Jobs at Novo Nordisk

Research Laboratory Technician

- Research & Development
- Denmark - Måløv

Are you interested in working with in vitro biology? If you find it exciting and inspiring to be part of a research team developing new insulin analogues for an improved treatment of diabetes, you may be our new colleague in the Insulin Biology department.

About the department
We are a department specialising in in vitro diabetes research with primary focus on insulin. We work in teams consisting of a scientist and one or more technicians, in close collaboration with the rest of the department. We contribute to many different research projects and are responsible for delivering high quality data and input to drive the projects forward. In the department, we are fourteen scientists, nineteen technicians, and several Post Docs and PhD students committed to the discovery of new and improved insulin analogues as well as new pharmaceutical peptides and proteins of therapeutic interest within diabetes care. We are located in modern facilities in Måløv as part of the Diabetes Research Unit.

The job
As a laboratory technician, you will participate in the in vitro characterisation and development of new protein based therapeutics for diabetes care. You will be employing a variety of analytical techniques such as ELISA, Western blotting, enzyme coupled assays, quantification of radioisotopes, cellular imaging, purification of DNA/RNA, and PCR by working with primary cell types and cultured cell lines. In collaboration with a scientist, you will participate in the planning and preparation of experiments as well as the development and establishment of new in vitro assays. You will also carry out the experiments in the laboratory and take active part in data handling and analysis. The working atmosphere is characterised by an open, cheerful and informal tone. Ultimately, your work will contribute to the improvement of the quality of life for millions of people with diabetes around the world.

Qualifications
You have an education as laboratory technician or similar and you have at least three years’ experience within research. Experience with biochemical, molecular and cell biological methods is considered an advantage. Since data handling and evaluation is part of your job, it is important that you have solid experience with Windows based programs. You have an independent approach to your work assignments, work in a systematic and focussed fashion and take responsibility for your work. In addition to your scientific profile you are an open minded person with a flexible and helpful attitude and good collaboration skills. We value sound humour as well as a healthy working environment.

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

Your application may in English or Danish.

Contact
For further information, please contact Tine Glendorf at +45 3075 6277.

Deadline
27 September 2013

Produktionskemiker

- Produktion
- Danmark - Hillerød

Har du lyst til, at arbejde med aseptisk fyldning via isolatorteknik? Og har du interesse for, at arbejde med procesforståelse og dokumentation af vores insulinfyldelinie.Så har vi det helt rigtige job til dig som kemiker for fyldelinien til processupport i Hillerød. Grib muligheden for en karriere med gode udviklingsmuligheder, en dynamisk hverdag og en stor kontaktflade i en international virksomhed.

Om afdelingen
Afdelingen producerer, fylder og inspicerer insulin af penne og har ansvaret for, at levere vores produkt i en høj kvalitet. Teamet består 23 engagerede medarbejdere der har ansvaret for driften i formulering, vask & sterilisation, fyld samt inspektion. Vores mål er, at være fagligt stærke og yde den bedste support til linierne og sikre stabilitet. Vi har en humørfyldt hverdag selvom der er travlt. Vi hjælper hinanden med respekt for hinandens profession.

Jobbet
Din primære opgave bliver at yde daglig support til driften af vores aseptiske fyldeproces. I tæt samarbejde med operatører, supportere, teknisk support og QA løser du en bred vifte af opgaver lige fra procesforbedringer, valideringer og afvigelsessager. Når der opstår udfordringer i vores produktion, er det dig, der sikrer overblikket, så problemerne kan løses hurtigt og effektivt. Din analytiske evne er vigtig, da den dagligt bruges ved de udfordringer hverdagen indebærer. Du bliver målt på din evne til at overholde deadlines og sikrer din succes ved at være en holdspiller. Du driver og prioriterer dine opgaver selvstændigt. Du er fagligt orienteret og sikrer, at afdelingen altid er i compliance med gældende lovkrav.

Kvalifikationer
Vi forestiller os, at du har en relevant akademisk uddannelse såsom produktions-, kemi-, maskin- eller procesingeniør, farmaceut. Uanset din baggrund skal du have viden om GMP – gerne relateret til aseptisk produktion eller fyldeprocesser. Har du tilmed erfaring fra farmaceutisk produktion (gerne FDA) samt kendskab til valideringsarbejde og LEAN, er det absolut et plus.

Som person er du lidt af en problemknuser og du skal være god til at prioritere dine opgaver selvstændigt samt være meget omstillingsparat. Du trives i en dynamisk hverdag, hvor din evne til at træffe beslutninger er helt essentiel. Da kvalitet og præcision er afgørende i lægemiddelindustrien, er det også vigtigt, at du er kvalitetsbevidst og har lyst til og erfaring med skriftlig dokumentation. Du har en fortrolighed med it og evner at sætte dig ind i nye systemer. Sidst, men ikke mindst, er du er udadvendt, bidrager med godt humør og dygtig til at kommunikere på tværs af faggrænser – både på dansk og engelsk.

Hos Novo Nordisk bruger vi vores kompetencer og dedikation til at hjælpe folk med diabetes og herved forbedre deres liv.

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

Kontakt
Vil du vide mere om stillingen, så er du meget velkommen til at kontakte Pia Morelli på +45 3075 7473.

Ansøgningsfrist
29. september 2013

Processupporter

- Produktion
- Danmark - Hillerød

Er procesforbedringer og valideringer lige dig? Og har du lyst til at arbejde med sterilisation og cleaning i en produktionsafdeling? Så har vi det helt rigtige job til dig som kemiker til processupport i Hillerød. Grib muligheden for en karriere med gode udviklingsmuligheder, en dynamisk hverdag og en stor kontaktflade i en international virksomhed.

Om afdelingen
Afdelingen producerer, fylder og inspicerer insulin og har ansvaret for, at levere vores produkt i en høj kvalitet. Teamet består 23 engagerede medarbejdere der har ansvaret for driften i formulering, vask & sterilisation, fyld samt inspektion. Vores mål er, at være fagligt stærke og yde den bedste support til linierne og sikre stabilitet.

