Jobs at Novo Nordisk

QA Academic, Qualification/Validation in Pilot Plants

- Research & Development
- Denmark - Gentofte

Are you looking for new challenges within QA and do you strive for making a difference in assuring the quality of facilities and equipment in CMC API Development?Can you combine your knowledge of quality and pharmaceutical production with your drive for results?Do you want ensure the quality of Novo Nordisk new products for clinical development?

About the department
CMC API QA has the responsibility of assuring that API (Active Pharmaceutical Ingredients) activities in development and support projects in Novo Nordisk A/S fullfill cGMP requirements.The department consists of 29 employees organised into two teams. You will be a part of the Process Compliance Team (PC-Team) in CMC API QA. You will join a team of 10 dedicated colleagues assuring that our pilot plants (cell banks, cell cultivation, purification and chemical synthesis) and development laboratories meet the internal and external requirements.The pilot plants and the development laboratories are located in Bagsværd, Gentofte, Måløv and Hillerød. During the week you will be moving between the different locations and the QA office. This way of working requires that you have the ability to be a team player on distance.

The job
With responsibility of one or several of our pilot plants you will be in charge of assuring quality of our production areas with regards to validation and qualification of equipment, environment and utilities. Document approval in connection with qualification, cleaning, maintenance and improvement of the quality system (SOP’s) and other documentation from the facility, will be included in your daily tasks. You will have a broad interface within the organisation and a dynamic working week with varying tasks. CMC Supply’s continuing high level of audit and inspection readiness is on top of your agenda. In CMC Supply QA we work with QA oversight where you, in close cooperation with your colleagues, will identify and contribute to the strengthening of our stakeholders’ compliance.

The responsibility of maintenance and improvement of the quality systems is also based on close cooperation between the pilot plants and QA. Great interpersonal skills and high spirits will therefore be a necessity. In cooperation with your colleagues in QA, you act as a consultant for our pilot plant and you will experience a lot of time spend on competent feedback with internal in QA colleagues and colleagues from the pilot plants.We operate in a LEAN orientated environment and you will have the opportunity to contribute with ideas and improvements and to drive the implementation of these. Working within QA your professional and individual skills will be challenged and you will find that your tasks will include many different clinical stages in the product development.

Qualifications
Ideally, you have a master in Pharmacy, Chemical Eng. or corresponding qualifications and a strong quality mindset. You have a few years of experience and knowledge of GMP, equipment / facilitation, qualification and cleaning from a QA area working in pilot plants or production. As we operate in an international environment you will have to master fluent English both spoken and written.Personally, you are ambitious and focus on results and quality and you contribute to the right level of compliance. You are decisive and embrace complex tasks via constructive dialogue and in cooperation with QA colleagues and collaborators in the pilot plants. Also, you thrive in a role where you use your knowledge and bring your arguments and negotiation skills in to play. You are able to adapt and challenge our way of doing things, so that we will get even better.

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 Lisbeth Voetmann +45 3075 0530 or Peter Søtofte Elten at +45 3079 8453.

Deadline
11 August 2013.

VP cLEAN Project Manager

- LEAN
- Denmark - Måløv

Are you motivated by driving and executing cLEAN®? Are you strong at project management, process optimization, problem solving, data analysis and eager to create continuous improvements? Are you keen to join an organization with an ambitious cLEAN® agenda? Then you might be the right person to take cLEAN® to the next level in CMC supply, Drug Product Development (DPD), a part of the Novo Nordisk A/S R&D organization.

About the department
cLEAN® is Novo Nordisk A/S´s version of LEAN.

You will be a part of R&D CMC DP Development, which consists of approximately 360 employees and is responsible for the development of formulations, production processes and belonging analytical methods, and production of SDF products to support Novo Nordisk’s clinical trials within all platforms and proteins. We are looking for 2 VP cLEAN® Project Managers, who will report directly to the 2 VP´s for Injectable Protein Formulation, IPF and for Oral Protein Formulation, OPF. In OPF we are on a voyage towards the development and production of oral formulations of proteins. Our ambition is to develop break-through products based on orally available versions of insulin and GLP-1.In IPF we are responsible for developing formulation and processes as well as analytical methods for new therapeutic proteins primarily soluble and freeze-dried injectables. Our ambition is to break new land and develop diabetes and biopharm products of the future.

The job
As part of DP Development you will drive cLEAN® activities across the business areas together with local management. You will ensure alignment with the business strategy and challenge the management team as appropriate. You will play a key role in Long Term Business Management and support the Master Planning process.In recent years a number of LEAN projects and initiatives have been carried out successfully in the business area and the level of ambition for further optimization is high. You will be responsible for driving cLEAN® projects as well as coordinating, prioritizing, following-up and facilitating alignment of cLEAN® activities incl. learning across the business. You will cooperate intensely with department cLEAN® coordinators, CVP cLEAN® and Business Partners in DP Development. You will also become a part of the R&D CMC cLEAN® network.

Qualifications
You have several years of experience with cLEAN®/LEAN, incl. facilitation of improvement activities, coaching, conducting training, executing workshops, driving own projects, coaching management in performance board meetings and using systematic problem solving as a corner stone in cLEAN® implementation. You probably have black belt qualifications. You have solid project management experience; documented results from cLEAN®/LEAN projects are a must. You base your conclusions on data analysis and have a structured approach to problem solving. You have strong change management and communication skills. You are an excellent team player with an involving and proactive style. You can work with people at all levels of the organization and you are good at creating an internal network. The person we are looking for has a relevant Master’s Degree (pharmaceutical, business, engineering or similar). Ideally, you have experience with supply chain and/or production in a complex and project oriented company. Experience from the pharmaceutical industry will be an advantage, but not excluding.

At Novo Nordisk, 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.

Contact
For further information, please contact Janus Kortsen at +45 3079 0506.

Deadline
18 August 2013.

