Jobs at Novo Nordisk

Senior system manager to create framework for IT portfolio

- Research & Development
- Denmark - Søborg

Are you interested in working with Clinical IT Systems? Do you want to be a key player in the link between end users and the system? Do you like a challenging and rewarding workplace? Do you like having a broad and daily contact with colleagues and users from around the globe?

About the department
Then you might be our new senior system manager. Clinical Systems Management, consisting of 25 functional system supporters, is responsible for support to users and super users, development of processes and systems that Novo Nordisk use for collecting and processing data for our clinical trials. Our department is working closely with internal as well as external partners.

The job
We are seeking a new colleague to take up a position as senior system manager, responsible for establishing a framework for system management of smaller IT systems and tools, and supporting local managers in using this framework. Novo Nordisk has a solid system management framework to ensure compliance to internal and external requirements for our corporate IT systems. However, there is a need to develop a simpler framework to support governance of our smaller business critical IT systems and tools. A number of smaller systems have been identified to pilot this framework, and the job will be to gradually ensure that all business critical IT systems and tools are supported and continually develop the needed framework in collaboration with our local quality department. The working place will be our office building in Søborg.

Qualifications
You have a B.Sc. or M.Sc within IT, natural sciences or other relevant degree, and extensive knowledge and experience from IT in the pharmaceutical industry. Knowledge of quality control and testing of IT to comply with internal and external requirements and Good Clinical Practice is a benefit. Most likely you have taken system management responsibility for clinical IT systems before within an operational role from daily second line support to system governance.

We expect you to be capable of working independently, taking responsibility and showing initiative, and are flexible and efficient. You have attention to detail and you are able to overview several challenging tasks in parallel without compromising on the quality of your work. As a person you are extrovert and have the power to influence. English proficiency is a must. Experience with project management will be an advantage.

At Novo Nordisk, we use our skills, dedication and ambition to help people with diabetes. We offer the chance to be part of a truly global work place, where passion and engagement are met with opportunities for professional and personal development.

Contact
For further information, please contact Rikke Søndergård at +45 3079 4096.

Deadline
5 January 2014

Kemiker til stabile produktionsprocesser for HPLC-kolonner

- Produktion
- Danmark - Køge

Vi har brug for din hjælp i en periode på 9-10 måneder.

Vil du anvende og udvikle dine professionelle kemiske og projektfaglige færdigheder i et samarbejde omkring stabile produktionsprocesser og levering af HPLC-kolonner til analyse af lægemidler?

Er du positiv, engageret og fleksibel, og trives du med en omskiftelig hverdag, hvor fokus sættes ud fra kundernes behov? Vi tilbyder en spændende arbejdsplads med skiftende udfordringer, hvor du kan opnå god erfaring med kolonneproduktion/stabilisering af produktionsprocesser. Du vil blive en del af et team i udvikling med fokus på faglighed, engagement og quality mindset.

Om afdelingen
FeF Chemicals A/S er et 100% ejet datterselskab af Novo Nordisk A/S og ligger i Køge. I dag er vores største produktgruppe substitueret kiselgel, der bruges til kromatografisk oprensning af Novo Nordisks lægemidler. Desuden producerer vi kvaternære ammoniumforbindelser, som vi markedsfører over hele verden. Vi er i dag ca. 140 ansatte i firmaet. Udviklingsafdelingen består af 6 kemikere og 12 laboranter fordelt på 3 teams. Vi er kompetencecenter for gelteknologi i Novo Nordisk, hvilket indebærer en tæt kontakt til forsknings-, udviklings- og produktionsafdelinger i koncernen.

Du bliver en del af Kolonnepak-teamet, som består af 3 laboranter, 3 kemikere og en teamleder. Teamet producerer analytiske HPLC-kolonner til analyse af lægemidler og brug i udviklings-, produktionsudvikling- og analyseafdelinger i Novo Nordisk og FeF.

For at stabilisere kolonneproduktionen gennemfører vi udviklingsprojekter, baseret på laboratorieforsøg. Vi fremstiller kromatografiske faser ved organisk syntese med kiselgel og producerer kolonner under ISO9001. Såvel udvikling som produktion dokumenteres, ligesom projektfremdrift rapporteres løbende.

Jobbet
Dit job bliver at sikre stabile produktionsprocesser og dokumentation herfor, så teamet kan levere HPLC kolonner i rette kvalitet til tiden. Du skal opbygge og forankre anvendt og videnskabelig vide n om kromatografiske kolonnematerialer og produktion af kolonner.

Arbejdet vil hovedsagelig bestå i at designe, planlægge og rapportere samt evt. i mindre omfang at udføre og dokumentere laboratoriearbejde.

Du vil i samarbejde med kemikere og laboranter blive ansvarlig for kemiske udviklingsforsøg med geler og kolonner/arbejde med forskellige produktionsprocesser. Du vil planlægge, drive, gennemføre og dokumentere stabile produktionsprocesser for HPLC-kolonner, herunder rapportere projektfremdrift.

