Jobs at Novo Nordisk

Reparatør eller tekniker til maskin vedligeholdelse

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

- Produktion
- Danmark - Kalundborg

Site Danmark Finished Products i Kalundborg søger dygtig elektriker eller automatik mekaniker,-fagtekniker med stor lyst til vedligeholdelse og problemløsning af vores 10 højteknologiske produktionslinjer.

Om afdelingen
Vi er en afdeling i rivende udvikling, og foruden daglig vedligehold kommer du til at medvirke i optimeringsprojekter af vore automatiske linjer. Vi har brug for dit engagement og dine kompetencer for at vedligeholde og optimere vore produktionslinjer til at være blandt de bedste i verden. Vi dækker alle processer i forbindelse med montage og pakning af Flexpen®, montage og pakning af InnoLet® samt pakning af Vials og Penfill®.

Om jobbet
Du bliver en del af et dynamisk produktionsmiljø, hvor fokus er på Lean og hvor løbende forbedringer, procesoptimering samt systematisk problemløsning og vedligehold (TPM) udgør en vigtig del af dagligdagen. Der stilles krav til vores medarbejdere om stor forandringsparathed og evne til at se muligheder frem for begrænsninger. Ligeledes er vidensdeling en vigtig del af vores daglige samarbejde på tværs af egen gruppe som på tværs i team og afdelinger i bygning. Som tekniker vil du indgå i vores produktionsteams, som består af operatører og teknikere og arbejder indenfor ovennævnte produkt,-produktionsområde.

Du kommer til i tæt samarbejde med dine kolleger at varetage planlægning og udførelse af service og reparation samt forebyggende vedligeholdelse og optimering af vores automatiske pakke- og montagelinjer på 2,- og 3-holdsskift. Vi anvender SAP PM til styring af vores vedligeholdelsesaktiviteter, hvorfor kendskab til SAP er en fordel. Udfordringerne er mange, hvorfor du forventes at bidrage på tværs af teamet, så vi fællesskab når i mål. Vi træner dig i vores systemer og du skal have lyst til at medvirke til løsning af tekniske vedligehold, problemstillinger og forbedringer, både selvstændigt, i teams og ikke mindst med andre faggrupper.

Kvalifikationer
Vi forestiller os, at du er uddannet indenfor automatik eller el - enten som automatikmekaniker eller automatikfagtekniker, elektriker eller anden tilsvarende uddannelse og har kendskab til fejlfinding på automatiske anlæg. Har du kompetencer og interesse indenfor Siemens S7, Scada, Allen Bradley, Vision og/eller MES systemer er det bestemt en fordel.

Det er nødvendigt, at du er hjemmevant på en pc, da brug heraf danner grundlag for en stor del af vores processer, ligesom det er vigtigt, at du har god kvalitetsforståelse, da vi arbejder indenfor ISO og GMP. Som person har du gode samarbejdsevner og et opsøgende service mindset. Du er fleksibel med stor ansvarsfølelse og en god portion gå-på-mod. Du er en teamplayer og en god kollega, der altid er parat til at give en hånd med. Endvidere lægger vi vægt på, at du har en god ordenssans samt et godt humør.

For eksterne kandidater vil der være tale om 24 måneders vikariat, mens fastansatte i Novo Nordisk forbliver dette. Alle ansøgninger vil blive vurderet løbende og samtaler vil ligeledes blive foretaget løbende.

Stillingen er indplaceret i løn kategori F3.

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 Michael Staunstrup +45 30 75 18 32 eller Joan Søgaard Jønsson +45 30 75 64 27. Alternativt kan Søren Heber kontaktes på +45 3075 7658.

Ansøgningsfrist
23.november 2013

Product Manager

- Marketing
- Denmark - Greater Copenhagen area

Are you looking for an opportunity to join Novo Nordisk as a Product Manager? Do you want to take part in launching new diabetes products in two important Nordic markets?

A position as Product Manager within the diabetes area of the Danish-Norwegian affiliate of Novo Nordisk is now available.

About the department
The job is located in Novo Nordisk Danish affiliate based in Copenhagen. As Product Manager you will be part of a dynamic Marketing team of 10, where you will work closely with three other Product Managers and collaborate with people across the entire affiliate.

The Job
Reporting to the Marketing Director, you will be accountable and responsible for the entire marketing process from brand planning to implementation in both Denmark and Norway. The main part of your responsibility will be to execute the product/marketing launch strategy but also to set the go to market strategy, preparing all pre-launch activities, as well as being able to translate strategies into tangible actions and tactics.

You will be in charge of developing a focused and impactful launch plan and the optimal marketing mix for the brand, and of setting a clear direction to your sales, medical and market access colleagues. You will be leading brand team and coordinate cross functional processes as well as initiate and analyse market research and continuously measure the impact of diabetes marketing actions. Disease awareness activities and communication will also be your responsibility, and you will be in charge of developing all relevant marketing and sales material.

Qualifications
You hold a relevant master’s degree (business, economics or the like) and have a minimum of 4-5 years of marketing and product management experience within the pharmaceutical industry. It’s an advantage if you possess knowledge of the diabetes area and have experience from working in an affiliate but it is not a requirement. Fluency in both spoken and written Danish and English is a requirement.

You have a positive can-do attitude and like to deliver your work in high quality. You are able to work on your own as well as contribute as part of a team. You are ambitious, set ambitious goals for the projects you manage and strive for excellence in the way you collaborate and drive results.

Contact
For further information, please contact Marketing Director Mads W.Ø. Larsen on +45 3079 7025.

Deadline
19 November 2013.

Business Analyst

- IT
- Denmark - Bagsværd

Does your motivation come from being challenged with a broad aspect of assignments? Is your ambition to create visible results? Do you strive to be one of the key drivers for our continuous focus to define and ensure that business needs are optimized via efficient processes and utilization of IT? We have the job if you have the engagement, drive and ambitions!

Novo Nordisk is one of the world’s most successful pharmaceutical companies and with a great growth potential. Our vision in Finance is to be the best finance operation in the global pharma industry. If you want to be part of this, we are currently looking for a Business Analyst to Procurement Consulting in Corporate Procurement, Corporate Finance.