Udstyrssupporter

- Produktion
- Danmark - Bagsværd

Vil du være med til at supportere vores insulinproduktion? Vil du være med til at sikre at vores mikrobiologiske laboratorium er i compliance med gældende GMP og ISO krav? Er du ansvarlig og energisk og brænder du for at arbejde med laboratorieudstyr? Så er du måske vores nye kollega.

Om afdelingen
QC Mikrobiologisk Laboratorium, QCM består af ca. 40 medarbejdere fordelt på 2 teams. Vi udfører mikrobiologisk analyse på vand og insulinprodukter, og vi har en stor kontaktflade til vores samarbejdspartnere i produktionen. Du bliver en del af support teamet som består af 4 kemikere, 8 laboranter og 3 operatører.

Jobbet
Som supporter i supportgruppen skal du være med til at sikre den daglige drift i laboratoriet. Vi har ansvar for den faglige support vedr. analyser og udstyr, og vi arbejder med udarbejdelse af instruktioner, afvigelser og ændringssager samt diverse forbedringsprojekter. Du vil være en af de drivende kræfter omkring vores udstyr, og du vil være med til at sætte retning for kvalificering, drift, support og optimering af analyseudstyr og processer i laboratoriet. Du vil skulle lave fejlsøgning og problemløsning i samarbejde med de andre supportere og analyselaboranterne, og du vil være den, der udarbejder dokumentationen af undersøgelserne. Vores udstyr tæller bl.a. isolatorer, inkubatorer, klimarum og ID udstyr samt diverse småudstyr som mikroskoper, vægte og pipetter. Ud over udstyr vil du også få mulighed for at arbejde med andre support opgaver relateret til de forskellige analyser.

Kvalifikationer
Du er uddannet laboratorietekniker, laborant el.lign., og du har erfaring fra arbejde i et GMP laboratorium, gerne mikrobiologisk. Du har stor lyst til og erfaring med laboratorieudstyr, og du er vant til at udføre kvalificering, support og vedligehold af udstyr – herunder udarbejdelse af diverse dokumentation. Interesse for og kendskab til IT systemer under ”21CFT part 11” vil være en fordel. Du er vant til problemløsning, og du har en omhyggelig og systematisk tilgang til dine opgaver. Du håndterer gerne instruktioner, afvigelser og ændringssager, og du er god til at formulere dig på dansk og engelsk i både skrift og tale. Du er udadvendt, initiativrig og har en masse gå-på-mod, og du er i stand til både at arbejde selvstændigt og som en del af et team. Du er fleksibel og i stand til at håndtere en travl hverdag med godt humør. Du er vant til forandring og omprioritering, og du er god til selvstændigt at håndtere mange opgaver samtidig.

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 ikke bare om at tjene til føden, men om at gøre en forskel.

Kontakt
Vil du vide mere om stillingen, så kontakt Lisette Hayford på +45 3079 1883 or Birgitte Grindsted på+45 3075 6764.

Ansøgningsfrist
31. juli 2013

Chemist HPLC-2

- Production
- Denmark - Gentofte

Are you our new scientific colleague in the dynamic HPLC team at Novo Nordisk in Gentofte? We are in rapid growth, working with the quality control of Biopharm’s broad portfolio of haemophilia products, and therefore we urgently need your solid HPLC and GMP insight.

About the department
The department validates the analytical methods for the new haemophilia products and the release testing of clinical phase 3 batches. In addition we support the three chemical site QC laboratories in Biopharm using our technical skills combined with systematic problem solving.

We work in an unpretentious and good atmosphere with knowledge share across teams and professional groups.

The job
You and your 16 colleagues share the responsibility for the day-to-day running of our HPLC methods and ensure that the analytical results comply with the current GMP standards. You will approve the analytical results and troubleshoot on the methods of analyses, and at the same time prepare instructions, non-conformity reports and change requests. Another part of your responsibility covers standardisation and optimisation of HPLC methods. You will participate in cross-organisational meetings and as such be in close dialogue with the development laboratories. In case of deviations, it is your job to go into dialogue with our colleagues in the production. Together you examine the cause and analyse the problem further, before you make your suggestion for solution of the incident. As such you will have a challenging and innovative job that requires your energetic, dynamic and flexible mindset.

Qualifications
You hold a Master of Pharmacy, Cand Scient or similar and have a solid HPLC background from several years in a GMP-controlled environment. Here you have been part of another busy environment, and you thrive in an unpredictable workday where you solve heavy challenges and adjust tiny details. You have extensive experience in validation and standardisation of HPLC analyses and you are able to create a crystal clear overview and prioritise your tasks – even when deadlines are closing in. You never compromise on quality, however, you are able to round off and finish your tasks on time in order to proceed to the next assignment with enthusiasm and energy. Besides being open-minded and committed, you know how to motivate and inspire your colleagues to perform even better. You use your LEAN knowledge to renew our work processes, and you follow a systematic and analytic practice in order to meet the many deadlines. Lastly, you speak and write Danish and English fluently.

In Novo Nordisk it is your skills, your commitment and your ambitions, which helps us to improve many people's lives. In return we offer you the opportunity to work with exceptionally talented colleagues, and we offer you a wide range of opportunities for professional and personal development.

We will interview candidates continually as we receive the applications. Deadline for application is 1 September

Contact
For further information, please contact Christina Alsted Frandsen at +45 3075 6552.

Deadline
1 September 2013.

Senior ingeniør til højteknologiske samle- og pakkelinjer

- Produktion
- Danmark - Måløv

Har du solid erfaring med kvalificering, og kan du være med til at gøre vores allerede højteknologiske samle- og pakkelinjer endnu bedre? Er det dig, kan du se frem til at blive en del af et stærkt teknik-team, der sikrer stabil drift og forsat udvikling på Biopharm Tablets & Finished Products i Måløv.

