Jobs at Novo Nordisk

Laborant med celle og GMP erfaring

- Forskning og Udvikling
- Danmark - Måløv

Vil du være med til at udvikle og validere cellebaserede bioassays? Og har du lyst til at være en del af en åben, dynamisk og social gruppe med et stærkt fokus på faglige evner og løbende forbedringer? Så er du måske den nye kollega, vi leder efter.

Om afdelingen
De to Bioactivity teams er en del af afdeling 318, CMC Bioassay, som er placeret i CMC DP Development, R&D, Novo Nordisk A/S. Teamet er fysisk placeret i Måløv og kører i hverdagen som et team, bestående af 9 akademikere, 10 teknikere og en teamleder.

Jobbet
Du vil efter en oplæringsperiode deltage i udvikling af bioassays til projekter i alle klinisk forsøgsfaser. Du bliver ansvarlig for at modtage, analysere, beregne og afgive svar på analyseprøver i LIMS. Det forventes at du tager aktivt del i optimering af vores arbejdsgange i teamet, samt i udarbejdelsen af dokumenter. Du vil udover analysearbejdet også deltage i vores daglige driftsopgaver, som bl.a. indbefatter pasning af mammale cellekulturer og vedligeholdelse af apparatur. Arbejdet kræver en god ordenssans idet det foregår under GMP.

Kvalifikationer
Du er laborant eller tilsvarende og har erfaring med analysearbejde og håndtering af mammale cellekulturer. Du har kendskab til GMP og er glad for at arbejde i et team. Du har udover en god humoristisk sans og godt humør, en naturlig ordenssans, er systematisk, selvstændig, motiveret og kan holde hovedet koldt i travle perioder.

I Novo Nordisk skaber vi værdi ved sætte patienterne først. Hvert tiende sekund bliver to personer diagnosticeret med diabetes, og næsten 366 millioner mennesker i hele verden har brug for os. At arbejde her handler ikke bare om at tjene til føden, men om at gøre en forskel.

Kontakt
Vil du vide mere om stillingen så kontakt Pernille Hulgaard på +45 3075 0835 eller Jesper R. Jørgensen +45 3079 7885 (uge 52-01 undtaget).

Ansøgningsfrist
15. januar 2014

Operatør til Deviceproduction

- Produktions operatør
- Danmark - Hillerød

Tør du prøve kræfter med vores højautomatiske produktionsudstyr? Vil du være med til at sikre leverancen af devices til vores kunder? Er du klar til at tage ansvar og vise initiativ i et miljø, hvor vi arbejder systematisk med cLEAN®, konstant udfordrer og stræber efter at gøre en forskel?

Så er du måske en af de nye engagerede kolleger, vi søger i D&S, Prefilled Moulding Team - Hillerød. Vi er et team med 34 medarbejdere, som producerer FlexTouch®, FlexPro® og FlexPen® komponenter.

Stillingerne er faste stillinger med ansættelse tidligst 1. februar 2014. Samtaler afholdes i januar 2014.

Her støber vi fremtidens devices
I vores afdeling har vi til opgave at plaststøbe komponeter til forskellige præfyldte devices og det bl.a. hos os, at fremstillingen af fremtidige præfyldte pensystemer skal foregå.

Du kan se frem til en hverdag med varierede opgaver, men hovedvægten i jobbet ligger på at overvåge og betjene produktionsudstyret, manuel og elektronisk inspektion af komponenterne og i nogen grad rengøring af og service på udstyret. Desuden vil du som en naturlig del af din hverdag arbejde med løbende forbedringer herunder optimering og standardisering af arbejdsprocesserne.

Vi har en målsætning om at være `Best in Class´ og arbejder hele tiden på at forbedre os bl.a. med hjælp fra cLEAN® værktøjer og gennem fokus på vores medarbejderes kompetenceudvikling. Alt i alt er vi en afdeling med en stærk ånd, hvor fleksibilitet og omstillingsparathed er nøgleord.

Du får i det daglige arbejde en bred kontaktflade med kolleger fra andre teams. Det kan være ved kvalitetsfejl, hvor du i dialog med plastteknikere og automatikteknikere bidrager til at lokalisere og rette fejl, således at man sammen finder en holdbar løsning, som afhjælper fremtidig gentagelse af problemet.

Vi arbejder i øjeblikket 3 holdskift, 7 dage om ugen (3 week-ender ud af 10).

Overblik og kvalitetssans
Du har gerne erfaring med at arbejde i en produktion, men din faglige baggrund er ikke så væsentlig. Det vigtigste er, at du tager ansvar og er meget bevidst om kvaliteten i dit arbejde. Du er handlingsorienteret og viser initiativ ved selv at byde ind og drive opgaver.

Da hverdagen byder på både små og store udfordringer og forandringer lige fra stop på maskiner til indkøring af nyt udstyr, skal du være åben over for ændringer og kunne bevare roen og overblikket i en omskiftelig hverdag. Du skal derfor også være klar til løbende at tilegne dig nye færdigheder. Vi vægter samarbejde højt, så du skal have en positiv indstilling og lysten til at løse opgaver i fællesskab med kolleger.

For at kunne løse de daglige opgaver skal du have flair for teknik og IT.

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
Har du spørgsmål til stillingen, så kontakt Grith Pilegaard Albrecht på +45 3075 8559.

Ansøgningsfrist
16 december 2013

Research Scientist

- Research & Development
- Denmark - Gentofte

The department of Protein Separation & Virology is seeking a candidate with a strong background in project management and protein purification.

About the department
The department is part of CMC API Development, R&D, and is responsible for developing, documenting and transferring scalable purification processes for API’s in order to bring the growing pipeline of new therapeutic proteins into clinical trials. The purification processes typically comprise unit operations such as chromatography, filtration, enzymatic reactions and tangential flow membrane processes, applying state of the art technologies and mechanistic modelling.

The working climate is informal with a high degree of flexibility. The work is performed in multidisciplinary project groups in collaboration with Discovery, Cell culture, Analytical, Formulation, and Quality departments. Thus, a wide interdisciplinary understanding of the development process for biopharmaceuticals is needed to support decision making and progress within this area.