About the department
We offer a job in an international environment. You will be part of a department consisting of 17 employees working with implementation and utilization of IT systems on a global scale.

The Job
Your primary task will be to transform business requirement into system configuration within the T&E area supported by the Concur standard application used in Novo Nordisk. You will play an active role in implementation projects and be responsible for system design, configuration, integration and testing of the application to support business needs. You will be part of an enthusiastic team that sets high standards and individual targets, but achieves them as a team.

You will be based in Denmark however, as part of an increased internationalization some travel activities can be expected.

Qualifications
You are among the best! You have completed a relevant Master's Degree (i.e. engineering or IT) with excellent results. Ideally you have 1-2 years of experience with configuration of standard systems (ideally Concur) from a large organization or consultancy firm.

You are motivated by driving change and improvements involving many stakeholders at all organisational levels. You have a high level of drive, initiative and persistence and you are result-oriented. Furthermore, you are ambitious and like to be challenged. You are analytical and structure your own work. Good communication and presentation skills are required in both Danish and in English.

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

Contact
For further information, please contact Thomas Malmvig at +45 3075 6358.

Deadline
29 November 2013.

OHS SVP partner

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

- Business Support
- Denmark - Kalundborg

Do you have a burning interest in Health & Safety (OHS) and can drive this agenda across business units.

Can you take a strategic and operational responsibility for implementing and optimizing Health & Safety issues.

Then you could be our new OHS SVP Partner in Diabetes API in Product Supply.

About the department
Diabetes API is an organization with around 1,800 employees located in Kalundborg, Denmark. We are responsible for all diabetes-related active ingredient production at Novo Nordisk. Our mission is to be the best supplier of Diabetes API and deliver API in high quality and regulatory compliance in a cLEAN, environmental sustainable and social responsible way.

As OHS SVP partner, you will join 12 highly skilled colleagues in DAPI Finance & EHS. We are responsible for Environment, Health and Service and financial performance management and support the management of business areas.

The Job
You will be dedicated to OHS work and will be responsible for ensuring that DAPI meets Novo Nordisk’s occupational health and safety policies and targets. More concretely you will be responsible for implementing the strategy and drive and optimize the OHS management system.

Furthermore you will drive and own the OHS coordinator network in DAPI and through this coordinate the OHS initiatives and projects across DAPI and you will be responsible for coordination of the work with the OHS VP coordinators maintaining an effective and synergistic network across the local sites.

You will also play an active role in the OHS network across Product Supply.

You will be involved in our wellbeing project across DAPI focusing on a healthy worklife. This includes developing and implementing this part of the strategy in close collaboration with internal and external stakeholders.

Qualifications
You have a proven track record from years of successful work in either Line of Business or Corporate Functions and you hold a relevant Masters Degree. You have strong analytical skills and a structured way of working combined with humour. With your natural skills in communication, stakeholder management and personal drive you effectfully ensure strategy execution and promote the OHS agenda throughout DAPI in alignment with the OHS strategy in Product Supply.

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

Contact
For additional information please contact Benedikte Lohse at +45 3079 2998.

Deadline
01 December 2013

IT Risk Coordinator

- IT
- Denmark - Bagsværd

Would you like to use your IT risk management experience to make a difference in a worldwide healthcare company? If so, you may be the new IT risk coordinator at Novo Nordisk, where the protection and integrity of our data is vital not only for the company, but for millions of patients.

About the department
The job is based at our IT Process Office, which is part of Novo Nordisk’s Corporate IT Governance organisation in Bagsværd, Denmark. The department supports the work of system managers and process owners in Bagsværd, Bangalore and other locations, which means that you can expect 15-20 days of travel per year.

The Job
In your new position, you will play a key role in the ongoing implementation and optimisation of the global IT risk management process at Novo Nordisk. You will train system managers in this process, motivating them to use it independently and proactively. You will also develop and continuously improve the training programme itself.

The IT risk coordinator is also responsible for the planning, execution and presentation of the regular, consolidated IT risk reports that are sent to our corporate Risk Office. Your position will involve close cooperation with colleagues in our IT Security department and in our system management organization, as well as with one other IT risk coordinator in the IT Process Office.

Alongside your risk coordinator duties, your job will include variety of global process support functions. In this capacity you will, among other things, help process owners identify and execute necessary changes and improvements to global IT processes.

Qualifications
You have a Master’s degree or the equivalent in IT, engineering or finance, plus at least 3-4 years of practical risk management experience. Risk management certification would be a definite advantage.

As a person, you are a team player who is inventive and geared towards finding practical, real-life solutions. You communicate well in English, both as a trainer and when presenting reports to management, and you have an eye for detail that helps you spot potential problems.

At Novo Nordisk, your skills, dedication and ambition help us change lives for the better. In return, 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 Manager Bo Vindberg at +45 3079 4923.

Deadline
24 November 2013

Energetic QA Team Member with Quality Mindset

- Quality, senior position
- Denmark - Hillerød

Do you have a mind for quality assurance? Can you guarantee the quality of newly developed health care devices? Then join Novo Nordisk’s Device Manufacturing Development (DMD) as our new Quality Assurance Professional and contribute to defeating diabetes worldwide

About the department
You will be part of a team of 13 dedicated colleagues, in Hillerød. Together, we are responsible for assuring the quality of Medical Devices developed by our R&D department every step of the way from the development processes to pilot production. We also assist the transfer into high volume production that takes the finished product to markets worldwide. The working relations are informal and the team values professional sparring and good humour highly.

The job
You will be responsible for status assignment of final assembled combination products for clinical trial. On an operational level, you ensure that the devices are assembled in full alignment with the given regulations. You review the requests for changes, e.g. of the production equipment, and review the cases of non-conformities in the production. You also provide quality support to the process responsible persons. Supporting the ideas for optimisation you approve the necessary documentation accordingly. Monitoring trends across processes are also one of your main objectives and your curiosity and thoroughness helps the organisation to identify issues for improvement.