Om afdelingen
Du kan glæde dig til at blive del af et voksende team, der kombinerer det bedste inden for en vifte af ingeniørdiscipliner med det bedste inden for teknik og håndværk. Vores mål er at have rendyrket verdensklasse i såvel teknologi som processer, metoder og systemer. Du bliver en vigtig medspiller i at leve op til den målsætning.

Jobbet
Dit job har fokus på to sideløbende opgaver: Kortsigtet driftssupport på den ene side og langsigtet udvikling af systemer, processer, metoder og teknik ved hjælp af LEAN og Systematisk Problemløsning (SPL) på den anden side.

Den daglige driftssupport dækker vores 11 højt automatiserede fylde- og pakkelinjer. Det handler meget om teknisk her-og-nu problemløsning, hvor du fjerner årsagen til problemet og samtidig sikrer, at vi fremadrettet undgår lignende tilfælde. Det kræver tæt dialog og godt samspil med dine kolleger, der betjener linjerne samt med dine ingeniør- og håndværker-kolleger i teamet. På udviklingsområdet gennemfører du selvstændigt små og store projekter, eksempelvis periodisk systemevaluering samt evaluering af sikkerhed og konfigurationsstyring. Herunder sikrer du konsistens og højt compliance-niveau i vores kvalificeringsdokumentation. Du udfører også risikoanalyser samt udarbejder ændringsansøgninger og kravspecifikationer, så vi altid lever op til gældende myndighedskrav. På den vis bidrager du også til vores fremadrettede strategiproces.

Kvalifikationer
Du er ingeniør og uanset baggrund har du erfaring med automatiseret pakke- og fyldeudstyr og et indgående kendskab til kvalificering og LEAN. Du kan derfor gennemskue avancerede automatik- og mekaniske systemer. Det gør, at du kortsigtet kan få en maskine hurtigt i gang, og at du langsigtet kan identificere, implementere og drive forbedringsprojekter – og dermed hæve udstyrseffektiviteten og skabe en stabil produktion. Måske har du allerede arbejdet i et GMP-reguleret miljø og har drevet egne projekter. Hvis ikke, er du mere end klar til udfordringen.

Du kommer ind i et miljø, der er kendetegnet ved et godt samarbejde på tværs af teams og faggrænser og en stor vilje til at bidrage til at nå de fælles mål. Vi regner derfor med, at du også møder med en positiv indstilling og godt humør. I afdelingen sker der hyppigt uforudsete ting, som kan medføre omprioriteringer og forandringer, så du skal have lyst og mod på en omskiftelig og til tider hektisk 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 Lars Solgaard på +45 3075 4945

Ansøgningsfrist
18. august 2013

Development Quality Engineer

- Quality
- Denmark - Hillerød

Are you ready to make a difference and proactively influence the future device development projects in Novo Nordisk? As Development Quality Engineer in Device Manufacturing Development (DMD) you will use your quality-focused mindset to make a serious difference and contribute to defeating diabetes worldwide.

About the department
You will be part of a team of 13 dedicated colleagues, including 10 QA Engineers, in Hillerød. Together, we are responsible for assuring the quality of devices developed by our development departments, processes to pilot production and transfer processes into high volume production that takes the finished product to markets worldwide.

The job
Your main objective is to be quality responsible in device development projects – devices for diabetic treatment. The devices to be developed are durable devices which include electronics. Your main focus will be on the electronic development tasks. Your quality tasks are to secure the development is done according to the written design control procedures, e.g. review and approve design inputs such as product requirements, component specifications for metal, plastic and electronics, product risk analyses and implementation of mitigations, review/approve engineering change orders and later in the development process you will prepare control specifications for in-coming and out-going inspection. Furthermore you must cover supplier evaluation and assure new suppliers are evaluated according to the quality requirements they are intended to be used for. The development departments will need your support in preparing development agreements if development is done at a supplier. It is your responsibility to secure that the design inputs still are prepared according to regulatory and quality requirements. Anticipate visits to suppliers in Europe and Asia between 10–30 days a year.

Qualifications
Your approach to this position is a relevant engineering degree (B.Sc. or M.Sc. level) within Electronics, Mechanics, Manufacturing or Medicine and Technology. You have knowledge with the requirements ISO 13485, 21 CFR Part 820 and ISO 14971. You have worked with development projects, supplier tasks in general, you know how to fulfil the regulatory and quality requirement when cooperating with suppliers that develop devices together with the development departments and you are familiar with an international environment.

On a personal level, you are known for dedicating yourself to working proactively to solve the tasks at hand and you are talented within coordination of tasks.Your ability to convince your colleagues to follow written procedures is excellent and you like to present the essence of the quality importance for those where you see a need. You are aware that convincing and presenting often is successful when you have prepared solid facts and data. Moreover, you have a high level of fluency in written and spoken English.

In Novo Nordisk it is your skills, your commitment and your ambitions, which helps us to improve many people's lives. In return we offer you the opportunity to work with exceptionally talented colleagues, and we offer you a wide range of opportunities for professional and personal development.

Learn more about Novo Nordisk Product Supply and working in QA using this link www.novonordisk.com/careers/QA

Feel free to submit your job application in either English or Danish, whichever you prefer.

Contact
For further information, please contact Malene Fugl Andersen at + 45 3075 8982.

Deadline
9 September 2013.

Teamkoordinator – QC laboratorium

- Produktion
- Danmark - Kalundborg

Har du lyst til et job, hvor du er med til at skabe succes og understøtte driften på et Novo Nordisk laboratorium? Så kan du blive teamkoordinator i vores QC laboratorium, som er en del af Novo Nordisk DAPI i Kalundborg. Vi er et større team bestående af 23 laboranter og 6 kemikere, og vi forsyner hele DAPI produktionen med kemiske analyser – lige fra gæring til finrens. Vi vil gerne frigive endnu mere tid til personaleledelse, og derfor har vores teamleder brug for en højre hånd til at sikre kvaliteten og rettidige leverancer. Det er her du kommer ind i billedet…

Om afdelingen
Du vil blive en del af et kemisk analyseteam bestående af 30 engagerede og dygtige laboranter og kemikere. Teamet er en del af QC laboratoriet i IM2, hvor der udføres både kemiske og mikrobiologiske analyser af vores produkter i Diabetes API. I afdelingen er vi ca. 80 medarbejdere fordelt i 4 teams.

