Jobs at Novo Nordisk

Area Training Supporter, akademiker

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

- Produktion
- Danmark - Kalundborg

Vil du gerne være en central person i en stor afdeling med opgaver som giver dig kontakt med mange mennesker hver dag? Kan du lide at træne og følge op på resultater?

Hvis det lyder interessant for dig har Site Danmark Ka i Kalundborg en spændende ny etableret position som trænings supporter. Siten består af ca. 400 medarbejdere og de primære processer er formulering, inspektion, montage og pakning af insulinprodukter.

Om afdelingen
Sammen med 15 yderst motiverede og dygtige kolleger udgør du Site Danmarks Packaging Support i Kalundborg. Vi behandler henholdsvis kvalitet og tekniske forbedringer til fuldautomatiske pakkelinjer samt øvrige generelle krav til vores omgivelser, herunder standardiseret træning. Din nye afdeling er især kendetegnet ved en uformel tone og et godt sammenhold, og vi hjælper gerne hinanden med at nå de fælles mål. Vi belønner engagement med plads til at udfolde og udvikle sig fagligt og personligt.

Jobbet
Dit primære område som ansvarlig træningssupporter vil være en hjælp til at sikre træning af medarbejdere i operationelle standarder som øger kvalitet. Andre opgaver inkluderer support til produktionens afdelinger i at koordinere træning.

Du skal kunne udvikle kompetencematrix planer, jobtræningsplaner, forberede oplæg og kreere et godt flow i afdelingens træningsaktiviteter. Du vil samarbejde med afdelingens shop floor trænere samt coache disse i brug af træningsmetoder. Du vil også fokusere på afdelingens trænings struktur og opdatere denne.

Du skal kunne præsentere dokumentation for danske og udenlandske myndigheder ved audits og inspektioner.

Du vil blive en del af afdelingernes tværgående trænings set up, som sikrer udveksling af træning og praktiske forhold som supporterer din udvikling.

Kvalifikationer
Du er uddannet farmaceut, kemi ingeniør eller lignende og ønsker at lære og udvikle dig indenfor den farmaceutiske produktion. Du er fortrolig med at arbejde i et GMP reguleret miljø og har indsigt og forståelse for god adfærd i farmaceutisk produktion. Du har kendskab til LEAN værktøjer og er kompetent til at tilvejebringe et højt niveau af træning til andre.

Du er god til kommunikation, fremstår professionel i samarbejde og du kan håndtere mange forskellige opgaver samtidig med at du bevare overblikket og går efter resultater. Du er en igangsætter, engageret, fleksibel og det er naturligt for dig at tage ansvar. Din attitude er positiv og du kan lide at være nøgleperson i en stor afdeling

Du behersker dansk og engelsk flydende – skriftligt og mundtligt

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, kontakt Birgitte Petersen på +45 3075 5587.

Ansøgningsfrist
15. december 2013

Product Surveillance Advisor

- Quality
- Denmark - Bagsværd

This is a highly versatile job where you will gain broad exposure to the company through regular interaction with stakeholders in R&D, Global Development and Product Supply along with our affiliates around the globe. You will frequently report directly to top management where your written and presentation skills must be excellent. If you find this challenging and inspiring, then you might be our new colleague in Global Safety.

About the department
Handling potential recall situations and surveiling global customer complaint data are the responsibility of CCC in Global Safety. We are located in House of Quality in Bagsværd.

The Job
The job is a 12 month temporary position starting 1st of February 2014.

You will be responsible for the surveillance and trending of data generated by clinical trials and customer complaints and for managing product recall situations from clinical trials and on marketed products. Our department is responsible for detecting, investigating and reporting complaint trends to top management and management forums. In product recall situations, you will be responsible for coordinating all relevant investigations and will handle the contact with regulatory authorities such as the FDA and EMA. We are also represented in various committees, e.g. safety committees and complaint surveillance groups where we provide input to local management, Product Supply and R&D.

Therefore, you will get the opportunity to work broadly within Novo Nordisk connecting with R&D, production sites, marketing departments and several of our international affiliates. In CCC, we work at the interface of our products and the patients and are responsible for maximizing the value of patient feedback by capturing the data and incorporating it back into Novo Nordisk processes.

Qualifications
You hold an academic degree in pharmaceutical sciences, engineering or a related natural science discipline and you have a strong quality mindset.

The ideal candidate has experience from CMC supply, Product Supply, QC, QA, Regulatory affairs or health authorities. Your analytical skills are excellent, and you can navigate in an organization under difficult circumstances and ensure a high level of communication. In your previous assignments you have demonstrated solid skills in writing reports and making presentations.

You are a positive and open minded team player who can co-operate at all organizational levels. You like a dynamic environment with many simultaneous tasks and changing priorities, while managing strict deadlines and meeting business targets.

Strong communication skills are required, so it is expected that you are fluent in English, both written and spoken.

We offer a very exciting job amongst good colleagues with diverse backgrounds in a positive working environment.

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 Lisbet Bærentzen at +45 3079 8080.

Deadline
15th of December 2013

QA kemiker

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

- Kvalitetssikring
- Danmark - Kalundborg

Vil du være med til at sikre kvaliteten af insulinproduktionen hos Novo Nordisk i Kalundborg?

Vi søger en kemiker til vores afdeling for Quality Assurance (QA) i IM2. Stillingen kræver en høj grad af selvstændighed, at du har sans for detaljer, og at dine formidlings og samarbejdsevner er stærke.

Om afdelingen
Måske er du vores nye kollega i QA i site Insulin Manufacturing II (IM2), hvor vi pt. er 35 engagerede og motiverede medarbejdere. Vi er en afdeling i vækst og du bliver en del af et af vores 3 teams, der yder kvalitets support til alle aktiviteter i produktionen både til drift og projektmæssigt. IM2 er ansvarlig for Novo Nordisks produktion af human insulin API, lige fra gæring til finrensning.

Jobbet
Som QA medarbejder, er du med til at sætte retning for kvalitet og compliance ud fra de myndighedskrav vi efterlever. Det bliver din opgave at sikre, at produktionen lever op til kvalitets og myndighedskrav herunder GMP, som er en forudsætning for vores produktion. I jobbet som QA kemiker får du en stor kontaktflade til produktionens afdelinger og det er derfor væsentligt at dine kommunikative evner er stærke og at du kan samarbejde på tværs i organisationen.

