dine evner, dit engagement og dine ambitioner, der hjælper os med at forbedre mange menneskers liv. Til gengæld tilbyder vi dig muligheden for at arbejde sammen med usædvanligt talentfulde kolleger, og vi tilbyder dig en lang række muligheder for professionel og personlig udvikling.

Yderligere oplysninger:Stillingen er til besættelse snarest muligt.

Kontakt
Nærmere information kan du få hos Helle Christensen på +45 3075 5721 eller Ulla Falkenberg på +45 3075 8890.

Ansøgningsfrist
24. november 2013

Regulatory Professional – CMC

- Regulatory Affairs
- Denmark - Søborg

Join a fast-changing environment where engaged people do their best every day to get Novo Nordisk medicines approved across the globe. Our people have a unique combination of scientific insight and the ability to navigate many agendas and stakeholders. This makes Regulatory Affairs a truly interesting place to work but also challenging. Are you up for the challenge?

About the department
The RA-Inflammation & Growth Hormone Area is part of Regulatory Affairs and is a dedicated and diverse team of around 25 people. You will work in the CMC department with nine experienced and engaged colleagues working closely with production and quality departments. We are breaking new ground in a dynamic environment, where our dedicated group prepares and executes the regulatory strategies and is responsible for global interactions with regulatory authorities. We work closely with many different stakeholders within Novo Nordisk headquarters and affiliates. Together we go an extra mile to succeed.

The Job
The position is located in Søborg and you will be part of a team of Regulatory Project Managers, Professionals and Associates. Your role will be to diligently secure the CMC input to global regulatory strategies and submissions for development and LCM projects. You will plan, coordinate and review regulatory documentation and chair internal working groups as our primary sparring partner for the Production and CMC Support units in Novo Nordisk. You will work closely with the Regulatory Project Manager, who is overall responsible for the regulatory part of our projects. In addition, you will be part of cross functional teams sharing your knowledge and getting new ideas. You will report to the Department Director.

Qualifications
As a minimum, we expect you to have a biology/health science university degree plus experience from pharmaceutical Industry working with regulatory aspects of CMC in development or Life Cycle Management projects. You can document solid scientific understanding and you have successfully worked in project teams respecting the contribution of everyone. You have demonstrated that you are organised, detail-oriented and a proactive problem-solver. You communicate well and are completely comfortable speaking and writing English and can deal with the challenges of international communication.On a personal level, you thrive in busy and changing circumstances and bring a can-do attitude and a healthy sense of humour. You keep focus on jointly moving the projects and are able to work independently, be challenged and find new solutions.

At Novo Nordisk, your skills, commitment and ambition help us change lives for the better. In exchange, we offer you a chance to work with extraordinary talent and to develop professionally and personally.

Contact
For further information, please contact Bente Brunbakke at +45 3075 7875.

Deadline
1 December 2013.

Analysekemiker til Biopharm QC New Haemophilia

- Produktion
- Danmark - Gentofte

Vil du arbejde med Biopharms brede portefølje af produkter, og hjælpe os med at være Fast to Market, og har du lyst til at være en del af en dynamisk afdeling med mangeartede opgaver, så er denne stilling lige noget for dig.

Om afdelingen
I Biopharm QC New Haemophilia er vi ansvarlige for support til vores produktioner og løbende optimeringer af vores mange processer. Laboratoriet er ansvarlig for at levere analyseresultater til frigivelse af kliniske fase 3 batches på Biopharm’s hæmofili portefølje. Afdelingen består af 50 medarbejdere organiseret i fire analyseteams samt en stabsfunktion, som varetager tværgående aktiviteter.