Jobbet
Dit job bliver at assistere afdelingens teamleder med at koordinere de daglige opgaver for teamet. Du har fokus på, at vi leverer analyser i den rette kvalitet til tiden. Med dit solide overblik over afdelingens kompetencer hjælper du med at sikre, at laboratoriet altid har de rette ressourcer fordelt de rigtige steder. I samarbejde med teamlederen faciliterer du systematisk problemløsning, ligesom du sikrer opfølgning og udarbejder uddannelsesplaner. Foruden disse opgaver deltager du på kundemøder, forbereder tavlemøder, søsætter optimeringsinitiativer, der mindsker procestid, ligesom du håndterer de udfordringer og løser de problemer, som kunne sætte din planlægning over styr. I det hele taget kan du se frem til et varieret job, der giver dig mulighed for at observere personaleledelse helt fra forreste række.

Kvalifikationer
Din uddannelse er en kandidatgrad i kemi eller et andet relevant fag. Du har erfaring fra et produktionsmiljø, hvor du har fået indsigt i GMP og ISO standarderne. Du får brug for dit høje energiniveau og din solide sans for struktur, og det motiverer dig især at optimere processer samt løse uforudsete opgaver. I tillæg til dine enestående koordineringsevner formår du at tænke strategisk, hvilket gør, at du kan planlægge både på kort og lang sigt. Som person skal du kunne trives i en udadvendt rolle, hvor du opsøger kolleger såvel som ledere og motiverer dem til at arbejde sammen og med interessenter for at nå fælles mål. For at få succes i stillingen skal du være en god lytter og i stand til at samarbejde på alle niveauer i en stor organisation. Sidst, men ikke mindst, har du en god forretningsforståelse.

Novo Nordisk i Kalundborg
Novo Nordisk i Kalundborg er en by i byen. Området er på 1.350.000 m2 med eget vejnet, kun godt en times kørsel fra København. 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 Søren Johnsen på +45 3075 8110.

Ansøgningsfrist
28. Juli 2013

At Novo Nordisk, our winning culture is focused on cross-functional and cross-cultural teamwork. We combine clinical research to develop new products, regulatory efforts to work with the FDA to bring these products to market, and sales and marketing to convey a strong, clear message to patients and physicians. We encourage employee involvement at all levels, which in turn helps to nourish development and innovation. When employees become involved, the result is a rich exchange of ideas and concepts. And that helps us give more to our customers, to our community and to society as a whole.

In an effort to match your background and experience with our potential future openings, we invite you to upload your resume by clicking on the apply button. Please note your resume will be kept confidential.

We look forward to continuing to provide you with information on Novo Nordisk career opportunities.

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We look forward to continuing to provide you with information on Novo Nordisk career opportunities.

International Medical Director/International Medical Manager

- Research & Development, Medical Doctor
- Denmark - Søborg

The Medical & Science, Degludec II department at Novo Nordisk A/S is seeking a physician to take on a position as International Medical Director/Manager working with diabetes projects in Novo Nordisk. We are looking for a medical doctor with documented clinical and scientific knowledge about diabetes. A candidate with experience from clinical development work within the pharmaceutical industry and knowledge about interaction with regulatory agencies will be preferred. The job will require strong interaction with highly engaged colleague’s world-wide and external stakeholders including treating physicians and therapeutic experts.

About the department
The department is medically responsible for planning and conducting clinical studies as well as medical input to regulatory documents and health authority interactions. The candidate will be involved in these activities closely interacting and collaborating with the NN organization globally.

The Job
Key responsibilities of the successful candidate will be to take up the role as Medical Specialist within the assigned projects. This includes being instrumental in creating regulatory documents, implement clinical development strategies for a drug candidate, updating Clinical Development Plans, executing clinical studies phases 1-3 and providing medical deliverables to the paediatric investigational plans for a drug candidate.

A specific focus will be to provide input to the content and quality of the regulatory documents, Clinical Part of the Submission Dossier as well as creating / writing relevant risk-assessment plans, medical content of trial outlines, protocols, clinical trial reports, paediatric investigation plans, IMPDs and publications and presentation of medical aspects of the clinical development program at internal and external meetings (including meetings with health authorities, congresses, investigator meetings etc.).

Qualifications
You have a medical degree including scientific training (PhD, DMSc or equivalent), and preferable knowledge within diabetes or metabolic conditions. It will be an advantage if you have previous experience from the pharmaceutical industry and experience from interaction with regulatory authorities e.g. NDA submissions, scientific advice or similar. You are a reliable, open-minded and dedicated team player, who thrives in a global environment of continuous development, and focuses on completion, quality and results. Interaction with internal and external experts require proficiency in English, high communication, coordination and planning capacities, as well as flexibility and a keen sense of quality. You may expect certain travelling activity of approximately 10%.

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

Contact
For further information, please call Pernille Poulsen on +45 3075 9214.

Deadline
12 August 2013.

IT Process Lead - Manufacturing Execution Systems

- Production
- Denmark - Bagsværd

If you have a strong knowledge of 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 IT/Process lead you will have the opportunity to personally impact the way we manage our manufacturing IT systems and processes across Product Supply.

About the department
You will join a colleague in Diabetes Finished Products IT which is a part of our Business Support department which consists of more than 30 employees. The department is dedicated to provide support and direction to our production facilities across the globe.

The job
Your overall objective is to secure a stable and harmonised use of Manufacturing Execution Systems across Product Supply. A vital part of this will be to monitor the process performance and data quality across our Manufacturing Execution Systems. You will identify areas of opportunity to further improve the performance of processes or manufacturing systems. With your global understanding of our manufacturing systems and processes you will analyse changes and understand the impact of such changes to our production facilities.

