Jobs at Novo Nordisk

Business system analyst

- IT, SAP Specialist
- Denmark - Bagsværd

Diabetes Finished Products, Site Denmark Bagsværd, Production IT.

If you have knowledge about SAP, Manufacturing Execution Systems and production processes, combined with the ability to communicate with multiple stakeholders from different layers in the organisation, we have just the right job waiting for you. As Business system analyst you will have the opportunity to personally impact the way we use and manage our IT systems and the processes for which they are used in Diabetes Finished Products, Site Denmark Bagsværd.

About the department
You will join a group of colleagues conducting process support in the inspection area and you will report to the department manager. You will support the whole Site Denmark Bagsværd when it comes to production IT and you will have heavy interaction with stakeholders across Site Denmark Bagsværd and other areas of Novo Nordisk.

The job
Your overall objective is to secure a stable and harmonised use of the SAP and PAS-X systems for the business processes of production and warehouse. A vital part of this will be to monitor the process performance and data quality across the two systems. You will identify areas of opportunity to further improve the performance of processes or systems. With your joint understanding of our warehouse and production processes and system knowledge you will analyse possible changes and understand the impact of such changes to our production facilities. The job requires interaction with people from other production facilities globally in order to share best practice, as well as process experts and system super users within Site Denmark Bagsværd. A part of your job will be to represent the warehouse and production processes in already established Area responsible super user forums to secure standard processes, data coherency and integration between the PAS-X and SAP solution. You will also be expected to supply input to various projects where you contribute to ensure alignment between the suggested project initiatives and the way we use SAP and PAS-X as part of our business processes.

Qualifications
You have a relevant academic degree. You have gained knowledge about Manufacturing Execution Systems, SAP and production processes. Experience from the pharmaceutical industry will be an advantage. With your ability to understand and create overview of complex issues you are able to identify potential optimisation areas. You are used to work independently and able to drive strategic initiatives. You have a structured approach to your work combined with excellent communication skills in written and spoken Danish and English. At Novo Nordisk, we have been changing diabetes since 1923. If you are ready to strengthen our position as an innovative pioneer and respected industry leader, we encourage you to join us to make the most of your talent.

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 Michael Aaris Rand at +45 3075 0043.

Deadline
12 January 2014

International Trial Manager, Maternity vacancy

- Research & Development
- Denmark - Søborg

If you are driven by taking responsibility for the planning and execution of clinical trials within quality, timeline and budget deliverables, you may be our new International Trial Manager.

About the department
Clinical Operations, Haemophilia is a team of 70 highly skilled and ambitious colleagues responsible for planning and execution of clinical trial activities in accordance with the Clinical Development Plans, hereby securing Novo Nordisk a world leading position within the treatment of haemophilia and rare bleeding disorders. The scope of our activities is phase 1 to 4 clinical trials in collaboration with our Novo Nordisk affiliates. Being a headquarter division our environment is characterised by a vast global network with high quality standards, challenging assignments and continuous career opportunities.

The job
We are seeking a new colleague to take up a temporary position as International Trial Manager for 10 months. As International Trial Manager you will be responsible for timely planning, executing and finalizing clinical trials using your operational and therapeutic experience. You will be leading the trial team and coordinate trial management activities in order to meet key deliverables and quality standards. Tasks will be solved through proactive planning, team work, clear communication and stakeholder management. You will be a main contributor during international meetings requiring you to have strong cross-cultural awareness and presentation skills. Your main responsibility will be the development of critical trial documents like the trial protocol, the clinical operational plan and the trial budget which will require you to have an eye for important details while keeping the overview. You will be expected to digest complex data outputs, analyse complex scientific challenges and to ensure a high level of quality in all you do.

Qualifications
You hold a university degree in health, biological, pharmaceutical science or equivalent with preferably two years of experience in trial or project management related positions. You have a broad knowledge of clinical trial methodology and you have excellent presentation, organizational and cooperation skills. A quality mind set is a must, together with a focus on meeting deadlines, communicating effectively and maintaining overview. You have a determined, analytic and structured personality with a pragmatic and quality based approach to your tasks. You strive in a dynamic and challenging cross-cultural environment and you are motivated by leading a team and developing solutions to complex challenges. You are an experienced IT user and capable of familiarizing yourself with advanced technologies. You are a dedicated team player with a natural drive and motivation who inspires trust and engagement amongst colleagues and partners. Fluency in written and spoken English is essential.

At Novo Nordisk, we strive for excellence. As a world leading pharmaceutical company, we offer our employees opportunities for continuous personal development and excellent career opportunities.

Contact
For further information, please contact Iris Koenig at+45 3079 3971 or Lars Bjørn Justesen at +45 3079 6501.

Deadline
12 January 2014

Auditor for the Business Ethics Assurance team in Group Internal Audit

- Business Support
- Denmark - Bagsværd

Business Ethics is a focus area within Novo Nordisk and the pharmaceutical industry. Group Internal Audit is looking for a new ambitious and international minded member for our Business Ethics team that primarily focuses on compliance within anti bribery, corruption and fraud.

About the department
Group Internal Audit is a department consisting of 19 people representing eight different nationalities. We are responsible for providing assurance to senior management and the Audit Committee on compliance with IT, Finance and Business Ethics requirements. Our team consists of a variety of backgrounds, working in a dynamic, ambitious and informal environment.

The job
We offer an exciting and challenging job that will provide you with an inside perspective to Novo Nordisk’s business processes and give you a broad network throughout the organisation. The wide range of interesting assignments are primarily related to business ethics reviews of affiliates worldwide, as well as ad-hoc management requests from our headquarters in Denmark and international business areas.

You will also be involved in cross-disciplinary projects where you will have the opportunity to take an active role in the performance and completion of a variety of assurance tasks, including planning, performing and completing internal projects and compliance investigations

The position is based at our headquarters in Copenhagen (Denmark) and will include international travel. Working with our team, you will obtain an exceptional insight into the global business operations and principles of the Novo Nordisk group.

Qualifications
You possess a M.Sc. or diploma in Accounting, Auditing or similar. You will preferably have two to four years’ experience working with Novo Nordisk, a large accounting firm or international company. You are motivated by working both as part of a team and on projects and have strong analytical skills combined with a pro-active mind-set. Other key personal qualifications include a high level of energy, good sense of humour and the ability to stay focused while working under pressure. You are fluent in written and spoken English, proficient with IT-tools and you are willing to travel 60+ days per year.