Jobbet
I Biopharm QC New Haemophilia søger vi en kemiker til en spændende stilling med hovedvægt på BIO analyser, herunder ELISA og enzymkinetiske analyser samt farmacopé metoder, så som pH, Karl Fischer og NIR.Du vil indgå i BIO-teamet bestående af en teamleder, kemikere og laboranter. Som vores nye medarbejder skal du være med til at sikre den daglige drift af vores analysemetoder til analyse af fase 3 produkter.Din opgave bliver at sørge for, at analysesvarene lever op til gældende GMP-regler samt udarbejdelse af diverse dokumenter som instruktioner, analyseforskrifter, afvigelsesrapporter og ændringsansøgninger. Du skal godkende analyseresultater og problemløse på analyserne.Du skal samarbejde med teamet og på tværs af afdelingen samt være i tæt kontakt med QA, produktionsafdelinger og QC laboratorier. Vi kan tilbyde dig et udfordrende og innovativt miljø med store muligheder for udvikling af dine faglige og personlige kompetencer.

Kvalifikationer
Du har en solid bioanalytisk baggrund og har erfaring og lyst til at arbejde med bioteknologiske analysemetoder herunder ELISA, SDS-PAGE og enzym kinetiske analyser på nye produkter.Du har viljen og evnen til hele tiden at forsøge at gøre tingene bedre, og forny arbejdsprocesserne.Du er uddannet farmaceut, cand. scient., ingeniør eller har en anden relevant uddannelse indenfor analytisk kemi. Du har erfaring med optimering og validering af kemiske analyser og GMP, og har solide IT-kundskaber og erfaring med anvendelse af statistik. Du skal kunne dansk og engelsk flydende, i skrift og tale.

Du er god til at skabe overblik og prioritere din tid. Du er systematisk og har en høj grad af ansvar- og kvalitetsbevidsthed. Som person er du åben og engageret og i stand til at motivere og inspirere dine kollegaer. Du har vist fra tidligere ansættelser, at du kan arbejde selvstændigt, og er god til at samarbejde og kommunikere med kollegaer. Du bevarer overblikket og et godt humør i et til tider meget travlt arbejdsmiljø.

I Novo Nordisk er det dine evner, dit engagement og dine ambitioner, der hjælper os med at forbedre mange menneskers liv. Til gengæld tilbyder vi dig muligheden for at arbejde sammen med usædvanligt talentfulde kolleger, og vi tilbyder dig en lang række muligheder for professionel og personlig udvikling.

Kontakt
Vil du vide mere om stillingen, så kontakt Lissi Falch Kaag på +45 3075 1015. Send din ansøgning online. Tiltrædelsesdato: 01. januar 2014.

Deadline
26. november 2013

Assistant in Biostatistics & Epidemiology - Aalborg

- Administrative
- Denmark - Aalborg

Biostatistics & Epidemiology are looking for an experienced administrative assistant for our department located in Aalborg.

About the department
Biostatistics & Epidemiology consist of approx. 125 employees – primarily statisticians, statistical programmers and epidemiologists - distributed in eight departments. The area is responsible for statistical and epidemiological support to the development of medicine. It is a very dynamic and well-functioning area with many stakeholders within the Danish organisation and across borders to our sister departments in USA, India, Japan and China, and our outsourcing partners in India.

The Job
As administrative assistant you will be part of a team consisting of six assistants supporting the area. You will have full responsibility for own tasks but also work closely with your assistant colleagues. You will be located in Aalborg, while your assistant colleagues are located in Søborg.The administrative job covers a broad range of tasks, e.g. booking of travel and settling of travel expenses, purchase, seminar-, meeting- and course planning, registrations in SAP, update of personnel binders, and general administrative assistance to the employees in the area. You will be responsible for supporting the department in Aalborg covering 16 employees, but also responsible for planning and follow up on budgets in Biostatistics and Epidemiology in SAP in close collaborations with the managers. We are a fast growing area and therefore you will also be involved in on-boarding of new employees.You will work in a challenging environment with on-going personal and professional development.

Qualifications
You are a team player, responsible and continuously have an eye on the details. You take initiative and like new challenges. You can handle simultaneous tasks and are able to complete them, even when you are busy. You are engaged, positive and willing to actively contribute to the department.You have some years’ experience from a similar position, where you have handled administrative tasks incl. budget planning and follow up in SAP. You are an experienced IT user, familiar with the Office-package and therefore fully versed in Word, PowerPoint and Excel. You should be articulate in both Danish and English as well oral as written.

At Novo Nordisk we use our skills, dedication and ambition to help people with diabetes and change their lives. By working with us you will have the opportunity to do the same in a global business environment.