The job
The major task involves formal project management as an API coordinator. In this role, you will prepare and execute API activities to support the project objectives and the CMC strategy. The successful API coordinator is responsible for interaction with the other members of the CMC group, as well as cross organisational stakeholders.

The API activities for which you are responsible are the development of purification processes for new biopharmaceuticals at laboratory scale as well as their transfer to pilot plants for the production of drug substance for clinical trials. Documentation of process robustness and scalability is an integrated part of the work process.

Qualifications
You should hold a scientific academic degree in engineering, biology, chemistry or another relevant discipline. Preferably, you have more than 3 years of experience within the field of protein purification at laboratory, pilot or production scale.

You possess drive and a positive mind-set and you strive to be in a decision-making role. When cooperating, you often take the leading role and you enjoy setting direction to others.

As a person, you are proactive, ambitious and like to be challenged. You continually strive to raise the bar and aspire to be in a decision-making role.

We are an organisation with a continuous need to develop new leaders and therefore leadership ambitions would be an advantage.

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 Niels Nørregaard Holst at +45 3075 8116.

Deadline
31 December 2013.

Research scientist

- Forskning og Udvikling
- Danmark - Måløv

Har du en stærk molekylærbiologisk baggrund og drømmer du om at sætte dine evner inden for koordinering og ledelse i spil? Og har du lyst til at være en del af en veletableret, fagligt stærk og social gruppe med fokus på god kundekontakt og løbende forbedringer? Så er det måske dig vi leder efter til vores nyoprettede stilling som research scientist.

Om afdelingen
Vores team 318.02 Molecular Biology er en del af afdeling 318 CMC Bioassay under CMC Drug Product Development, R&D, Novo Nordisk A/S. Teamet består af 2 akademikere, 5 laboranter og en teamleder og er fysisk placeret i Måløv.

Vores ekspertise ligger inden for udvikling af analysemetoder ved brug af både klassiske og moderne molekylærbiologiske teknikker som vi tilpasser løbende i forhold til den enkelte organisme, der arbejdes med; gær, E. coli eller mammale celler.

Jobbet
Jobbet vil indebære udførelse af molekylærbiologiske leverancer krydret med ledelsesmæssige opgaver så som koordinering, projektledelse, opgavestyring, kontakt til interne kunder osv. Du vil blive LEAN-uddannet og drive forbedringsprojekter og optimering af arbejdsgange.

Du vil som research scientist være fagligt ansvarlig for molekylærbiologisk analysearbejde i forbindelse med afprøvning af nye stammer, test af celleprøver fra procesoptimering samt frigivelse af cellebanker fra udviklings- og markedsførte produkter.

Du vil komme til at arbejde med den praktiske udførelse af en eller flere af vores analysemetoder, dvs. alt fra opformering af celler, oprensning af DNA, gel-kørsel og Southern blots til PCR, qPCR, DNA sekventering og automatisering. Dokumentation og afrapportering af laboratoriearbejdet er underlagt GMP, og det vil være dit ansvar at udarbejde interne rapporter såvel som ekstern dokumentation til sundhedsmyndigheder.

Du vil endvidere blive involveret i problemløsning og support ud af afdelingen hvor det forventes at du bringer dig selv og dine erfaringer i spil for at løse opgaven på bedste vis.

Når du har fået opbygget tilstrækkelige kompetencer og et omfattende kendskab til virksomheden, vil du komme igennem et teamleder assessment med henblik på at varetage en stilling som teamleder, hvis du har de fornødne evner.

Kvalifikationer
Du er molekylærbiolog, ingeniør eller tilsvarende og har dokumenteret erfaring med molekylærbiologiske analyseteknikker. Du tager naturligt en ledelsesrolle, er systematisk, selvstændig og motiveret og kan holde hovedet koldt i travle perioder. Du kender til GMP og forstår vigtigheden af dokumentation af udført arbejde. Du er glad for at arbejde i et team og betragter IT som en integreret del af dit arbejde. Du forstår og er aktiv bruger af LEAN-tankegangen (løbende optimeringer og forbedringer) og har en god humoristisk sans.

Jobbet kræver forandringsparathed samt evner og lyst til at gennemføre løbende forbedringer/optimeringer af processer og arbejdsrutiner. Selvstændighed er en forudsætning, men du skal også kunne samarbejde med forskellige faggrupper, hvorfor der kræves gode samarbejds- og kommunikationsevner.

I Novo Nordisk er det dine evner, dit engagement og dine ambitioner, der hjælper os med at forbedre mange menneskers liv. Du får chancen for at arbejde sammen med usædvanligt talentfulde kolleger og mulighed for at udvikle dig fagligt som personligt.

Kontakt
Hvis du er interesseret i at høre mere, og din profil passer til ovenstående, så ring til os: Birgitte Bojer Jørgensen på +45 3079 3592, eller Vibeke Sønder på +45 3075 8087.

Ansøgningsfrist
22.december 2013

Student Assistant Epidemiology

- Student and Internships
- Denmark - Søborg

Are you looking for a student assistant job with possibilities to make a difference personally and professionally? Do you thrive with working as a personal assistant? Are you dedicated to making the best possible effort?

About the department
The Department of Epidemiology is a department within Global Development, and focuses on contributing with epidemiological knowledge to various stakeholders in the Novo Nordisk organisation. As a student assistant in Epidemiology you will assist the team of 12 epidemiologists in analysing, validating, and communicating epidemiological knowledge.

The job
You will be involved in various projects incl. non-interventional post-marketing studies, and preparation of epidemiological reports to stakeholders. The tasks will include validation of data in abstracts and proofreading of publications, and preparation and validation of presentations. In addition updating the department website and assisting in literature reviews and data analyses.

Qualifications
You are studying a relevant BSc/MSc programme related to epidemiology, and you have preferably 2 years until graduation. You have a strong interest and understanding of epidemiology and biostatistics, are proficient in MS Office (especially Excel and PowerPoint), and are fluent in spoken and written English. Familiarity with SAS and PubMed is an asset.