Jobbet indeholder mange facetter. Det er dig, der sikrer kvaliteten, når produktionen har afvigelser, ved ændringssager og frigivelse samt i forbindelse med projekter inden for blandt andet kvalificering og validering. Det gør du ved at udfordre og godkende forslag og løsninger samt coache produktionen til at levere i den rette kvalitet.

Dine kompetencer og dit erfaringsniveau afgør, hvilke konkrete opgaver du kommer til at håndtere.

Kvalifikationer
Du er ingeniør, farmaceut eller har anden relevant naturvidenskabelig uddannelse. Har du erfaring fra farmaceutisk produktion er absolut en fordel.

Gennem din erhvervserfaring har du vist, at du som person arbejder proaktiv og engageret. Du har løst opgaver med succes, ved at bevare overblikket, og kan træffe beslutninger om prioritet i en omskiftelig hverdag.

Du beskrives som en person med et godt humør og en åben tilgang til dine omgivelser. Du skal selvstændigt kunne drive processer og med en god energi kunne håndtere udfordringer, også i de mere travle perioder.

Du skal søge dette job i Novo Nordisk fordi dine evner, dit engagement og dine ambitioner, vil hjælpe os med dagligt at forbedre mange menneskers liv. Vi tilbyder dig muligheden for at arbejde sammen med usædvanligt talentfulde kolleger, og vi tilbyder dig en lang række muligheder for professionel og personlig udvikling.

Du kan lære mere om Novo Nordisk Product Supply og arbejdet i QA ved at bruge linket www.novonordisk.com/careers/QA

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 Mette Ulsø på +45 3079 5212.

Ansøgningsfrist
8. december 2013

Senior Project Manager

- Business Support
- Denmark - Bagsværd

We are looking for a Senior Project Manager to play a key role in driving supply chain improvement projects in Devices and Supply Chain Management (D&S).

About the department
You get the opportunity to join a high performing team responsible for developing the Global Supply Chain in Novo Nordisk. We assess and identify future strategic supply chain projects across Product Supply in order to meet the ambitious supply chain targets. We manage the supply chain project portfolio within Product Supply and execute strategic projects anchored in the PS supply chain management strategy.

The job
As senior project manager your primary role is to drive supply chain improvement projects. You main role will be to develop solid project plans; meet objectives, milestones and costs. You will identify required project resources and settle allocation with managers. You will set direction, manage, motivate and coach project team members and anchor benefit realisation with process owners in line of business.

It is you responsibility to identify key stakeholders to the project and proactively engage stakeholders in dialogue across Product Supply. You will communicate project progress/performance to all relevant stakeholders from senior management to directly affected employees. Furthermore you will ensure alignment of expectations and support from cross functional stakeholders throughout the project. Day to day operation is a mix of above responsibilities and includes a high degree of independence and interaction with our stakeholders.

Qualifications
You hold a master degree within production engineering, cand. merc. in supply chain or similar. You have at least 5 years of experience from a similar position, preferably within business processes, leadership or project management. You are capable of working with a high degree of independence on all organisational levels.

It is essential that you have a solid business understanding combined with strong analytical skills. You show strong leadership and you are used to communicate clearly with diverse stakeholders at various organisational levels. You have an ability to build strong relations and to work cross-functionally and internationally. On a personal level you work independently, are motivated by optimisation and improvements, deliver high quality output and set pride in keeping deadlines.

It is an advantage if you have experience with the pharmaceutical industry or similar production environment.

You must be fluent in both written and spoken English.

The main part of the job will be performed at the location of D&S Business Support, but will also involve activities in other Novo Nordisk sites in Denmark and abroad. Some travel activities are expected.

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 Claus Høgholm +45 3075 2436.

Deadline
6 December 2013

Associate Category Manager

- Sourcing
- Denmark - Hillerød

Join Novo Nordisk (37.000 employees) and help us maintain the position as the world leader in diabetes care by making a difference within strategic sourcing. We have an engaged and people focused culture, which is strongly founded on the Novo Nordisk Way.

About the department
Strategic Sourcing is the central sourcing unit in Novo Nordisk’s Product Supply division, and we are responsible for the strategic sourcing activities related to Novo Nordisk’s worldwide pharmaceutical production sites as well as global management of suppliers. Strategic Sourcing is currently based in Hillerød, but will move to Bagsværd in April 2014.

The job
The Primary Packaging category includes packaging materials in direct contact with our pharmaceutical products. As Associate Category Manager you will work together with the Category Manager for Primary Packaging who is heading up the category.

You will have an opportunity to work both individually as well as in close collaboration with Strategic Sourcing colleagues as well as with many stakeholders across the organization. You will be responsible for selected sourcing activities in the category, including supplier relationship management, category - and item strategies, risk mitigating activities, selection & approval of suppliers, negotiation and contracting, various reporting activities and budgeting processes, etc.

Qualifications
We are seeking candidates with a Master degree in Business administration, or equivalent educational level. The candidate must have minimum two years of relevant working experience with procurement and/or related and relevant areas within a multinational organization. You must be fluent in English (both written and oral).

The job requires you to manage a broad range of contacts in Novo Nordisk as well as with suppliers worldwide. Hence, solid communication skills and the ability to work in a complex and dynamic organization while retaining focus on overall goals are prerequisites. As the category activities are global, you should expect 20-30 days of travel activity annually. Engagement and a positive attitude, demonstrated by good cooperation skills, are further required.

At Novo Nordisk, we create value by putting patients first. Every ten seconds two people are diagnosed with diabetes, and close to 366 million people worldwide need us. Working here is not just a way to make a living, but a way to make a diffrence.

Contact
For further information, please Contact Mikkel Husby at +45 3075 5683

Deadline
07 December 2013.

Moulding Process Engineer

- Production
- Denmark - Hillerød

In this job, you will work with state of the art equipment, if you possess experience and in-depth knowledge within injection moulding and/or tools. Can you set strategic direction and motivate others, then go for this job. Device manufacturing & Sourcing (DMS) seeks a talented engineer with experience within the field injection moulding and tools.