Kvalifikationer
Du er uddannet cand.scient i kemi, kemisk ingeniør eller lign., gerne med en Ph.D., og med indsigt og viden om kemiske reaktioner og kromatografi. Du har mere end 3 års kemisk laboratorieerfaring indenfor organisk syntese og HPLC-analyse og har en skarp analytisk sans. Du er dygtig til at opbygge viden, vidensdele, dokumentere og afrapportere laboratorie- og projektarbejde. Det er en fordel, hvis du har erfaring med dokumentation (ISO/GMP).

Du bidrager med dine kemiske færdigheder på højt niveau omsat til praksis. Din tilgang er analytisk og databaseret.

Du leder projekter og implementerer forbedringer ved brug af statistiske værktøjer og forsøgsdesign (DOE) i tæt samarbejde med kolleger og kunder.

Du holder overblik og hjælpe med at prioritere opgaver, ligesom du koordinerer med interessenter. Du udarbejder udviklingsrapporter og anden videnskabelig, teknisk og kvalitetsmæssig dokumentation.

Som person har du let ved at omgås kolleger på alle niveauer i organisationen, og du gør dit for at bidrage til den positive stemning i teamet. Du tager ansvar for, at vi både som team og individer, når de mål forretningen har brug for. Du forstår betydningen af kundefokus og opbygger gode relationer til samarbejdspartnere. Du kan lide at tage ansvar og vise vejen, samtidig med at du som teamspiller har fokus på at spille andre stærke.

Hvis du er indstillet på at dokumentere levering af HPLC-kolonner og stabile produktionsprocesser, kan vi tilbyde dig samarbejde med kompetente og engagerede kolleger og mulighed for professionel og personlig udvikling. Arbejdet foregår i en uformel atmosfære, hvor vi har fokus på som team at levere i rette kvalitet til vores kunder.

Kontakt
Vil du vide mere om stillingen, er du meget velkommen til at kontakte Kirsten Modvig på telefon 2429 4119

Ansøgningsfrist
6. januar 2014

Postdoctoral Researcher

- Research & Development
- Denmark - Greater Copenhagen area

An international Postdoctoral position in the field of functional genetics in multiple sclerosis is available for a highly skilled scientist in collaboration between Novo Nordisk Research Center Seattle, US and the Nuffield Department of Clinical Neurosciences, Clinical Neurology, University of Oxford, United Kingdom.

About the department
The project will mainly be performed in the laboratory of Professor Lars Fugger, University of Oxford, where the Postdoctoral Researcher will join a team of scientists and clinicians with a range of genetic, immunological and neurological expertise to work in an interdisciplinary environment in which research, teaching, clinical training and clinical care interact. The University of Oxford is a stimulating organisation, which enjoys an international reputation as a world-class centre of excellence in research and teaching.

The Novo Nordisk Research Center Seattle is home to the company’s Inflammation R&D Centre where researchers leverage Novo Nordisk’s strong knowledge within the field of proteins, in order to further build the company’s clinical pipeline of products for the treatment of chronic inflammatory diseases. Globally, about 6,000 Novo Nordisk employees are involved in research and development activities with main R&D facilities located in the Copenhagen area (Denmark), Beijing and Seattle.

The Job
The project will focus on elucidating the functional basis of selected genetic variants identified in multiple sclerosis GWAS using a combination of genetic, biochemical and immunologic approaches.

The overall goal of the project is to apply genetic approaches towards improved disease treatment of multiple sclerosis and potentially other autoimmune diseases.

The candidate will be employed by Novo Nordisk. However most of the work will take place in the laboratory of Professor Lars Fugger, University of Oxford, and a minor part in the Novo Nordisk Research Center Seattle. Visits to the Novo Nordisk research headquarter in Denmark will also occur. The candidate must therefore expect some extent of travelling between these locations.

The position is for a fixed-term period of two years and is available as soon as possible. The recruitment process will be conducted in cooperation between Novo Nordisk and University of Oxford.

The position is offered as part of the Novo Nordisk R&D STAR Programme (Science, Talent, Attraction and Recruitment). This programme supports the brightest graduate students in biotechnology, life, medical and engineering sciences, who want to pursue a career in pharmaceutical R&D.

Qualifications
A PhD in Immunology is essential, with up to 3 years postdoctoral research experience. Prior research experience investigating the immunological and/or genetic association of an autoimmune disease would be highly advantageous.

The successful candidate must have excellent English language skills and be able to

communicate results clearly as demonstrated by both oral presentation and publication history. A keen willingness to show initiative in developing novel techniques and strategies to achieve research goals is also required.

At Novo Nordisk, we strive for excellence. Your curiosity, skills, dedication and ambition will help us change lives for the better. We offer you an opportunity to work in an extraordinary stimulating scientific environment.

Contacts
If you would like to know more about the position please contact Jacques Peschon by email, JQPS@novonordisk.com

Deadline
14 January 2014.

Process Supporter

- Production
- Denmark - Måløv

Are you committed to support a GMP production in Novo Nordisk? Right now, we are looking for a production chemist with a high quality mindset and GMP experience to join us in the HRT bulk production, a part of Biopharm Tablets & Finished Products.