You are dedicated, have excellent interpersonal skills, a good feeling for details, and have a positive mind-set.

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.”

The position is located in Søborg and the working time is estimated to be 15 hours per week, but mutual flexibility is expected.

Contact
For further information, please contact Anne Louise Svendsen at +45 3075 2799 or Sofia Inez Iqbal Kring at +45 3075 5255.

Deadline
3 January 2014

Produktions ingeniør

- Produktion
- Danmark - Bagsværd

Er procesforbedringer lige dig? Og har du lyst til at arbejde med aseptisk produktion hos verdens førende producent af insulin? Så har vi det helt rigtige job til dig som produktionsingeniør til processupport i Bagsværd. Grib muligheden for en karriere med gode udviklingsmuligheder, en dynamisk hverdag og en stor kontaktflade i en international virksomhed.

Om afdelingen
Du bliver en del en afdeling som sikrer drift og frigivelse fra én af vore fyldelinjer i Bagsværd. Som en del af Proces Support & Teknisk Support får du ca. 10 kolleger, som tæller både ingeniører, farmaceuter, kemiker og supportere. Tilsammen har vi ansvaret for den daglige driftssupport til fyldelinjen.

Jobbet
Din fornemmeste opgave bliver at yde daglig support til driften af vores aseptiske fyldeproces så vi opretholder en stabil og kontinuerlig produktion. I tæt samarbejde med operatører, supportere, teknisk support og QA løser du en bred vifte af opgaver lige fra procesforbedringer, valideringer og afvigelsessager. Når der opstår udfordringer i vores produktion, er det dig, der sikrer overblikket, så problemerne kan løses hurtigt og effektivt. Du spiller således en nøglerolle i arbejdet med at sikre drift og frigivelse af produkterne – og du, at afdelingen altid er i compliance med gældende lovkrav. Deltagelse i større og mindre optimerings- og standardiseringsprojekter bliver også en del af din nye hverdag.

Kvalifikationer
Vi forestiller os, at du har en relevant akademisk uddannelse såsom produktions-, kemi-, maskin- eller procesingeniør, farmaceut, biolog, mikrobiolog eller lignede. Uanset din baggrund skal du have viden om GMP – gerne relateret til aseptisk produktion. Har du tilmed erfaring fra farmaceutisk produktion (herunder FDA) samt kendskab til valideringsarbejde og LEAN, er det absolut et plus. Som person er du en problemknuser, og du trives i en dynamisk hverdag, hvor din evne til at træffe beslutninger er helt essentiel. Da kvalitet og præcision er afgørende i lægemiddelindustrien, er det også vigtigt, at du er kvalitetsbevidst og har lyst til og erfaring med skriftlig dokumentation. For at få succes i stillingen er fortrolighed med IT og evnen til at sætte dig ind i nye systemer alfa og omega. Sidst, men ikke mindst, er du er udadvendt og god til at kommunikere på tværs af faggrænser – både på dansk og engelsk.

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 er du meget velkommen til at kontakte Søren Dam på +45 3079 1815.

Ansøgningsfrist
31. december 2013

Produktions Ingeniør

- Produktion
- Danmark - Bagsværd

Er procesforbedringer lige dig? Og har du lyst til at arbejde med aseptisk produktion hos verdens førende producent af insulin? Så har vi det helt rigtige job til dig som produktionsingeniør til processupport i Bagsværd. Grib muligheden for en karriere med gode udviklingsmuligheder, en dynamisk hverdag og en stor kontaktflade i en international virksomhed.

Om afdelingen
Du bliver en del en afdeling som sikrer drift og frigivelse fra én af vore fyldelinjer i Bagsværd. Som en del af Proces Support & Teknisk Support får du ca. 10 kolleger, som tæller både ingeniører, farmaceuter, kemiker og supportere. Tilsammen har vi ansvaret for den daglige driftssupport til fyldelinjen.

Jobbet
Din fornemmeste opgave bliver at yde daglig support til driften af vores aseptiske fyldeproces så vi opretholder en stabil og kontinuerlig produktion. I tæt samarbejde med operatører, supportere, teknisk support og QA løser du en bred vifte af opgaver lige fra procesforbedringer, valideringer og afvigelsessager. Når der opstår udfordringer i vores produktion, er det dig, der sikrer overblikket, så problemerne kan løses hurtigt og effektivt. Du spiller således en nøglerolle i arbejdet med at sikre drift og frigivelse af produkterne – og du, at afdelingen altid er i compliance med gældende lovkrav. Deltagelse i større og mindre optimerings- og standardiseringsprojekter bliver også en del af din nye hverdag.

Kvalifikationer
Vi forestiller os, at du har en relevant akademisk uddannelse såsom produktions-, kemi-, maskin- eller procesingeniør, farmaceut, biolog, mikrobiolog eller lignede. Uanset din baggrund skal du have viden om GMP – gerne relateret til aseptisk produktion. Har du tilmed erfaring fra farmaceutisk produktion (herunder FDA) samt kendskab til valideringsarbejde og LEAN, er det absolut et plus. Som person er du en problemknuser, og du trives i en dynamisk hverdag, hvor din evne til at træffe beslutninger er helt essentiel. Da kvalitet og præcision er afgørende i lægemiddelindustrien, er det også vigtigt, at du er kvalitetsbevidst og har lyst til og erfaring med skriftlig dokumentation. For at få succes i stillingen er fortrolighed med IT og evnen til at sætte dig ind i nye systemer alfa og omega. Sidst, men ikke mindst, er du er udadvendt og god til at kommunikere på tværs af faggrænser – både på dansk og engelsk.

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 er du meget velkommen til at kontakte Søren Dam på +45 3079 1815.

Ansøgningsfrist
31. december 2013

Project Manager

- Project Management
- Denmark - Gentofte

Steno Diabetes Center is looking for a Project Manager for the Steno-REACH project who can coordinate the development of an international Steno satellite in Malaysia.

Do you have experience in driving international projects and are you successful in meeting deliverables and milestones? If so, you may be just the colleague we are looking for.