About the department
DMS is focused on introduction of moulded components for medical devices, maturation of the production setup to excellence and sourcing the components to sister sites abroad. The area is at a high development pace and we need an experienced engineer in Mould Pipeline & Validation (MPV), which is a team responsible for ordering and approval of injection moulds for plastic parts for disposable pen systems produced internally in Hillerød DK and on various production sites worldwide.

The job
We can offer you a workplace with an international atmosphere, surrounded by talented and dedicated colleagues with whom you can exchange experiences

You will have a very high degree of influence and planning of your own job and daily tasks, as well as working with the highest quality and complexity of equipment within injection moulding and tooling.

You will be responsible for specific moulds from ordering to final validation and handover to production. This process includes all the documentation such as user requirement specification and change request forms, contact to mould maker to ensure adherence to timeline and quality, participation in Factory Acceptance Test at Mould maker, review of steel measurement reports, creation and review of validation documentation and reports and problem solving when specifications or requirements are not met.

Qualifications
You have a background as tool maker, plast processing technician, production technologist or likewise experiences, together with hands-on skills.

You have minimum 3 years of engineering with mass production of precision plastic components. Furthermore, you have a high quality mind-set and possess good interpersonal skills, are process oriented and have the ability to communicate simple and uncomplicated. It is also important you support the rest of us in creating a positive spirit and a good department. Communication in English in speech and writing is a necessity, since you will cooperate with international suppliers and customers. The position also includes travel.

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 Laura Sørensen at +45 3075 0463.

Deadline
11 December 2013.

Pakkeriassistent

- Produktions operatør
- Danmark - Måløv

Har du lyst til at være en del af et team, som har ansvaret for pakning af kliniske produkter, som pakkes i henhold til GMP? Kan du holde overblikket og bevare roen i en hverdag, som kan være både hektisk og omskiftelig?

Så er du måske en af den nye engagerede kollega, vi søger i Clinical Supplies Packaging(CSP) i Packaging teamet, som er en del af CMC.

Om afdelingen
Du bliver en del af CSP i Måløv sammen med 65 kollegaer, der er delt i 3 teams (Packaging, Process Support og Shipping). CSP har ansvaret for at pakke og distribuere produkter til kliniske studier over hele verden, og arbejder tæt sammen med resten af den kliniske Supply Chain i CMC for at nå de overordnede mål om at levere den rette kvalitet, i rette mængde og til tiden – dette er af afgørende betydning for at sikre effektiv udvikling af Novo Nordisk produkter. Afdelingen er i konstant udvikling med mange spændende udfordringer.

Jobbet
Teamets primære ansvar består i at forberede pakkemateriale til pakning (herunder bl.a. print af etiketter) og pakke produkter til kliniske studier. Pakningen foregår både manuelt og på en automatiseret pakkelinie. Dette job er dog udelukkende til den manuelle pakning.

Du vil indgå i et team med meget dedikerede medarbejdere, og som består af 4 pakkeriteknikere, 2 håndværkere, 1 planlægger, 1 lab/tech og 20 operatører.

Som pakkeriassistent er du primært ansvarlig for manuel pakning og etikettering af vials, penfills, og dumaer til kliniske studier, men din rolle kan udvides til fremtagning af produkter fra lageret, kontrolopgaver, samt udfærdigelse af batchdokumentation. Du kan også forvente at deltage i Lean aktiviteter samt løse mange ad hoc opgaver i relation til pakkeprocessen.

Jobbet er et dagholdsjob og er midlertidigt frem til midten af 2015.

Kvalifikationer
Der kan være flere uddannelsesmæssige tilgange til jobbet, men vi forestiller os, at du har en relevant baggrund, der matcher udfordringerne i jobbet, gerne suppleret med en uddannelse på operatørniveau som f.eks. industrioperatør. Det er en fordel, hvis du har erfaring med og forståelse for arbejdsgangene ved pakkeordrer til kliniske studier og kendskab til farmaceutiske produkter, arbejdsprocesser og dokumentationskrav.

Jobbet kræver, at du kan håndtere komplekse pakkeopgaver, samt at du har et kvalitetsmindset, der sikrer, at du aldrig går på kompromis med kvaliteten af det, du leverer. Dit arbejde kommer til at foregå i samarbejde med mange forskellige medarbejdere og du skal derfor have gode samarbejds og kommunikationsevner, samt være en udpræget team-player.

Da vi tit arbejder under tidspres er det vigtigt, at du kan holde hovedet koldt i pressede situationer. Selvom du indgår i et team, er det vigtigt, at du kan arbejde selvstændigt, og at du har en positiv og konstruktiv tilgang til opgaveløsning og forandringer. Kendskab til GMP og LEAN er en fordel, men ikke et krav. Sidst men ikke mindst forventer vi, at du er fleksibel, positiv og har et godt humør.

Ansættelse ønskes snarest muligt.

Fast dagholdsstilling til medarbejdere med min. 3 års anciennitet eller medarbejdere, der har været via revalideringsforløb

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 Martin Baunø Nielsen på +45 3075 1760.

Ansøgningsfrist
13. december 2013

Team Leader

- Quality
- Denmark - Bagsværd

Do you have an interest in people management? Can you set direction for a team of academics and act as inspiring sparring partner for your employees? Do you want to further develop quality mind set and make a difference for our stakeholders? Then you may be our new team leader.

Drug safety is an integral part of drug development and is now in focus more than ever. In this job, millions of people with diabetes worldwide depend on our medical evaluation of the benefit/risk profile of the Novo Nordisk insulin products.

About the department
Safety Surveillance Diabetes Insulin & Devices is an international department of highly committed and skilled professionals with medical or pharmaceutical background. We have the global responsibility for the safety surveillance and safety communication for the Novo Nordisk insulin products and devices, marketed or in clinical development.

The Job
As a Team Leader you will be responsible for a team of 5 medical doctors and pharmacists. This team has responsibility for the ongoing assessment and communication of benefit risk for some of Novo Nordisk insulin products

On the managerial level, you will focus on developing your team further and securing timely delivery of high quality assessments of safety profile.

Close collaboration and communication with other functional areas in Novo Nordisk, especially with clinical and non-clinical development teams and with the regulatory affairs team is required.