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 Tobias Brun Hansen +45 3075 7880.

Deadline
13 January 2014

Department Assistant

- Administrative
- Denmark - Bagsværd

Are you a skilled and experienced administrative assistant looking for new challenges?

Would you like to use your excellent knowledge of Novo Nordisk admin systems to support project managers to lead improvement in quality?

Then this might interest you.

About the department
Quality Projects (QP) is part of Quality Development – based in Corporate Quality. We are a skilled group of project managers and process specialists who work to improve the Quality Management System (QMS) collaborating closely with customers throughout the company.

The job
The job covers a broad range of admin tasks, e.g. maintenance and support of Globeshare team and publishing sites, project budget follow up, design, development and maintenance of reports and portfolio reporting, event planning, project assistance and ad hoc administrative tasks and support to the CVP area.

You will be responsible for providing a full range of administrative support in QP as well as supporting other employees in Quality Development as required. You will be the contact person for project managers in NN Quality in connection with monthly project reporting as well as larger project management events.

You will work in a challenging environment under constant development. You have an eye for details and are able to work independently and to prioritise and manage your own time. You will have full responsibility for your own tasks working closely with your assistant colleague in the CVP area.

Qualifications
You have administrative qualifications and experience of Novo Nordisk systems and you are a skilled user of Globeshare and SAP. You have solid expertise with the MS Office Package; mainly Excel, PowerPoint and Project.

You are a team player. You take initiative and like new challenges. You can handle simultaneous tasks and are able to complete them, even when you are busy. You are engaged, positive and willing to actively contribute to the department. Preferably you have some years’ experience from a similar position.

Your oral and written communication abilities in both English and Danish are excellent.

If you think you fit this profile then we look forward to hearing from you in Quality Projects!

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 additional information, please contact Louise Muijen on +45 3075 3936.

Deadline
8 January 2014

Teknisk processupporter til Pakkeri

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

- Produktion
- Danmark - Kalundborg

Vil du arbejde med verdensklasse produktion af Novo Nordisks montage og pakning af insulinprodukter i Kalundborg. Og er du klar til et markant ansvar med fokus på kvalitet, produktion og processer samt faglig og personlig udvikling? Så er du sikkert vores nye kollega i processupporter teamet, der består af 13 højt engagerede medarbejdere? Vi skaber fortsat stor vækst og gode resultater og har derfor brug for en processupporter med højt energiniveau og gerne lederambitioner.

Om afdelingen
Du kommer til at indgår i Prefilled Device Support, Site Ka i Kalundborg. Vi supporterer driften af montage og pakkelinier, optimerer processer og sikrer udstyrets valideringstilstand, så vi kan holde antallet af afvigelser på et minimum. Vi håndterer ændringer og løser problemer effektivt og i komplet overensstemmelse med gældende krav.

Jobbet
Dit ansvar er at supporter montage og pakkelinjer i afdelingen Prefilled Device, således at kravene til validering, kvalitet, compliance og GMP er overholdt. Du vil få ansvaret for en konkret produktionslinje, hvor din hverdag byder på tekniske udfordringer og du løser pludseligt opståede problemer i produktionen, også her anvender du LEAN værktøjerne. Du sørger hele tiden for at skabe fremdrift i dine opgaver bl.a. ved at involvere relevante kolleger fra andre områder til opgave og problemløsning. Du deltager i inspektioner både eksterne og interne audits.

Din primære kontaktflade er operatører, reparatører og ledere i produktionen samt logistik og QA. Du sikrer din succes ved at holde fokus på dels kvalitet og leadtime på dine opgaver samt sikre en god relation til dine interessenter.

Du trives som en del af et engageret team, hvor vi lægger stor pris på samarbejde og trivsel. Derfor er det helt essentielt, at du er både åben og udadvendt og samtidig har en god portion empati. Teamet står over for en spændende udfordring, som er at skabe stabile processer, samtidig med at kapaciteten øges. Ud over det øges kravet om compliance hele tiden. Området er i det hele taget i en rivende udvikling, hvor vi har mange bolde i luften og mange interessenter at forholde os til.

Kvalifikationer
Du har en videregående uddannelse med et videnskabelig eller teknisk fokus som fx proces eller produktionsingeniør gerne suppleret med relevant erfaring. Du er dit ansvar bevidst og formår at træffe de nødvendige beslutninger for at løse udfordringer med sans for effektivitet og kvalitet. Du har et godt overblik og en skarp analytisk sans, som gør det nemt for dig at skære ind til benet og gennemskue sammenhænge fx mellem processer, materialer og udstyr.

Er du nyuddannet skal du besidde et stort drive for at lykkes i stillingen, og du skal indstille dig på en stejl læringskurve. Du taler og skriver flydende engelsk og dansk.

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 Ole S. Iversen på +45 3075 2649.

Ansøgningsfrist
14. januar 2014

Technical Writer, Process Support Kalundborg

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

- Produktion
- Danmark - Kalundborg

Har du lyst at sætte dit præg på en afdeling i rivende udvikling, så læs endelig videre, for vi søger en ny kollega til Site Danmark Kalundborg, hvor vi sikrer, at forskellige insulinprodukter bliver monteret og pakket korrekt.

Om afdelingen
Sammen med 30 yderst motiverede og dygtige kolleger udgør du Proces Support, SDK Ka i Kalundborg. Vi er to teams, som behandler henholdsvis kvalitet og tekniske forbedringer til fuldautomatiske montage- og pakkelinjer samt øvrige generelle krav til vores omgivelser. 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
Du får ansvaret for at supportere vores support funktion med at skrive SOP’er med teknisk og kvalitetsmæssigt indhold samt indsætning af billeder der henvender sig til processerne der arbejdes efter. Du hjælper ligeledes med at optimere på procedurerne så vi er i compliance. Målet er at levere høj kvalitet af SOP’er som er enkelt og godt beskrevet og er i overensstemmelse GMP-kravene.