Steno-REACH project

Steno Education Center is a rapidly expanding department within the Steno Diabetes Center. We focus upon developing professional education for doctors and other health care professionals in all aspects of diabetes management. As part of our expansion strategy, we have received funding for the Steno-REACH project from the Novo Nordisk Foundation to develop an education satellite in Malaysia. The satellite will be established during 2014 and 2015. It is planned that a large part of the Steno Diabetes Center teaching taking place in Asia will run from this satellite. Our educational focus will be on translating knowledge of diabetes management into everyday clinical care.

Job description

As a project manager you will be responsible for the day to day managing of the project, workflow design , and driving the project forward within budget, scope and timeline. It will be your responsibility to liaise with content owners/developers within the project, i.e the Project Managers for e-learning and programme development.

You will also be responsible for the project structure, including identifying and clarifying problems, recommending solutions, and prioritising issues. You will also identify and handle relevant stakeholders, secure frequent communication on project progress with the steering committee, collaborators and stakeholders, and secure proper and timely feedback.

You will be working in close collaboration with experienced researchers, doctors, nurses and course administrators within Steno Education Center. You will be based at Steno Diabetes Center in Copenhagen and your daily working environment will be filled with enthusiastic and motivated people with a good sense of humour.

Qualifications

You must be experienced and hold a higher education and at least 4 years of independent project management experience from an international company. You must also have experience with finance processes, roadmaps and project planning tools, and preferably have worked with project planning in an Asian country. We expect that you work effortlessly with project methodology and can be a knowledge person to the project regarding tools and methods.

You should work proactively, show initiative, be a motivating team player, and be good at negotiating. Proficiency in English is required. You should be a strong communicator both orally, and in writing. We expect you to be culturally aware and understand how this influences the project. You must have a high degree of flexibility, and be able to shoulder additional workload when necessary. Some travel may be expected.

You must be able to work independently and be able to drive a process, create structure and a framework for the project and be comfortable with reporting progress to the steering committee.

Salary and hiring

Salary and hiring will depend upon educational degree and qualifications and will be in accordance with Danish legal agreements. The position is initially for a 5 year period.

Application

Deadline December 29th 2013. The position is to be filled as soon as possible. Job interview will take place weeks 3 and 4.

Questions regarding the position may be addressed to Head of Education, Steno Diabetes Center. Ulla Bjerre-Christensen +45 30 75 62 64. A job description can be requested by contacting course administrator Dorte Gundtoft DGCH@steno.dk.

About Steno Diabetes Center

Steno Diabetes Center is a world leading institution within diabetes care and prevention. Steno is owned by Novo Nordisk A/S and is a 'not for profit' organisation working in partnership with the Danish healthcare system. Steno treats around 5600 people with diabetes.

Senior Medical Writer

- Research & Development
- Denmark - Søborg

Clinical Reporting is looking for a senior medical writer. You will be offered a challenging job with a significant amount of individual responsibility, and good personal development opportunities in an international and dynamic atmosphere.

About the Department
Clinical Reporting is the medical writing function at Novo Nordisk and is part of Global Development. We are currently 60+ employees, primarily medical writers and clinical publishers. We are a diverse group with different nationalities and professional backgrounds working together in a pleasant and informal atmosphere. We are responsible for preparing clinical documents for submission to regulatory authorities worldwide as well as abstracts and posters for scientific conferences and manuscripts to scientific journals.

The job
As a medical writer, your main tasks involve preparation of complex clinical documents within Novo Nordisk’s different therapy areas. Planning and coordination of activities in a cross-disciplinary setting is a central part of the job. Your main collaboration partners include clinicians, statisticians, regulatory affairs professionals, trial managers and data managers from Novo Nordisk headquarters and international affiliates. All documents are written in English and must comply with internal Novo Nordisk standard operating procedures as well as external guidelines.

Qualifications
You have a university degree within natural sciences (MD, M.Sc., M.Sc.Pharm. or equivalent) including skills within statistics and scientific research methods, and you have experience with medical writing. You master written and spoken English at a professional level, and you have a flair for, and a genuine interest in scientific communication. You are a strong team player who adapts easily to a changing environment with tight deadlines, and you are good at planning, coordinating and reaching consensus. You are thorough, structured and conscientious, and you have a good sense of humour.

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 development.

Contact
For further information, please Contact Trine Kruse on + 45 3079 6107, Lisbet Westergaard on + 45 3079 9817 or Mette Pierri Stensler-Thomsen on + 45 3075 2575.

Deadline
10 January 2014

Medical Writing Specialist

- Research & Development
- Denmark - Søborg

Clinical Reporting is looking for a medical writing specialist. You will be offered a challenging job with a significant amount of individual responsibility, and good personal development opportunities in an international and dynamic atmosphere.

About the Department
Clinical Reporting is the medical writing function at Novo Nordisk and is part of Global Development. We are currently 60+ employees, primarily medical writers and clinical publishers. We are a diverse group with different nationalities and professional backgrounds working together in a pleasant and informal atmosphere. We are responsible for preparing clinical documents for submission to regulatory authorities worldwide as well as abstracts and posters for scientific conferences and manuscripts to scientific journals.

The job
As medical writing specialist, your main tasks involve preparation of complex clinical documents within Novo Nordisk’s different therapy areas. Planning and coordination of activities in a cross-disciplinary setting is a central part of the job. Your main collaboration partners include clinicians, statisticians, regulatory affairs professionals, trial managers and data managers from Novo Nordisk headquarters and international affiliates.

Another important component of the job is mentoring and training of other medical writers, which requires the ability to provide constructive feedback. The medical writing specialist is also expected to drive sharing of better practices across projects/processes.

All documents are written in English and must comply with internal Novo Nordisk standard operating procedures as well as external guidelines.