About the department
The job is located in Biopharm T&FP HRT Bulk production, which is a tablet production producing HRT (Hormone Replacement Therapy) products including the processes; granulation, compression and coating. The department consists of 50 employees and is based in Måløv, Denmark and consists of three teams; Production, Tech Support and Process Support. The Process Support Team consists of 10 dedicated supporters.

The job
The primary responsibilities of this position will be to support the operators in the daily production and secure that we live the requirements of our quality management system and that we work systematically according to the LEAN principles implemented in the department. Furthermore, you will handle deviations from standard procedures, implement corrective actions, handle change requests, write protocols, reports and various documentations related to the HRT bulk production. You will also be a part of the team releasing the bulk batches. In this job, you will be in close contact with professional colleagues both in the department as well as in QA and QC department, Product Support and our Technical Team.

Our department is highly motivated and this position offers you a unique opportunity to strengthen your experience in a GMP production environment, realise personal as well as department goals and see the benefits of your work. You will experience an enthusiastic working climate where we take a personal responsibility for quality, delivery and each other.

Qualifications
You hold an academic degree (Cand. Pharm, chemical engineer or the equivalent). You have experience from pharmaceutical and knows how to perform in a GMP environment. Preferable you have knowledge of the LEAN principles. On a personal level you have a positive can-do attitude, you are engaged, systematic and take responsibility to ensure deadlines are met. You enjoy working with major challenges and can maintain an overview in a busy work day while complying with the requirements for manufacturing of drug products. You are fluent in both written and spoken Danish and 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 Charlotte Lex on +45 3075 2559.

Deadline
6 January 2014

QA Chemist

- Quality
- Denmark - Gentofte

Would you like to help securing release of Novo Nordisk A/S haemophilia portfolio, growth hormone portfolio and Glucagon filled product? Do you thrive when working in a team; handling multiple tasks of high complexity? Then you might be the person we are looking for in Biopharm QA Aseptic Production.

About the department
Biopharm QA AP is responsible for quality assurance of two existing aseptic filling plants in Gentofte, the building of a new filling plant in Kalundborg and all utility systems in the Gentofte production areas. Our key tasks are to review and approve all sorts of GMP documentation such as validation reports, change requests, non-conformities and batch documentation in order to be able to release filled product for packaging.

As QA Chemist in Biopharm QA AP you will join a group of 45 highly skilled and competent colleagues working in four teams lead by separate associate managers. By joining us you will get the chance of professional and personal development and you will get an excellent and unique overview of current authority expectations and demands in the pharmaceutical industry.

The Job
We have two vacant position situated in two different releasing teams for the filling plants in Gentofte. Both jobs include QA review of several types of documents related to release of pharmaceutical products. The documents comes from all types of processes in a filling plant, such as formulation, wash and sterilisation processes, filling, freeze-drying, and visual inspection. One of the vacant positions includes evening work with QA presence in the production area approximately two-three times pr. month.

Your main responsibility will be to quality assure the filling plants and thereby contribute to assure product quality and compliance with the current GMP rules and guidelines. On top of that QA is a major player at internal audits and external authority inspections, where you are expected to participate.

When started you will undergo an individual training program, where you can expect to be given more responsibility gradually.

Qualifications
You hold an academic degree that qualify you as QP (Qualified Person) according to the Danish Medical Agency. Preferable your academic background is topped with experience either from the pharmaceutical industry. However we would also like to hear from talented newly academic graduates.

You must thrive in a role where you are required to take leadership in order to achieve the shared targets in cooperation with your stakeholders. You have a strong quality mind-set, meet your deadlines, and know how to prioritise between different tasks in a dynamic environment. You are a dedicated team player who inspires trust amongst colleagues and partners. Your language skills cover proficiency in both Danish and 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.

Your application is welcome in Danish or English.

Contact
For further information, please contact QA Director Rikke Wissing Jensen at +45 3075 1566.

Deadline
2 January 2014

Supporter til Mikrobiologisk laboratorium

- Produktion
- Danmark - Bagsværd

Vil du være med til at supportere vores mikrobiologiske laboratorium? Er du kvalitetsbevidst og har masser af drive og selvstændighed, og vil du være med til at sikre at vores laboratorium er i compliance med gældende GMP og ISO krav? Har du erfaring med arbejde i et mikrobiologisk GMP laboratorium? 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 5 kemikere, 9 laboranter/speciallaboranter og 3 operatører.

Jobbet
Som supporter i QCM har du sammen med dine kolleger ansvar for at analyserne er i drift. Vi supporterer alle vores analyser, som inkluderer kimtælling, steriltest, miljøprøver og bioindikatorer, endotoxin test samt identifikation af mikroorganismer. Vores daglige opgaver er primært faglig support til laboranterne, udarbejdelse og opdatering af instruktioner, håndtering af afvigelser og ændringssager samt sikre at udstyret er kvalificeret, vedligeholdt og i drift.

Som supporter er du den, der leder problemløsninger, og du vil stå i spidsen for at drive forbedringer i afdelingen inkl. træning af dine kolleger. Ved audits og inspektioner vil du kunne komme til at fremlægge efterspurgt dokumentation.