Du kommer ligeledes til at løse forskellige opgaver, der relaterer sig til kvalitet. Du skal fremlægge og redegøre for relevante dokumenter ved myndigheds inspektioner og interne audits. Du vil få rigtigt godt indblik i den måde, vi arbejder med LEAN i Novo Nordisk. Desuden kommer du til at samarbejde med mange forskellige kolleger på tværs i vores organisation og får en hverdag med variation i opgaverne, derfor er kommunikation også en vigtig del at din dagligdag.

Kvalifikationer
Du har en kandidatuddannelse med flere års erfaring, som har givet dig rigtig god indsigt i GMP og udarbejdelse af SOP’er. Du er god til at formulere dig skriftlig og kan lide at arbejde med dokumentation. Du er dit ansvar bevidst og formår at løse opgaverne med sans for effektivitet og kvalitet samt har et godt overblik, som gør at du kan gennemskue sammenhænge fx mellem processer og udstyr. Dine kolleger kender dig som en omgængelig person, som formår at gå i dialog om opgaverne. Med andre ord er du god til at samarbejde og opbygge relationer til alle slags interessenter. Sidst, men ikke mindst, behersker du dansk og engelsk flydende – mundtligt som skriftligt.

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 Birgitte Petersen på +45 3075 5587.

Ansøgningsfrist
9 January 2014

Laborant, barselsvikar

- Forskning og Udvikling
- Danmark - Måløv

Har du lyst til et afvekslende job, hvor du arbejder med en række forskellige teknikker inden for immuncellebiologi og karakterisering af antistoffer? Så læs videre, og se, om du er vores nye laborant. Stillingen er et 12 måneders vikariat med start 1. februar 2014.

Om afdelingen
Din nye afdeling bliver Immuno Biology-afdelingen, som er en del af Novo Nordisk Biopharmaceutical Research Unit. Her indgår du i et dynamisk team af laboranter, som forsker i nye muligheder for at behandle kroniske inflammationssygdomme. Du kommer til at arbejde på flere forskningsprojekter sideløbende, hvor du både anvender kendte metoder og teknologier samt udvikler nye.

Jobbet
Dine primære arbejdsopgaver bliver at udvikle nye projektspecifikke in vitro analyser til at karakterisere potentielle lægemiddelkandidaters ønskede effekter og mulige uønskede bivirkninger. Som en del af karakteriseringsarbejdet står du for bearbejdning af data, udvælgelse af lægemidler samt undersøgelser af bivirkningsprofiler i forskningsfasen inden de kliniske forsøg påbegyndes. Du kommer bl.a. til at arbejde med cellebaserede analyser med primære humane immunceller som f.eks. PBMC’er og oprensede blodcelletyper, ligesom du arbejder med humane cellelinjer og fuldblod. Desuden får du indsigt i arbejdet med cytokine release assays, antibody-dependent cellular-cytotoxicity (ADCC) og antibody-dependent cellular phagocytosis (ADCP) samt teknikker til bl.a. dyrkning af primære mammale celler og cellelinjer og oprensning af celler fra blod.

Kvalifikationer
Du er uddannet laborant og har erfaring med celle dyrkning og at analysere humane celler fra blod og foretage FACS-analyser. Det er vigtigt, at du er systematisk og omhyggelig i dit arbejde, og at du er god til at samarbejde med kolleger. Samtidig formår du at løse dine opgaver selvstændigt, og dit engagement og din motivation er høj. Du er kendt for din fleksible indstilling, og du arbejder hjemmevant med Office-pakken, herunder Excel, Word og PowerPoint. Kender du GraphPad Prism eller lignende databehandlingsprogrammer, vil det være en fordel. Da vi arbejder i et internationalt miljø, skal du beherske engelsk flydende i både skrift og tale.

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 Charlotta Folkesson på +45 3075 6817.

Ansøgningsfrist
17. januar 2014

Line kemiker

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

- Produktion
- Danmark - Kalundborg

Får du energi af at gå forrest og og tage ansvar? Er du dygtig til at afslutte dine opgaver og projekter? Og trives du bedst på et stærkt hold, der både er fagligt og socialt velfunderet? I så fald er du måske vores nye kollega i proces-support.

Om afdelingen
Biopharmaceuticals er en del af Novo Nordisks produktion, hvor vi producerer en række af Novo Nordisks produkter. Vi er i alt 1.800 medarbejdere fordelt på flere af Novo Nordisks sites på Sjælland. Du bliver en del af Biopharmaceuticals produktion i Kalundborg, hvor vi producerer den aktive ingrediens i produktet NovoSeven® (hæmofili-præparat). Produktionsprocessen består af mammal celledyrkning med efterfølgende kromatografisk oprensning og vi producerer døgnet rundt, året rundt. Vi udgår i alt 111 medarbejdere på det 3.500 mand store site i Kalundborg.

Jobbet
Sammen med dine kolleger er du ansvarlig for at vores celledyrknings og oprensningsproces kører stabilt og er i compliance med krav og regler. Du følger op på driften, håndterer afvigelser i samarbejde med produktionen og QA, afrapporterer i forhold til myndighedskrav samt håndterer ændringer. Dine ansvarsområder er en kombination af at være på gulvet og at håndtere administrative opgaver ved skrivebordet. Dine opgaver vil blandt andet inkludere vask og validering af udstyret som du har ansvaret for. Opgaverne på gulvet er sammen med kolleger i og uden for teamet, hvor du ofte er den, der driver processen. Bag skrivebordet sikrer du dokumentation i forbindelse med de enkelte sager. Du bliver en succes ved at være målrettet og nå dine opgaver til tiden. Du skal agere som en holdspiller, der evner at gå forrest og vise vejen, når der er behov for det. Du er en del af et hektisk miljø, og for at lykkes i det skal du kunne lide at kaste dig ud i tingene. Da du er en del af et fagligt dygtigt team med en stærk holdånd har du et godt fundament for at fremme din karriere og personlige udvikling.

Kvalifikationer
Du har en akademisk naturvidenskabelig uddannelse, ingeniør, cand. polyt, cand. scient eller cand. pharm. Du taler og skriver engelsk og dansk. Din erfaring og dit kompetenceniveau afgør omfanget af opgaver og ansvar, hvilket gør det til et udfordrende job hvad enten du er nyuddannet eller har erfaring. Som person er du ambitiøs og brænder for at komme i mål med dine opgaver og vise dine kvaliteter. Du er en holdspiller og trives i et miljø, hvor der stilles høje krav til kvalitet, effektivitet og overholdelse af tidsplaner. Din troværdighed, positive indstilling og dit smittende engagement gør det nemt for dig at samarbejde med kolleger uanset organisatorisk placering.