Your job responsibilities will also include becoming an active member of the Safety Surveillance Management Team.

Qualifications
You have a medical degree (MD) and have at least 5 years of experience in the pharmaceutical industry, preferably from a drug safety department or a medical department. Management experience will be an advantage.

As a person, you are reliable, energetic and innovative, open-minded and dedicated team player who thrives in a global environment of continuous development. You have focus on the quality of work and the results of the team.

Above all, you have genuine interest in people, willing to facilitate their development to reaching their full potential in the job.

Interaction with internal and external partners require proficiency in English, excellent communication, coordination and planning skills.

At Novo Nordisk, we create value by putting patients first. Every ten seconds two people are diagnosed with diabetes, and close to 366 million people worldwide need us. Working here is not just a way to make a living, but a way to make a difference.

Applications must be written in English.

Contact
For further information, contact Liliana Hansen at +45 3075 0964.

Deadline
8 December 2013

Operatør til Tabletproduktion

- Produktion
- Danmark - Måløv

Kan du spænde vidt med forskellige opgaver på flere procestrin og samtidig sørge for at udstyret er rengjort og klar til brug? Vil du være med til at sikre produktkvaliteten fra start til slut i fremstillingsprocessen? Vil du bringe din GMP forståelse i spil og dokumentere dit arbejde?

Så er du måske den nye engagerede kollega, vi søger i Biopharmaceuticals T&FP, afd. 129 i Måløv.

Vi er et team med 15 medarbejdere ud af en afdeling på 45 medarbejdere, som producerer hormontabletter til systemisk og lokal hormonbehandling bl.a. Vagifem®.

Stillingen er en fast stilling.

Vi har styr på proces og udstyr
Du kan se frem til en hverdag med mange og varierede arbejdsopgaver. Du kommer bl.a. til at afveje, granulere, tablettere og arbejde med coating af tabletter, prøveudtagning samt daglig rengøring af udstyret.

I afdelingen har vi meget fokus på kvalitet. Derfor arbejder vi hele tiden med at sikre et højt kvalitetsniveau og udfører således omfattende dokumentation af vores arbejde. Det bliver også din opgave at sørge for, at produkterne lever op til kvalitets- og myndighedskrav herunder GMP, som er en forudsætning for vores produktion. Vi arbejder med daglig målstyring, og cLEAN® er en vigtig del af vores hverdag.

Du vil i det daglige arbejde få en bred kontaktflade med kolleger fra andre teams i afdelingen som f.eks. processupportere og teknisk support.

Vi arbejder i 2 holdskift, 5 dage om ugen.

Initiativ og kvalitetssans
Du har gerne erfaring med at arbejde i en produktion, gerne en tabletproduktion og kender GMP, men din faglige baggrund er ikke så væsentlig. Det vigtigste er, at du tager ansvar og er meget bevidst om kvaliteten i alt dit arbejde. Du er handlingsorienteret og viser initiativ ved selv at byde ind og drive opgaver. Samtidig har du lyst til at arbejde i et miljø, hvor der kræves en stor del dokumentation.

Du skal også være klar til løbende at tilegne dig nye færdigheder og håndtere de udfordringer og forandringer, som ligger foran dig. I vores team er samarbejde vigtigt, så du skal have en positiv indstilling og lysten til at løse opgaver i fællesskab med kolleger.

For at kunne begå dig i vores produktion skal du have teknisk flair og være fortrolig med brug af IT.

Du har dansk, matematik og engelsk på mindst 9. klasses niveau og/eller en uddannelse som for eksempel industrioperatør, procesoperatør, håndværker eller lignende, og du skal dokumentere dette, når du søger stillingen.

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 Jeanette Goth på +45 3079 3903 i tidsrummet kl. 10-14.

Ansøgningsfrist
11. december 2013.

Kemiker

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

- Produktion
- Danmark - Kalundborg

Motiveres du af pulsen i en produktionsafdeling? Vil du være en del af et stærkt supporterteam med en høj faglighed, højt energiniveau, udfordrende processer og skarpe deadlines?

I så fald kunne det være dig vi er på udkig efter.

Om afdelingen
Du indgår som et vigtigt led i Novo Nordisks insulinproduktion Diabetes Active Pharmaceutical Ingredients (DAPI). Området omfatter 9 fabrikker og huser 1.700 medarbejdere, der primært arbejder i Kalundborg. Produktionen består af gæring, grovrens og finrens. Resultatet bliver en bred vifte af innovative insuliner til gavn for patienter over hele kloden.

Den ledige stilling er i Purification Plants (PPIV), som er en finrensningsfabrik, hvor vi producerer insulin Detemir. Afdelingen består af ca. 80 medarbejdere med forskellige ansvarsområder, fordelt på 4 forskellige teams.

Jobbet
Dit mål er at bidrage til en stabil produktion i absolut topkvalitet og altid i overensstemmelse med gældende kvalitets- og GMP-regler. En helt afgørende del af dette er en standardiseret proces, og her spiller du en nøglerolle. Grundlæggende deler du således din indsats mellem at håndtere afvigelser, supportere vores driftsoperatører og arbejde på optimere vores proces, således at vi til enhver tid lever op til stadig stigende kvalitetskrav. Du vil således bruge meget tid på gulvet i produktionen, for så at tage dine iagttagelser med til skrivebordet, hvor du udarbejder dokumentation. Det kan også være opgaver, som løses i samarbejde med kollegaer på tværs af fabrikker i DAPI. Jobbet giver dig et stærkt fundament for at fortsætte din karriere som fx projektleder på bl.a. optimeringsprojekter eller som leder – hvis du ønsker det.

Kvalifikationer
Du er kemiker, ingeniør, farmaceut eller lignende, og du har solid erfaring med procesanlæg og processtyring. Du er således vant til at arbejde efter systematiske kvalitetssystemer, og du er selv bannerfører for høj kvalitet. Det er helt naturligt for dig at tage ansvar for dine opgaver og nå dine deadlines. Samtidig er det afgørende, at du trives i et travlt miljø, der er i stadig forandring. Du kan derfor både prioritere mellem mange sideløbende opgaver og være med til at drive forandringer, der forbedrer vores kvalitet. Da vi er mange involveret i processen på tværs af faggrupper, afhænger din succes også i høj grad af din evne til at skabe og pleje relationer med mange forskellige mennesker – samt selvfølgelig din lyst til at arbejde målrettet for, at vi lykkes som et hold. Derudover skal du kunne begå dig på engelsk i skrift og tale.