Jobbet
Den primære udfordring består i, at yde daglig support til driften af vores vask og sterilisations område. I tæt samarbejde med operatører, supportere, teknisk support og QA løser du en bred vifte af opgaver lige fra procesforbedringer, valideringer og afvigelsessager. Du bliver målt på din evne til at overholde deadlines. Du sikrer din succes ved at være en holdspiller og have en positiv tilgang. Når der opstår udfordringer i vores produktion, er det dig, der sikrer overblikket og driver processen, så problemerne kan løses hurtigt og effektivt. Du er fagligt orienteret og sikrer, at afdelingen altid er i compliance med gældende lovkrav.

Kvalifikationer
Vi forestiller os, at du har en relevant akademisk uddannelse såsom farmaceut, kemi-, mejeri - eller procesingeniør. Uanset din baggrund skal du have viden om GMP – relateret til sterilisering og rengøringsprocesser. Har du tilmed erfaring fra farmaceutisk produktion (gerne FDA) samt kendskab til valideringsarbejde og LEAN, er det absolut et plus.

Som person trives du i en dynamisk hverdag, hvor din selvstændige evne til at træffe beslutninger er helt essentiel. Da kvalitet og præcision er afgørende i lægemiddelindustrien, er det også vigtigt, at du er kvalitetsbevidst og har lyst til og erfaring med skriftlig dokumentation. Du er udadvendt og god til at opbygge gode relationer og skabe et fagligt netværk. Sidst, men ikke mindst, er du god til at kommunikere på tværs af faggrænser – både på dansk og engelsk.

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

Kontakt
Vil du vide mere om stillingen, så er du meget velkommen til at kontakte Pia Morelli påpå +45 3075 7473 eller Stener Larsen på +45 3079 8381.

Ansøgningsfrist
28. september 2013

QC Chemist - Biopharm QC, Ka

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

- Production
- Denmark - Kalundborg

Do you have a drive and do you want to ensure the right quality on the analysis in Biopharm? Then you might be our new chemist in a QC laboratory where excellent performance is on top of the agenda. Become part of Biopharm QC in Kalundborg, where we support the production of the NovoSeven®.

About the department
Novo Nordisk, Biopharm QC, Ka performs chemical and biological analysis on API and we are on the verge of implementing new analyses for support to Biopharm AP. To keep up with the implementation of the new analyses while supporting the present production, we are in need for another ambitious HPLC QC Chemist.

The department consists of 48 dedicated employees divided into three teams. We have a busy and stimulating environment with lots of opportunities to develop both your professional and personal competencies. We are looking for a chemist for team QC Chemistry II (HPLC/VAND). Today the team consists of 9 laboratory technicians, 4 chemists and 1 Associate Manager.

By joining 48 enthusiastic colleagues in this department, you will have an opportunity to make a difference for people with haemophilia worldwide.

The Job
As a QC chemist, your objective is to secure the daily routine of analysis results and delivering these to our stakeholders. You do fast and quality compliant problem solving, this is crucial in order to meet the production targets. You have to be able to evaluate and solve challenges based on your analytical skill on a high GMP level. It is important that you can handle several tasks at the same time and can finish them in due time. You will have the responsibility of writing different documents such as SOP’s, qualification reports, change requests etc.LEAN is an important part of our daily work. You will be involved in systematic problem solving, optimisation and standardisation of processes to bring our products faster to market. We have a high focus on improvement of our processes both with regard to quality, costs and lead time.In this challenging environment and to make sure that we take action, you communicate your observations and ideas to relevant managers and other stakeholders.

Qualifications
Your background is a relevant Master’s degree within the natural sciences, and as such you could be a Chemist, Chemical Engineer, Biologist or Pharmacist. On top of this, you have solid insight into GMP processes and in particular you have experience in working with the HPLC technique. To achieve success in this job, you are tuned in on sharpening and acquiring new skills to become the best at what you do. You can easily picture yourself thrive in a complex organisation where processes and circumstances change, and you deal with colleagues of different backgrounds. Besides your quality-mindset, you have a winning attitude and focus on achieving your goals. You also have a positive, cooperative spirit and are known for taking action and following through on your tasks. Eventually, you master English as well as Danish.

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

Contact
For further infomation please contact Martin Skipper at +45 3079 9663.

Deadline
30 September 2013

Global Forecasting Manager

- Marketing
- Denmark - Søborg

Are you excited by understanding complex market dynamics and assessing the impact of strategic decisions and initiatives? Do you have the numerical and analytical skills to analyse and project the performance of Novo Nordisk products in markets around the globe? Can you process and combine information from various sources to synthesize assumptions and forecast future market development?

About the department
Strategic Analytics, Insights & Forecasting department, part of the ‘Commercial Planning’ area in Marketing & Medical Affairs focuses on analysing market dynamics, identifying trends and forecasting market development, as well as providing insightful analyses to senior management and other parts of the organisation.

The job
You will be part of a highly motivated, customer-centric and performance-driven team in a position which offers: Broad insight into the Novo Nordisk worldwide business. Ongoing participation in cross-functional projects . International exposure and collaboration with teams across departments and geographies. Dynamic development opportunities.

Your responsibilities in this challenging job opportunity will include: Participating in the Strategic Planning Process and developing the long term forecast for key Novo Nordisk products. Assessing the sales potential of products in the mid to late development phases. Identifying & synthesizing data and critical information from various sources, to shape recommendations and inform strategic decision-making. Communicating key insights and analyses to relevant stakeholders within the organisation.

Establishing and maintaining a partnership with teams within HQ, regional and affiliate organisations.

Qualifications
The ideal candidate will have the following qualifications: A degree in business/Economics/Mathematics/ Engineering and a Master’s degree in a related field. MBA considered an asset. Experience in product sales forecasting and market analysis, preferably within the pharmaceutical industry. Robust numerical and analytical problem-solving skills. Ability to work independently, with a track record in delivering high quality outcomes within predefined timelines. Ability to collaborate with team and key customers, maintaining a strong customer focus and positive outlook. Good communication and influencing skills. High level of proficiency with Excel. Experience in SAP and programming skills in SAS considered an asset. Fluent in English.