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 talentfulde kolleger, og vi tilbyder dig en lang række muligheder for professionel og personlig udvikling.

Novo Nordisk i Kalundborg er en by i byen. Området er på 1.350.000 m2 med eget vejnet. Vi er 3.500 mennesker i alt fordelt på 16 fabrikker, og vi producerer bl.a. 50 % af verdens insulin. Vi arbejder helt på forkant af udviklingen inden for teknologi, systemer, metoder og processer. Er du vores nye kollega, tør vi godt garantere dig nogle muligheder, du vil have meget svært ved at finde andre steder.

Kontakt
Vil du vide mere om stillingen så kontakt Jakob Momme på +45 3075 3932.

Ansøgningsfrist
19. Januar 2014

Operatør til steril nat rengøring, 12 måneder vikariat

- Forskning og Udvikling
- Danmark - Måløv

Ønsker du at arbejde i et dynamisk og foranderligt miljø og mærke pulsen fra produktionen – så har vi lige jobbet til dig.

Vi søger en rengørings assistent til rengøring af produktionsfaciliteten i Aseptik Pilot Plant (APP). Afdelingen, som er en del af R&D CMC Clinical Supplies, består af 48 medarbejdere og er placeret i henholdsvis Gentofte og Måløv. APP omfatter produktionsområderne: Vask & sterilisation, præparation, påfyldning & frysetørring, miljø & rengøring samt vedligehold & kalibrering.

Om afdelingen
Vi befinder os i grænsefladen mellem udvikling og produktion og har bred kontakt til mange funktioner i virksomheden. Vores primære opgave er at producere aseptisk fremstillede færdigvarer til brug i prækliniske og kliniske studier i forbindelse med virksomhedens udviklingsprojekter. Produkterne er derfor skiftende – ofte nye – og produceres efter gældende cGMP regler. Vi har en travl hverdag og samtidig lysten og viljen til cLEAN arbejde. Fleksibilitet er en selvfølgelighed.

Jobbet
Som en del af rengøringsteamet (4 pers.) vil du få ansvar for at sikre at vores produktions lokaler er rengjorte og klar til produktion. For at kunne varetage denne funktion vil du blive dragtcertificeret og trænet i at arbejde under aseptisk forhold.

Kvalifikationer
Du er operatør eller rengøringsassistent. Vi forventer, at du har erfaring med aseptisk rengøring eller produktion, ligesom erfaring med cGMP er en fordel.

Du er indstillet på at arbejde Søndag-onsdag 19.00 - 02.30 og fredag 06.00-14.00.

Vi leder efter en kollega med godt humør og som med initiativ, selvstændighed og ansvar tager fat på nye opgaver. Vi forventer, at du er god til at strukturere og planlægge arbejdet og ikke lader dig slå ud af en omskiftelig hverdag.

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 Janne Brast på +45 3075 8228 i hverdage mellem 08.00-11.00.

Ansøgningsfrist
10. januar 2014

Proces supporter

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

- Produktion
- Danmark - Kalundborg

Kunne du tænke dig, sammen med engagerede og fagligt ambitiøse kolleger, at være med til at bygge en afdeling i Kalundborg op? Biopharms nye pakkeri er en strategisk vigtig satsning, der skal sikre den fremtidige kapacitet til at pakke Novo Nordisks hæmofili-produkter samt GlucaGen® Hypokit. Det giver et dynamisk arbejdsmiljø, hvor vi på samme tid skal sikre stabile leverancer af livsvigtig medicin til vores kunder, håndtere forberedelsen af en ny pakkelinie samt støtte og udføre flere projekter i afdelingen.

Er produktionssupport, problemløsning og procesoptimeringer det, der gør hverdagen spændende og udfordrende? Og lægger du samtidig vægt på, at det sker det på en struktureret og LEAN måde, så de gode idéer forankres i hverdagen?

Om afdelingen
Biopharm T&FP, Kalundborg er en del af Biopharmaceuticals (Biopharm). Afdelingen består pt. af ca. 40 dygtige medarbejdere, der alle beskæftiger sig med pakning af NovoSeven® og på sigt flere hæmofiliprodukter og GlucaGen® Hypokit. Afdelingen forventes at vokse betragteligt over de kommende år.

Dine kommende kolleger består af ingeniører, farmaceuter, farmakonomer, automatik og tekniske supportere, projektledere, operatører, og håndværkere. Afdelingen er opdelt i 3 teams, et produktionsteam, et teknisk team og et proces-supportteam. Dit kommende team, Team Support, er en supportfunktion for produktionen, der varetager de cGMP-mæssige opgaver.

Jobbet
I Biopharm lægger vi vægt på, at alle tager et personligt ansvar for kvalitet, opgaver og hinanden. Vi sætter ambitiøse mål, samtidig med at vi fokuserer på stabil leverance til vores kunder. Dit arbejde vil bl.a. bestå i support til produktionen, udarbejdelse af afvigelser, ændringssager, trendrapporter, SOP opdateringer, interne reklamationer, samt selvstændigt at drive LEAN-aktiviteter, som f.eks. systematisk problemløsning og proceskonfirmering. Du vil også være en af de supportere der beskæftiger sig med frigivelsen af vores produkter.

Din arbejdsdag vil således være afvekslende og til tider hektisk, da driften af vores fuldautomatiserede pakkelinie er essentiel for gennemførelse af produktionen. Arbejdet vil foregå i tæt dialog med mange medarbejdergrupper både i og udenfor afdelingen. Det betyder at vi stiller lige store krav til selvstændighed og det at være en god teamplayer.

Kvalifikationer
Til tiltrædelse snarest søger vi to kolleger, der har en relevant videnskabelig baggrund som farmaceut, produktions-, kemi- eller maskiningeniør. Gerne med 3-4 års erfaring indenfor færdigvareproduktion af medico- eller medicinalprodukter, men nyuddannede kan også komme i betragtning til stillingen. Du må gerne have stor og dokumenteret forståelse for GMP. Det vil være en fordel, hvis du har erfaring med brug af LEAN i forbindelse med systematisk problemløsning.