You can look forward to entering into an energetic and positive working environment where cooperation is a keyword.

Qualifications
You hold an academic degree and preferable your academic background is topped with a shorter or longer work experience from the pharmaceutical business or a company in the food industry. Moreover, you have a high level of fluency in written and spoken English.

On a personal level, you are known for dedicating yourself to working proactively to solve the task at hand. Using your ability to think outside the box, you are still able to come up with solutions or suggestions that comply with quality requirements. You are a team player and a skilled communicator, and you thrive on unfolding your high level of energy and spirit in an international, dynamic environment.

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

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

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

Contact
For further information, please contact Dean Kloe at +45 3075 8948.

Deadline
25 November 2013.

Intern to CMC Process Support

- Student and Internships
- Denmark - Gentofte

At Novo Nordisk, we share a passion for changing patients’ lives, and we are always looking for talented individuals who want to join us in this effort. Our internships provide exciting learning opportunities for students who bring new ways of thinking to our company.

About the department
The internship is in CMC Process Support, a department in CMC Supply responsible for lean and statistical support across the organisation. In terms of lean, in Novo Nordisk called cLEAN®, the department is responsible for building competences through our cLEAN® Academy and driving strategic improvement projects across CMC Supply. The other main responsibility is statistical support to our development processes and building statistical competences across CMC Supply.

The job
You will primarily support two project managers in their role of driving strategic improvement projects. In this role you will conduct analyses, prepare business cases and support improvement workshops as well as implementing and anchoring solutions. You will also be part of the training team where you will train colleagues across CMC Supply within our field of expertise.

Qualifications
We are looking for an intern who is passionate about lean/SixSigma and has interest in and flair for data analysis. You are currently studying on your master’s degree in Supply Chain Management, engineering or other relevant fields. General knowledge of the pharmaceutical industry or experience with improvement methodologies is preferred. Our preferred candidate has through previous student’s job(s) demonstrated to be service minded, ambitious, and thriving in a busy environment. Fluently in both oral and written English and excellent interpersonal skills are required.

You are an outgoing person with a strong personal drive and dedication, and your curiosity and ability to quickly assess complex problems makes you capable of generating improvement input to the processes and systems surrounding you. In addition, you thrive in a busy environment and bring a can-do attitude and a sense of humor to work.

Practicalities
Qualification: Students in their first or second year of their master studies

Period: The internship position is a full-time position for 4-6 months (depending on your studies)

Start date: Preferably 01-FEB-2014.

Contact
For further information, please contact Helle Rasmussen, +45 3075 5021, or Ole Ekelund, +45 3079 1083.

Deadline
30 November 2013.

Tekniker

- Produktion
- Danmark - Hillerød

Vil du være med til at sikre at Device produktionen i Device Manufacturing Sourcing DMS i Hillerød kører stabilt og efter reglerne? Så læs endelig videre, og se, om det er dig, vi søger til jobbet som teknisk supporter. Du kan se frem til at få 25 engagerede teknikere som dine nærmeste kolleger.

Om afdelingen
Du bliver en del af afdelingen Pre-assembly Production, som producerer Flex-Touch og Flex-pro på vores nye højteknologiske udstyr, og vi kan tilbyde et arbejdsmiljø, hvor dagene aldrig er ens og du kan derfor se frem til mange forskellige opgaver, som vil udfordre og udvikle dig.

Jobbet
Som medansvarlig for den daglige drift på husets produktionslinjer får du til opgave at sikre en effektiv og korrekt servicering af vores udstyr. Når der er behov for akut og kompleks problemløsning, er du en del af teamet der koordinerer indsatsen for en hurtig og effektiv løsning og sørger for dokumentationen efterfølgende. I det hele taget bliver dokumentationen en vigtig del af dit job, da afdelingen anvender et system, der gør det muligt at dele viden, best practice med de andre kollegaer. Du er med til at vedligeholde og optimere vores automatiske produktionslinjer som driftsteknisk team på rulleskift, og det er derfor vigtigt at du har en positiv indstilling over for at arbejde uden for normal arbejdstid.

Kvalifikationer
Vi forestiller os, at du er automatiktekniker eller har El teknisk baggrund/industri elektriker og gerne med kendskab til fejlfinding og optimering på automatiske anlæg fra lignende avanceret montage produktion. Det er nødvendigt, at du kan begå dig på engelsk og at du er vant til at anvende IT, da det danner grundlag for en stor del af vores processer. Det er desuden vigtigt, at du har god kvalitetsforståelse, da vi arbejder indenfor ISO/GMP.

Stillingen er kategoriseret som F3.

Vi forventer du er indstillet på at arbejde på skiftehold, pt. 2. holds skift, senere 3. hold skift incl. weekender

Som person har du gode samarbejdsevner og et opsøgende service mind-set. Du er fleksibel med stor ansvarsfølelse, og har en god portion gå-på-mod. Du er teamplayer og en god kollega, der altid er parat til at give en hånd med. Endvidere lægger vi vægt på, at du har en god ordenssans og er i stand til at holde mange bolde i luften og er indstillet på at gøre en forskel.

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 om stillingen, så kontakt Jesper Jensen på +45 3075 7286.

Ansøgningsfrist
20 november 2013

Administrativ

- Administrative
- Denmark - Hillerød

We are looking for a Personal Assistant to the Director for Biopharm Mammalian Cell production in Hillerød. You will work closely with the Director and the management team and you will be a part of the team of Assistants in Biopharm. The position requires strong organisational skills and a high degree of independence as well as detail orientation.

About the department
Biopharm Mammalian Cell Production is a production area with 70 employees in 3 teams located in Hillerød.

The job
As a department Assistant your key area of responsibility will be to support the Director in establishing smooth operation of various processes. Your tasks will include monthly reporting, close follow up on department budget, administration of training and preparation for new employees, central role in audits, organising and following up on projects and organisational requirements.Furthermore you will be a member of the team of assistants in Biopharm and play a role in cross-organisational initiatives.