Qualifications
You have a university degree within natural sciences (MD, M.Sc., M.Sc.Pharm. or equivalent) and ≥5 years of medical writing experience. In addition, you have a good understanding of the pharmaceutical industry, including clinical development and regulatory processes and requirements. Your professional skills also include statistics and scientific research methods, and you have experience with writing publications for scientific journals. You master written and spoken English at a professional level, and you have a flair for, and a genuine interest in scientific communication. In addition, you should be able to communicate in a reliable, professional and trustworthy manner. You are a strong team player who adapts easily to a changing environment with tight deadlines, and you are good at planning, coordinating, managing stakeholders and reaching consensus. You are thorough, structured and conscientious, and you have a good sense of humour.

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 development.

Contact
For further information, please Contact Trine Kruse on + 45 3079 6107, Lisbet Westergaard on + 45 3079 9817 or Mette Pierri Stensler-Thomsen on + 45 3075 2575

Deadline
10 January 2014

Træningskoordinator

- Administration
- Storkøbenhavn

Er du vor nye kollega i Site Denmark (SDK) Training hvor vi arbejder med at strukturere og dokumentere træning? Aktuelt er vi på udkig efter kompetente kollegaer til Bagsværd og Kalundborg der kan styrke vores team og tage del i at løse de mange opgaver vi har med at sikre kvaliteten.

Vil du have en central rolle i en udfordrende dagligdag i et team med der har kontakt med hele organisationen. Arbejder du struktureret med blik for detaljen og samtidig kan se på tværs i organisationen? Så har vi et spændende job til dig som træningskoordinator i SDK Training.

Om afdelingen
SDK Training består fremadrettet af 19 medarbejdere der sørger for at implementere træningsstandarder og dokumentere, samt strukturere træning i SDK Denmark.

Jobbet
Du bliver en af de 14 medarbejdere der arbejder med vores træningssystem ISOtrain hvori vi dokumenterer træning. Du vil blive en del af vores “One Point of Entry” hvor vi samlet modtager alle henvendelser fra SDK Denmark og dermed løser opgaver på tværs af organisationen.

Du vil bl.a. blive en aktiv del implementering af standarden “Competence Management” der strukturerer og illustrerer hvordan træning planlægges og gennemføres. Du vil i samarbejde med ledere, trænere og træningskollegaer medvirke til at sikre at træning gennemføres i overensstemmelse med vores standarder.

Klargøring af dokumentation og aktiv deltagelse ved både nationale og internationale audits og inspektioner vil være en del af jobbet.

Kvalifikationer
Du har en uddannelsesmæssig baggrund med afsæt i administrativ opgaveløsning. Ideelt set har du erfaring fra farmaceutisk produktionsvirksomhed. Du behersker dansk og engelsk skriftligt såvel som mundtligt.

Du er god til kommunikation, i samarbejde og du kan håndtere mange forskellige opgaver samtidig med at du bevare overblikket. Du arbejder struktureret og systematisk og er serviceminded. Du kan forfølge et mål og arbejde i overensstemmelse med en standard. Du er en igangsætter, engageret, fleksibel og det er naturligt for dig at tage ansvar. Din attitude er positiv og du har et højt energiniveau. Du kan lide at være nøgleperson i en travl hverdag med mange relationer og er drevet af at lære nyt.

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.

Anfør i din ansøgning hvilken af de to arbejdssteder (Bagsværd og Kalundborg) du foretrækker.

Kontakt
For yderligere information, kontakt Associate Manager Benjamin Risum på +45 3079 2298.

Ansøgningsfrist
23 December 2013

Process Engineer

- Production
- Denmark - Hillerød

Device manufacturing & Sourcing (DMS) seeks 1 talented engineer with experience within the field of injection moulding.

In this job, you will be responsible for the performance of our 40 injection moulding machines at our production site in Hilleroed. If you have a structured way of working, and the ability to involve and motivate others, go for this job.

About the department
Process Support in Hillerød is part of Device Manufacturing & Sourcing (DMS) and is responsible for the injection moulding and decoration of plastic components for devices such as Vagifem®, FlexPen® and the next generation of pre-filled devices. The department employs about 75 members of staff and faces a multitude of exciting challenges in the next few years with the launch of several new products.

The job
You will be measured against and take up the position as processowner of our 40 injection moulding machines we have in operation at our internal production-site in Hilleroed. Your main tasks will be to ensure the validated state, specify new equipment standards and qualify the equipment in order to ensure that it meets the requirements of the pharmaceutical industry. Besides that you will be expected to take lead on Structured Problem Solving, follow up on service and maintenance agreements, and coordinate daily tasks using both internal and external resources.

Qualifications
You are a qualified engineer or similar and have experience within injection moulding (preferably machine) and/or having experience with similar challenges from another area of pharmaceutical production. You have experience of qualifying and document the validated state of equipment within the pharmaceutical industry. You have good fundamental technical skills and you are familiar with practical problem solving.

You are outgoing, have strong communication skills and enjoy communicate with others.

As a person you can stay focused in a sometimes busy working day and you always approach tasks and colleagues with a positive attitude and energy.

Your commitment makes you persistent and you see a task through from start to finish. You have a build-in quality mind-set – and have the ability to have an overall view of many tasks. Besides that you are able to do the above mentioned things with a smile and a positive approach.

The position is based at Moulding Equipment Support, a team of 20 engaged Engineers and Technicians, in the division of Device Manufacturing Sourcing, which employs approx. 375 people. DMS works within component manufacturing and pre-assembly of Novo Nordisk pre-filled insulin pens, and provides many exciting career development opportunities.

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. Your skills, dedication and ambition help us change lives for the better. In addition, we offer you an opportunity to work with extraordinary talent and benefit from a range of possibilities for professional and personal development.

You are very welcome to apply to this position in danish.

Contact
For further information please contact Jens Antonsen at +45 3079 2676.

Deadline
1 January 2014

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%

Senior Research Scientist

- Research & Development
- Denmark - Måløv

Do you want to develop and validate immunoassay's? And do you enjoy working in an open, dynamic and social atmosphere with a strong focus on technical and scientific skills? If so, then you may be our new senior research scientist in Team IBA, Department 318 CMC Bioassay.

About the department
You will be a part of a team consisting of 12 technicians and 6 academics in the total of 55 colleagues working in Department 318 CMC Bioassay. The department is located in Novo Nordisk Park, Måløv, greater Copenhagen area, within R&D in Novo Nordisk A/S. The department develops and applies various methods for the measurement of Potency of API and Drug Product, DNA/RNA characterization and ELISA methods.