Du tager ansvar og finder løsninger i selv pressede situationer og sikrer samtidig involvering og ejerskab blandt dine kollegaer. Som person er du kendt for at være positiv og løsningsorienteret, og god til at etablere samarbejde på tværs af faggrænser. Du er åben og ærlig, samt i stand til at give og modtage konstruktiv feedback. Vi arbejder i en GMP reguleret virksomhed, hvorfor du lægger vægt på detalje, struktur og kvalitet i dit arbejde.

Da Novo Nordisk A/S er en international virksomhed, er det et krav at du behersker engelsk og dansk, såvel mundtligt som skriftligt.

I Novo Nordisk stræber vi efter at være de bedste. Vi er førende i verden indenfor diabetesbehandling og en større spiller indenfor behandling af blødninger, behandling med væksthormon og behandling med hormonterapi. Vi giver vores medarbejdere mulighed for en stærk professionel udvikling.

Kontakt
Vil du vide mere om stillingen så kontakt Morten Kring på +45 3075 2694.

Ansøgningsfrist
19. januar 2014

Tekniker med klasse C erfaring

- Forskning og Udvikling
- Danmark - Bagsværd

Har du lyst til at være med til at designe, kvalificere og indkøre et helt nyt anlæg til oprensning af fremtidens insuliner og GLP-1’er i pilotskala, så er muligheden her.

Vi er i gang med at bygge et nyt pilotanlæg for at øge fremstillingskapaciteten indenfor vores portefølje af diabetes produkter til udviklingsformål og klinisk afprøvning. Store dele af det nye anlæg bliver designet til klasse C. Til den opgave søger vi en dygtig og engageret tekniker med indgående erfaring med at arbejde i klasse C.

Om afdelingen
Afdelingen er Diabetes Purification 2 i Bagsværd, som hører under området CMC API Development. Vi er en helt ny afdeling, der i de næste 2-3 år udgør brugergruppen på projektet.

Vi tilbyder en spændende tekniker stilling, hvor du i tæt samarbejde med de øvrige medarbejdere i teamet får til opgave at bringe det nye pilotanlæg i stabil drift.

Jobbet
Du vil gennemgå en oplæring, afhængig af din bagrund, og vil få et selvstændigt ansvarsområde indenfor procesudstyr eller utility. Du får derudover en vigtig opgave i at bruge din erfaring fra klasse C til at sikre simple, praktiske løsninger i vores klasse C lokaler, som medfører at vi kan opnå stabile resultater i vores miljømonitorering. Når anlægget er indkørt og i drift, vil dine primære opgaver således være at indgå i driften, så vi kan levere API til klinisk afprøvning.

Jobbet kræver, at du har tæt samarbejde med de andre i teamet samt vores samarbejdspartnere, herunder det rådgivende ingeniørfirma, QA og teknisk support.

I teamet arbejder vi med LEAN og stræber efter hele tiden at forenkle vores arbejdsprocesser, og dine idéer og løsninger vil være værdifulde for, at vi løbende kan forbedre vores procedurer og reducere overflødige rutiner.

Kvalifikationer
Du er uddannet kemotekniker, procesteknolog eller lignende. Det er essentielt, at du har praktisk erfaring med farmaceutisk produktion i klasse C lokaler. Denne erfaring kan enten være fra færdigvare eller fra API.

Vores drømmekandidat har derudover erfaring med en eller flere af nedenstående discipliner: proces kontrolsystemer (f.eks. DeltaV og Unicorn), procesteknik og processtyring, kromatografi, miljømonitorering, vaskevalidering. Du må ikke være bange for papirarbejde.

Du skal være professionel og tage ansvar for deadlines og leverancer, og være positivt indstillet overfor den foranderlige verden, vi befinder os i. Vores arbejde udføres og dokumenteres i henhold til GMP, og det forventes derfor, at du besidder en systematisk tilgang til dine opgaver og har en god ordenssans.

Vi tilbyder et spændende og afvekslende job i et åbent og dynamisk arbejdsmiljø, hvor du vil opleve stor frihed til at løse opgaverne på din måde. Du vil i teamet få en flok engagerede og hjælpsomme kolleger, der ligesom du synes, at det er vigtigt, at det er sjovt at gå på arbejde.

På Novo Nordisk bruger vi vores evner, engagement og ambitioner til at hjælpe mennesker med diabetes, og vi fokuserer på personlig performance og udvikling for vores medarbejdere.

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 Casper Vinther på +45 3075 5469 eller Thomas Busch på +45 3079 0533.

Ansøgningsfrist
17. januar 2014

Quality Process Manager

- Quality
- Denmark - Bagsværd

Novo Nordisk’s success continues, and we are expanding our production facilities. This brings even bigger and more exciting challenges to our purchasing organisation. And we need your analytical outlook and quality mindset to optimise our QMS processes accordingly. If you are anxious for such a challenge, then a job in Product Supply could be perfect for you.

About the department
Purchasing Standard & Analysis is a team in the purchasing department of Product Supply. It employs 9 highly motivated and talented colleagues who support the purchasing department in Sourcing Operations. Our primary objective is constant enhancement of our supply chain processes and standards to provide a streamlined purchasing flow for the supply chain activities. We are in close and daily dialogue with production planning, warehousing, quality control, quality assurance and central support functions.

The job
Your job as Quality Process Manager will entail responsibility for the continuous improvement and optimisation of quality processes in order to adhere our quality policy and objectives within purchasing. The overall goal is to ensure high levels of quality for the day-to-day work in Purchasing where each step must be aligned with our own and the authorities’ quality regulations and be based on our LEAN principles.

You will be our project manager for our improvement projects in accordance with our Quality Compliance Plan for Purchasing, which you will be responsible for.

You engage constructively with relevant experts who you will be in close dialogue with in respect to conduct quality management reviews in an efficient manner. You identify and drive the activities and make sure that your colleagues are enlightened and prepared to follow the new principles and guidelines.