Qualifications
You have an administrative education or hold a bachelor degree and have a minimum of 4 years relevant working experience. You demonstrate good business understanding and master professional communication skills. You have flair for numbers and solid IT skills. You are fluent in English both written and spoken. You have a strong Quality mindset and understand the GMP principles that are the basis for our business. Experience from a similar position in Novo Nordisk is an advantage. We are looking for a person who is enthusiastic and engaged. You are reliable, loyal and service-minded. You have a can-do attitude; enjoy working under tight deadlines and master good coordination skills. You work in a structured manner with a sense for the details. It is important that you can work independently, be proactive, and always strive to find solutions to the challenges that keep coming up in a busy environment.

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

Contact
For further information, please contact Jane Karina Nielsen on +45 3079 8795.

Deadline
24 November 2013

Technician for Stem Cell Development

- Research & Development
- Denmark - Bagsværd

Are you passionate about early applied development within cell replacement therapy? Do you want to be part of a team that work on the development of a stem cell based therapy leading to a cure for diabetes and its complications? Then join CMC Stem Cell Development at Novo Nordisk A/S, Denmark. Our objective is to develop cell replacement therapy into a viable option for treating Diabetes Mellitus by developing procedures for pilot scale cultivation and purification of beta cells derived from stem cells.

About the department
In the initial phase you will contribute to building a strong new department in CMC Support and assist in clarifying the need for the technical processes, implementing cGMP and aseptic production.

The department is located in CMC API Development, where we are approximately 350 employees, located in CMC supply under Novo Nordisk Research and Development.

The job
The goal is: Through innovation within the area of bioprocess development and the possibility in the differentiation of stem cells to combine and turn this into a clinical application. As part of the development team, you will; execute and evaluate the experimental work towards establishing a robust procedure for manufacture of beta cells to be used for the clinical trials.

Currently, robust and scalable procedures for the manufacture of beta cells derived from embryonic stem cells do not exist. However, with the team, you will ensure that the project delivers according to plans and deadlines. In all your work, you promote high technical and quality standards and contribute to the positive, enthusiastic working environment.

Qualifications
The optimal candidate have a background in mammalian cell cultures preferable in human embryonic stem cells, molecular biology and/or developmental biology, and/or have extended knowledge with GMP and aseptic production and/or have worked in manufacture of drug substances for clinical trials.

Our candidate is proactive, outgoing and possess a strong desire to get the job done. You have a creative mind set and a positive outlook on your work, this enables you to get to the bottom of challenges and provide new methods and perspectives. At the same time, you have a well-structured approach to your work. You are a team player and comfortable working in a dynamic work environment. You have relevant experience, and you are able to communicate in English, written as well as spoken.

Novo Nordisk is build on skills, commitment and ambitions, this is what helps us to improve and develop new products that ultimately change and improve many people's lives. We offer you an opportunity to join Novo Nordisk and work with exceptionally talented colleagues, and we offer you a wide range of opportunities for professional and personal development.

Contact
If you find this interesting and would like further information, please contact Sanne Bové at +45 3075 5635 or Jørn Meidahl +45 30 79 2634 or Kirsten McGuire +45 30 79 6637.

Deadline
30 November 2013.

Global Medical Advisor

- Marketing
- Denmark - Søborg

Novo Nordisk has a leading position in Global Medical Affairs Diabetes and in this area we are seeking a Global Medical Advisor

About the Department
Novo Nordisk is recruiting a Global Medical Advisor to join the Global Medical Affairs team in the Company Headquarters outside of Copenhagen, Denmark. This is a unique opportunity to work for a world leader in diabetes care and help improve the lives of people with diabetes worldwide.

Global Medical Affairs is responsible for delivering consistent scientific communication across phases in clinical trial programmes. We provide input to phase I-III trial design and drive post-approval study strategy.

The Job
The Global Medical Advisor belongs to a highly motivated group of Medical Doctors with clinical, research and marketing experience, and can maximize best practice sharing. By working closely with Global Product Managers, the Global Medical Advisor gives directions and input to the product strategy and positioning. Furthermore, the Global Medical Advisor establishes and maintains the link to Key Opinion Leaders (KOL) by ensuring the strategic approach and positioning is appropriately challenged. This position also builds the global KOL strategy (including meetings), and ensures it is properly executed and on-track.

Internally, the Global Medical Advisor works together with highly professional and specialized people within clinical reporting, drug discovery, publication planning, clinical development, regulatory, health economy, marketing, communication and affiliates. The Global Medical Advisor will be involved in the global publication planning giving input to the publication strategy and participates actively in the review process for publication.

Externally, the Global Medical Advisor acts as a liaison between Novo Nordisk and Key Opinion Leaders. The Global Medical Advisor is a strategic partner within an interdisciplinary project team and provides input to clinical development plans from a marketing and communication perspective. The role must maintain relationships with external experts and cultivate relationships with new opinion leaders, through Global Advisory Board meetings, etc. The Global Medical Advisor is an internal and external resource, developing, reviewing and approving educational and promotional material, incl. slide kits, CME programs, web-sites, etc. This position is also responsible for scientific programs and activities at international scientific meetings.

Qualifications
The candidate must have a background as Medical Doctor with relevant clinical experience and preferably a research background (clinical or basic science) and/or business education. Previous experience from a pharmaceutical company is a plus. The candidate must be action oriented, with a strong drive, and focus on results; Extrovert, engaged and customer-oriented; Team-player with good peer relationships; Well structured and perseverant; High integrity and good at solving problems; Flexible attitude, willingness to travel and motivated for personal development; fluent in both oral and written English (company language) and strong presentation skills.

Location: The position is based in Denmark in Søborg (10 kilometres from the centre of Copenhagen). Worldwide travel should be expected.

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

Contact
For further information, please contact Anne Mette Rosenfalck +45 3075 3203.

Deadline
25 November 2013.