Contact
For further information, please contact Malene Højbjerre at +45 3079 6209.

Deadline
8 December 2013.

Chemist

- Quality
- Denmark - Bagsværd

Do you want to manage and improve a variety of material analyses in a highly professional QC laboratory? In that case you should apply for the new position as Chemist in QC Raw Materials. If you are as ambitious as we are, you can look forward to an exciting job in an environment where we seek to be best in class in everything we do.

About the department
Your new department, QC Raw Materials, consists of 59 employees who are located in Bagsværd and Kalundborg. You will join the analytical team in Bagsværd, which is responsible for the chemical control of raw materials for the production across Novo Nordisk. We cooperate with a variety of functions, including purchase, storage and QA.

The Job
You will work closely with the chemists and laboratory technicians in your team to approve the raw materials and thereby enable a continuously high pace in the production. You will be responsible for several analytical methods and for securing that the analytical flow is aligned with our customers’ expectations along with regulatory compliance. Your primary focus will be chromatographic analyses (HPLC and GC-MS) however a broad understanding of analytical methods is an advantage. You will among other things be responsible of method development and validation, pharmacopeial monitoring and updates, handling of change requests, non-conformities and OOS. A high GMP and compliance mind-set is thus required. In general, the assignments carried out by the department are diverse as we deliver to various parts of Novo Nordisk. This gives a variety of analytical challenges and strong collaboration with your colleagues is therefore an essential key to success.

You will further support the laboratory technicians in their daily operations to ensure that the analytical performance and equipment live up to the industry standard.

Qualifications
You hold an MSc in Pharmacy, Engineering or another relevant field within the natural sciences. Your degree is supplemented with several years of experience from a similar job in which you have gained in-depth knowledge of working with GMP in a laboratory environment. Strong practical and theoretical experience within chromatographic analyses will be required. You have a high level of energy to drive yourself and your colleagues forward. You are result-oriented and take pride in delivering on your milestones, and you motivate your colleagues with a positive, forthcoming attitude. You work well independently, although it also motivates you to cooperate with colleagues and stakeholders across functions and departments. Lastly, you must have fluency in written and spoken Danish and English.

At Novo Nordisk, we strive for excellence. As a world leader in diabetes care and a major player in haemostasis management, growth hormone therapy and hormone replacement therapy, we offer our employees opportunities for continuous growth.

Contact
For further information, please contact Jacob Kirkegaard Jensen at +45 3075 6914.

Deadline
1 December 2013

Global Publication Manager

- Marketing
- Denmark - Søborg

Novo Nordisk Global Medical Affairs Diabetes is looking for a Global Publications Manager.

About the department
Novo Nordisk is recruiting a Global Publications Manager to join the Global Medical Affairs team in the Company Headquarters outside of Copenhagen, Denmark. This is a unique opportunity to work for a world leader in diabetes care and help improve the lives of people with diabetes worldwide.

Global Medical Affairs is responsible for delivering consistent scientific communication across phases in clinical trial programmes.

The job
In this key position you will report to the Global Medical Director, and be responsible for managing the strategic global publication plans, collaborating closely with medical affairs colleagues, commercial colleagues from marketing, as well as clinical development, discovery, regulatory, and global affiliate offices.

You will be chairing publication meetings with key stakeholders from medical affairs, medical and science teams and regional offices in cooperation with the Global Medical Advisors/Director.

To succeed you need to provide impact and combine your knowledge and experience with outstanding interpersonal and influencing skills. You easily build constructive relationships across multi-disciplinary departments and with key opinion leaders, and are able to select and manage agencies to deliver to budget and target.

You have professional project management skills and are action-oriented with ability to deliver results in a fast-paced environment. Previous therapy experience within diabetes is of advantage but not a requirement.

Qualifications
Proven expertise in a similar position together with several years of experience of medical/science journal publishing – either with a publisher, medical communication agency or a pharmaceutical company is required.

You have an excellent knowledge and understanding of congress, journal and web publication possibilities, as well as international publication guidelines and application to the pharmaceutical industry.