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 Yiannis Mallis on + 45 3079 6876.

Deadline
22 September 2013.

Academic for Quality Assurance of API Development

- Quality
- Denmark - Gentofte

Do you want to unfold your profound QA knowledge and your huge appetite for creating results in a pharmaceutical production environment? If so, please apply for the position as QA Academic in a job that includes many different clinical stages of the product development.

About the department
In Chemistry, Manufacturing & Control (CMC) API QA we assure that each and every Active Pharmaceutical Ingredient (API) activity in our development and support projects live up to the cGMP requirements. The development portfolio is expanding and thus we seeking a new colleague to help us support the growth.We are 29 colleagues in three teams. You will join the downstream team and have 12 dedicated colleagues. Our mission is to assure that our manufacturing processes, intermediates and finished API (purification and chemical synthesis) meet the internal and external requirements. Furthermore we’re responsible for release of API for all of Novo Nordisk’s clinical trials. The production facilities and the development laboratories are located in Bagsværd, Gentofte and Måløv, and you will move between the different locations and the QA office on a day-to-day basis.

The Job
You assure best-in-class quality of our new manufacturing processes and API for clinical trials. Document approval in connection with development, manufacture, stability and release of API for clinical trials as well as maintenance and improvement of the quality system (SOP’s) will constitute some of your daily tasks. In addition, you will participate in our development projects and in close cooperation with your colleagues you identify and contribute to the strengthening our stakeholders’ compliance level and act as a consultant for them.We operate in a LEAN-dominated environment, and you will have the opportunity to contribute with ideas for improvements and drive the subsequent implementation as well. Working within QA will definitely challenge your professional and individual skills, and you will find that your tasks cover many different clinical stages of the product development.

Qualifications
You hold a Master’s degree in Pharmacy, Chemical Engineering or possess equivalent qualifications besides a strong quality mindset. You have at least 3 years’ experience with GMP, product release, production or quality assurance. As we operate in an international environment, you must speak and write English fluently.You are ambitious and determined on creating world-class results and ensure quality of the highest order. Moreover, you thrive in a role where you use your knowledge and bring your arguments and negotiation skills into play. You are able to adapt but also challenge our way of working so that we constantly improve our methods and processes.

At Novo Nordisk, you will be part of a company respected equally for its financial results and its business ethics. Across geographical, cultural and professional communities we develop and deliver innovative medicines.

Contact
For further information, please contact Peter Søtofte Elten at +45 3079 8453.

Deadline
06 October 2013.

Supportkemiker

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

- Produktion
- Danmark - Kalundborg

Får du energi af en dynamisk hverdag med megen omskiftelighed og spændende udfordringer? Kan du ikke lade være med at tage ansvar, og er du typisk den, der sætter skub i de daglige opgaver? I så fald er du måske vores nye kollega i Purification Support.

Om afdelingen
Du er en del af Novo Nordisks insulinproduktion (DAPI), hvor vi i IM2 leverer human insulin til færdigvarefabrikker i hele verden. Du bliver en del af driftssupport-teamet i finrens, hvor vi er 20 kolleger bestående af teknikere og kemikere. Vores mål er at sikre at produktionen af Human Insulin forløber så stabilt som muligt.

Jobbet
Dit ansvar er helt overordnet sammen med dit team at sikre en stabil produktion. Din primære kontaktflade er QA, operatører og laboratorier, og din arbejdsplads er på Novo Nordisks site i Kalundborg.

Du bliver procesansvarlig på en delproces, hvilket betyder at din dag bliver en blanding af at være på gulvet med dine kolleger og at håndtere de administrative opgaver ved dit skrivebord. Dine opgaver er at følge op på produktionen, håndtere hændelser og ændringssager, dokumentere justeringer og dermed sikre videndeling på tværs samt drive ændrings- og optimeringsprojekter. Alt sammen skal understøttes af viden om og forståelse for kvalitet, et LEAN mindset samt en engagerende og involverende tilgang til samarbejdet med produktionen. Dit erfaringsniveau påvirker opgavernes kompleksitet og kan dermed tilpasses dig, hvad enten du er nyuddannet eller erfaren.

Du bliver en del af et socialt velfungerende team med en stor faglig erfaring, der står over for en spændende udfordring, som er at skabe stabile processer, samtidig med at kapaciteten øges gennem optimering.

Kvalifikationer
Du har en akademisk naturvidenskabelig uddannelse, hvor du har tilegnet dig en god procesforståelse. Det kan være som kemiingeniør men også maskiningeniør, Cand. Pharm eller relevant cand.scient, hvor du via erfaring eller fag har tilegnet dig procesforståelse. Er du nyuddannet skal du besidde et enormt drive for at lykkes i stillingen, og du skal lykkes med en stejl læringskurve. Du taler og skriver flydende engelsk og dansk.

Da du bliver en del af en stor organisation er det vigtigt, du har erfaring med at skabe relationer, og at du får du energi af et miljø, hvor du hele tiden skal omstille dig og prioritere dine opgaver. Ud over det har du både på og uden for dit studie bevist, at du er en af driverne, når der skal tages handling, og at du smitter dine omgivelser med dit vindende væsen og gode humør.

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

Kontakt
Vil du vide mere om stillingen så kontakt Peter Sørensen på +45 3079 2718.

Du kan lære mere om Novo Nordisks største produktionssite ved at bruge linket www.novonordisk.com/kalundborg-careers.

Ansøgningsfrist
13. oktober 2013

Kvalitetskoordinator

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

- Produktion
- Danmark - Kalundborg

Kan du lide at gøre en forskel og har du lyst til at være en del af Novo Nordisk fortsatte vækst og gode resultater? Hvis du kan svare ja til de spørgsmål og du samtidig har lyst til at arbejde med produktion af lægemidler med høj kvalitet – Så er du måske vores nye kollega. Vi søger en dygtig og engageret kvalitetskoordinator som er indstillet på at drive kvalitets og compliance opgaverne i et dynamisk miljø i en af de mest traditionsrige fabrikker i Diabetes API (DAPI).

