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Dygtige ledere til Novo Nordisk Kalundborg (Kalundborg, Danmark)

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Dygtige ledere til Novo Nordisk Kalundborg

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

- Produktion, Teamleder
- Danmark - Kalundborg

Brug dine GMP-evner i verdens største insulinproduktion

Novo Nordisk er verdens førende virksomhed inden for diabetesbehandling. Vores ambitioner og dygtige medarbejdere har bragt os meget langt. Og vi er slet ikke færdige. Derfor investerer vi massivt i hele vores værdikæde. Det gælder globalt og ikke mindst i vores produktions-setup. Vores fabrikker i Kalundborg er en hjørnesten i dette. Og det er her, du kommer ind i billedet.

Om afdelingen
Vores succes gør, at vi mangler dygtige teamledere med ledererfaring i en hel række teams i Kalundborg. Jobbene spænder bredt, og vi har derfor brug for profiler med forskellig erfaring og specialisering. Nogle skal lede akademiker-teams i business support-funktioner og andre skal lede teams i selve produktionen. Teamene er typisk på 8-20 medarbejdere.

Jobbet
De forskellige teams arbejder fx med processupport, QA, QC, projekter, EHS & IT, vedligehold eller logistik, planlægning, indkøb og økonomi m.m. Som teamleder er du en vigtig nøglefigur når du driver dit team og dermed Novo Nordisk frem til nye, store resultater. Med din positive og smittende energi får du dit team til at spille sammen, så I når selv de mål, I troede, var tæt på umulige. Du sætter retningen, inspirerer og vejleder dine medarbejdere, så de er klar over: hvad målene er, hvorfor deres indsats er så vigtig, og hvordan de arbejder smart og efter gældende regler og myndighedskrav.

I den sammenhæng driver du løbende optimeringer af vores systemer og processer ud fra vores LEAN-tankegang. Forandring til det bedre er således en helt central del af vores verden, og som leder går du forrest i at tænke nyt og hele tiden stræbe efter at blive bedre. Du bliver en del af afdelingens lederteam og er i tæt dialog med teamlederkolleger på tværs af afdelinger. Det er jeres ansvar at implementere Novo Nordisk’s strategi og værdier i afdelingen. Du kan se frem til et job, hvor du får mulighed for en stærk faglig, personlig og ledelsesmæssig udvikling.

Kvalifikationer
Du har en længerevarende uddannelse og konkret ledererfaring. Du kan derfor kombinere den nødvendige faglige indsigt med en åben og anerkendende ledelsesstil, som du bruger til at involvere og engagere dine medarbejdere. Samtidig har du gennemslagskraft og kan træffe og gennemføre selvstændige beslutninger. I forlængelse heraf trives du i en foranderlig kultur med ambitiøse målsætninger og høj grad af kompleksitet. Har du ikke arbejdet med LEAN, har du erfaring med systematisk optimering og problemløsning. Vil du arbejde i eller supporterende til produktionen, skal du have GMP/GxP erfaring fra et reguleret miljø underlagt høje kvalitetskrav.

Novo Nordisk i Kalundborg

Novo Nordisk PS Kalundborg er i sig selv en by i byen, kun godt en times kørsel fra København. Området er på størrelse med 270 fodboldbaner. Vi er 2.700 mennesker i alt fordelt på 15 fabrikker, og vi producerer ca. 50 % af verdens insulin. PS i Kalundborg kan helt kort sammenfattes til: udviklingsmuligheder uden ende. Skulle du have lyst til at flytte til Kalundborg, kommer du til en by tæt på skov og vand, med gode skoler, sports og fritidsfaciliteter og meget mere. Har du brug for det, har vi gode erfaringer med at hjælpe tilflyttere med at finde ny bolig. Besøg vores hjemmeside og læs mere om de forskellige job og PS Kalundborg.

Vi glæder os til at høre fra dig: novonordisk.com/kalundborg-careers

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 stillingerne, så kontakt Lili Behjat Kristensen på LBEK@novonordisk.com

Ansøgningsfrist
31. januar 2013

Finance Partner (Kalundborg, Denmark)

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Finance Partner

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

- Finance
- Denmark - Kalundborg

Would you like to join our team controlling all diabetes active product ingredient (DAPI) production at Novo Nordisk?