You are a business or science graduate (PhD or MSc equivalent) and skilled at maintaining a brand’s scientific integrity while translating data into crisp scientific messages.

At Novo Nordisk, we strive for excellence. As a world leader in diabetes care and a major player in haemostasis management, growth hormone therapy and hormone replacement therapy, we offer our employees opportunities for continuous growth.

Contact
For further information, please contact Lise Baltzer +45 3079 8782.

Deadline
28 November 2013.

Moulding Process Engineer

- Production
- Denmark - Hillerød

Device manufacturing & Sourcing (DMS) seeks 1 talented engineer with experience within the field of injection moulding and tools. In this job, you will be responsible for the performance of specific injection moulding tools and can you set direction and motivate others, then go for this job.

About the department
Moulding Support Components (MSC) is part of DMS Moulding Support and consists of 13 moulding process engineers and process technicians. You will work in an international atmosphere, and be surrounded by talented and dedicated colleagues with whom you can exchange experiences. We are a team of process experts and are responsible for process support of injection moulded plastic parts produced internally in Hillerød DK and on various production sites worldwide.

The Job
We need 1 experienced moulding process engineer who will be responsible for expert moulding/tool support on Novo Nordisk owned moulding tools at one of our strategic moulding suppliers.We can offer you an international workplace with a high degree of influence and planning of your own job and daily tasks, as well as working with the high quality and complexity of equipment within injection moulding and tooling.As an engineer in DMS Moulding Support Components you will support moulding and tool projects in our production with focus areas such as lean, problem-solving, optimization and documentation.

Qualifications
You hold a degree in engineering, or likewise experiences, together with hands-on skills. You possess a great business sense and are a motivating player who achieves specified goals. You have minimum 3 years of experience with mass production of precession moulded plastic components and have a thorough knowledge within injection moulding, moulding tools and/or validation. Furthermore, you possess good interpersonal skills and are process oriented with the ability to communicate simple and uncomplicated. Communication in English in speech and writing is a necessity, since you will cooperate internal and with international suppliers and customers.

At Novo Nordisk we use our skills, dedication and ambition to help people with diabetes and change their lives. By working with us, you will have the opportunity to do the same in a global business environment.

Contact
For further information, please contact Paw Holmgaard Krogh at +45 3075 4269.

Deadline
22 November 2013.

Specialist - Talent Management & Leadership Developement

- Human Resources
- Denmark - Bagsværd

Can you grow a leader-led talent management culture to build a strong pipeline of talents? If you are also gifted with HR and LEAN skills, this could be your chance to significantly impact our global talent and leadership development initiatives through effective programmes and processes.

About the department
You will report to the Director of People & Organisation (P&O) and be part of a team of dedicated and highly professional HR and Communication colleagues. You will be working in an environment of strong values, high standards and energizing relations. Your home base could be at any of our production sites in Denmark, France, US, China and Brazil, and you must be ready to travel between the sites. You can expect a large degree of interaction with colleagues across the globe, leaving you with a challenging and inspiring job that could easily pave the way for your future career.

The Job
As Talent Management & Leadership Development Specialist you will have a key role ensuring that our pool of future leaders, project managers and specialists are always of the highest quality. You are responsible for the entire portfolio of leadership development activities and talent management processes in Diabetes Finished Products (DFP) and for roll-out at our production sites all over the world, as well as ensuring the processes are being followed. You refine and adapt the processes to our business needs - and make sure they are implemented on a global scale. In short, your job is to build effective leadership development activities and a strong culture of leader-led talent management to grow our talent pipeline.

This job will provide you with a large network all over the world, and as you will be working across all our organisational levels. You can expect diversified and challenging assignments, and around 30–40 travel days per year.

Qualifications
You hold a relevant Master’s degree and have at least 5 years of relevant experience e.g. from a global HR function or working internationally for a consulting business. Your LEAN toolbox is full, and you are used to applying the tools in your working day. You work systematically and efficiently and are willing to go the extra mile to achieve the milestones and goals. Your insight into human behaviour is broad and reflects both empathy and integrity and as such the ability to coach and consult colleagues at all levels. In addition, you use a motivating and resourceful method, and you have got what it takes to create respect and to make an impact in the organisation. Lastly, you have a convincing attitude and the ability to collaborate with a broad range of stakeholders.