Teamleder Trainee

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

- Produktion, Teamleder
- Danmark - Kalundborg

I Novo Nordisk arbejder vi hele tiden målrettet på at skabe en god pipeline til vores Teamlederstillinger. Et af vores succesrige tiltag er at ansætte allerede dygtige eksterne Teamledere i stillinger for kommende Teamledere i et uddannelsesforløb. Dette er en succes, da Novo nordisk er en kompleks virksomhed, hvor særligt produktions Teamlederne fra dag 1 skal præstere på et meget højt niveau.

Så kan du gå forrest og motivere, inspirere og lede produktionsoperatører og/eller Drifts Supportere og vil du rigtig gerne være med til at producere Novo Nordisks insulin, så har vi dit nye job klar til dig. Du kommer til at udfolde dig i en succesrig afdeling i rivende udvikling, hvilket giver masser af muligheder og udfordringer. Vi står netop nu foran en større opskalering af produktionen og indførelse af et nyt produkt i produktionen. I IM1 Support er vi en værdifuld støtte for produktionen i den proces.

Til Insulin Manufacturing I (IM1) i Kalundborg søger vi dig, som ønsker at bruge dine evner og interesse indenfor ledelse. IM1 er verdens største insulin fabrik, med 360 medarbejdere, der varetager alle processer fra gæring til oprensning, samt alle support funktioner såsom logistik, projektledelse og automation.

Novo Nordisk i Kalundborg er en by i byen. Området, der ligger en god times kørsel fra København, dækker 1.350.000 m2 og rummer mange fabrikker, laboratorier og eget vejnet. Vi producerer ca. 50 % af verdens insulin, og er på forkant med udviklingen indenfor teknologi, systemer, metoder og processer. Hvis du er vor nye kollega, kan vi garantere dig nogle udfordringer og karrieremuligheder, som du vil få svært ved at finde andre steder.

Om afdelingen
Du bliver en del af afdelingen IM1 Support. Vi leverer support til produktionen i form af projektledelse, drift og udvikling af automation/IT løsninger, råvareindkøb, logistik, finans og koordineringsopgaver på tværs af vores store insulinfabrik. Kulturen er udpræget resultatorienteret med stort fokus på at lykkes. Afdelingen består p.t. af ca 60 medarbejdere – og der mandes i øjeblikket op til at kunne støtte udviklingen i fabrikken med at øge produktionskapaciteten og producere et nyt produkt.

Jobbet
Du får mulighed for at lære jobbet som Teamleder i Novo Nordisk at kende ved at assistere en dygtig teamleder med interessante ledelsesopgaver. Teamlederens og dine væsentligste opgaver er at udøve personaleledelse, sørge for den daglige drift og via medarbejderne få gennemført de vigtigste optimeringer/projekter, som er forankret i teamet, herunder sørge for, at rammerne er plads ift. bemandingsplaner, opstilling af mål på både team- og medarbejderniveau, ansættelser, eventuelle afskedigelser og oplæringsplaner for nye medarbejdere etc. Dit overordnede mål er at sikre en stabil og leveringsdygtig support, hvor vi leverer i rette kvalitet, til rette tid og til lavest mulig omkostning.

Din helt afgørende udfordring sammen med Teamlederen er at få teamet til at spille aktivt og positivt med i forhold til de udfordringer og forandringer de møder i deres hverdag. Du skal på daglig basis og i mange sammenhænge forklare, hvorfor det er rigtigt og nødvendigt at ændre rutiner, arbejdsgange, roller og strukturer i organisationen.

Du refererer til afdelingslederen, og indgår i ledergruppen i afdelingen. Desuden deltager alle teamledere og du i IM1s ledelsesgruppe, hvor emnerne af mere strategisk karakter bliver drøftet. Jobbet giver derfor en bred berøringsflade og store muligheder for personlig og faglig udvikling.

Kvalifikationer
Du har en teknisk eller akademisk uddannelse, og/eller har fået skabt en god all round teknisk forståelse gennem din karriere som leder i et GMP-reguleret farmaceutisk produktionsmiljø. Din viden ligger særligt i spændet mellem produktion og processer med en kobling til, hvad forandring i den sammenhæng kræver af ledelse. Du kender også til LEAN og har lyst til at arbejde aktivt med det som del af din hverdag.

Din faglige identitet er først og fremmest som leder, og du trives derfor med at sætte retning og løse de problemer, der dagligt opstår i et højeffektivt produktionsmiljø. Du ved derfor også, at du får brug for dine gode kommunikationsevner, din naturlige empati og din fleksible indstilling ift. at få skabt løsninger, hvor alle involverede føler, at de er hørt. Derudover skal du kunne bruge MS Office og særligt Excel samt være god til både dansk og engelsk. Vi søger en kandidat, der er ansvarsbevidst, målrettet, initiativrig, og har den faglige nysgerrighed i behold. Jobbet kræver forandringsparathed samt evner og lyst til at gennemføre løbende forbedringer/optimeringer af processer og arbejdsrutiner. Selvstændighed er en forudsætning, men du skal også kunne samarbejde med forskellige faggrupper, hvorfor der kræves gode samarbejds- og kommunikationsevner.

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

Kontakt
Vil du vide mere om stillingen, så kontakt Mette Krogh telefon +45 3075 6166.

Ansøgningsfrist
30. november 2013.

Personlig assistent for VP

- Produktion
- Danmark - Hillerød

Er du god til at holde mange bolde i luften og arbejde på tværs af et stort område? Har du lyst til at skabe fælles rammer og arbejdsgange, som samler afdelingerne inden for VP området. Er du udadvendt, positiv og frisk på udfordringer? Så er du måske den nye VP assistent.

Om afdelingen
Vi er knap 350 medarbejdere fordelt på fem afdelinger, hvor vi fylder insulin i penfills og monterer og pakker FlexPen og FlexTouch. Vi er et område med høj aktivitet og stor udvikling, fordi vi kører 24/7 og samtidigt er launch site for Novo Nordisk nye produkter. Derfor er forandringsparathed og løsningsorientering vigtige kompetencer i vores område.