The job requires high level of interaction with people from headquarters as well as from our production facilities. A part of your job will be to represent Manufacturing Execution Systems in the newly established IT Business Process Forum to secure data coherency and seamless integration to SAP, our global ERP solution. You will establish and drive a super user network covering global use of our Manufacturing Execution Systems. You will also be involved in various projects where you contribute to ensure alignment with the standards and processes related to manufacturing systems. You can look forward to 15-20 travel days per year.

Qualifications
You have a relevant master’s degree backed by a minimum of 3 years’ experience. Alternatively you have a background from the IT consultancy industry. You have gained profound knowledge within 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 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.

Contact
For further information, please contact Thomas Zakarias at +45 3079 1039.

Deadline
8 August 2013.

GMP koordinator

- Kvalitetssikring
- Danmark - Kalundborg

Kunne du tænke dig, sammen med engagerede og fagligt ambitiøse kolleger, at være med til at bygge en helt ny afdeling i Kalundborg op? Det nye pakkeri er en strategisk vigtig satsning i Biopharm, der skal sikre den fremtidige kapacitet til at pakke alle 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 og håndtere projektfasen for en ny pakkelinie, der skal levere til markedet allerede i Q4 2013. Har du en kombination af QA viden og forståelse for et GMP-styret produktionsmiljø og er du drevet af at arbejde med, og sætte retningen for kvalitet i et sådant miljø, så har du det helt rigtige fundament for at søge denne spændende stilling i vores nye afdeling i Kalundborg.

Om afdelingen
Afdelingen er en del af Biopharm T&FP Finished Products, som består af 6 afdelinger. Du får ca. 40 dygtige og motiverede kolleger. Som kvalitetskoordinator bliver du afdelingens kvalitets ansvarlig, refererer til afdelingslederen, og er med i ledergruppen, som består af en afdelingsleder, 2 teamledere og en afdelingssekretær. Derudover vil du være en del af kvalitetsgruppen på tværs af afdelingerne i T&FP, hvor I har mulighed for sparring på tværs, og drive handlinger til opretholdelse af et højt complianceniveau.

Jobbet
Da vi er en ny afdeling, vil dit fokus blandt andet være at opbygge de rette kvalitetssystemer og -fora samt sikre, at afdelingen når og efterlever de gældende kvalitetsmål fastsat af myndigheder, vores eget koncernniveau og afdelingen selv. Din opgave vil endvidere være at sikre, at vi hele tiden flytter os mod højere kvalitetsniveauer. Rollen er derfor at fungere som brobygger mellem QA og produktionen. I tæt samspil med afdelingens ledergruppe formulerer du helt konkret vores kvalitetsmål. Det er i den forbindelse din opgave at udtænke og implementere de planer, der gør, at vi når målene. Som en naturlig del af rollen har du også ansvar for at sikre, at afdelingen altid er inspektionsparat til både interne audits og myndighedsinspektioner. En helt afgørende forudsætning for din succes bliver at skabe en god dialog med kollegaer i produktionen om, hvorfor målene er vigtige, og hvordan medarbejderne helt konkret kan bidrage til at nå målene. Det kræver evnen til at kunne stille ufravigelige krav på en måde, der forvandler kravene til et fælles mål.

Kvalifikationer
Din baggrund er en videregående uddannelse, sikkert med en naturvidenskabelig vinkel. Du har allerede arbejdet hands-on med kvalitet i et GMP-styret miljø, og nu er du klar til at tage et endnu større ansvar. Dine gode kommunikationsevner og din udadvendte og afslappede personlighed gør, at det falder dig naturligt at skabe tætte relationer til mange mennesker. I forlængelse af dette, trives du med at navigere i en kompleks organisation med mange interessenter. Da du kommer til at køre meget på egen hånd, er det også helt nødvendigt, at du kan sætte egne mål og selvstændigt sikre, at de nås. Derudover skal du kunne arbejde ubesværet på engelsk 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 Klaus Arneskov Mathiesen på +45 3079 1624.
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Ansøgningsfrist
31. august 2013.

LEAN flow Specialist

- LEAN
- Denmark - Søborg

Since 2002, striving for operational excellence, LEAN has been the driver behind our production philosophy. Today, it is a true part of our DNA and visibly integrated in our strategy. From top management to local offices and production facilities our every action is concerned with reducing waste in the work processes and with doing things right the first time around. And it works!

About the department
You will join the cLEAN® Office in Søborg. We provide the global Product Supply organisation with concepts, sparring and coaching enabling the Line of Business to achieve the fast to market targets and solve the business challenges in a LEAN way.

The job
Your overall focus is to develop the flow capabilities to continuously meet strategic and operational goals and needs of Product Supply. As part of the specialist team you evaluate and challenge our LEAN strategy, programmes and master plans. You will be hands-on responsible for the development and improvement of flow standards incl. delivery of training programmes to develop LEAN Project Managers at Black belt level. Accordingly, you render specialist support to the LEAN roll-out within flow. You also manage the methods and systems that we use to evaluate and measure the effect of our efforts. Another part of your job will be to integrate flow competencies within other business activities, improvement projects, and the business strategy – and you will function as Project Manager for a number of cross-organisational projects. You can look forward to major influence and impact.

Qualifications
You hold a degree at master’s level within e.g. engineering or business administration. In addition, you have 5-10 years of solid experience from a large, multi-site environment where you have implemented flow in the supply chain across business functions like Planning, Purchase, Manufacturing and Quality. You have a certified LEAN education at Black belt level or similar, and your toolbox is loaded with LEAN methodologies and experience – all the way from the analysis throughout concept development until final implementation. You are used to functioning as Project Manager, and you are able to drive and lead several teams that work with multiple parallel business process improvements. You have excellent communication and stakeholder management skills enabling you to build trust and explain managers and employees why changes are necessary, and how they will benefit from contributing with a positive mindset. Naturally you also have the stamina it takes to succeed in such a challenging and influential role. A high level command of English, written and spoken, is required.