Du har tæt samarbejde med både resten af afdelingen og vores mange samarbejdspartnere andre steder i organisationen, og du vil derfor komme til at samarbejde med mange forskellige personalegrupper.

Stillingen er et 2-årigt vikariat.

Kvalifikationer
Du er uddannet laborant, laboratorietekniker el.lign., og du har erfaring indenfor mikrobiologisk analyse og håndtering af udstyr (vedligehold, kalibrering, kvalificering mv.). Du er vant til at arbejde med ISO 9000 og GMP, og du arbejder med LEAN som en naturlig del af din hverdag.

Du er engageret og har lyst til at sætte dig ind i nye opgaver, og du har en positiv tilgang til at løse udfordringerne på en systematisk, enkel og effektiv måde. Du er struktureret og kvalitetsbevidst, og det at nå teamets deadlines og mål er en selvfølgelighed.

Du er en teamplayer, og dine gode kommunikationsevner gør det let for dig at formidle viden på både dansk og engelsk. Du trives godt i en travl hverdag, hvor vi hjælper hinanden på tværs af teams og afdelinger, og du motiveres af at få noget fra hånden.

Du er ikke bange for at tage initiativet, og du driver gerne forskellige opgaver og projekter selvstændigt. Du er fleksibel med stor ansvarsfølelse og du har masser af drive og godt humør. Du er åben og ærlig, og du er i stand til både at modtage og give konstruktiv feedback.

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 Marianne Foss Hansen på + 45 3075 9846.

Ansøgningsfrist
5. januar 2014

Validation Process Engineer

- Production
- Denmark - Hillerød

Device manufacturing & Sourcing (DMS) seeks a talented engineer with experience within the field validation and qualification.

If you have a great quality mindset and always strive for improvements and possess in-depth knowledge within validation and qualification then go for this job.

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

The Job
You will be responsible for various validation activities such as execution, writing and reviewing validation plans, protocols, and reports associated with Installation Qualification, (IQ), Operational Qualification (OQ) and Performance Qualification (PQ) to ensure quality and compliance. You will also be responsible for continually improving the validation documentation and related standard operating procedures as well as you will be involved in problem solving when specifications or requirements are not met.

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

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

Qualifications
You have a background as validation engineer or similar experience.

You have some experience with validation and/or qualification of production tools within the pharmaceutical industry or other regulated industry. Furthermore, you have a good understanding of GxP and a high quality mind-set. You possess good interpersonal skills, are process oriented and have the ability to communicate simple and uncomplicated. It is also important you support the rest of us in creating a positive spirit and a good department. Communication in English in speech and writing is a necessity, since you will cooperate with international suppliers and customers. The position also includes travel.

At Novo Nordisk we use our skills, dedication and ambition to help people with diabetes and change their lives. By working with us, you will have the opportunity to do the same in a global business environment.

Contact
For further information, please contact Laura Sørensen at +45 3075 0463.

Deadline
1 January 2014

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 organization? You will be leading a highly competent QA team of 8 employees responsible for the quality assurance of Biopharm Manufacturing Development. Since the team is newly established, we are now looking for a new colleague to lead the team.

About the department
“Biopharm QA QC & Support” consists of two teams, one responsible for quality assurance of QC analyses and the other responsible for quality assurance of development activities. Our key tasks are to review and approve GMP documentation such as validation reports, change requests and non-conformities in order to be able to insure delivery of high quality products in compliance.

The Job
As Associate Manager in Biopharm QA Support team you will be the leader of 8 highly skilled and motivated QA professionals, forming a new team since 1 November 2013. The team provides quality assurance for the manufacturing development activities in Biopharm and as associate manager you will be involved both as QA person handling cases and as a representative of the department manager. 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 our patients. You act as a competent sparring partner to your team you coach and empower your employees to deliver excellent results. You collaborate with the Manufacturing Development departments in a professional and amicable way and collaborate to overcome disagreements while never compromising on quality mindset and compliance.

Qualifications
You have a solid working experience from a QA organization which ideally is from a similar role in a pharmaceutical company and your experience is paired with 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 that you can stand firm in favour of product and user safety, as well as compliance. 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 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 Ulla Thinggaard at +45 3075 2104.

Deadline
03 January 2014

Distribution Quality Coordinator

- Supply Chain and Logistics
- Denmark - Bagsværd

Are you ready to be exposed internationally and to gain in-depth expert knowledge of Novo Nordisk’s worldwide distribution? This job will give you both. As Distribution Quality Supporter in Supply Chain Planning you will have direct access to our string of global customers and be part of a busy environment due to successful growth in volume.

About the department
Shipping & Customer Service in Søborg handles shipping of finished products and raw materials. 37 dedicated colleagues ensure fast and reliable global import/export of Novo Nordisk’s products to our affiliates and direct customers around the world in the right quality and at competitive prices.