Om Afdelingen
Du vil blive en del af leder/stabs teamet i afdelingen bestående af afdelingslederen, 6 teamledere og en cLEAN koordinator og vil der ud over samarbejde tæt med afdelingens 20 engagerede og dygtige teknikere og kemikere. Afdelingen er en del af Insulin Manufacturing II og består af ca. 150 medarbejdere der finrenser human insulin. Insulin Manufacturing II er en del af Diabetes API der beskæftiger godt 2.500 medarbejdere fordelt på 9 fabrikker, som tilsammen producerer ca. 50% af den insulin der hver dag benyttes af diabetikere over hele verden. Afdelingen og funktionsområdet er kendetegnet ved sine engagerede og målrettede medarbejdere som dagligt arbejder for, at området fortsat kan være førende indenfor produktion af API, som anvendes til Novo Nordisk forskellige diabetes produkter.

Jobbet
Du kan se frem til en spændende og udviklende stilling med gode muligheder for selv at påvirke din dagligdag og dine opgaver. I jobbet som kvalitetskoordinator kan du udvikle dig fagligt inden for blandt andet GMP og koordinatorrollen og dette kan give adgang til karrierer indenfor kvalitetsområdet, andre koordinatorstillinger eller ledelsesvejen.

Du vil få det daglige ansvar for kvalitets- og compliancerelaterede opgaver i afdelingen. Dette indebærer bl.a., at det er din opgave at medvirke til, at vi efterlever og implementerer kvalitetskrav fra myndigheder og fra Novo Nordisk’s kvalitetssystem. I den sammenhæng vejleder og motiverer du dine kollegaer og sammen sørger I for, at vi når vores kvalitetsmål i afdeling og området. En del af dette vil være at sikre planlægning og opfølgning på afdelingens QAP, NC’er og CR-sager. Du står for områdets QMR-proces samt planlægning og gennemførelse af interne audits, kunde audits og myndighedsinspektioner, ligesom du som medlem af områdets kvalitetsgruppe sikrer en løbende udvikling og optimering af vores kvalitetsstyringssystem. Du kommer til at arbejde internt med afdelingens kvalitetsmål, men ligeledes på tværs af afdelingerne i IM2, hvor du vil få et tæt samarbejde med de øvrige kvalitetskoordinatorer i andre afdelinger i IM2.

Kvalifikationer
Du har helt sikkert solid erfaring med kvalitet og/eller GMP produktion og gerne en relevant naturvidenskabelig uddannelse (Farmaceut, kemiingeniør, cand. scient. el. lign.). Det er vigtigt at du har gode kommunikationsevner fordi du som kvalitetskoordinator kommer til at bidrage væsentligt til det gode samarbejde med mange faggrupper. Det er endvidere vigtigt, at du arbejder systematisk og kan prioritere dine opgaver. Du har det store overblik, når du skal træffe kvalitetsmæssige beslutninger, men har også fagligheden med så du kan dykke ned i detaljen om nødvendigt. For at få succes i stillingen skal du være engageret og udvise høj grad af selvstændighed. Du trives i en hverdag med høj intensitet og stramme deadlines og ser det som din fornemmeste opgave at få fulgt opgaverne til dørs.

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 Stig Bruse Andersen på +45 3079 9901.

Ansøgningsfrist
6. oktober 2013

Business Analyst

- Business Support
- Denmark - Bagsværd

Are you motivated by complex analytical challenges? Can you handle large data sets and make sense of the numbers? And can you handle a diverse set of stakeholders with different views of the data? If you can answer yes to these questions, you may be the Business Analyst we are looking for in Business Support, Sourcing Operations, Bagsværd.

About the department
Sourcing Operations (SoOp) is the central purchasing area in Product Supply, responsible for purchasing and distributing/warehousing the thousands of materials going into the production worldwide. We are 12 dedicated colleagues in Business Support, among others responsible for supporting this complex setup in becoming still more effective and efficient. We are currently looking for a strong analytical and ambitious Business Analyst, who can analyse big data sets to uncover interdependencies and bottle necks in the flow of materials.

The Job
As a Business Analyst your main role will be to drive data analysis and participate in improvement projects, both in SoOp and broader in Novo Nordisk. You will enjoy a high degree of independence in your work, and get the opportunity to e.g. define KPIs, reporting tools, and necessary analysis. An important part of your job will be to work with the SoOp organization, ensuring the right understanding and usage of data, hence providing you with the opportunity to thoroughly getting to know the supply chain within Novo Nordisk and work with a team of highly dedicated colleagues.

Qualifications
You hold a relevant Master's degree (i.e. in Business, Engineering or Supply Chain Management) with excellent results, and you have some years of experience from a similar position. Ideally, you have system understanding of SAP BW, as well as a high competency level of MS-Excel and basic knowledge of PPT.

As a person, you have excellent process understanding, an analytical mind-set and you know how to get to the core of complex problems and make them understandable for others. You have the ability to work independently, develop your own expertise, explore various possibilities and structure your own work. Furthermore, you possess good communication skills and are keen on coordinating and navigating between many stakeholders in a busy environment. Lastly, you speak and write English fluently.

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

Contact
For further information, please call Anne-Kristine Prag on +45 3075 7094.

Deadline
14 October 2013.

QA Professional

- Quality
- Denmark - Gentofte

Would you like to join us in making a difference to people in need of glucagon and growth hormone. Would you like to be responsible for quality assurance of qualification and validation tasks? A job is waiting for you in a challenging and developing environment.

About the department
In Biopharm QA API Gentofte you will join a team with 6 engaged employees. Together we assure quality and compliance in the production of growth hormone and glucagon. The working relations are informal and the team values professional sparring and good humour highly. The team responsibility covers the release of the product, approval of instructions and qualification and validation, processing of change and nonconformity cases and various other tasks.