At Novo Nordisk, you will help patients around the world. As their needs evolve, so does our challenge to find better and more innovative ways to improve their quality of life.

Contact
For further information, please contact Marianne Baatrup Thystrup at +45 3079 6662.

Deadline
11 August 2013.

Associate Manager

- Management
- Denmark - Gentofte

Looking for a job where you set direction for your team and maintain standards on high quality?

About the department
In Biopharm Aseptic Production in Gentofte you will join a department of 110 colleagues, be part of a group of Associate Managers and head your own team of highly specialized and skilled professionals. The team ensures support to the formulation, filling and freeze drying of GlucaGen®. You will play a key part in helping people with diabetes all over the world.

The job
As Associate Manager you will direct a process support team of 8 motivated Chemists. Your overall objective will be to make sure that the production works in compliance with our regulations and standards. In cases where production deviates from standard, your employees solve the problem according to procedures and hereby ensure solid and robust solutions. To succeed, you will need a team of highly qualified and motivated colleagues. It is your job to shape a work environment that inspires to job enthusiasm and matches the requests and capabilities of your team. For this, you set up KPIs and follow up to make sure that behavior and results are correctly measured. If necessary, you support complicated non-conformities and ensure training of your colleagues. You set an example and point the way, and you take pride in securing a high level of quality in everything you do.

Qualifications
You have solid managerial experience combined with a Master’s degree in one of the natural sciences and have acquired a sound understanding of a production set-up. You are highly familiar with quality standards and know when to react to support the correct yield and production volume. If you know the pharmaceutical industry, it will be a plus. LEAN, GMP and ISO 9001 are natural elements in your workday, and you have a keen eye for improving and optimizing your and your team’s working conditions and procedures. In this way, you focus on the targets and have the will and the skills to fulfill them. You have a positive mindset and thrive in the decision-making role where decisiveness, self-consciousness and conflict management are key words, and you know how to win acceptance through direct and clear communication.

At Novo Nordisk, we work together to prevent, treat and eventually cure diabetes. Nearly 366 million people worldwide are living with diabetes today, with two people diagnosed every ten seconds. Working here is not just a way to make a living, but a way to make a difference.

Contact
For further information, please contact Peter Thomas Olesen +45 3075 0187.

Deadline
15 August 2013

Akademiker med miljø- og GMP-viden til finrensningspilot

- Forskning og Udvikling
- Danmark - Bagsværd

Har du styr på kravene til internt miljø? Ved du hvordan en trend skal se ud og hvad vi gør hvis der er sporedannere? Vi søger en naturvidenskabelig profil med evne til at drive og afslutte opgaver og som kan finde gode løsninger ud fra anlæg, arbejdsprocesser og compliancekrav. Vi har i afdelingen kontrollerede lokaler samt klasse D og C.

Om afdelingen
Afdelingen er Downstream Pilot Plants, afd. 201 i Bagsværd, som hører under området CMC API Development. Afdelingen består af 3 teams, heraf to kampagne teams der oprenser proteiner til toksikologiske og kliniske studier og et supporterende team, der understøtter driften.Den ledige stilling er i Supportteamet, der består af 4 teknikere og 3 kemikere. Vi løser en lang række meget varierende opgaver i forbindelse med drift og vedligehold af eksisterende anlæg og udstyr, kvalificering og implementering af nyt udstyr, monitorering af forsyninger og miljø, systematisering af afdelings arkiv, prøvekoordinering samt vedligeholdelse og udvikling af kvalitetssystemer og processer. Du vil i teamet få en flok højt engagerede og hjælpsomme kolleger der oftest har et lunt glimt i øjet.

Jobbet
Afdelingen er vokset betydeligt i mandskab gennem det sidste år, og kravene til kvalitetsniveauet skærpes løbende. Du får en nøglerolle i arbejdet med at holde overblik og agere på afdelingens miljøopgaver.Konkrete opgaver bliver at sikre korrekt niveau af monitorering, struktureret problemløsning eller udarbejdelse af NC’er ved overskridelser i tæt samarbejde med prøvetagere og andre kolleger. Og ikke mindst proaktivt at tage de rigtige aktioner for at sikre at afdelingen også fremadrettet er i compliance.

Du vil blive en del af områdets erfa-gruppe indenfor internt miljø.Afhængig af dine kompetencer og interesser og vores behov i teamet vil du få andre ansvarsområder. Du har stor mulighed for selv at præge opgaverne og dermed din dagligdag.

Kvalifikationer
Du har en naturvidenskabelig uddannelse som f.eks. cand. scient., ingeniør eller farmaceut. Du har nogle års erfaring fra en lægemiddelvirksomhed, og har godt styr på mikrobiologi, GMP og kravene til internt miljø. Måske ved du også noget om renset vand systemer og rengøring af klassificerede lokaler. Viden om proteinkemi eller erfaring med inspektioner vil være en fordel. Kendskab til systemerne PEMS og LIMS er også en fordel, men ingen forudsætning.Du har en positiv tilgang til at løse udfordringer på en systematisk, enkel og effektiv måde. Du er en teamplayer, og du kan formidle viden på både dansk og engelsk. Du er engageret, struktureret, kvalitetsbevidst og tager ansvar for både dine egne og afdelingens opgaver. Du trives i en hverdag hvor opgaverne veksler og du når dine mål.Vi tilbyder et spændende job i et åbent og dynamisk arbejdsmiljø med gode muligheder for faglig og personlig udvikling.

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 kemiker Pia Lavgaard Sørensen på tlf. 30 79 17 08 eller teamleder Vibeke Bohn Edwards på tlf. 30 79 84 63.