Qualifications
You are an experienced quality profile with at least 5 years knowledge from a similar job. You are used to operating in a GMP-regulated environment and hold a degree in one of the natural sciences. Either you have been working in a QA or QC function, or you have acquired your quality mindset and project management skills elsewhere. And you know that supplying our customers with products of highest quality at competitive costs are the keys to our continued success. You know how to handle large groups of stakeholders, and your professional expertise, convincing attitude and strong impact make you a trusted expert for successful handling of the increased focus on quality. As your job requires prompt and efficient problem-solving, you must be analytical and able to clarify the dilemma and suggest applicable solutions. As such, you are able to dig into detail to get to the core of the issues without losing your general view. It goes without saying that your quality mindset is excellent.

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 Louise Hørlyck at +45 3075 5198 or Annette Wiese Nørbjerg at +45 3079 2619.

Deadline
20 January 2014

Graduates! Kick-start your European business career

- Graduate
- Denmark - Bagsværd

Professional development

What has surprised you?

Begin the journey of a lifetime in September 2014

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

Start your career climb
During the programme you will develop invaluable skills working with a broad range of business processes across Novo Nordisk’s business areas and markets. In addition to intensive cross organisational business training, the programme also offers you leadership and teamwork skills development.

Scope of the programme
This programme offers insights into how to drive business and cross organisational sales in Europe through well-founded marketing, business and pricing strategies.

1 rotation in our headquarters in Denmark
2 rotations in one of our European affiliates and/or headquarters in Switzerland.

For further information, visit Novonordisk.com/Business-Programmes

A global career
After successfully completing the programme, you will embark on your career at Novo Nordisk with a permanent position - perhaps as an Executive assistant, Internal Consultant or International Product Manager. While you could be based in Denmark, your broad network and international experience from the programmes will enable global career opportunities.

Requirements
To join one of the European Business Management Graduate Programme you must hold a master’s degree in the field of Business, for example within Economics, Management, International Business, Marketing and have no more than 1 year of work experience since finishing your studies. You are a strong individual who is result-oriented, ambitious and able to adapt to change in a fast-paced environment.

You must master at least one of the following languages: German, Spanish, French, Italian, Dutch, Polish or Swedish.

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.

Contact
Programme Director, Ove Munch Ovesen: +45 3079 3445
Programme Assistant, Birgitte Blangsted: +45 3079 3539

Apply online before 9 February 2014
Apply before 9 February 2014 by submitting your motivational letter, CV (in English) and a scanned copy of your latest grade transcript.

In addition to the European Business Management Graduate Programme we have many other graduate programmes which all lead to life-changing careers.

Purchasing Quality Coordinator

- Quality
- Denmark - Bagsværd

Are you committed to quality and eager to unfold your structured and meticulous mindset in a GMP-regulated setting? Then you could be our next Quality Coordinator to improve and preserve the use of our quality standards in Purchasing for Novo Nordisk.

About the department
Purchasing Standard & Analysis is a team in the purchasing department of Product Supply. It employs 9 highly motivated and talented colleagues who support the purchasing department in Sourcing Operations. Our primary objective is constant enhancement of our supply chain processes and standards to provide a streamlined purchasing flow for the supply chain activities. We are in close and daily dialogue with production planning, warehousing, quality control, quality assurance and central support functions.

The job
You will be in charge of the Change Request and Non-Conformity cases in the department. This means that you will be the department expert for CR as well as NC cases.

A very important part of your job will be to promote the quality mindset to the purchasers and convince them of the authority and eligibility of quality.

You will act as sparring partner for the purchasers, drive CR cases for the ones that are not yet entitled to handle CR-cases and you will train our CR owners.

In case of non-conformities, you challenge our purchasers what should be done to prevent a recurrence and you make sure that the right precautions are taken and implemented. On top of that, you will support the purchasers in handling NC on their own and occasional conduct training.

All in all, you secure a smooth progress and a positive result of the NC and CR cases and thereby maintain superior quality of our purchasing processes.

Qualifications
You are an experienced quality profile with at least 3 years’ expert knowledge from a similar job. You thrive in a role where quality and compliance are key words. If you are used to working in a GMP-controlled environment, it will absolutely give you a head start. Either way, your mind is set on structure and compliance, and you never compromise on quality in your work. Moreover, you are comfortable teaching colleagues our quality mind set, and your systematic approach makes this possible. You are used to handling complex tasks and to deliver quality work, and you have a diplomatic and constructive way of communicating your requirements. Last but not least, you are a team player and a skilled communicator who thrive working in an international dynamic 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 Louise Hørlyck at +45 3075 5198 or Annette Wiese Nørbjerg at +45 3079 2619.

Deadline
20 January 2014

Project Coordinator

- Project Management
- Denmark - Hillerød

Join Novo Nordisk and help us maintain the position as the world leader in diabetes care by making a difference within development of medical device production.

About the department
Device Manufacturing Development (DMD) is a young project organisation comprising of more than 250 dedicated employees striving to make us the best manufacturing development partner of medical devices. Our dedication is to build and maintain superior quality into our device products. Our challenge is to execute an increasing portfolio of diverse projects in a complex, high volume, international and highly regulated area.

DMD Business Support is situated in Hillerød near Copenhagen and responsible for portfolio management, Lean, finance and strategy and we are looking for a project coordinator to join the team.

The job
As a Project Coordinator in Business Support, you will be dedicated to the Product Maintenance Project Office ensuring that cross organizational device projects, are prioritized appropriately and coordinated efficiently for superior project execution.

You will work closely with the project office senior project manager and will continually support, develop and improve portfolio management within the product maintenance area, and serve as a sparring partner/support for project managers.

Qualifications
You have an academic degree in engineering or similar, with 2 years of experience of engineering / technical project management in a GMP environment.

As a person you are extrovert, responsible, pro-active and co-operate easily at all levels. You work independently, have a strong drive with focus on execution and results and proactively seek the information you need.

You are analytical and demonstrate proactive stakeholder management at all levels. Last but not least, you communicate fluently in written and spoken English.

We can offer you a challenging job where you have the opportunity to influence your work and develop your professional and personal skills in a dynamic working environment with highly competent colleagues.

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 Peter Fairhurst between 17th – 24th December & 6-10th January at +33609719504.

Deadline
12 January 2014

Intern

- Student and Internships
- Denmark - Bagsværd

Novo Nordisk is seeking an intern in FLIR Executive Office in Bagsværd from 01 February 2014 to support our efforts in supporting management decision and managing our quality function.