The job
You are responsible for qualification and validation of the challenging and changing facilities for manufacture of hGH and glucagon. The facilities face major changes and challenging tasks within IQ, OQ, PQ computer and cleaning validation. An important element of the job involves cooperation with the project team, production department and process QA. Quality is the key words and therefore it is natural for you to have an ongoing dialogue and good relations with your stakeholders regarding how we ensure quality and compliance. The position offers you a unique opportunity to leave your mark on the department while realising your goals and seeing the benefits of your work. When you start you will undergo an individual and intense training program.

Qualifications
You have a Master of Science degree. You are familiar with GMP and the requirements of the authorities in the pharmaceutical industry. Ideally you have several years of experience within validation and qualification. You work systematically and can take a comprehensive view and you are not afraid of taking decisions. Moreover, you are purposeful and able to prioritise several tasks in a changing environment

Precise communication is absolutely essential and you must be capable of taking part in constructive cooperation concerning the various tasks and have the kind of impact that means you can stand firm in favour of product and user safety. Your language skills cover proficiency in both Danish and English.

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

At Novo Nordisk we use our skills, dedication and ambition to help people in need of glucagon and growth hormone. By working with us you will have the opportunity to do the same in a global business environment.

Contact
For further information, please call Lotte Solvang Christensen on +45 3075 8846 or Ulla Falkenberg on +45 3075 8890.

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

Deadline
29 September 2013.

QA Associate Manager

- Quality
- Denmark - Gentofte

Do you want responsibility for developing people and optimizing processes in a core part of Novo Nordisk’s QA organisation? You will be part of a highly competent QA team responsible for the quality assurance of growth hormone. Since our current Associate Manager has been promoted internally, we are now looking for a new colleague to join our team.

About the department
In Biopharm QA API Gentofte you will join a team with 6 engaged employees, team hGH. The team assures quality and compliance in the production of growth hormone. The working relations are informal and the team values professional sparring and good humour highly.

The team responsibility covers the release of the product, approval of instructions, validation, processing of change and non-conformity cases, and various other tasks

The job
As Associate Manager in Biopharm QA API team growth hormone you are the leader of 6 highly skilled and motivated QA professionals. The team provides quality assurance for the hGH purification process and as associate manager you are involved both as QA as a representative of the department management. You set a good example and lead the way to ensure that your employees obtain the right behaviour and achieve the targets all to the benefit of the end user.

You act as a competent sparring partner to your team - coaching and empowering employees to deliver excellent results. You collaborate with the production department in a professional and amicable way and collaborate to overcome disagreements while having in mind the importance of quality mindset and compliance.

Qualifications
You have solid working experience from a QA organization which ideally is from a similar role in a pharmaceutical company and your experience is backed by a relevant Master of Science degree. You set and communicate a clear direction for your team. You display a high level of personal engagement, drive, persistence and integrity.

Precise communication is essential and you must be capable of taking part in constructive cooperation concerning the various tasks and have the kind of impact that means you can stand firm in favour of product and user safety. Your language skills cover proficiency in both Danish and English.

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

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

Contact
For further information, please call Lotte Solvang Christensen on +45 3075 8846 or Ulla

Falkenberg on +45 3075 8890.

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

Deadline
29 September 2013.

Materials Expert

- Research & Development
- Denmark - Hillerød

Are you looking for a job where you unlock your engineering talent and work with state-of-the-art technology? Please apply for a position as Material Expert and contribute to the development of the world’s most innovative injection devices. In this job you will impact the everyday of people with diabetes and other chronic diseases.

About the department
You will join a team of 6 highly skilled Engineers in the Materials team in Hillerød. We are part of Device R&D Competency Centre and support medical device projects with selection of materials, measurement of material properties, failure analysis, biosafety and environmental assessments. You will have a key role among innovative device engineers who invent and create the world’s future injection devices.

The job
As representative of the Competence Centre you will take a role as material expert and contact person for the device development projects. You will support the projects with your knowledge and expertise as well as facilitate contact to other relevant experts from the Competence Centre when needed. Based on your strong skills you will support the projects with requirement based materials selection within at least one of the topics below:

Thermoplastics and rubbers, preferably including short fiber reinforced materials coatings for metallic components, e.g. springs, contacts etc.

Electromechanical/mechatronics

Metallic components

An in-depth understanding of high volume manufacturing processes for plastic and metallic parts will be highly advantageous. You will assist the projects in evaluating material candidates based on review of technical data and use your experimental expertise to produce material data if relevant data are not available.

You work closely together with experts within design, structural calculations, processing and sourcing. Another important task is to identify best practice and create improvements for methods, techniques and approaches. Lastly, you review device designs and train R&D engineers in selection of materials.

Qualifications
Optimally, your solid experience with materials is combined with a Master’s or a Bachelor’s degree within Mechanical Engineering. Alternatively, you have another engineering degree and profound knowledge of measurement of material properties – in particular plastics. Either way, you are able to manoeuvre in the interface of a cross-functional organisation and set directions for your own results. You thrive in a job where you solve complex problems in an international environment, and you are comfortable keeping track of many stakeholders. This calls for excellent collaboration and communication skills, a convincing attitude and the ability to secure buy-in from your stakeholders. Lastly, you are able to make yourself heard in a large organisation.

At Novo Nordisk, decisions and actions are based on their positive impact on society, the environment and on their potential to generate a profit. That makes for a responsible culture with a healthy and engaging working environment.

Contact
For further information, please contact Team leader Sisse Louise Lund at +45 3079 2456.

Deadline
29 September 2013.

Quality & cLEAN Coordinator (Professional)

- Production
- Denmark - Bagsværd

Do you have experience with GMP, and can you handle a great variety of tasks from identifying and driving projects over writing Standard Operating Procedures to setting and following up on goals? If you thrive on working with quality and compliance in a LEAN manner, you could be our new Quality & cLEAN coordinator.