Jobbet
Du bliver ansvarlig for at støtte VP’en, ledelsesgruppen i området og samtidigt skabe en sammenhæng i huset gennem et godt arbejde med assistentgruppen og lederne. Du planlægger ledermøder og seminarer, står for kommunikation i huset og indgår i SDK kommunikationsgruppen. Du bliver ansvarlig for assistent gruppen i huset og skal sammen med to eksisterende og flere nye assistenter skabe et godt samarbejde i gruppen, så I understøtter huset i fællesskab. Du bliver også kulturbærer for huset og får mulighed for at implementere kulturinitiativer som Take Action, succes fejringer og andre tiltag der skaber stemning og sammenhold. Desuden bliver du koordinator på de officielle besøg til Novo Nordisk som ofte kommer forbi 25A.

Kvalifikationer
Du er struktureret og kan bevare overblikket i en hverdag med mange forskellige opgaver og samarbejdspartnere. Du løser en bred vifte af opgaver, fra kalenderstyring og praktisk hjælp, til styring af projekter og større events. Du har blik for detaljen, er god til at kommunikere på dansk både mundtligt og skriftligt og kan skrive nyhedsbreve, præsentationer og andet i et fængende og korrekt sprog. Du kan arbejde i Excel og Powerpoint, og din flair for IT hjælper dig til hurtigt at lære vores mange interne IT-systemer at kende. Du går positivt til nye udfordringer og har lyst til at være del af et hus med højt tempo og masser af udvikling.

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

Kontakt
Spørgsmål rettes til VP Anne Reker Cordt på telefon +45 3079 0518.

Ansøgningsfrist
19.november 2013.

Laborant

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

- Produktion
- Danmark - Kalundborg

Laboranter til mikrobiologisk team i QC laboratorium

Brænder du for at arbejde med mikrobiologi, og har du lyst til at være med til at sikre at kvaliteten af vores produkter er helt i top? Vil du være en del af et engageret, velfungerende og kompetent laboratorieteam? Så er du måske vores nye kollega.

Om afdelingen
Vi søger to engagerede laboranter (en fast stilling og et barselsvikariat) til det mikrobiologiske analyseteam, som består af 13 personer. Teamet supporterer områdets fire finrensningsfabrikker med mikrobiologiske analyser og endotoxin analyser.

Afdelingen består af ca. 90 engagerede medarbejdere, fordelt på 5 analyseteams. Hvert analyseteam indgår i et tæt samarbejde med produktionen og de øvrige QC laboratorier på siten. Analyseresultaterne danner basis for styring af produktionen og frigivelse af vores moderne insulinprodukter.

Jobbet
Dit daglige arbejde vil primært bestå i at sikre den daglige drift fra analyse til resultatfrigivelse. Det er afgørende at GMP niveauet er helt i top i alle trin i både det praktiske arbejde med udførelsen af analysen og omkring dokumentationen og godkendelsesprocessen. Vi arbejder i en LEAN kultur, hvor vi fokuserer på, at optimere vores arbejdsgange i laboratoriet gennem løbende forbedringer og fokus på struktureret problemløsning. I den forbindelse samarbejder vi også med de øvrige QC laboratorier i området.

I teamet har vi stor fokus på trivsel og på at have et arbejdsmiljø, hvor vi får det bedste frem i hinanden. Vi har en vinderkultur, og vi er alle motiverede for at ville være det bedste team, inden for vores felt. Du er med til at sikre, at vi driver vores analysearbejde på en god og effektiv måde, herunder sikre, at vi leverer analyseresultater til vores kunder i produktionen i rette mængder, rette tid og vigtigst af alt i den helt rette kvalitet.

Kvalifikationer
Du har en relevant uddannelse som laborant/bioanalytiker og interesse for eller gerne erfaring med den farmaceutiske industri. Du har erfaring med de klassiske mikrobiologiske analyser som dybde- og membranfiltreringsanalyser og også gerne kendskab til LAL/endotoxin.

Du er initiativrig, fleksibel og parat til at tage ansvar. Som person er du nysgerrig og har viljen til at finde årsager og løsninger på dagligdagens udfordringer. Du skal kunne lide at arbejde i en struktureret verden, hvor vores mål og resultater hver dag følges, og hvor vi i fællesskab gør, hvad vi kan for at opnå det, vi løber efter. Derudover trives du i en omskiftelig og til tider travl hverdag, og du har en positiv indstilling til forandringer. Du er en fighter, en holdspiller og du er altid villig til, at gå den ekstra mil for dine kollegaer, så vi løfter i flok.

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 høre mere om stillingen, er du meget velkommen til at kontakte Randi Poulin Pedersen, på +45 3079 8162.

Ansøgningsfrist
24.november 2013.

Udstyrs ansvarlig

- Produktion
- Danmark - Gentofte

Har du lyst til at bruge din tekniske viden i et produktionsmiljø, hvor kvalitet og en høj oppetid er afgørende? Så kan du blive vores nye kollega i Biopharm Filling i Gentofte.

Om afdelingen
Du bliver en del af en afdeling, som har det tekniske ansvar for produktionsudstyret i Biopharm Filling. På fabrikken er vi 107 kolleger, der tilsammen står for formulering, påfyldning, frysetørring og inspektion af lægemidlet GlucaGen® til det globale marked. I teknisk support arbejder du sammen med 6 ingeniører og 3 maskinmestre.

Jobbet
Dit mål er at yde support til produktionsudstyret, så vi sikrer, at den daglige drift kører uden nedbrud og i henhold til kvalitetskravene. Du skal bl.a. foretage troubleshooting på maskiner og systematisk problemløsning, ligesom du implementerer forbedringer og udarbejder dokumentation i forhold til GMP og andre regulativer. Du kommer til at arbejde tæt sammen med dine kolleger i afdelingen. Derudover deltager du i større og mindre projekter f.eks. som at optimere nuværende udstyr samt implementere af nyt udstyr. Alt dit arbejde foregår i tæt sparring med forskellige faggrupper både i og uden for afdelingen. Du kan se frem til en afvekslende men til tider en travle arbejdsdage i et job med gode udviklingsmuligheder og udfordrende opgaver.