The Job
You will be responsible for developing and validating immunoassay's for the project portfolio covering clinical phase 1, 2 and 3. You are expected to take an active part in optimization and standardization of workflow in the department, participate in cross organizational project groups and be involved in document writing. In addition, collaboration with other departments both in Quality Control and in Research Units, including troubleshooting and transfer of analytical methods, will be part of the challenge.

Qualifications
You hold a university degree within natural sciences with proven skills within immunoassay, molecular biology, protein chemistry and biochemistry. Especially experience with ELISA and SPR method development is important. Experience with qualification of analytical equipment is an advantage. You are familiar with lean and continuous improvement and/or have an open mindset regarding standardization and optimization of work flow. If not already acquainted with GMP, you are ready to participate in GMP courses, and you understand the necessity of documentation and traceability. As a person you are able to work both independently as well as contributing to teams. You have a positive attitude and good communication skills.

Contact
For further information, please call Per Jeppesen at +45 3075 0049. or Lise Leonardsen Rønnedal at +45 3075 7030.

Deadline
14 December 2013

Senior Clinical Disclosure Professional

- Research & Development
- Denmark - Søborg

Novo Nordisk recently announced our commitment to a high level of transparency of our global clinical research activities by volunteering to make Clinical Study Reports public via NovoNordisk-Trials.com for products marketed in EU and US. Consequently, a substantial amount of Clinical Study Reports are to be made ready for disclosure and uploaded to the external web-site. This is a new challenge and to assist us in making this happen, and to take part in other activities to ensure transparency of Novo Nordisk global clinical research activities, we are seeking two new colleagues for the Global Clinical Registry department.

You will be working with colleagues worldwide, be part of establishing work processes, and planning and overseeing the conduct of the activities. You have a university degree, MSc within natural science, and have several years of experience working with clinical research either as e.g. a medical writer, or clinical trials manager.

About the department
Global Clinical Registry is part of Novo Nordisk Clinical Reporting area, and currently employs 6 people. In total the Clinical Reporting group consists of more than 50 people working with reporting and publishing of clinical reports. The group consist of different nationalities as well as professional backgrounds.

The availability of the information on clinical research to the public is governed by legal requirements. It is a challenge for the department to be up-to-date with the progress of the portfolio of clinical research activities in order to meet the legal requirements. Information on the clinical research in terms of study initiation, completion, results availability and scientific publications is captured via the Clinical Trial Management System (CTMS), and a disclosure IT system, PURE, is used to keep track of the deadlines.

Global Clinical Registry oversees and performs registration of our worldwide clinical activities. We manage timely release of results information to clinicaltrials.com, to NovoNordisk-trials.com, and to the EU Clinical Trials Register which, from next year, also will hold results of clinical trials. It is also our responsibility to keep aligned with national requirements for clinical trial registries in other countries. Finally we cover the maintenance of our clinical disclosure IT system and NovoNordisk-trials.com.

As part of Clinical Reporting, the job brings the option of being involved in other activities. Flexibility in relation to the growing Novo Nordisk portfolio of drug development projects calls for allocation of the resources where they are needed the most.

The Job
You will be working across the entire Novo Nordisk portfolio of clinical research activities, and in close collaboration with colleagues such as clinicians, statisticians, regulatory affairs professionals and trial managers from Novo Nordisk headquarters and international affiliates.

The purpose of your job will be to ensure disclosure of clinical research reports to the public in accordance with Novo Nordisk new disclosure code of conduct and to engage in other of the departments’ disclosure activities.

New challenges are ahead of us and the purpose of the 2 new jobs is to engage in shaping new work processes, planning activities, ensuring the job is done timely and to the right level of quality, and engage in use of and update/introduction of the use of IT systems.

One of the positions will be focused towards project management of report disclosure activities, whereas the other will be focused towards the use of IT tools.

Qualifications
Our preferred candidates have a university degree within natural sciences (MD, M.Sc., M.Sc.Pharm. or equivalent). Skills within statistics, scientific research methods, and experience in writing scientific reports, publications for scientific journals or similar will be considered a benefit. You must master written and spoken English at a professional level. Furthermore both jobs require planning and coordination of activities, and some level of project management skills is desirable.

You are a strong team player who adapts easily to a changing environment who works with at times tight deadlines. You are thorough, structured and conscientious.

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 Merete Jørgensen +45 3079 1728.

Deadline
16 December 2013

Graduates! Kick-start your R&D Regulatory Affairs career

- Graduate
- Denmark - Søborg

Professional development

What has surprised you?

Start your career climb in September 2014

Novo Nordisk’s Regulatory Affairs Programme is a great springboard for launching life-changing careers. As a global pharmaceutical company and the world leader in diabetes care we can give you the opportunity to use your recently-acquired master’s degree to make a difference.

Start your journey
Novo Nordisk Regulatory Affairs makes medicine available to patients all over the world by ensuring fast regulatory approval in all our markets. Regulatory Affairs is a fast-changing field and 600 dedicated employees around the globe need both keen negotiating skills and scientific insight to serve as Novo Nordisk advocates.

During the programme tight deadlines, cross-departmental collaboration, project management and the challenges of international communication will be part of your work day.

Scope of the programme
The Regulatory Affairs Graduate Programme is a 2-year expedition consisting of three 8-months rotations:

2 rotations in our corporate headquarters in Denmark
1 rotation in one of our large global affiliates such as USA, China, Japan, India or Brazil

A global career
After successfully completing the programme you will embark on your career at Novo Nordisk in a permanent position – most likely as a Regulatory Professional. While you would probably be based in Denmark, your broad network and international experience from the programme will enable global career opportunities.

Requirements
To join the Regulatory Affairs Graduate Programme you must hold a recent master’s degree in Natural Science, for example within Pharmacy, Chemical Engineering, Biology, Biotechnology or a related field. You have no more than 1 year of work experience since finishing your studies. It is your drive, intellect, commitment and ability to take control of your own development that will get you a position on our Programme.