About the department
You will join QC Packaging Materials in Bagsværd. We are responsible for quality control of printed and primary packaging materials to production departments in Denmark and abroad. Today we are 39 employees in two teams. You will be referring to the department manager and will become part of our management team. Our focus is to deliver high quality adhering to agreed deadlines and budgets every time.

The job
Your overall objective is to help us set and meet the department goals within quality and compliance, and make sure that our way of doing things represent best practice. You coordinate and are operationally responsible for quality and cLEAN projects where you

define milestones and ensure that we meet the agreed deadlines. As such, you will be in charge of different improvement projects in the department and be part of cross-organizational groups. As quality coordinator you will have an important role in ensuring high standards in compliance with regulations and procedures. You are also responsible for the departments input to the Quality Management Review (QMR), and you play an active role in audits and inspections. Following up on targets and facilitating our incidents handling are other tasks on your agenda. All in all, you can look forward to an exciting and challenging job.

Qualifications
Your background is a master’s degree most likely within the natural sciences. You have experience with quality, GMP and ISO9001, including hands-on experience with quality control. In addition, you share our interest in meeting high standards in everything we do. If you do not have practical experience with LEAN already, you are eager to learn all about it. You are known to be very structured, and you can analyze an incident and pinpoint the cause and afterwards adjust methods/procedures/processes in order to prevent the problem from recurring. As quality and cLEAN coordinator you must also thrive on having contact to many people, and you can use your good communication and interpersonal skills to make your contacts co-players on your quality agenda. To succeed, it is also vital that you can independently plan and drive your own tasks. Likewise your ability to balance when to compromise and when to stand firm will be crucial.

Finally, you must master English and Danish, written and spoken.

At Novo Nordisk, you will help millions of 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 Marie-Louise Haldbo at +45 3075 4206.

Deadline
28 September 2013.

QA Chemist - Temp.

- Quality
- Denmark - Bagsværd

Do you want a key role in ensuring the quality of the insulin products and compliance with regulatory requirements? If so, then seize the opportunity and join QA of the aseptic production (AP) in Site Denmark.

About the department
In QA AP we are responsible of assuring quality and compliance in the aseptic production of insulin products in Site Denmark. It is our responsibility that the documentation related to the aseptic production is in compliance with regulatory requirements and the Novo Nordisk quality management system.

In QA AP you will join a department of 46 highly motivated and dedicated employees which is divided in three teams - two teams in Bagsværd and one team in Hillerød. In a close collaboration with the production we ensure a high level of quality and play a key role in releasing insulin products to diabetics all over the world.

We are at the moment looking for a QA chemist (maternity temp, 12 month) to our chemist- and principal scientist team in Bagsværd.

The Job
As a QA chemist you will be a decisive factor in making sure that the released products lives up the current GMP and regulatory requirements. You will be involved in the handling of incidents in the production and participate in systematic problem solving together with process support and production. Likewise, you will perform different tasks related to quality assurance, e.g. approval of batch documentation and production related documents. We operate in a LEAN environment where we focus on optimising our processes. You will therefore be involved in the implementation of new initiative which can optimise our daily work.

Qualifications
You hold an academic degree and preferable your academic background is topped with work experience from the pharmaceutical industry. On a personal level you are known for you positive mindset, flexibility and persistence. You have a strong quality mindset, meet your deadlines, and know how to prioritise between different tasks in a dynamic environment. You like and are good at coordinating different tasks for both yourself and other people and you demonstrate an ability to find the right solutions with your colleagues. Your language skills cover proficiency in both Danish and English.

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

Contact
For further information, please contact Henriette Kyed, +45 3075 2194.

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

Deadline
29 September 2013

Administrator

- Administrative
- Denmark - Bagsværd

Do you want to be part of a team that handles customer complaints from around the world? Then we might just have the right job for you.

About the Department
The Customer Complaint Center (CCC) is responsible for processing and monitoring customer complaints received through Novo Nordisk’s international subsidiaries for all Novo Nordisk’s products. We work closely together with departments monitoring side effects, and with production sites and laboratories.

CCC comprises 50 colleagues organized into 4 teams. We have an informal, busy and collaborative environment along with contact with colleagues throughout Novo Nordisk world-wide. We now seek a colleague for a 12 months temporary position (until 30. Sept. 2014) in the team responsible for investigating customer complaints within Prefilled Devices.

The Job
You will be part of a dynamic team consisting of 12 dedicated employees. Responsibilities include registering, processing and responding to complaints on Novo Nordisk products in our customer complaints IT system. This covers receiving complaints from affiliates around the world to documenting the final investigation results. Product testing/examination and batch trending are integral parts of the complaint handling process as well as maintaining a network of contacts within HQ, affiliates and production sites throughout the world. Additionally you will assist with related administrative and procedural activities as required or requested

Qualifications
You have an education as nurse, pharmaconomist or medical secretary or otherwise have experience with and knowledge of medicinal terminology.You have administrative and GxP experience. Familiarity with Novo Nordisk products is advantageous.

You are reliable, loyal and service-minded. You have a can-do attitude, enjoy working according to tight deadlines and master good coordination and cooperation skills. You have solid IT skills and work in a structured manner with a sense for details. It is essential that you can act independently, but also as a team player who thrives on contributing to any team you are part of. You have the ability and willingness to adjust quickly to new situations in a continuously developing environment. Fluency in written and spoken English is essential.

At Novo Nordisk 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
If you have questions, please contact Morten Gadgaard +45 3079 7487.

Deadline
30 September 2013.

Chemist

- Research & Development
- Denmark - Bagsværd

Do you dream about working with optimization and support? Do you have substantial experience with protein purification? Then you might be our new chemist for the purification team in Diabetes API (DAPI) Process Support.

About the department
You will join Manufacturing Development (MDev) where you can look forward to become part of a dynamic and well-functioning team consisting of 6 research scientists, 6 laboratory technicians and a project manager. We enjoy scientific challenges; we work independently with great responsibility and with a high level of commitment. We have many contacts/stakeholders in the organization including DAPI, CMC (development), RA (regulatory affairs), QA and others. The department is located in Bagsværd, but has also offices in Kalundborg, and you should expect to work there approximately 1 day a week.