Ansøgningsfrist
11. august 2013

Senior Project Manager

- LEAN
- Denmark - Søborg

Since 2002, striving for operational excellence, LEAN has been the driver behind our production philosophy. Today, it is a true part of our DNA and visibly integrated in our strategy. From top management to local offices and production facilities our every action is concerned with reducing waste in the work processes and with doing things right the first time around. And it works!

About the department
You will join the cLEAN® Office in Søborg. We provide the global Product Supply organisation with concepts, sparring and coaching enabling the Line of Business to achieve the overall strategy and solve the business challenges in a LEAN way.

The job
In this challenging and exciting senior role you will have the following main objectives: One is to ensure excellent planning and coordination across our LEAN project portfolio. Another is development and standardisation of principles, systems and tools including ensuring proof of concepts by pilot execution.

More in detail you will, on an ongoing basis and based on the project portfolio, consult the Product Supply management at all levels to initiate and run cross-functional LEAN development programs. You take lead and execute complex change and improvement projects including pilot projects to ensure proof of concepts and to create acceptance and organisational buy in on the developed concepts. Part of the role is to be senior advisor, consultant and coach for senior management to ensure local ownership of the developed solutions – at all levels of the organisation. This includes training and coaching of employees in the principles, methods and new ways of working. You also ensure systematic exchange of knowledge across departments, projects and production areas. The job requires approximately 20 travel days per year to sites in the global Product Supply organisation.

Qualifications
You have an academic degree and at least 10 years’ experience as Manager/Project Manager working with change management and LEAN. You have documented your ability to initiate and manage large and complex projects in a multi site environment – and you are used to turn your knowledge into new tools, systems and methods. Your stakeholder management and communication skills are excellent, and you have the professionalism and charisma it takes to coach and convince people at senior management level. At the same time you can explain colleagues at operator level why changes are necessary and how they personally will benefit from contributing with an open and positive mindset. Your LEAN education is at Black belt level or similar, and a natural part of your work routines is to stay updated on the latest developments within LEAN principles and methodologies. Finally, you must have an excellent command of English, written and spoken.

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 Marianne Baatrup Thystrup at +45 3079 6662.

Deadline
11 August 2013

Senior LEAN Consultant

- LEAN
- Denmark - Søborg

Since 2002, striving for operational excellence, LEAN has been the driver behind our production philosophy. Today, it is a true part of our DNA and visibly integrated in our strategy. From top management to local offices and production facilities our every action is concerned with reducing waste in the work processes and with doing things right the first time around. And it works!

About the department
You will join the cLEAN® Office in Søborg. We provide the global Product Supply organisation with concepts, sparring and coaching enabling the Line of Business to achieve the fast to market targets and solve the business challenges in a LEAN way.

The job
You will contribute to the development, execution and implementation of concepts that reflects the needs of Product Supply on strategic and operational level. In practice you coordinate LEAN projects/initiatives of varying complexity based on project briefs. Across all activities you ensure that relevant stakeholders are taken into account in goal setting, and you drive the projects forward by continuous follow up, communication and goal attainment. You identify potential problems and solve these by communicating to the project team in a clear and motivating manner.

Another part of your job will be to coach and train project team members and line of business employees and to prepare, develop and conduct workshops. In this role you will function as internal consultant for various departments and business areas in Product Supply. You will also contribute to the development and standardisation of principles, systems and tools. You must ensure proof of concepts by pilot execution aligned with business plans and goals and with focus on performance and productivity improvements. The job requires approximately 20-30 travel days per year to sites in the global Product Supply organisation.

Qualifications
You have an academic degree and at least 5 years’ experience driving LEAN activities in a production or administrative environment where you have demonstrated high quality performance and the ability to deliver within tough deadlines. You are a skilled Project Manager and have solid experience working with LEAN as coach and trainer. Your certified LEAN education is at green belt level or similar and you have excellent analytical skills. With your engagement and persistency you drive your activities from start up to final implementation. Having many contacts from operators to senior management, across all kinds of professional backgrounds, requires excellent stakeholder management and communication skills including the ability to explain complex subjects in an easy understandable way – in English written and spoken.

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 Marianne Baatrup Thystrup at +45 3079 6662 or Charlotte Guldmann at +45 3075 1196

Deadline
11 August 2013

Director

- Quality
- Denmark - Bagsværd

Are you ready for a remarkable career opportunity? This could be your chance to set direction for a business critical area of Novo Nordisk Diabetes Finished Products. As Director for Quality Support you will have direct access to the top management, as your projects and activities will have their keen interest.

About the department
DFP Quality Support provides quality support and expertise to DFP, including the production sites worldwide. Our mission and yours is to support the optimisation and harmonisation of products, processes, methods and technologies and to support the fast-to-market strategy.

The job
You will report directly to the Corporate Vice President for DFP Quality and lead a team of 16 highly qualified and competent employees – nine of these are chemists and specialists, who will report directly to you. This is a unique career opportunity. You will be overall responsible for ensuring that products manufactured under contract for Novo Nordisk to the EU market are checked, released and subjected to stability studies. Furthermore, you make sure they are in compliance with the regulatory standards. This includes monitoring the quality of the products on a global scale. As such, you vouch for the compliance of our products no matter where the product has been manufactured. The overriding target is to secure smooth and efficient harmonisation and thereby support the fast-to-market strategy.

You set the standards for your team of experts and make sure they possess the correct resources to meet with the demands of tomorrow. This implies that you attend to day-to-day people management and follow up on performance, KPIs and other measuring tools.

Qualifications
You hold an MSc in Pharmacy or a comparable degree and have strengthened your theoretic knowledge with further training within the areas of GMP, quality control, quality assurance and regulatory compliance. You have been working for at least three years in a managerial position where you have successfully led your colleagues to deliver outstanding performance.