Joining Novo Nordisk appeals to you, not because of the competitive salary we offer, but because the work we do is so rewarding - as we make a difference to the lives of people with chronic conditions around the world.

For more details, visit Novonordisk.com/ Regulatory-Affairs-Graduate

Contact
For further information please contact Programme Manager Jakob Wolter: JkWo@novonordisk.com, Graduate Mark Root: MJhR@novonordisk.com, or visit our Graduate blog at http://blogs.novonordisk.com/graduates/

Deadline 9 February 2014
Apply before 9 February 2014 by submitting your motivational letter (one page in English where you explain your motivation for applying), CV (in English) and a scanned copy of your latest grade transcript.

In addition to the Regulatory Affairs Graduate Programme, we have 9 other graduate programmes which will all lead to life-changing careers.

Laborant

- Kvalitetssikring
- Danmark - Bagsværd

I Novo Nordisk skaber vi værdi ved at sætte patienterne først. Hvert tiende sekund bliver to personer diagnosticeret med diabetes, og næsten 366 millioner mennesker i hele verden har brug for os. At arbejde her handler om at gøre en forskel. Hvis du finder sådanne udfordringer inspirerende, og samtidigt motiveres af kemiske analyser og med at yde support, er du måske vores nye laborant.

Om afdelingen
Vi er en afdeling på cirka 70 medarbejdere som har en central supportfunktion World Wide i forhold til analyse af diabetespræparater. Vi er involveret i udviklingsprojekter og efterfølgende i at sikre implementering af analysemetoder og tilhørende udstyr på alle produktions sites laboratorier.

Afdelingen er delt op i 4 teams med hvert deres ansvarsområde. Du vil blive tilknyttet det team, som varetager support på kemiske analyser på Humane insulin produkter og GLP-1 analoger. Teamet består i dag af 17 personer – fordelt imellem 6 kemikere, 10 laboranter/teknikere og en teamleder. Vi arbejder primært med HPLC, men også med pH, atomabsorption, partikeltælling, turbidimetri og mikroskopi.

Jobbet
Vi søger en analyselaborant til et fast job. Ansvaret som analyselaborant inkluderer alt omkring den praktiske del forbundet med kørsel af analyser, reagensfremstilling, beregning af resultater og analysesupport til produktions sites i samarbejde med kemikerne. Opgaverne er især relateret til stabilitetsprøver men også til optimeringer, valideringer samt sammenligningsstudier.

Kvalifikationer
Du har en uddannelse som laborant eller tilsvarende, og har erfaring og interesse for proteinkemi, HPLC-analyser og kromatografi. Gennem dit praktiske arbejde med GMP, er du i stand til at sikre et højt kvalitetsniveau af analyserne. Du har et indgående kendskab til LIMS, Empower, cLEAN og gerne også til LimsLink.

Du har ved tidligere ansættelser vist at du kan arbejde selvstændigt, samt udvist engagement i et konstruktivt samarbejde med dine kollegaer. Du er god til at skabe overblik, og prioritere din tid. Du er kvalitetsbevidst, og du evner at have fokus på dokumentation af arbejdsgange. Vi forventer desuden, at du er resultatorienteret og parat til at tage et ansvar. Du skal være omstillingsparat og kunne arbejde under tidspres, idet vi arbejder i et dynamisk arbejdsmiljø hvor tingene af og til går stærkt. Du har et godt humør, og evner at bibeholde det i alle situationer.

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.

Jobbet ønskes besat hurtigst muligt.

Kontakt
Nærmere oplysninger om jobbet kan fås ved henvendelse til: Ea Pettersson på +45 3079 5384.

Deadline
15. december 2013

Graduates! Kick-start your global finance career

- Graduate
- Denmark - Greater Copenhagen area

Professional development

What has surprised you?

Join one of our Finance Graduate Programmes

Novo Nordisk’s Finance Graduate Programmes are great platforms for launching life-changing careers. As a global pharmaceutical company and the world leader in diabetes care, we treat more than 20 million patients across the world. We can give you the opportunity to use your recently acquired master’s degree to make a difference in changing how people live with Diabetes.

Start your journey in September 2014
Our Finance Graduate Programmes are designed to provide you with comprehensive knowledge of the Novo Nordisk finance operation and a solid understanding of the underlying business. During the programmes you will develop skills within financial planning, project management, business intelligence, risk management and other core finance skills. You will develop through training, access to senior mentors and a steep learning curve.

Kick-start a global career
After successfully completing the programmes you will be equipped with the skills to embark on your career at Novo Nordisk with a permanent position typically within the Corporate or European Finance organisations, or in a business analyst role related more directly to sales and marketing. While you could be based in Denmark or elsewhere in Europe your broad network and international experience from the programmes will enable global career opportunities.

Choose your programme
We offer two Finance Graduate Programmes that during a 2-year journey consist of four 6-months rotations:

Global Finance Graduate Programme
3 rotations in our headquarters in Denmark
1 rotation in a global sales affiliates or production site

European Finance Graduate Programme
2 rotations in our European headquarters in Zurich
1 rotation in our headquarters in Denmark
1 rotation in a large European sales affiliates

Requirements
You must hold a master’s degree in a relevant subject, for example within Finance, Management Accounting, Economics or International Business and have finished at the top of your class. You should have no more than 1 year of work experience since finishing your studies. Joining Novo Nordisk appeals to you, not because of the competitive salary we offer, but the work we do. Also, you strive for working in a global, international and culturally diverse organisation with all of the opportunities this entails.

For further information, visit Novonordisk.com/Finance-Graduates

Contact

Global Finance Graduate Programme
Graduate Programme Coordinator, Annemarie Birkedal Andersen: +45 30 79 02 65, abay@novonordisk.com

European Finance Graduate Programme
Programme Manager for European Finance, Peter Egsgaard: +41 79 777 43 56, pteg@novonordisk.com

Apply online before 9 February 2014
Apply for the Global, European or both Finance Graduate Programmes in the same application. Simply indicate at the beginning of your application which programmes you are applying for.