At Novo Nordisk, you will get the opportunity to build a career among talented professionals. Across borders and job functions, we share an ambition to continuously treat and defeat diabetes.

Contact
For further information, please contact Jesper Cassøe Andersen at +45 3075 9525.

Deadline
2 December 2013

Kemikere til aseptisk produktion

Du kan lære mere om Novo Nordisk�s største produktionssite ved at bruge www.novonordisk.com/kalundborg-careers

- Produktion
- Danmark - Kalundborg

Da der sker nye og spændende tiltag har vi behov for flere erfarne kemikere til vores support-teams inden for miljø, formulering, fyld & inspektion samt vask & sterilisation. Hvis du er ambitiøs og har en positiv ’can do’ tilgang, vil du passe perfekt ind hos os.

Om afdelingen
Vi er 183 kolleger i AP Filling & Supply og er placeret på Novo Nordisks site i Kalundborg, hvor vi er 3.500 ansatte i Novo gruppen. Vores overordnede ansvar er at formulere og fylde insulin og sende det til pakning.

Jobbet
Som kemiker AP Filling & Supply er du ansvarlig for at sikre compliance og håndtere afvigelser (NC’er) og optimeringer (CR sager). Du er ansvarlig for dokumentation og for at drive processerne samt mindre projekter, som involverer flere i organisationen. Du vil arbejde metodisk med dine opgaver, da vi har fokus på at optimere både LEAN adfærd og anvendelse af LEAN metoder. Jobbet er særligt interessant, da vi har to fantastiske support-teams, hvor vi får det meste til at lykkes og hvor du har en faglig bredde, der er svær at finde andre steder. Lige nu er vi i gang med et projekt, hvor vi skal opgradere og kvalificere en linje til aseptisk produktion, hvilket åbner op for en række spændende muligheder.

Du lykkes ved at være synlig, have gode relationer til produktionen og ved at have en go-look-see tilgang i din support til produktionen. For at lykkes kræver det ligeledes, at du forstår processerne og har gode relationer til vores interessenter, som kan være QA, QC, pakkeriet, RA, leverandører og ikke mindst alle medarbejdere i produktionen.

Kvalifikationer
Du har en akademisk uddannelse, fx cand.scient, ingeniør, pharmaceut eller dyrlæge. Dit erfaringsniveau påvirker opgavernes kompleksitet og kan dermed tilpasses dig, hvad enten du er nyuddannet eller erfaren. Det er vigtigt, at du har erfaring fra jobs med team-arbejde, hvor du har været vant til at arbejde med fælles mål. I de jobs du har haft (fuldtid eller deltid), har du vist, at du er dygtig til at bygge relationer og er i stand til at engagere dine kolleger, når du har ansvaret for en opgave. Du har også vist, at du går ind til selv svære udfordringer med en positiv og optimistisk tilgang og med en vilje til at få tingene til at lykkes.

Site Kalundborg er en by i byen, kun godt en times kørsel fra København. Området er på 1.350.000 m2 med eget vejnet. Vi er 3.500 medarbejdere i alt fordelt på 16 fabrikker, og vi producerer bl.a. 50 % af verdens insulin. Site Kalundborg kan helt kort sammenfattes til: udviklingsmuligheder uden ende.

I Novo Nordisk er det dine evner, dit engagement og dine ambitioner, der hjælper os med at forbedre mange menneskers liv. Til gengæld tilbyder vi dig muligheden for at arbejde sammen med usædvanligt talentfulde kolleger, og vi tilbyder dig en lang række muligheder for professionel og personlig udvikling.

Da vi ansætter løbende, skal du sende din ansøgning snarest.

Kontakt
Vil du vide mere om stillingen, så kontakt Thorid Lassen på +45 3075 8009 eller Jeppe Frøslev på +45 3075 2272.