I Novo Nordisk er det dine evner, dit engagement og dine ambitioner, der forbedrer mange menneskers liv – i samspil med usædvanligt talentfulde og passionerede kolleger.

Kontakt
Er du interesseret i at høre mere om stillingen, så kontakt Marianne Espenhain på +45 307 57812.

Ansøgningsfrist
6.december 2013.

Regulatory Affairs Associate

- Regulatory Affairs
- Denmark - Søborg

Novo Nordisk Regulatory Affairs makes medicine available to patients all over the world by ensuring rapid regulatory approvals in all our markets. Regulatory Affairs is a fast-changing and complex landscape, therefore, a high level of professionalism and a thorough business understanding is essential for the employees in our unit in order to make a difference to our business.

We are currently looking for a Regulatory Associate, with an interest in CMC to join our team working with all tasks related to ensure that all our marketed products and our early development projects are in compliance.

About the department
Our team (Regulatory Affairs CMC Insulins and Oral Proteins) is lifting tasks to ensure succesfull lifecycle management of our marketed insulin products as well as ensuring succesfull clinical trial applications for products handled in our team. Our team consist of 18 employees and we are located in Søborg.

The job
In Regulatory Affairs, you will work in a fast-paced environment where no two days are alike. Tight deadlines, cross-departmental collaboration and the challenges of international communication. Your work day will consist of preparing and providing documentation for authorities, support the team, handle various IT systems for archiving of documents and information, and some administrative tasks, will be part of your busy workday.

You will be expected to make an impact, ask questions and challenge the status quo if that is what it takes. You will find that Novo Nordisk offerst first-rate professional training, relevant support and talented, friendly colleagues working in an enjoyable atmousphere.

Qualifications
Your background education is Pharmaconomist, B.Sc. in English, or equivalent. You have preferable experience from working in regulatory affairs or similar area. You have a flair for IT systems and experience with MS Office as you will be responsible for managing data entry and electronic filing in our various databases and document management systems as well as assist with preparation, submission and approval of worldwide aplications covering insulin products in close collaboration with your colleagues. You communicate in written business English and are comfortable using English in your daily work.

On a personal level, you thrive in a busy environment and bring a can-do attitude to your work. You have good coordination and planning skills and maintain a healthy sense of humour even when the pressure is on. Your are a strong team player, but also enjoy working independently. You are able to challenge the status quo and find new solutions to the challenges you may face. You are systematic, flexible in your approach and goal oriented, and have a quality mindset.

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 Lene Vindelev Dalsgård Nielsen at +45 3075 3358.

Deadline
30 November 2013

Senior Project Coordinator

- Regulatory Affairs
- Denmark - Søborg

Are you the new Regulatory Senior Project Coordinator in Regulatory Operations, Regulatory Affairs?

Would you like to be part of driving and improving one of the core processes in Regulatory Affairs by improving processes across 6 VP areas in Regulatory Affairs (RA)? If so, you may be the regulatory project manager we are looking for.

About the department
You will be located in the department Regulatory Operations Business Support and you will be responsible for supporting the SVP-area Regulatory Affairs by driving improvement projects across RA. In addition you will be the Data responsible and expert in supporting the newly established Change Handling IT system, novoGloW.

Regulatory Operations is a VP-area consisting of 150 employees in Denmark and India. The VP area is responsible for Regulatory operational activities from labelling development and management, publishing activities, RA affiliate coordination, IT projects and support to Clinical Trail Applications.

The Job
As a Senior Project Coordinator your primary task will be independently to drive improvement projects across RA and report to the newly established governance body in Regulatory Affairs consisting of CMC directors across 6 VP ares. The job offers frequent senior management interactions, leadership responsibility and has cross functional reach. Your job will be to set the right direction for sub projects and, at the same time, making sure that your project is implemented and anchored in the organisation. The projects will vary in size and complexity but will all have a cross-organisational take-off.

In addition you will be responsible for the following activities;

• Ensure that results are delivered according the project plans

• Involve relevant stakeholders and ensure timely communication in relevant countries

• Prepare, mobilise and run projects

• Communication/change management responsibility before, under and after execution of projects

• Coordinate with relevant functions in NN outside RA

Qualifications
You have completed a relevant Master's Degree (IT, business administration, engineering or the like) with excellent results and have backed your theoretical background with at least 3 years’ practical experience. You have acquired solid experience as Project Manager. You have an understanding of the classic cLEAN tools.

Within IT you are able to understand IT architecture and data structures. You can identify possibilities for improving interactions between system and process, and for analysing and improving processes based on data.

Earlier you have successfully handled business critical projects at strategic level, and, as such, you are comfortable interacting with stakeholders at any organisational level and is use to work across organisational and geographical boundaries. Leading others in project contexts comes natural to you, and you use your energy and understanding of other people to involve the right competences in the right processes and carry projects ideas through with success.

You write and speak English fluently. You have a high level of drive, initiative and persistence and you are result oriented. In addition, you are ambitious and like to be challenged. You are analytical, structured and comfortable managing a team on your own.

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 Shakeel Zaki Dar at +45 3079 0608.

Deadline
12 December 2013

Process Supporter

- Production
- Denmark - Gentofte

Are you able to keep focus, prioritize and get to the root cause of problems in a hectic working environment? Are you motivated by keeping the production running? Do you take pride in ensuring documentation meet GMP standards? Then you could be the next colleague to strengthen our support team.

About the department
We are a small production facility located in Gentofte, responsible for the purification of Glucagon. Organised in Product Supply, Biopharm API, we are 30 colleagues who work closely together and take pride in having a challenging and fun working environment. In the Process & Support team we are 10 chemists, technicians and engineers who, together with the department’s two specialists, support the production team and ensure timely release of high quality Glucagon to current GMP standards.