The job
You are overall responsible for transport validation of Novo Nordisk’s products. This means that you make protocols and work out documentation for the appointed transport lanes. As such, it is your job to test and document that the products stay within the specific standards of tolerance from the moment they leave the ramp at Novo Nordisk until they reach the final destination somewhere in the world. You will have a key role preparing and presenting validation documents for Danish and international authorities, and you participate in the audits and inspections, giving a detailed account of the validation methods and the results. It is also part of your job to support the department and unit in quality related issues such as to coordinate internal and external inspections, act as unit GxP training coordinator as well as unit review coordinator. Further you are responsible for handling the change requests and non-conformities. You are expert in SOP writing and assist your colleagues with guidance in all quality issues. Another key task will be to contribute to managing the daily use and maintenance of the IT system used for temperature monitoring during transport and validation in connection with upgrade and changes to the system.

Look forward to a job where you will be in contact with stakeholders from all over the world and play a major role in our efforts to live up to all QA and QC requests.

Qualifications
Either you are an Engineer, or you have a similar academic background including at least 2 years’ QA or QC experience. You are used to manoeuvring in an international setting with stakeholders who work by other sets of rules than you. This requires confidence in your own professional competences and personal ballast that allow you to know when to be resilient and when to stand your ground. You use an analytic and structured method of working to prepare the right documentation and seek information on your own. You must thrive working in a specialist function as the go-to-person who possesses solid in-depth expertise within your field of work. This job also requires an open and appreciative, yet determined mind-set, and you navigate your way round colleagues, foreign authorities and other stakeholders with a good balance of support and continuous follow-up. You never compromise on quality in your work, and you take pride in delivering within your deadlines and keeping your customers satisfied.

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 Christina Grauballe at +45 3075 2053.

Deadline
7 January 2014.

QA Academic for Development Products

- 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 14 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 both in a national and an international environment, you must speak and write Danish and 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 Tenna Aggerholm Møller at +45 3079 9918 or Peter Søtofte Elten at +45 3079 8453.

Deadline
13 January 2014

GMP partner

- Production
- Denmark - Hillerød

Are you ready to take the next step in your career - you now have the opportunity!!

You will be key player in ensuring quality and compliance for a large business area in Site Hillerød consisting 5 departments, more than 20 managers and app. 350 employees. You will be a key member of the ambitious, local management team and primary sparring partner for the Vice President and directors on critical GMP issues.

About the department
We are looking for GMP Partners to our sites in Hillerød 25A where we focus on both aseptic production and on medical devices. The GMP-partner and coordinator setup is a matrix organisation, where you will head up 5 GMP Coordinators across the different departments.

The job
As GMP Partner you have the overall responsibility for setting the targets on quality for your area and for making sure that they will be met. As such, you bring in the latest knowledge within GMP when you challenge our business managers to bring GMP and quality to the top of the common agenda. You ensure that the area is in compliance with the authorities’ and Novo Nordisk’s regulations, including ISO9001:2008, and you will become your area’s representative in Site Denmark’s cross-organisational GMP group/GMP board. You are also responsible for Quality Management Review (QMR), and you play an active role in audits and inspections, having the GMP Coordinators as your skilled co-workers.

You will participate in SDKs GMP network meetings with your peers for sparring, sharing and development of GMP and QMS related topics. The network is owned and facilitated by the QMS function.

The job involves contact and interaction to many different stakeholders in the organisation, from operators, maintenance, cLEAN professionals, project managers and to all line management levels. Your role calls for strong change management and communication skills and ability to create the right quality and compliance mindset.

Qualifications
You hold a degree at minimum master’s level. Your academic background is topped with experience from a pharmaceutical production where you have gained solid experience within quality, GMP and ISO9001. Maybe you already work in Novo Nordisk as a manager, project manager, specialist or as an experienced professional.

You are used to creating results in projects. To succeed, you must thrive in a role where you take leadership, initiate and coordinate a large number of actions and projects. You thrive by challenging the managers in good GMP practise. You know how to anchor your solutions into systems and this requires an excellent overview, a structured mind-set and way of working. Working cross-organisationally, your networking skills will also be crucial as well as your ability to balance when to compromise and when to stand firm. Finally, you must master English and Danish, 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 Anne Reker Cordt at +45 3079 9308.

Deadline
10 January 2014

International PostDoc

- Research & Development
- Denmark - Måløv

The position is offered as part of the Novo Nordisk R&D STAR Programme (Science, Talent, Attraction and Recruitment). This programme supports the brightest graduate students in biotechnology, life, medical and engineering sciences, who want to pursue a career in pharmaceutical R&D.

About the department
Translational Haemophilia Pharmacology is offering an international Postdoc fellowship to a highly motivated and ambitious candidate. Translational Haemophilia Pharmacology is a research unit focusing on research and development of drug candidates for the treatment of haemophilia; we support the Novo Nordisk haemophilia portfolio with knowledge generated in animal models of haemophilia.

The Job
The project will first focus on optimizing and validating a thrombin generation assay for use with samples from dogs, prior to and after therapeutic intervention. Subsequently the assay will be used to predicting the bleeding phenotype and response to treatment in dogs with haemophilia A and B as a model for human haemophilia. The project is conducted in close collaboration with leading researchers from the University of North Carolina at Chapel Hill.

The starting date is February 1, 2014 or later, and the position is on a temporary contract. Part of the PostDoc project will take place at Translational Haemophilia Pharmacology in Måløv, Denmark and the other part in the lab of Dr. Tim Nichols in close collaboration with Dr. Alisa Wolberg at the University of North Carolina, Chapel Hill. Travel expenses between the US and Denmark will be reimbursed by Novo Nordisk.