Kvalifikationer
Du er formentlig uddannet maskiningeniør, og du har lyst at arbejde med teknisk kompliceret udstyr. Det er et plus, hvis du har erfaring fra et GMP-reguleret produktionsmiljø, hvor du f.eks. har udarbejdet afvigelser og ændringssager. Uanset hvad har du forståelse for, hvorfor det er nødvendigt med fyldestgørende dokumentation. Du formår at kombinere din pragmatiske tilgang til problemløsning med din teoretiske viden. Du er social og positiv anlagt, og du arbejder proaktivt og løsningsorienteret. Videndeling falder dig naturligt, og du arbejder systematisk og med dedikation til at skabe gode resultater sammen med dine kolleger. Med dine gode samarbejdsevner og kommunikationsevner kan du ubesværet arbejde på tværs af faggrupper. Endelig formår du at jonglere flere bolde uden at miste dit gode overblik, ligesom du behersker engelsk flydende skriftligt og mundtligt.

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 Kasper Siewert på +45 3075 9572.

Ansøgningsfrist
1.december 2013

Associate Supply Professional

- Supply Chain and Logistics
- Denmark - Bagsværd

The Purchasing department, part of Novo Nordisk Sourcing Operations in Bagsværd, is looking for an Associate Sourcing Professional for the Filing and Tableting team, for a one year maternity leave replacement.

About the department
We are a team of 13 dedicated colleagues, and are responsible for setting up and maintaining effective supply chains for sourcing of production materials, as well as ensuring the supply of these materials to all Novo Nordisk Filing and Tableting production and development departments worldwide. Your main responsibility will be inventory and order management of the Process Aids category, including both daily operations and improvement projects.

We are looking for a highly motivated and result oriented candidate, who takes pride in delivering high quality work, on time and in a pro-active way.

The job
Our ambition is to deliver high quality services to manufacturing sites and their production departments. You will be responsible for specific items, and will ensure deliveries to production in full and on time. To achieve this, you will be in direct contact with our production sites in Denmark and abroad, and with suppliers, you will monitor inventory level of your items, prioritise needs from production and coordinate activities with other functions in Sourcing Operations to secure availability of released material, and you will place purchase orders with international suppliers and follow up on deliveries to NN warehouses and with NN release flow.

Additionally, you will participate in or drive improvement projects.

Qualifications
We expect you to have a higher education (preferably Master’s Degree) within a relevant discipline e.g. Supply Chain Management, Engineering, or alike, with 0-2 years of purchasing or supply chain experience. Excellent data management skills, an analytical mindset and an ability to work independently with Excel and SAP will be assets.

As a person you have a high energy, a positive mindset and are open towards other people and new ideas. You work independently and you like a dynamic environment with many simultaneous tasks and changing priorities, while managing strict deadlines. You thrive in international environments, with people of diverse backgrounds. You master English and Danish fluently, both written and spoken.

We offer you an exciting job among great colleagues and in a positive working environment, potentially providing a platform for other positions in the department or Novo Nordisk.

Contact
For further information, please contact Maud Le Crom at +45 3075 6476.

Deadline
20 November 2013.

Document Specialist

- Research & Development
- Denmark - Måløv

Is your IT mind set on structure and quality, then join Novo Nordisk, Non-Clinical Development department in Måløv and help us meet the internal and regulatory demands for non-clinical documentation.

About the Department
You will have 6 dedicated and focused colleagues in Submission & Study Support, who supports more than 60 scientists in different departments in Research & Development. Look forward to a job where you will juggle with several IT programmes and have a central role in a key function of Novo Nordisk. All pharmaceutical companies are committed to live up to the very strict rules and regulations for documentation, and Novo Nordisk is furthest advanced in this process.

The job
The prime objective for you and your colleagues will be to support fulfilment of internal and regulatory demands for non-clinical documentation. You make sure that the documents are in the right format and in compliance with international requirements for electronic submission (e-CTD). Moreover, you support internal and external partners in document and template handling and train and support your colleagues in the use of our electronic document management system. You will be handling large amounts of reports in several IT systems, and this challenging and interesting job is all about making these systems collaborate and work together.

Qualifications
There are many entries into this interesting job, however an academic degree will be an advantage i.e. within information science or similar. The all-important and indispensable requirement is that you have the right mindset, are curious and take pride in solving highly critical issues and tricky challenges. Besides, it is important that you are an experienced IT system user, have technical flair and knowledge of electronic document management systems. You are an advanced user of MS Word (preferably with VBA knowledge) and Adobe Writer, and you easily switch between various IT programmes in order to find the best suitable programme for the given task. This calls for an excellent eye for details and a quality mindset above average, and if you are already familiar with Good Laboratory Practice regulations, it is a great plus. You thrive in a hectic environment and do not lose your general view even when priorities change and you are compelled to readjust. You are a dedicated team player but you also take on individual responsibility and see disseminating information as a challenge. Lastly, you have a good sense of humour, proficiency in spoken and written English and good communication skills.

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 Sandie Philipsen +45 3075 3713.

Deadline
25 November 2013.

Associate Sourcing Professional

- Supply Chain and Logistics
- Denmark - Bagsværd

The Purchasing department, part of Novo Nordisk Sourcing Operations in Bagsværd, is looking for an Associate Sourcing Professional for the Filing and Tableting team, as replacement of one of our team members moving to another position in Novo Nordisk.

About the department
We are a team of 13 dedicated colleagues, and are responsible for setting up and maintaining effective supply chains for sourcing of production materials, as well as ensuring the supply of these materials to all Novo Nordisk Filing and Tableting production and development departments worldwide. Your main responsibility will be inventory and order management of the Glass (vials and cartridges) and Foil items, including both daily operations and improvement projects.

We are looking for a highly motivated and result oriented candidate, who takes pride in delivering high quality work, on time and in a pro-active way.

The Job
Our ambition is to deliver high quality services to manufacturing sites and their production departments. We are responsible of the supply to all Novo Nordisk filling and tableting sites worldwide, and your position will include close cooperation with our colleagues in US, Brazil, France, China and Denmark.