The job
You will join our group of four chemists responsible for the production processes. Depending on your background and interests you will be the primary responsible for one of the purification steps, cleaning validations and/or environmental monitoring. You will be working closely with the 14 dedicated operators in the production team to ensure the production is carried out according to current standards. You will handle deviations in non-conformity reports, review documentation for release and write instructions. You will identify possible process optimizations in close corporation with the production team and lead the continuous improvements within your area. When our facility is being audited you will represent the department and confidently present relevant documentation. You will ensure to maintain the good relations with our stakeholders through your close collaboration with QA, Support and the laboratories.

Qualifications
You hold a degree as a pharmacist, chemical engineer or equivalent. You have a natural understanding of GMP as our license to operate. You have the ability to keep focus in a highly complex working environment. You use LEAN tools and systematic problem solving methods in order to find the root cause of problems and develop better standards in order to prevent them from reoccurring. You have a positive, will-do attitude and take responsibility to ensure deadlines are met. You start every day with enthusiasm and your great communication skills make it naturally for you to work closely with colleagues from different parts of the organisation. Besides being fluent in Danish you master English on a professional level.

If you want to become our new colleague, we will look forward to receiving you application in Danish or English, as you prefer.

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 contcat Pernille Nyvang Jørgensen +45 3075 6948.

Deadline
8 December 2013

Analysekemiker til Biopharm QC Support

- Produktion
- Danmark - Gentofte

I Biopharm QC Support søger vi en analysekemiker til en spændende stilling med hovedvægt på BIO analyser herunder ELISA, enzymkinetiske analyser, clot og chromogen til vores hæmofiliprodukter.

Har du lyst til at være en del af en dynamisk afdeling med mangeartede opgaver inden for metodeoverførsel og validering på Biopharm’s hæmofili portefølje – så er denne stilling lige noget for dig.

Om afdelingen
Biopharm QC Support er ansvarlig for optimering og validering af kemiske og bioteknologiske analysemetoder til Biopharms hæmofili portefølje. Derudover varetager vi support til Biopharms QC laboratorier, som har ansvar for analyser til frigivelse af markedsførte produkter. Afdelingen er beliggende i Gentofte og består af 40 medarbejdere organiseret i tre teams samt en stabsfunktion, som varetager tværgående aktiviteter.

Organisatorisk hører afdelingen hjemme i Biopharm Manufacturing Development (Biopharm MDev), som supporterer produktionsområderne, validerer analysemetoder og driver regulatoriske projekter.

Jobbet
Du vil blive en del af afdelingens BIO Validation team, som består af teamleder, kemikere og laboranter. Teamet har ansvaret for at validere, overføre og optimere bioteknologiske analysemetoder. Implementering af ny teknologi sker løbende i relation til behovet i nye projekter.

Som vores nye medarbejder vil du få ansvar for optimering, validering samt overførsel af analysemetoder, herunder udarbejdelse af protokoller, rapporter og analyseforskrifter. Du skal problemløse på analyserne og lede små og mellemstore projekter på tværs af afdelingen og funktionsområdet.

Du skal samarbejde med teamet og på tværs af afdelingen samt være i tæt kontakt med QA, analyse-udviklingsafdelinger, produktionsafdelinger, QC laboratorier samt Regulatory Affairs.

Kvalifikationer
Du er uddannet farmaceut, Cand. Scient., ingeniør eller har en anden relevant uddannelse indenfor analytisk kemi og har minimum 4 års erhvervserfaring. Du har arbejdet med bioteknologiske analysemetoder herunder ELISA og enzym kinetiske analyser samt optimering og validering af analysemetoder. Du har solide IT-kundskaber og erfaring med anvendelse af statistik. Det er en fordel at du har arbejdet under GMP.

Du skal kunne dansk og engelsk flydende, i skrift og tale.

Du er systematisk og har en høj grad af ansvars- og kvalitetsbevidsthed. Du kan håndtere komplekse problemstillinger og må gerne have kendskab til systematisk problemløsning. Som person er du åben og engageret. Du er i stand til at motivere og inspirere dine kollegaer og kan agere som sparringspartner. Du er god til at prioritere din tid og skabe overblik selv med mange bolde i luften. Og i et til tider meget travlt arbejdsmiljø bevarer du et godt humør.

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 Ann Cherie Zier Grønbech på + 45 3075 8918

Ansøgningsfrist
09. december 2013

Project Manager

- Project Management
- Denmark - Måløv

Do you thrive with planning and implementing projects of complex technical nature in an engaging environment?

About the department
In Novo Nordisk, CMC Optimisation we are looking for an experienced and reliable project manager to lead GMP and investment projects at our facilities in Bagsværd, Gentofte, Måløv and Hillerød. The department is organizationally part of CMC Supply, which is an area under "Research & Development".

The job
As project manager within CMC Optimisation you will enter into a small team of project managers with the responsibility for implementation of facility and utility upgrades, new equipment, overhauls and improvements including full qualification and documentation packages. You will be a part of a small cross-functional project management team that excel in managing projects and are motivated by the challenge of improvement. You will typically manage investment projects, often in collaboration with external suppliers, and manage complex changes when we rebuild or optimize equipment in our facilities.

We offer a full and exciting job opportunity for both personal and professional development.

You thrive with communicating with stakeholders and you understand the importance of follow-up on budgets, timeliness, structured working methods and thorough documentation. You are expected to carry the projects forward in accordance with approved goals, agreed milestones and granted resources. You are experienced in managing projects for pharmaceutical manufacturing.

In all of your work you will ensure compliance with GMP and Novo Nordisk standards. In connection with e.g. FAT or audits you can foresee some yearly travel days (5-10 days).

Qualifications
You either hold a BSc or MSc in a technical field, or you have another technical background that qualifies you for this challenge. With a minimum of 5 years’ experience of similar responsibilities from the pharmaceutical industry, you have extensive experience in managing projects in a GMP-regulated environment and use LEAN as a natural tool to simplify and optimise processes and procedures. You take natural leadership and you have good people skills making the stakeholders and project team satisfied and effective.

Novo Nordisk’s company language is English. Danish language skills are needed in daily communication with your project team and skilled workers in the facilities.

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 Steen Weber Jensen, +45 3079 2979.

Deadline
10 December 2013.

Chemist

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

- Research & Development
- Denmark - Kalundborg

Are you a highly skilled and structured chemist? And do you want to make a difference for Novo Nordisk production of insulin? If you are we might have the right job for you in Manfacturing Development (MDev), biotechnological support.