Ansøgningsfrist
8. december 2013

Project Manager

Learn more about the largest site in Novo Nordisk�s global production network using this link www.novonordisk.com/kalundborg-careers

- Production
- Denmark - Kalundborg

Are you motivated by bringing ideas to life and facilitating improvements and changes that are critical for our ability to meet our business needs? Do you have what it takes: Production experience, business mindset, strong communication skills and project manager experience? Then this may be your opportunity to pursue a challenging job in a global organisation.

About the department
Insulin Manufacturing (IM2) Projects is anchored in Diabetes Active Pharmaceutical Ingredients (DAPI) in Kalundborg. IM2 is developing rapidly, therefore we continuously execute large investments in our factories. You will join a team of 8 dedicated project managers with different backgrounds and experience. It is a team with strong focus on knowledge sharing and learning. We qualify, drive and facilitate the execution and implementation of both small and large investments and strategic projects. Processes, regulatory requirements and interactions between manufacturing areas constitute the focal point of most improvement projects. We work in close collaboration with stakeholders including Global Project office, Global Investment Management and the Manufacturing Development (MDEV) organisation.

The job
As Project Manager you apply appropriate project management methodologies and tools, define, challenge and manage project scope. Your primary role is to drive improvement projects and manage the project team, suppliers, the steering committee and reference group to ensure engagement, cooperation and results. You will be accountable for cost, timelines and deliverables. You will identify and assess project risks and facilitate senior management’s decisions on project direction and continuation. You will ensure alignment of expectations and support from crossfunctional stakeholders throughout the project. You will support communication and implementation of solutions. You will take part in the development of our project management methodologies and tools. Day to day operation is a mix of above responsibilities and includes a high degree of independence and interaction with our stakeholders.

Qualifications
We are seeking a candidate with an engineering background, with +7 years of experience from the pharmaceutical industry within production. You have a successful track record and documented skills in managing complex, crossfunctional, interdisciplinary projects and overcoming various unforeseen difficulties. You have some experience working at the interface of MDEV and production development and are used to communicating clearly with diverse stakeholders at various organisational levels. Experience in developing sourcing strategies to ensure high level management commitment and contract negotiation will be a plus.

You possess strong cross functional leadership skills, including an ability to build relationships and ensure trust and commitment from both internal and external stakeholders. You must possess personal power to influence others and to retain focus while having a high level of execution. The job requires you to create a strong network internally in Novo Nordisk as well as with suppliers worldwide. You must therefore have excellent communication skills, both orally and in writing, and be capable of working in a complex interdisciplinary organization.

You must be fluent in Danish and English (both written and oral) and master Microsoft Office.

Engagement and a positive mindset, combined with a willingness to make a difference and walk the extra mile are personal competencies needed in order to be a success in this job. You must be able to work both independently as well as within a team. You are innovative, dynamic and

enthusiastic.

At Novo Nordisk, your skills, dedication and ambition help us change lives for the better. In exchange, we offer you an opportunity to work in an exciting environment and benefit from a range of possibilities for professional and personal development.

Contact
For further information, please call Anker Lionett at +45 3079 8172.

Deadline
28 November 2013.

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Technical Trial Manager (Søborg, Denmark)

Laborant til analyse laboratorium (Bagsværd, Danmark)

Laborant (Kalundborg, Danmark)

Industrial PhD fellow (Måløv, Denmark)

QA tekniker (Gentofte, Danmark)

Pharma Field Sales-Diabetes Care Specialist (DCS)-Marine Park, NY Job (MARINE PARK, NY, US)

Training Partner (Hjørring, Denmark)

Administrativ assistent med ambitioner (Gentofte, Danmark)

Regulatory Professional - CMC (Søborg, Denmark)

Analysekemiker til Biopharm QC New Haemophilia (Gentofte, Danmark)

Assistant in Biostatistics & Epidemiology - Aalborg (Aalborg, Denmark)

Chemist (Bagsværd, Denmark)

Global Publication Manager (Søborg, Denmark)

Moulding Process Engineer (Hillerød, Denmark)

Specialist - Talent Management & Leadership Developement (Bagsværd, Denmark)

Kemikere til aseptisk produktion (Kalundborg, Danmark)

Project Manager (Kalundborg, Denmark)