The candidate will become part of two laboratories located in high impact centres of excellence within haemophilia and thus exposed to world class science and in addition serve as a liaison between the University of Chapel Hill and Novo Nordisk A/S.

Qualifications
You hold a PhD in medicine, veterinary medicine, pharmacology, biology or related disciplines. Solid knowledge on in vivo research in general and haemostasis research in particular is desirable. Experience with haemophilia research is considered an advantage. We require very good communication skills 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 call Bo Wiinberg on+45 3075 3030.

Deadline
15 January 2014

Business Analyst

- Production
- Denmark - Hillerød

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

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

DMD Business Support is a department in the DMD project organisation responsible for finance, LEAN, project portfolio management, business processes and strategy. We are looking for an ambitious Business Analyst to join the team situated in Hillerød near Copenhagen.

The job
As a Business Analyst in Business Support, you will participate in a wide range of activities within performance management, business development and strategy implementation, such as Balanced Scorecard, business analysis, business support and optimization. You continually help support, improve and develop the business processes in the business unit, and serve as a sparring partner for project managers and management.

Qualifications
You have an academic degree in business administration or similar. You have at least 3 years of experience from similar job which enables you to set direction and contribute in improving business processes.

As a person you are extrovert, service minded, responsible and co-operate easily at all levels. You work independently and proactively seek the information you need. Your approach to problem solving is based on systematics and your ability to see things in a larger perspective.

You are known to have sharp analytical skills and masters excel at high level. Last but not least, you communicate fluently in written and spoken English.

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

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

Contact
For further information, please contact Rasmus Henriksen +45 3075 3230.

Deadline
5 January 2014

OHS Project Manager

- Human Resources
- Denmark - Bagsværd

In this job, you will be part of an organisation that supports a rapidly growing organisation globally whose role is to ensure that Novo Nordisk provides a healthy and safe working environment for all. If you find challenges like this exciting and inspiring, you may be our new Occupational Health and Safety Consultant.

About the department
The job is located in Corporate Occupational Health and Safety (COHS) which is a corporate staff function and a part of Corporate People & Organisation situated in Bagsværd. COHS is Novo Nordisk's Centre of Excellence in the field of occupational health and safety globally with 28 dedicated colleagues within ergonomics, psycho-social and technical working environment. COHS’s role is to inspire and support the OHS work throughout the global organisation, enabling line of business to realise Novo Nordisk’s OHS ambitions by providing easy-to-use guidance, tools and data.

The Job
Your main responsibility will be to drive cross-organisational OHS projects to support the implementation of our corporate OHS strategy. In addition to your role as project manager, you will work as a consultant for the organisation and support management at all levels and OHS representatives within a broad range of OHS topics. Development and implementation of easy-to-use guidance and tools on OHS topics will be also be a focus area for you.

Qualifications
You hold a bachelor or master degree within business, science or the like and have at least 3 years of experience within occupational health and safety, preferably from an international company.

You have experience as a project manager and are able to drive low/medium complex projects independently with strong focus on stakeholder management. You have a high level of drive and work well in a dynamic environment. You are proactive and eager to contribute to the continuous development of the area.

You are result-oriented, like to be challenged and are able to conceptualise ideas into simple and standardised tangible business concepts. You have a well-structured approach to your tasks and are capable of maintaining an overview also under time pressure. Furthermore, you have excellent verbal and written communication skills.

English is our corporate language, and hence it is a prerequisite that you speak and write English fluently. You work comfortably in MS Office (experienced in PowerPoint). It is also important that you approach tasks and colleagues with a positive attitude, energy and good humour.

At Novo Nordisk, decisions and actions are based on their 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 Nina Gylche Møller at +45 3079 4756.

Deadline
2 January 2014

Processupporter til Produktion

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

- Produktion
- Danmark - Kalundborg

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

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

Jobbet
Dit ansvar er at supporter montage- og pakkelinjer i afdelingen Prefilled Device, således at kravene til kvalitet, compliance og GMP er overholdt. Du vil få ansvaret for en konkret produktionslinje, hvilket bl.a. indebærer at håndtere hændelser, ændringssager og deltage i optimeringsprojekter. Du kommer til at løse forskellige opgaver, der relaterer sig til kvalitet, herunder at forbedre vores SOP’er, behandle afvigelser og løse pludseligt opståede problemer i produktionen, og du bruger dagligt LEAN værktøjerne. Målet er at levere høj kvalitet til tiden og i komplet overensstemmelse med GMP-kravene.

Du deltager i inspektioner - både eksterne og interne audits.

Du skal sikre videndeling på tværs af sites og lokationer, og du kommer til at samarbejde med mange forskellige kolleger på tværs af produktionen og får en hverdag med stor variation i opgaverne, derfor er kommunikation også en vigtig del at din dagligdag.