About the department
You are part of Novo Nordisk’s production of insulin and will be situated in MDev. Our responsibilities are to improve existing processes and analysis methods, implement new analysis methods and processes for new products, support daily operation and manage complex optimization projects. You will join Analytical Support in MDev and be part of the biotechnological team which provide analytical and technical support, conduct projects concerning optimisation/validation of analysis and we deliver analytical answers to our customers. We are working with ELISA, fibrillation analysis, DLS, FT-IR, Southern and Western blot and bioassays (cell-based in vitro assays for the determination of biological activity/identity).

The Job
You support the production on analytical questions and execute projects within biotechnological support and development. You qualify equipment, conduct optimisation projects and you validate and receive analysis methods from developmental laboratories and transfer methods to QC laboratories. That includes writing protocols, reports, analytical procedures and documents for registration. You solve various tasks such as writing SOPs, non-conformities and other GMP documents. Your stakeholders are your colleagues in MDev and Analytical Support, the production, QC laboratories, QA, the organisational are which develop analysis methods and regulatory affairs.We have a culture where you have many possibilities for influencing the development of the team and the production.

Qualifications
You have minimum 3 years of relevant experience from the pharma industry or research (or hold a Ph.D) with a strong focus on protein chemistry. Moreover, you exhibit hands-on experience with optimisation of biochemical methods and problem solving within antibody-based analysis and bioassay, including mammalian cell culture. Flair for equipment and maintenance is a plus. Since we are a support team, you have an urge to provide support such as analysis work and problem solving and you have shown that you are capable of handling and prioritising a huge workload. You are used to work within a team and communicate to various stakeholders. Furthermore, you have shown a high level of analytical skills and commitment that you have used to impact your stakeholders and you strive to get success with your tasks. You are committed to your tasks and reach your goals.

At Novo Nordisk’s production site in Kalundborg, Western Zealand, you will find a world class production environment and we are proud to say that we produce a substantial amount of the World’s insulin and are on the forefront when it comes to technology, systems, methods, and processes. The site is the workplace for more than 2.400 dedicated Novo Nordisk employees and this makes it the largest production site in Novo Nordisk’s global production network. Covering 270 football fields the site is also quite impressive in size. Novo Nordisk in Kalundborg is a city within the city. The area, which is located roughly an hour from Copenhagen, even has its own system of roads as well as a leisure centre where employees can do sports. If you are our new colleague, we guarantee challenges and career opportunities that will be hard to find elsewhere.

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 Miriam Bønnelykke at +45 3075 5475.

Deadline
8. December 2013.

Global Product Manager

- Marketing
- Denmark - Søborg

Novo Nordisk is recruiting a Global Product Manager to join the Modern Insulin & Devices 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.

About the department
As Global Product Manager in Future Devices you will in close cooperation with Device R&D be commercially responsible for the development of innovative delivery systems for our drug portfolio within diabetes and Biopharm.

You will be part of a highly skilled, diverse and high performing team of Global Product Managers working towards making our devices the most preferred in the market, you will be reporting to the Vice President of Devices, NovoMix and OADs. We provide commercial and strategic input to device innovation and development projects and secure that the needs of people with diabetes are in the centre of our innovation and development activities.

The job
You will be responsible for identifying, analysing and crystallising key customer needs in relation to development of new innovative delivery systems. You will couple this information with portfolio and affiliate commercial needs and hereby ensure that future delivery systems add maximum value to our customers and our business.

Additionally, you will be responsible for developing the product strategy, preparing the products for global launch and securing alignment with our portfolio strategies. You will collaborate intensively with other headquarter functions such as Device R&D, Product Supply, Global Marketing Brand Teams as well as our key affiliates.

Specifically we are looking for a colleague who will be responsible for a portfolio of devices of which some are in early device innovation and others closer to launch. This means that you will be overall commercially responsible for setting the business direction for the early stage devices, preparing the business case in cooperation with our evaluation team and being Global Marketing’s representative in the Device Core Teams. In addition, you will manage a portfolio of devices closer to launch. You will bring the individual devices to launch by optimising the strategy, establishing positioning, determining the roll-out plan and creating the launch package in close cooperation with our key affiliates, Brand Teams, advertising agencies and the Core Teams.

In essence, this is a job with a high degree of strategic assignments and where results are achieved through collaborations with stakeholders.

Qualifications
This is a position that requires strong leadership, so you hold a Masters degree in business, economics or similar, and have three-five years of commercial experience from the pharmaceutical industry, preferably within diabetes in US, UK, Canada, Japan or similar countries.

You are ambitious, interested in innovation, interested in making a difference to the lives of people with diabetes and you find it motivating to take commercial lead in a development project team. You possess very strong strategic and analytical skills and excel at engaging and impacting a variety of stakeholders on a global level in a large organisation. Your approach to tasks is structured.

You have an ability to adapt to a dynamic environment and handle multiple tasks across company functions, you are known for your leadership, and have a proven track record as a strong team player. Furthermore, you have a global mindset and are fluent in both spoken and written 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
If you need further information, please contact Anders Krabbe at +45 3075 6179 or Mikael Sørud at +45 3079 4361.

Deadline
9 December 2013.

Vi søger 18 kontorelever til 2 års udviklingsrejse...

- Elev
- Danmark - Bagsværd

Bliv en del af virksomhed i vækst
Et job som elev er starten på en personlig og faglig udviklingsrejse, der åbner for en række muligheder. Kickstart din karriere ved at brug 2 år hos Novo Nordisk til at finde dine styrker. Novo Nordisk er en global virksomhed i vækst. Det betyder at vi ansætter mere end 4.000 medarbejdere årligt. Når du er færdig med din elevtid, så kender du virksomheden og vores produkter og kan søge videre i den retning du brænder mest for.

Vi søger 18 kontorelever

Vi søger 12 kontorelever med start 1. september 2014 (heraf 3 til Kalundborg) og yderligere 6 kontorelever med start 1. februar 2015.