About the department
Novo Nordisk is one of the world’s most successful pharmaceutical companies. FLIR Executive office consists of a management support unit and an internal consultancy both supporting our CFO in facilitating decisions and driving key projects throughout Novo Nordisk’s global organisation.

Together with FLIR Consulting, FLIR Executive Office makes up a young, diverse area consisting of 12 dedicated employees with backgrounds from top-tier consultancies or with previous Novo Nordisk experience.

The job
As an intern in FLIR Executive Office, you will drive management support and quality management processes as well as one or more projects focused on developing the quality function in Finance, Legal and Investor Relations. You will be working closely together with the department Quality Manager and your tasks will vary widely, including analyses, information gathering, problem solving and independently driving own work streams.

In your work you will be exposed to the Finance, Legal and Investor Relations organisation and get hands-on experience with Novo Nordisk's quality management system as well as best practice project management methods and tools.

Qualifications
You are a master degree student in Economics, Business Administration, Supply Chain Management, Engineering or similar in the first or second year of your studies. You take an interest in consulting as well as process, quality and project management.

You are among the best in your class, proficient in English and are used to working independently as well as in teams. You approach tasks in a structured way with a good sense for detail. Finally you have a positive attitude.

Your development is important to us. Training and personal development plans are key tools to ensure your tasks continue to challenge you while developing or sharpening your toolbox.

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 questions, please contact Kasper Olsen at +45 3075 1087.

Deadline
15 January 2014

EXPERIENCED SYSTEMS ENGINEERS

- Research & Development
- Denmark - Hillerød

EXPERIENCED SYSTEMS ENGINEERS! ENHANCE YOUR CAREER IN ONE OF THE WORLD’S LEADING COMPANIES WITHIN MEDICAL DEVICES - Located in the greater Copenhagen area, Denmark

Are you looking to enhance your career within systems engineering and requirement management, look no further!

Novo Nordisk A/S, a global healthcare company with 90 years of innovation and leadership in diabetes care, is looking for experienced engineers who can strengthen our system engineering capabilities ranging from defining requirements to validating product design.

About the department
Device Research & Development is an area within Global R&D, responsible for the development of medical devices for self-treatment within all business areas of Novo Nordisk A/S. Device Research & Development has a long and outstanding track-record of developing the best, most innovative and widely-used injection devices in the world. You will join an international team of 12 highly skilled engineers and designers, responsible for the development of a next generation injection device.

We are located at a state-of-the-art R&D facility in the greater Copenhagen area.

To learn more about Device Research & Development, please visit: www.novonordisk.com/device-rd

The job
You will become a member of the Systems Engineering team (part of the development team), which is responsible for design control processes in the project like defining and managing requirements, safety risk management, design verification and validation including usability engineering. You will especially focus on defining and integrating user/stakeholder requirements and safety risk management. We are presently implementing updated systems engineering processes, enhancing our focus on effectiveness and quality; you will play an important role in implementing and shaping these processes in the development project.

You will be given a broad range of responsibilities and experience a variety of tasks, working with stakeholders at all levels. The job will enhance your professional and personal development, providing you with an opportunity to further develop your skills within specialist expertise and project management.

Qualifications
You hold an academic degree within Engineering with at least 5 years of experience with systems engineering and/or requirement management. Your experience preferably comes from either pharma, automotive, aerospace, energy or other industries where quality and regulatory compliance is vital to succeed. You have experiences with one or more of the following processes: definition of technical product requirements, architectural design, complexity management, safety risk management and/or verification and validation. You have the ability to analyse and understand complex structures and systems, and communicate them in a comprehensible way. You are self-motivated, ambitious and result-oriented. You are good at collaborating in teams as well as with stakeholders at all levels. Proficiency in oral and written English is essential.

At Device Research & Development we use our skills, dedication and ambition to help people with chronic diseases, and change their lives. You will get the opportunity to take part in this, and in addition enhance your career, benefiting from the possibilities for professional and personal development provided by Novo Nordisk A/S.

Device R&D is an organisation with many international employees and we welcome non-local applicants. We have great experience helping people move to Denmark and will support relocation.

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 Salim Bouaidat on +45 3075 8658.

Deadline
19 January 2014

TALENTED ENGINEERS WITH POTENTIAL TO GROW!

- Research & Development
- Denmark - Hillerød

TALENTED ENGINEERS WITH POTENTIAL TO GROW! KICK-START YOUR CAREER IN ONE OF THE WORLD’S LEADING COMPANIES WITHIN MEDICAL DEVICES - Located in the greater Copenhagen area, Denmark

Join Device Research & Development at Novo Nordisk A/S and get a life-changing career!

Novo Nordisk A/S, a global healthcare company with 90 years of innovation and leadership in diabetes care, is looking for newly graduated engineers to take up positions as systems engineers.

About the department
Device Research & Development is an area within Global R&D, responsible for the development of medical devices for self-treatment within all business areas of Novo Nordisk A/S. Device Research & Development has a long and outstanding track-record of developing the best, most innovative and widely-used injection devices in the world. You will join an international team of 12 highly skilled engineers and designers, responsible for the development of a next generation injection device.

We are located at a state-of-the-art R&D facility in the greater Copenhagen area.

To learn more about Device Research & Development, please visit: www.novonordisk.com/device-rd

The job
You will become a member of the Systems Engineering team (part of the development team), which is responsible for design control processes in the project like defining and managing requirements, safety risk management, design verification and validation including usability engineering. You will especially focus on defining and integrating user/stakeholder requirements and safety risk management.

You will be given a number of different responsibilities and experience a variety of tasks, working with both internal and external stakeholders. The job will enhance your professional and personal development, providing you with an opportunity to develop skills within specialist expertise and project management.

Qualifications
You hold an academic degree (or graduate within the next 6 months) in Engineering and are looking to kick-start your career within systems engineering and requirement management. You have the ability to analyse and understand complex structures and systems. You are independent, flexible and result-oriented with a ‘can-do’ attitude. You have a solid academic background with an international profile and must be able to learn fast, excel at cross-functional collaboration and communicate at all levels. You must be prepared to invest significant personal effort in your work and proactively take ownership of your areas of responsibility. Finally, the strongest candidates have relevant system engineering experience obtained while studying or after graduation like writing requirements, planning verification/validation activities or doing risk analysis. Proficiency in oral and written English is essential.