You will be responsible for your assigned items to ensure deliveries to production in full and on time. To achieve this, you will be in direct contact with our production sites and our suppliers, you will monitor inventory level of your items, prioritise needs from production and coordinate activities with other functions in Sourcing Operations to secure availability of released material, and you will place purchase orders with international suppliers and follow up on deliveries to NN warehouses.

Additionally, you will participate in or drive improvement projects.

Qualifications
We expect you to have a higher education (preferably Master’s Degree) within a relevant discipline e.g. Supply Chain Management, Engineering, or alike, with 0-2 years of purchasing or supply chain experience. Excellent data management skills, an analytical mindset and an ability to work independently with Excel and SAP will be assets.

As a person you have a high energy, a positive mindset and are open towards other people and new ideas. You work independently and you like a dynamic environment with many simultaneous tasks and changing priorities, while managing strict deadlines. You thrive in international environments, with people of diverse backgrounds.

You master English fluently, both written and spoken.

We offer you an exciting job among great colleagues and in a positive working environment, providing a good platform for development within in the department or Novo Nordisk.

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 Maud Le Crom at +45 3075 6476.

Deadline
20 November 2013

Operatør til Deviceproduktion

- Produktions operatør
- Danmark - Hillerød

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

Så er du måske den nye engagerede kollega, vi søger i DMS, Pre-assembly Team (Hillerød). Vi er et team med ca. 25 maskinoperatører, som betjener 3 højautomatiske produktionslinjer.

Stillingen er en fast stilling, hvor forskellige skifteholdsplaner må forventes jf. gældende regler, herunder også natarbejde.

Her støber vi fremtidens devices
I vores afdeling har vi til opgave at samle motormodulet til FlexTouch® og FlexPro®, som er en engangspen, der kan benyttes til vækst hormon og insulin.

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

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

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

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

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

Du har dansk, matematik og engelsk på mindst 9. klasses niveau og/eller en uddannelse som for eksempel industrioperatør, procesoperatør, håndværker eller lignende, og du har mulighed for at dokumentere dette.

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

Kontakt
Har du spørgsmål til stillingen, så kontakt Anders Pedersen på tlf. 3079 7896 eller Kenneth Jessen på tlf. 3075 0721

Ansøgningsfrist
18.november 2013

Talent Researcher

- Human Resources
- Denmark - Greater Copenhagen area

Can you ensure Novo Nordisk succeed to recruit the right people with the right competencies, for the right place, at the right time and thereby help Novo Nordisk to be a winning company!

Then you may be our new Talent Researcher in Novo Nordisk Product Supply supporting the largest site in Novo Nordisk’s global production network: Site Kalundborg.

About the department
Product Supply is responsible for the manufacturing and supply of all products sold by Novo Nordisk. We are more than 10,000 employees located in Denmark, USA, China, Brazil and France, and it is up to us to make sure that our high-quality products are available when our customers need them. In Product Supply’s HR function you find our team of highly motivated and ambitious Recruitment Consultants. Our challenge is to support Product Supply’s Managers with recruitment and constantly improve, develop and strengthen our recruitment process. We are located in Søborg (soon Bagsværd) and Kalundborg and support our customers all over Denmark. By this position we are adding elements of search strategies to secure on boarding the right talents. The position is temporary and of one year’s duration and you will be working from both Bagsværd and Kalundborg.

The job
Your main task is to drive proactive sourcing of external talents to our hard-to-fill positions in the largest site in Novo Nordisk’s global production network. By researching the potential candidate market in relevant industries through networks, social media and other information sources available, you identify and establish the first contact to potential candidates. Through this process, you build and maintain solid candidate pipelines. Working closely with your recruitment- and HR partner colleagues as well as hiring managers in Kalundborg is a daily part of your job – in order to ensure that the search efforts are aligned with the business needs.

This is a position in a dynamic environment with good opportunities for personal and professional development. Driving to different sites on Zealand on a weekly basis must be expected.

Qualifications
You probably hold an academic degree and have 4-6 years of experience with recruitment and talent research. You are ambitious, flexible and able to work very independently, and you thrive in an ever-changing environment. Based on your proactive, structured approach you have a strong track record of building up pipelines for hard to fill positions. Experiences from the Life-Science industry will be appreciated. Sense of simplicity will be highly appreciated when it comes to building the search function and candidate pipelines. Since we are a global company, you need to be proficient in English.

At Novo Nordisk we use our skills, dedication and ambitions 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. And if you are our new colleague, we guarantee challenges and career opportunities that will be hard to find elsewhere.

Contact
For further information, please contact Thomas Rasmussen at +45 30 75 54 76 or Annelise Vidø at +45 30 79 49 16.

If you want to learn more about the largest site in Novo Nordisk’s global production network please use this link novonordisk.com/kalundborg-careers.

Deadline
17 November 2013.

Reparatør eller tekniker til maskin vedligeholdelse (Kalundborg, Danmark)

Product Manager (Greater Copenhagen area, Denmark)

Business Analyst (Bagsværd, Denmark)

OHS SVP partner (Kalundborg, Denmark)

IT Risk Coordinator (Bagsværd, Denmark)

Energetic QA Team Member with Quality Mindset (Hillerød, Denmark)

Intern to CMC Process Support (Gentofte, Denmark)

Tekniker (Hillerød, Danmark)

Administrativ (Hillerød, Denmark)

Technician for Stem Cell Development (Bagsværd, Denmark)

Global Medical Advisor (Søborg, Denmark)

Teamleder Trainee (Kalundborg, Danmark)

Personlig assistent for VP (Hillerød, Danmark)

Laborant (Kalundborg, Danmark)

Udstyrs ansvarlig (Gentofte, Danmark)

Associate Supply Professional (Bagsværd, Denmark)

Document Specialist (Måløv, Denmark)

Associate Sourcing Professional (Bagsværd, Denmark)

Operatør til Deviceproduktion (Hillerød, Danmark)

Talent Researcher (Greater Copenhagen area, Denmark)