Som kontorelev får du mulighed for at prøve dig selv af.
Du vil få indblik i flere arbejdsområder via din rotation i 3 forskellige afdelinger. Din rotation kan f.eks. indeholde indkøb, personale, produktion, marketing, kommunikation eller afdelingen, som står for intern facilitering. Du har mulighed for at få indflydelse på, hvilke afdelinger du skal være i praktik.

Du planlægger stort set selv din arbejdsdag ud fra de arbejdsopgaver, du får ansvar for. Du vil få kundekontakt og ikke mindst et bredt netværk. Stillingen er et 2-årigt forløb og du får en elevvejleder i hver rotation, som følger dig gennem uddannelsen.

Du kan se frem til at blive en del af et internationalt miljø, hvor du bliver udfordret fagligt og personligt. Som elev i en stor organisation vil du indgå i et stort netværk på tværs af organisationen, som også giver dig mulighed for at deltage i faglige og sociale arrangementer sammen med de andre elever.

Derudover har du mulighed for at læse akademimerkonom eller HD om aftenen, hvis du opfylder adgangskravene.

For at komme i betragtning skal du være i gang med eller have en 3-årig HHX eller HGS.

Vedhæft dine eksamensbeviser og dit cv indeholdende personlige data, dine interesser og evt. erhvervserfaring.

Kontakt
Har du spørgsmål, kan du kontakt Anne-Marie Nielsen på + 45 3079 3475 eller Hanne Lissi Hansen på + 45 3079 6361.

Ansøgningsfrist
10. februar 2014

19 laborantpraktikanter søges til internationalt forskningsmiljø

- Elev
- Danmark - Bagsværd

Vi søger 19 laborantpraktikanter
Start 1. september 2014

Bliv en del af et udfordrende, internationalt forskningsmiljø
Vil du arbejde i en branche, der har fingeren på pulsen? Er du dynamisk har du gå-på-mod og kan du lide at arbejde systematisk? Så bliv laborantpraktikant i Novo Nordisk, som en del af et engageret team, der brænder for at skabe gode resultater. Du skal være i gang med eller have gennemført den teoretiske del af din laborantuddannelse. Har du derudover erfaring fra f.eks. fritidsjob eller udlandsophold, så kan det være en fordel.

Hvordan er uddannelsen?
Som laborantpraktikant får du bl.a kendskab til avanceret protein- eller molekylærbiologi, moderne bioteknikker som f.eks gensplejsning og godt indblik i det almene laboratorie- og driftsarbejde. Vi benytter os af det nyeste udstyr og teknikker inden for alle områder. I løbet af din 1-årige praktiktid vil din vejleder og dine kolleger sørge for, at du lærer relevante teknikker og apparatur at kende.

Du kan se frem til at blive en del af et udfordrende og internationalt forskningsmiljø, hvor du kan udvikle dig både fagligt og personligt. Samtidig har vi også plads til at have det sjovt.

Arbejdssted: Dit arbejdssted kan være enten i Bagsværd, Gentofte, Hillerød, Måløv, Kalundborg.

Ansøgning
Skriv i din ansøgning, hvilke arbejdsområder, teknikker, medicinske forsøg mv. du gerne vil arbejde med.

Vedhæft dine eksamenspapirer og cv med oplysning om personlige data, dine interesser og evt. erhvervserfaring.

Kontakt
Vil du vide mere om stillingen,så kontakt Anne-Marie Nielsen på + 45 3079 3475 eller Hanne Lissi Hansen på + 45 3079 6361.

Ansøgningsfrist
10. januar 2014

Vi søger 2 økonomielever til 2 års udviklingsrejse…

- Elev
- Danmark - Bagsværd

Bliv en del af virksomhed i vækst
Et job som elev er starten på en personlig og faglig udviklingsrejse, der åbner for en række muligheder. Kickstart din karriere ved at brug 2 år hos Novo Nordisk til at finde dine styrker. Novo Nordisk er en global virksomhed i vækst. Det betyder at vi ansætter mere end 4.000 medarbejdere årligt. Når du er færdig med din elevtid, så kender du virksomheden og vores produkter og kan søge videre i den retning du brænder mest for.

Vi søger 2 økonomielever
Start 1. september 2014

Vil du arbejde i en branche, der har fingeren på pulsen?
Er du dynamisk, har du gå-på-mod og kan du lide at arbejde med tal, så bliv økonomielev i Novo Nordisk.

Som økonomielev får du mulighed for at prøve dig selv af. Du vil få indblik i flere arbejdsområder via dine rotationer i 4 forskellige afdelinger og arbejdsområder: kreditorbogholderi og rejseafregning, finansregnskab, løn samt økonomistyring herunder budgetplanlægning og opfølgning.

I løbet af den 2-årige elevtid vil du få mulighed for at komme til Indien i 4 uger og arbejde i vores datterselskab.

Du kan glæde dig til at blive en del af et internationalt miljø, hvor du bliver udfordret både fagligt og personligt. Som elev i en stor organisation vil du få et stort netværk på tværs af organisationen og mulighed for at deltage i faglige og sociale arrangementer bl.a. sammen med de andre elevgrupper. Derudover har du mulighed for at læse HD om aftenen.

For at komme i betragtning til elevstillingen skal du være i gang med eller have bestået en 3-årig HHX.

Vedhæft dine eksamensbeviser og dit cv indeholdende personlige data, dine interesser og evt. erhvervserfaring.

Kontakt
Har du spørgsmål, kan du kontakte Lene Crone Glaas på + 45 4442 3972.

Ansøgningsfrist
19. januar 2014

Area Training Supporter, akademiker (Kalundborg, Danmark)

Product Surveillance Advisor (Bagsværd, Denmark)

QA kemiker (Kalundborg, Danmark)

Senior Project Manager (Bagsværd, Denmark)

Associate Category Manager (Hillerød, Denmark)

Moulding Process Engineer (Hillerød, Denmark)

Pakkeriassistent (Måløv, Danmark)

Team Leader (Bagsværd, Denmark)

Operatør til Tabletproduktion (Måløv, Danmark)

Kemiker (Kalundborg, Danmark)

Regulatory Affairs Associate (Søborg, Denmark)

Senior Project Coordinator (Søborg, Denmark)

Process Supporter (Gentofte, Denmark)

Analysekemiker til Biopharm QC Support (Gentofte, Danmark)

Project Manager (Måløv, Denmark)

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