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

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

Kvalifikationer
Du har en akademisk naturvidenskabelig uddannelse. Det kan være som ingeniør, cand. Pharm, relevant cand.scient, eller anden relevant uddannelse. Din uddannelse er gerne suppleret med nogle års erfaring fra et job i en farmaceutisk produktion, som har givet dig rigtig god indsigt i GMP. Du er dit ansvar bevidst og formår at træffe de nødvendige beslutninger for at løse udfordringer med sans for effektivitet og kvalitet. Du har et godt overblik og en skarp analytisk sans, som gør det nemt for dig at skære ind til benet og gennemskue sammenhænge fx mellem processer, materialer og udstyr.

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

I Novo Nordisk 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 derudover vide mere om stillingen, så kontakt Ole S. Iversen på + 45 3075 2649.

Ansøgningsfrist
4. januar 2014

Graduates! Kick-start your global marketing career

- Graduate
- Denmark - Bagsværd

Professional development

What has surprised you?

Begin the journey of a lifetime in September 2014

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

Start your career climb
Want to bring life-changing products to people all over the world? Novo Nordisk’s Global Marketing Graduate Programme aims to develop highly qualified Global Product Managers with a broad understanding and hands-on experience of global and local pharmaceutical marketing and sales challenges. You will experience a variety of tasks and projects from cross-departmental project work and internal/external stakeholder management to pre-launch, launch, and lifecycle processes.

Scope of the programme
The Global Marketing Graduate Programme is a 2-year expedition consisting of three 8-months rotations within the marketing and sales departments of Novo Nordisk:

1 rotation in Global Marketing headquarters in Denmark
2 rotations in our global affiliates whereas one will be within sales

For more details, visit Novonordisk.com/ Global-Marketing-Graduate

A global career
After successfully completing the programme you will have the necessary skills to embark on a career in global marketing at Novo Nordisk with a permanent position – perhaps as a Global Project or Product Manager. While you could be based in Denmark, your broad network and international experience from the programme will enable global career opportunities.

Requirements
To join the Global Marketing Graduate Programme you must hold a master’s degree in a relevant subject and have no more than 1 year of work experience since finishing your studies. Joining Novo Nordisk appeals to you, not because of the competitive salary we offer, but the work we do. Also, you strive for working in a global, international and culturally diverse organisation with all of the opportunities this entails.

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

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

In addition to the Global Marketing Programme, we have many other graduate programmes which will all lead to life-changing careers.

Graduates! Kick-start your global business career

- Graduate
- Denmark - Bagsværd

Professional development

What has surprised you?

Begin the journey of a lifetime in September 2014
Novo Nordisk’s Business Processes Graduate Programmes is a great springboard for launching a life-changing career. As a global pharmaceutical company and the world leader in diabetes care we give you the opportunity to use your recently-acquired master’s degree to make a difference. We treat more than 20 million patients across the world.

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

Scope of the Business Processes Graduate Programme
Are you interested in gaining global experience with a wide variety of processes across all Novo Nordisk business areas? The programme spans from working with production, regulatory affairs, financial planning to sales and marketing.

We offer a two 2-year programmes of three 8-months rotations:

- 2 rotations in our corporate headquarters in Denmark
- 1 rotation in one of our global affiliates

Visit www.novonordisk.com/Global-Business-Graduate for more information about the programme and the rotations, meet the programme manager on video and read blogs from current graduates.

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

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

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

Contact
Programme Director, Ove Munch Ovesen: +45 3079 3445

Programme Assistant, Birgitte Blangsted: +45 3079 3539

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

Click on the blue apply button below.

Chemist in QC

- Quality
- Denmark - Bagsværd

Do you want to manage and improve a variety of material analyses in a highly professional QC laboratory? In that case you should apply for the new position as Chemist in QC Raw Materials. If you are as ambitious as we are, you can look forward to an exciting job in an environment where we seek to be best in class in everything we do.

About the department
Your new department, QC Raw Materials, consists of 59 employees who are located in Bagsværd and Kalundborg. You will join the Analytical team in Bagsværd, which is responsible for the chemical control of raw materials for primary pack and for excipients. We cooperate with a variety of functions, including purchase, storage and QA.

The job
You will work closely with the Chemists and Laboratory Technicians in your team to approve the raw materials and thereby enable a continuously high pace in the production. You will be responsible for implementation of new equipment and methods for elemental impurities ICP-MS, and for development and validation.

A high GMP and compliance mind-set is a must, you have to be familiar with working after pharmacopoeia, handling of change requests, non-conformities and OOS.

Continuous improvements and systematic problem solving by means of LEAN will also be part of your responsibility. You will support the Laboratory Technicians in their daily operations to ensure that the analytical performance and equipment live up to the industry standard. It will be an advantage if you have experience in project planning. In general, you can foresee different project assignments that enable us to work faster and smarter within the department and across the organisation. This could also be your opportunity to build a strong network within Novo Nordisk while developing your skills further.

Qualifications
You hold an MSc in Pharmacy, Engineering or another relevant field within the natural sciences. Your degree is supplemented with experience from a similar job in which you have gained in-depth knowledge of working with GMP in a laboratory environment. You have a high level of energy to drive yourself and your colleagues forward. You are result-oriented and take pride in delivering on your milestones, and you motivate your colleagues with a positive, forthcoming attitude. You work well independently, although it also motivates you to cooperate with colleagues and stakeholders across functions and departments. Lastly, you must have fluency in written and spoken Danish and English.