Submit your motivational letter, CV (in English) and a scanned copy of your latest grade transcript.

In addition to the Global Finance Graduate Programmes we have many other graduate programmes which all lead to life-changing careers.

Associate 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

Do you take pride in working in a successful and world leading organisation? Do you want to work with business support and lead a team with a high variety of tasks?

We are seeking a team leader for our Business Support.

Novo Nordisk in Kalundborg is about 1 hour drive from Copenhagen, covering 1,350,000 m2 with several factories and laboratories. We produce approx. 50% of the world´s insulin and is at the forefront of technology, systems, methods and processes.

Can you lead, motivate, and inspire, and are you eager to deliver value adding services to our production. You get to express yourself in a successful department which is developing rapidly, giving plenty of opportunities and challenges. IM1 is to scale up production and you will play a central role in the exciting process.

About the department
In Insulin Manufacturing I, Business Support (IM1 BS), in Kalundborg you will be part of a dynamic department with 50 competent employees. Your team influence more than 350 people across the plant. This job will give you the opportunity to join a world leader within diabetes care. Main objective of the department is to support the world´s largest insulin plant, within disciplines of Business support, Process automation, Authority coordination, and Project Management.

The job
As Team Leader you will be responsible for a team of 12 employees responsible for finance, logistics, facility, raw material, risk management, and change management projects.

Currently, our plant is preparing to expand with new products, wherefore we are looking for you ambitious and strategic team leader, who appreciate different challenges and foster innovation.

Qualifications
To cope with the challenge you have a degree in Business Economics and experience as people management. In addition, you have at least 5 years of relevant experience, preferable from the pharmaceutical production with documented cGMP experience.

Your managerial style is open and positive, and you have already demonstrated that you are able to lead and motivate the team members to take pride in delivering on their objectives. You are goal-oriented and able to maintain your strong overview in a busy and dynamic environment.

Lastly, you have proficiency in both English and Danish.

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 Mette Krogh at +45 3075 6166.

Deadline
31 st of december

Laborant (Inflammation)

- Forskning og Udvikling
- Danmark - Måløv

Afdelingen for Immunfarmakologi på Novo Nordisk A/S i Måløv søger en dygtig og engageret in vivo laborant i en vikarstilling fra snarest muligt og indtil den 30. juni 2014. Vi har brug for en entusiastisk og motiveret kollega som – sammen med de øvrige akademiske og tekniske kolleger – kan bidrage til vores arbejde indenfor forskning i inflammationssygdomme.

Om afdelingen
Afdelingen er en del af Biopharmaceuticals Research Unit, som har til opgave at udvikle protein-baserede lægemidler til behandling af kroniske, inflammatoriske/autoimmune lidelser. Vi har et godt samarbejde i et dynamisk arbejdsmiljø, og vores daglige arbejdsplads er i Måløv, vest for København. Vi har flere veletablerede dyre-modeller og cellulære assays og søger hele tiden at implementere ny og relevant teknologi. Vi deltager i identifikationen af nye projekt-muligheder og vi repræsenterer farmakologien i projekt-grupper på tværs af organisationen, hvor vi altid bestræber os på at levere resultater af en høj kvalitet.

Vikarstillingen hører desuden ind under en arbejdspakke i det Europæiske konsortium, IMI (Innovative Medicines Initiative). IMI konsortiets hovedopgave er at fremme udviklingen af bedre og mere sikker medicin i Europa. Som et led i denne opgave understøtter IMI samarbejder mellem industri og universitetsverdenen for at optimere innovationen indenfor lægemiddeludvikling. IMI er et foretagende mellem EU og Sammenslutningen af Pharmaceutisk Industri i Europa (EFPIA).

Jobbet
Dine opgaver vil fokusere på en sygdomsrelevant in vivo musemodel for den autoimmune sygdom, leddegigt, og du vil være ansvarlig for alle aspekter af forsøgene, herunder planlægning og induktion af modellerne, scoring, behandling og indledende data-analyse. De teknikker vi bruger omfatter bl.a. immuniseringsteknikker, scoring/måling af inflammation i vores dyremodeller, flow-cytometri (FACS), celle-biologiske teknikker, ELISA og Bioplex. Erfaring med en eller flere af disse teknikker vil være meget ønskeligt.

Kvalifikationer
Du er uddannet laborant eller tilsvarende og har erfaring med in vivo farmakologi og dyreforsøg (i mus) samt teknikker såsom ELISA, Bioplex, flow cytometri, celle-oprensning og celle-kultur assays. Derudover må du gerne have erfaring fra den farmaceutiske industri. Du har et stort engagement, sætter ære i at udføre et godt stykke arbejde og er god til at omgås dine kolleger. Da en stor del af vores arbejde strækker sig over flere dage, er det vigtigt, at du er pligtopfyldende og til at regne med hver dag.

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 Claus Haase på + 45 4443 9309 eller Mette Thorn på + 45 3075 2408

Ansøgningsfrist
29 december 2013

Laborant med celle og GMP erfaring (Måløv, Danmark)

Operatør til Deviceproduction (Hillerød, Danmark)

Research Scientist (Gentofte, Denmark)

Research scientist (Måløv, Danmark)

Student Assistant Epidemiology (Søborg, Denmark)

Produktions ingeniør (Bagsværd, Danmark)

Produktions Ingeniør (Bagsværd, Danmark)

Project Manager (Gentofte, Denmark)

Senior Medical Writer (Søborg, Denmark)

Medical Writing Specialist (Søborg, Denmark)

Træningskoordinator (Storkøbenhavn)

Process Engineer (Hillerød, Denmark)

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

Senior Research Scientist (Måløv, Denmark)

Senior Clinical Disclosure Professional (Søborg, Denmark)

Graduates! Kick-start your R&D Regulatory Affairs career (Søborg, Denmark)

Laborant (Bagsværd, Danmark)

Graduates! Kick-start your global finance career (Greater Copenhagen area, Denmark)

Associate Manager (Kalundborg, Denmark)

Laborant (Inflammation) (Måløv, Danmark)