The job
DAPI Process Support provides support to DAPI’s production departments (located in Kalundborg) within the areas: process optimization, troubleshooting and transfer of new processes from development to production. We are responsible for the completion of process characterization of development projects. As we support the API production, your job will be to contribute to continuous stable operations and quality in the running productions. You will, among other things, be working with exciting optimization projects focusing on improving quality, capacity and cost efficiency. Your field of work will, among other things, be: commenting on process deviations, planning and reporting on laboratory experiments, preparation and maintenance of SOP’s and scientific discussions with our production.

The position offers opportunities to be creative and to test optimization proposals in our laboratories. Since the job is mostly self-organized, it is very important that you are able to prioritize work assignments as well as being comfortable in a changing and sometimes hectic environment. In this job you can look forward to the possibility of personal as well as professional development.

Qualifications
We imagine that you hold an educational background as Engineer, Cand. Scient., Pharmacist or similar and have several years of experience within protein chemistry, protein purification or similar. As a person you work independently, are able to handle a complex workday and are comfortable with a close and cheerful collaboration with your team and department. You are responsible, flexible, and have the courage and urge to engage in new assignments and stick to them until the job is finished. It is important that you are a good communicator, since you are in daily contact with other chemists, technicians, production employees, project managers, analytical laboratories and others. Beyond this, we expect you to be an open and outgoing person with a positive mindset which will be an advantage in our working environment where a good laugh is appreciated even when things are getting hectic.

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.

Feel free to submit you application in either English or Danish.

Contact
For further information, please contact Kristoffer Laursen at +45 3079 5458.

Deadline
6 October 2013.

Research Scientist/Principal Scientist

- Research & Development
- Denmark - Måløv

Novo Nordisk is a protein-based, focused healthcare company. For the past 90 years Novo Nordisk has pioneered therapeutic proteins to address unmet medical needs. Today, more than 6,000 employees work with R&D across the globe.

About the department
The Structural biology department is an integral part of the Diabetes Protein Engineering function with the task of providing structure based design of therapeutic proteins and peptides with improved pharmacological and formulation properties for the treatment of diabetes.

We are 10 enthusiastic individuals located in Måløv, Denmark, with expertise within protein modelling, X-ray crystallography, small angle X-ray scattering and protein chemistry.

The job
As a key member of discovery research projects you will proactively utilize, communicate and leverage bio-structural information to guide the design of biopharmaceutical molecules within a multi-dimensional chemical and formulation space.

You will provide protein homology models, perform advanced data mining and analysis and apply molecular dynamics calculations in interpretation of experimental data such as NMR and SAXS with the ultimate goal of designing compounds with improved biological, physical and pharmacological properties.

You will have the opportunity to influence your own development and grow into a key role at the interface of between protein chemistry, structural biology, formulation and pharmacology.

Qualifications
You hold a PhD in Computational Chemistry, modelling or a related discipline and have at least three years of post-doctoral experience. Previous experience from pharmaceutical industry would be a plus.

You have expert knowledge of computational aspects of 3D molecular structure and design (such as protein homology modelling, MD simulations), preferably coupled with hands-on experience in SAXS or NMR. Additional relevant skills within advanced large scale data analysis techniques and protein protein docking are highly desirable, as is familiarity with commercial molecular modelling and data-mining software.

You are fluent in English and good to share results and interact with scientist of different disciplines

You are enthusiastic about driving discoveries and have demonstrated scientific excellence by publication in peer reviewed journals and patents. You are skilled in extracting information and articulating clear and convincing hypotheses.

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 Gerd Schluckebier at +45 3079 4119.

Deadline
18 November 2013

Arkiveringsvikar

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

- Administration
- Danmark - Kalundborg

Søger du nye udfordringer, er muligheden her. Vi søger en engageret og serviceminde vikar i 9 mdr til arkivering for vores laboratorie i Kalundborg.

Om afdelingen
Kompetent vikar til arkivering søges til IM1 Laboratory i verdens største insulinfabrik (IM1) i Kalundborg. Vores fabrik består af flere afdelinger, der tilsammen har ansvar for fermentering og oprensning af insulin samt for laboratorium og support, - alt i samme enhed.

Laboratoriet består af 40 medarbejdere fordelt i 2 team og en ledergruppe.

Stillingen kræver nært samarbejde med vores dokumenthåndterings- og arkiveringsgruppe i Business Support afdelingen. Gruppen består af 3 personer, der sikrer, at al dokumentation håndteres korrekt fra sagsoprettelse til sagsafslutning, herunder korrekt arkivering.

Jobbet
Du vil i samarbejde med arkiveringsgruppen, teamleder og lokal laboratorie arkivar planlægge overførsel af lokalarkiv til centralarkiv. Herefter vil du være ansvarlig for at al dokumentation bliver korrekt registreret og flyttet.

Vi forventer derfor, at du har lyst til at arbejde struktureret og har lyst til kontinuerligt at arbejde med at sikre dokumentationen er korrekt opbevaret og systemet gennemskueligt og gør os i stand til at finde data på kort tid.

Kvalifikationer
Du har en uddannelse som teknisk assistent eller lignende og har lyst til administrativt arbejde. Du sætter som nævnt kvalitet i højsædet, og vi vil lægge vægt på, at du har gode samarbejdsevner, er systematisk og analytisk.Vi forventer, at du er initiativrig og engageret, er i stand til at arbejde selvstændigt, samt er god til at bevare overblikket selv med mange bolde i luften. Har du erfaring med cGMP, LEAN eller vores it-systemer, (Docsys eller OmniRIM), er dette naturligvis en fordel.