To be a success in this special position you must have proven theoretical and practical experience from manufacturing and quality assurance of pharmaceutical products. This professional background is what you will draw on to create a successful and high-performing team of colleagues. You use your empathic attitude to understand the problems and challenges of your team, and you pursue solutions until all challenges are properly resolved. This means that you are comfortable making decisions even difficult ones and setting direction for your team.

At Novo Nordisk, you will help some 366 million people who are living with diabetes. We expect high performance and the ambition to make your mark on our business. In exchange, we offer global opportunities for professional and personal development.

Contact
For further information, please contact Søren Hansen at +45 3079 2416, or Jonna Hindkær at +45 3079 8022.

Deadline
30 July 2013.

LEAN Partner Diabetes Finished Products - Bagsværd

- LEAN
- Denmark - Bagsværd

Do you have the drive to work closely with team leaders and employees on the production floor, using your LEAN thinking/tools to improve how we deal with daily problems?

About the department
In order to improve stability and quality, we are strengthening the LEAN setup on the site, and have already established LEAN Partners for each of the business areas (Finished Production, Aseptic Production, Quality Assurance, Quality Control and Environmental) supporting Vice Presidents in setting our direction regarding LEAN. As we need someone to drive LEAN in each department as well as work with other departments to solve the most important problems we are now seeking LEAN Partners reporting to our Department managers in Bagsværd.

The job
As LEAN Partner to our department manager your main role will be to continuously improve LEAN competencies and support different LEAN activities - all focused on improving stability and quality across our production sites in Denmark.

You will therefore be spending most of you time on the production floor, supporting leaders in development of systems (e.g. performance boards, problem solving, process confirmation) to see, solve, and follow-up on problems, in a way that secures sustainable results and thereby coach others to use and continuously improve these systems. When it comes to solving problems you will in some occasions be responsible for driving the process, supporting others in implementing and sustain defined solutions and ensure confirmation of new standards.

Besides leaders in your area you work closely together with a wide team of LEAN Partners, HR Partners and Training Partners within your assigned area. An outcome of this will be cross functional LEAN projects, defining and supporting improvement projects in your area and ensure on-boarding of new leaders in respect to the LEAN framework in Novo Nordisk Product Supply.

You report to the Department manager and are part of the department management group and you have a dotted line to the LEAN Partner for the Vice President.

Qualifications
You hold a B.Sc., M.Sc. or similarly and through your studies and working experience you have gained a good understanding and have a great interest in being part of process production setup. You can give examples of being part of complex problem solving; demonstrate a systematic approach to problem solving, experience with applying different LEAN tools and experience that demonstrates a desire to drive change.

On a personal level, you have excellent communications skills both oral and written in Danish and English and show a natural interest in others. You are known as a fast learner with a desire to develop yourself and others and have a naturally strong personal drive and thrive driving your tasks independently. Are you talented and have the ambitions, taking up this job as LEAN Partner might develop you into a manager.

In Novo Nordisk is your skills, your commitment and your ambitions, which helps us to improve many people's lives. In return we offer you the opportunity to work with exceptionally talented colleagues, and we offer you a wide range of opportunities for professional and personal development.

Contact
For further information, please contact Mogens Auchenberg +45 3079 4588 and Christian Goldbach +45 3075 0192 or Simon Riis Enghoff +45 3079 7521.

Deadline
11 August 2013

LEAN Partner Diabetes Finished Products - Hillerød

- LEAN
- Denmark - Hillerød

Do you have the drive to work closely with team leaders and employees on the production floor, using your LEAN thinking/tools to improve how we deal with daily problems?

About the department
In order to improve stability and quality, we are strengthening the LEAN setup on the site, and have already established LEAN Partners for each of the business areas (Finished Production, Aseptic Production, Quality Assurance, Quality Control and Environmental) supporting Vice Presidents in setting our direction regarding LEAN. As we need someone to drive LEAN in each department as well as work with other departments to solve the most important problems we are now seeking LEAN Partners reporting to our Department managers in Hillerød.

The job
As LEAN Partner to our department manager your main role will be to continuously improve LEAN competencies and support different LEAN activities - all focused on improving stability and quality across our production sites in Denmark.

You will therefore be spending most of you time on the production floor, supporting leaders in development of systems (e.g. performance boards, problem solving, process confirmation) to see, solve, and follow-up on problems, in a way that secures sustainable results and thereby coach others to use and continuously improve these systems. When it comes to solving problems you will in some occasions be responsible for driving the process, supporting others in implementing and sustain defined solutions and ensure confirmation of new standards.

Besides leaders in your area you work closely together with a wide team of LEAN Partners, HR Partners and Training Partners within your assigned area. An outcome of this will be cross functional LEAN projects, defining and supporting improvement projects in your area and ensure on-boarding of new leaders in respect to the LEAN framework in Novo Nordisk Product Supply.

You report to the Department manager and are part of the department management group and you have a dotted line to the LEAN Partner for the Vice President.

Qualifications
You hold a B.Sc., M.Sc. or similarly and through your studies and working experience you have gained a good understanding and have a great interest in being part of process production setup. You can give examples of being part of complex problem solving; demonstrate a systematic approach to problem solving, experience with applying different LEAN tools and experience that demonstrates a desire to drive change.

On a personal level, you have excellent communications skills both oral and written in Danish and English and show a natural interest in others. You are known as a fast learner with a desire to develop yourself and others and have a naturally strong personal drive and thrive driving your tasks independently. Are you talented and have the ambitions, taking up this job as LEAN Partner might develop you into a manager.

In Novo Nordisk is your skills, your commitment and your ambitions, which helps us to improve many people's lives. In return we offer you the opportunity to work with exceptionally talented colleagues, and we offer you a wide range of opportunities for professional and personal development.

Contact
For further information please contact Mogens Auchenberg +45 3079 4588 and Christian Goldbach +45 3075 0192 or Simon Riis Enghoff +45 3079 7521.

Deadline
11 August 2013

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Senior ingeniør til højteknologiske samle- og pakkelinjer (Måløv, Danmark)

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