At Device Research & Development we use our skills, dedication and ambition to help people with chronic diseases, and change their lives. You will get the opportunity to take part in this, and in addition enhance your career, benefiting from the possibilities for professional and personal development provided by Novo Nordisk A/S.

Device R&D is an organisation with many international employees and we welcome non-local applicants. We have great experience helping people move to Denmark and will support relocation.

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 Salim Bouaidat on +45 3075 8658.

Deadline
19 January 2014

Category Manager (IT)

- Sourcing
- Denmark - Bagsværd

Do you have a strong business mind-set and are you looking for a job with the possibility to utilize and further develop your skills and competences within negotiations, contracting, supplier management, category management and stakeholder management?

About the department
Corporate Procurement is, in close cooperation with affiliates and stakeholders, responsible for purchasing, sourcing and contracting of the global indirect spend in Novo Nordisk. Corporate Procurement has more than 100 employees and is a part of Corporate Finance. This position is in the IT Sourcing Team. We are commercial experts with responsibility for leading the sourcing processes and negotiations.

The job
Your will have the role as Lead Negotiator for IT projects and as Category Manager for certain IT categories. You will have to manage and align with stakeholders to prepare and adhere to negotiation strategies, category strategies and commercial sourcing processes. As Category Manager you will be the driving force in developing and implementing category strategies for your categories and lead Supplier Relationship Management. You will be a part of an enthusiastic group that sets high standards and individual targets, but achieves them as a team.

Qualifications
You have at least 5-7 years relevant sourcing or contracting experience and a track record in delivering above average results. You may have experience from sourcing or selling within IT categories. You have strong strategic, reasoning, and analytical skills. You have the ability to effectively plan, prioritise and execute. You are robust, self-motivating, very result oriented, always raising the bar for yourself and encouraging your peers to follow. You communicate and sell your ideas effectively and have the ability to work with various stakeholders, colleagues, and management. You are fluent in English. You probably hold a relevant Master’s degree in Business, Law or IT.

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 Jan B. Lausten +45 3075 7819.

Deadline
16 January 2014.

Erfaren kemiker / ingeniør / farmaceut der vil udfordres og udvikles i

- Produktion
- Danmark - Gentofte

Har du erfaring fra et GMP-reguleret miljø og ambitioner om ikke bare at være med, men om at være bedst, så har vi det helt rigtige job til dig. Du kan se frem til et virkelig varieret job, hvor din indflydelse går hånd i hånd med dine udfordringer og derfor også dine muligheder for at udvikle dig. Du får naturligvis en grundig introduktion via vores introforløb.

Om afdelingen
Du bliver en del af Biopharm AP filling HAC i Gentofte. Vi er en specialiseret aseptisk fyldeafdeling med ca. 200 medarbejdere. Sammen producerer vi bløderpræparatet NovoSeven® samt indkører og fylder Novo Nordisks nye proteinbaserede lægemidler. Vi arbejder med følgende processer: Vask og sterilisering af udstyr, formulering, sterilfiltrering, steril påfyldning, frysetørring, capping af vials og visuel inspektion. Du indgår i vores Proces Support team. Her får du 19 gode og engagerede kolleger, der har ansvar for validering og support til produktionen.

Jobbet
Det vigtigste kendetegn for dit nye job er næsten, at det er så alsidigt – og at din indsats virkelig har betydning. Som supporter for dine kolleger i produktionen er dit fokus, at vi kører med så få afbrydelser som muligt. I den sammenhæng er du blandt andet med til at håndtere her-og-nu problemer samt følge op på afvigelser – og dele din viden med operatørerne, så vi hele tiden bliver bedre og arbejder smartere. Et andet vigtigt område bliver udarbejdelse af valideringsdokumentation primært for autoklave og sterilisationsprocesser.

Som en naturlig del af din vigtige rolle deltager du også i tværorganisatoriske projektgrupper med fokus på optimeringer i henhold til de nyeste krav fra myndighederne. I den sammenhæng får du ansvar for en del af dialogen med regulatoriske myndigheder i forbindelse med inspektioner.

Kvalifikationer
Du er en erfaren kemiker, farmaceut, ingeniør eller lignende, og du har solid erfaring med GMP-reguleret fremstilling af lægemidler og myndighedskrav til den farmaceutiske industri. Derudover har du indgående kendskab til validering og sterilisationsprocesser. Du kan lide at arbejde med dokumentations- og databearbejdning i kombination med behov for din hurtige handling på akutte problemstillinger. Her får du også brug for din evne til at prioritere og din tro på, at der altid findes en løsning. Du trives med at arbejde koncentreret med mange data, hvor du for alvor får gavn af din strukturerede og analytiske arbejdsform. Da du kommer til at samarbejde med en masse mennesker på alle niveauer, får du også brug for dine gode kommunikations- og samarbejdsevner.

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, kontakt Louise Bruun Jørgensen +45 3079 8788.

Ansøgningsfrist
25. januar 2014

Business system analyst (Bagsværd, Denmark)

International Trial Manager, Maternity vacancy (Søborg, Denmark)

Auditor for the Business Ethics Assurance team in Group Internal Audit (Bagsværd, Denmark)

Department Assistant (Bagsværd, Denmark)

Teknisk processupporter til Pakkeri (Kalundborg, Danmark)

Technical Writer, Process Support Kalundborg (Kalundborg, Danmark)

Laborant, barselsvikar (Måløv, Danmark)

Line kemiker (Kalundborg, Danmark)

Operatør til steril nat rengøring, 12 måneder vikariat (Måløv, Danmark)

Proces supporter (Kalundborg, Danmark)

Tekniker med klasse C erfaring (Bagsværd, Danmark)

Quality Process Manager (Bagsværd, Denmark)

Graduates! Kick-start your European business career (Bagsværd, Denmark)

Purchasing Quality Coordinator (Bagsværd, Denmark)

Project Coordinator (Hillerød, Denmark)

Intern (Bagsværd, Denmark)

EXPERIENCED SYSTEMS ENGINEERS (Hillerød, Denmark)

TALENTED ENGINEERS WITH POTENTIAL TO GROW! (Hillerød, Denmark)

Category Manager (IT) (Bagsværd, Denmark)

Erfaren kemiker - ingeniør - farmaceut der vil udfordres og udvikles i (Gentofte, Danmark)