Novo Nordisk i Kalundborg

Novo Nordisk i Kalundborg er en by i byen. Området er beliggende en god times tid fra København og dækker over 1.350.000 m2 med eget vejnet. Vi producerer ca. 50 % af verdens insulin. Vi arbejder helt på forkant af udviklingen inden for teknologi, systemer, metoder og processer. Er du vores nye kollega, kan vi garantere muligheder, du vil have svært ved at finde andre steder.

Kontakt
Vil du vide mere om stillingen, så kontakt Annette Musiat på +45 3075 0902.

Ansøgningsfrist
23 November 2013

Business Information Scientist - Vikariat

- Forskning og Udvikling
- Danmark - Bagsværd

Er du interesseret i medieovervågning og informationsanalyse? Og har du lyst til at bidrage med dit talent og dine evner i bl.a. kampen mod diabetes? Så er det måske dig vi søger til vores team, Business Information Research. Vi leverer vigtig information til mange forskellige afdelinger i Novo Nordisk, herunder Research & Development, som vi hører til. Vi har, hurtigst muligt, brug for dig til et 6 måneders vikariat til en stilling i et dynamisk team bestående af yderligere 5 dygtige kolleger.

Om afdelingen
Global Information & Analysis (GLIA) består af +40 medarbejdere i Danmark og USA. Vi arbejder professionelt med informationssøgning og analyser internt i Novo Nordisk.

Jobbet
Din fornemmeste opgave som Business Information Scientist er at iværksætte informationssøgning i henhold til den enkelte kundes behov. På den måde er dit arbejde med til at danne beslutningsgrundlag for dine kunder, som spænder fra forskningsenheder til ledelsesniveau. Du har brug for et skarpt blik for informationsanalyse og grundig medieforståelse. Med et forretningsorienteret fokus foretager du også hver morgen den daglige medieovervågning på relevante områder sammen med dine kolleger i teamet.

Kvalifikationer
Din uddannelsesmæssige baggrund kan være kandidat i informationsvidenskab og kulturformidling, bibliotekar eller en kandidatgrad inden for en af samfundsvidenskaberne. Det er ikke så vigtigt om du har års erhvervserfaring med i bagagen, det er vigtigere at du besidder en god portion udadvendthed, et stærkt forretningsorienteret fokus, et innovativt mindset tilsat både selvstændighed og engagement. Desuden behersker du naturligvis flydende engelsk og dansk.

I Novo Nordisk baseres beslutninger og handlinger på deres indflydelse på samfundet, miljøet og muligheden for at skabe økonomisk overskud. Det skaber tilsammen en ansvarlig kultur med et sundt og engageret arbejdsmiljø.

Kontakt
Vil du vide mere om stillingen, så er du meget velkommen til at kontakte Karen Gleerup på +45 3079 7123.

Ansøgningsfrist
24. november 2013

Dynamic Quality Consultant for manufacturing

- Quality, senior position
- Denmark - Gentofte

We seek a Quality Consultant to ensure that our work is compliant with GMP and in line with Novo Nordisk QMS and to ensure that our aseptic production is in compliance with regulatory requirements.

About the department
Our department covers the complete API manufacturing process, from fermentation and recovery to liquid purification and freeze drying. We are organized in four teams, where two teams cover production (fermentation and purification) and two support teams.As a GMP Consultant you will join the management team consisting of four team leaders, two specialists and the department manager to whom you will report directly. You will be the primary responsible for the ensuring the compliance level which will be one of the primary focus areas in the department in the coming years.You will become part of a team which have a high level of self-governance. The working relations are informal and the team value professional sparring and good humour highly.

The Job
Together with the Management team you will be responsible for ensuring that we comply with Novo Nordisk’s quality system. As such, you participate in determining the quality objectives, and through planning and follow-up on quality activity plans and conduction of quality management reviews you ensure that the standards are met. In this respect, you will cooperate across the entire area and have close interaction with Quality Assurance. In this way, you provide sparring and consulting on quality and compliance inquires, as well as you interpret processes and come up with quality enhancing initiatives on the problems and improvements that you face in your everyday.In addition, you will drive and coordinate the quality work and secure continuous improvements of audits and inspections, as well as you coordinate and conduct training within GMP.

Qualifications
You hold an academic degree (e.g. engineer, chemist or pharmacist), and you have more than 2-3 years of practical experience with GMP and ISO9001 in pharmaceutical production or QA. You might even have experience with line management and/or project management, and are capable of working in all levels of the organisation. You take pride in reaching you targets on time, and are able to do so with limited guidance from your superior.

As a person you have an infectious energy and a drive for creating results in close cooperation with others. You have daily contact with many different types of employees, and the ability to communicate and create strong relations is therefore a necessity in order to be successful in the position as GMP consultant.

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.

Feel free to submit your job application in either English or Danish, whichever you prefer. Applications are reviewed on a rolling basis so please apply as soon as possible.

Contact
For further information, please Contact Søren Jensen on + 45 3079 1257.

Deadline
26 November 2013.

Research Laboratory Technician (Måløv, Denmark)

Produktionskemiker (Hillerød, Danmark)

Processupporter (Hillerød, Danmark)

QC Chemist - Biopharm QC, Ka (Kalundborg, Denmark)

Global Forecasting Manager (Søborg, Denmark)

Academic for Quality Assurance of API Development (Gentofte, Denmark)

Supportkemiker (Kalundborg, Danmark)

Kvalitetskoordinator (Kalundborg, Danmark)

Business Analyst (Bagsværd, Denmark)

QA Professional (Gentofte, Denmark)

QA Associate Manager (Gentofte, Denmark)

Materials Expert (Hillerød, Denmark)

Quality & cLEAN Coordinator (Professional) (Bagsværd, Denmark)

QA Chemist - Temp. (Bagsværd, Denmark)

Administrator (Bagsværd, Denmark)

Chemist (Bagsværd, Denmark)

Research Scientist-Principal Scientist (Måløv, Denmark)

Arkiveringsvikar (Kalundborg, Danmark)

Business Information Scientist - Vikariat (Bagsværd, Danmark)

Dynamic Quality Consultant for manufacturing (Gentofte, Denmark)