At Novo Nordisk, you will join a patient-centred culture of talented professionals. We respect individuality and empower you to make the most of your potential.

Contact
For further information, please contact Britta Johansen at +45 3075 7463.

Deadline
13 January 2014.

Moulding Process Engineer

- Production
- Denmark - Hillerød

Device manufacturing & Sourcing (DMS) seeks a talented engineer with experience within the field injection moulding and tools.

If you have a great quality mindset and always strive for improvements and possess in-depth knowledge within injection moulding and tools, then go for this job.

About the department
DMS is focused on introduction of moulded components for medical devices, maturation of the production setup to excellence and sourcing the components to sister sites abroad. The area is at a high development pace and we need an experienced engineer in Mould Pipeline & Validation (MPV), which is a team of 10, responsible for ordering and approval of injection moulds for plastic parts for prefilled devices produced internally in Hillerød DK and on various production sites worldwide.

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

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

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

Qualifications
You have a background as tool maker, plast processing technician, production technologist, engineer or likewise experiences.You have hands-on experience within engineering with mass production of precision plastic components and in-depth knowledge within injection moulding and/or tools. Ideally, you also have GMP experience. As a person, you have a high quality mind-set, good analytical skills and are able to work independently. You have the ability to collaborate with diverse stakeholders and can communicate in English in speech and writing since you will cooperate with international suppliers and customers. The position also includes travelling (approximately 30 days a year).

At Novo Nordisk we use our skills, dedication and ambition to help people with diabetes and change their lives. By working with us, you will have the opportunity to do the same in a global business environment.

You are welcome to send your application in Danish or in English, whichever you prefer.

Contact
For further information, please contact Laura Sørensen at +45 3075 0463.

Deadline
6 January 2014

Senior Research Scientist

- Research & Development
- Denmark - Måløv

We are looking for a motivated Senior Research Scientist with solid in vivo Pharmacology experience to help us run pharmacology and pharmacokinetic studies.

About the department
The Diabetes Pharmacology PK/PD department is organised within the Diabetes Research Unit of Novo Nordisk A/S in Måløv. We are 8 scientists, 13 technicians, and 1 PhD student in the department, and we are responsible for running pharmacology and pharmacokinetic studies of peptide compounds in the discovery phase of diabetes and obesity research projects.

The job
You will be responsible for planning and running non-clinical PK and PD studies, mainly in dogs and pigs, and analyse and report the results from these studies. You will participate in cross-functional project teams with colleagues from many different scientific backgrounds. Developing and optimizing the models and methods we use will also be part of the job, and it is expected that you actively take part in developing the department to continued scientific excellence. You will be encouraged to maintain old and establish new contacts to external collaborators. As a scientist in the department, you will refer directly to the department manager, and your main internal contacts in your daily work will be scientist colleagues, technicians and project members, as well as managers in Novo Nordisk R&D in Denmark and China.

Qualifications
You hold a degree in Pharmacology, Pharmacy, Biology, Medicine, Veterinary medicine or a related area, and have a PhD degree or equivalent work experience. You have solid knowledge of and hands-on experience with designing and running in vivo pharmacology studies. It will be an advantage if you also have working experience from the pharmaceutical industry; experience in performing pharmacokinetic analyses; hands-on experience doing in vivo pharmacology studies in dogs and/or pigs; and profound knowledge within the area of diabetes, obesity, and diabetic complications.

You are flexible, open to new ideas, ambitious, result oriented and have a good sense of humour. You are good at communicating and at collaborating in teams and have authority. You are fluent in English.

At Novo Nordisk we use our skills, dedication and ambition to help people with diabetes and change their lives. By working with us you will have the opportunity to do the same, and in addition benefit from a range of possibilities for professional and personal development.

Contact
For further information, please contact Director Henrik Duelund Pedersen at +45 3079 4148.

Deadline
5 January 2014

Senior system manager to create framework for IT portfolio (Søborg, Denmark)

Kemiker til stabile produktionsprocesser for HPLC-kolonner (Køge, Danmark)

Postdoctoral Researcher (Greater Copenhagen area, Denmark)

Process Supporter (Måløv, Denmark)

QA Chemist (Gentofte, Denmark)

Supporter til Mikrobiologisk laboratorium (Bagsværd, Danmark)

Validation Process Engineer (Hillerød, Denmark)

QA Associate Manager (Gentofte, Denmark)

Distribution Quality Coordinator (Bagsværd, Denmark)

QA Academic for Development Products (Gentofte, Denmark)

GMP partner (Hillerød, Denmark)

International PostDoc (Måløv, Denmark)

Business Analyst (Hillerød, Denmark)

OHS Project Manager (Bagsværd, Denmark)

Processupporter til Produktion (Kalundborg, Danmark)

Graduates! Kick-start your global marketing career (Bagsværd, Denmark)

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

Chemist in QC (Bagsværd, Denmark)

Moulding Process Engineer (Hillerød, Denmark)

Senior Research Scientist (Måløv, Denmark)