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.

About the department
As Finance 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.

In a highly skilled environment, you will be responsible for delivering high quality management information and proactive business sparring to management. You will have the responsibility for one of our production facilities. In close cooperation with 3 colleagues in the Finance Partner team, you will be responsible for financial planning and controlling and for execution of various other financial processes. You will participate in ad hoc analyses etc.

The job
You will have a wide variety of contacts, in a production-oriented, high-performance environment, and you will be involved in a broad range of financial decisions. Your contacts, ranging from senior management to local controllers, will facilitate building a solid network beneficial to your professional and personal growth. You will also gain a broad and in-depth understanding of the Novo Nordisk business.

Qualifications
You have a Masters degree in management accounting, business administration or the equivalent. You have some years of relevant work experience with superior and documented results. You have outstanding analytical skills combined with a structured, result-oriented approach.

You are fluent in written and spoken English and have good communication skills. You demonstrate initiative and have a high level of engagement. A high level of Excel skills are necessary and you must enjoy working with complicated Excel models.

You are happy in a dynamic and changeable work environment in which some days will involve very individual efforts while on other days you will work in the team and participate in meetings.

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

Deadline
15 December 2013.

Senior International Trial Manager (Søborg, Denmark)

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Senior International Trial Manager

- Research & Development, Trial Manager
- Denmark - Søborg

Do you have extensive experience in driving global clinical trials and do you want to exert your influence by managing large global trials in Inflammation and Growth Hormone, including trials in Rheumatoid Arthritis (RA), Crohn’s Disease (CD), Systemic Lupus Erythematous (SLE), ulcerative colitis (UC) and Growth Hormone Deficiency disorders? Are you prepared to embrace and tackle constant changes as part of your work each day? Then we may have just the right job for you.

About the department
Inflammation & Growth Hormone is the newest therapeutic area in Novo Nordisk. In Clinical Operations, Inflammation & Growth Hormone, we are now approx. 40 employees and we continue to grow as the pipeline matures. We are responsible for the planning, conduct, and finalisation of clinical trials within Inflammation & GH. We collaborate globally, with CROs and to a growing extent, with our Novo Nordisk affiliates. We are characterised by a world-class team spirit and quality mind-set, by our change readiness and an open, trust-based and creative working environment. Our working environment is characterised by interesting and demanding assignments and continuous professional development opportunities.

The job
The job as Senior International Trial Manager demands that you are capable of directing and driving large global phase 2b/3 trials. You will be responsible for ensuring that project key deliverables are met in time, at a high quality and within budget. You will be chair of the international study group, for which you will plan and conduct team meetings with focus on stakeholder engagement, knowledge sharing and decision making. This includes vendor management of CROs participating in the trial execution. You will participate in and contribute to relevant investigator and monitor meetings.

The job requires that you apply a structured and analytical approach during development of relevant trial documents such as trial protocol, informed consent, recruitment strategies, risk analysis plans, communication plans and trial budgets. You are detail-oriented, while able to maintain overview, digest complex data and evaluate the adequate level of quality.

You are expected to be able to identify better practices and create improvements and you will be able to chair cross-project/cross-functional tasks forces. You may act as trainer across projects and mentor new staff.

Qualifications
You hold an academic degree within natural sciences or healthcare. You are a clear communicator and can inspire and motivate a team to deliver their best in an ever-changing environment. You have a strong knowledge of clinical trial planning and execution and a minimum of 5 years’ experience in managing large clinical trials.

You have a quality mind-set and know how to prioritise between different tasks in a dynamic environment which requires a high degree of flexibility. You work independently while also being a dedicated team player. You have excellent cross-cultural awareness and like to contribute to multi-cultural project groups. You are fluent in written and spoken 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.

You will be part of a successful, expanding company in which working is not just a way to make a living, but a way to make a difference.

Contact
For further information, please contact Louise Høyer at +45 3075 1535 or Marianne Willert at +45 3079 3277

Deadline
07 January 2014.

Laborant til laboratorieforsøg-produktion af HPLC-kolonner (Køge, Danmark)

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Laborant til laboratorieforsøg/produktion af HPLC-kolonner

- Produktion
- Danmark - Køge

Vil du samarbejde omkring stabile produktionsprocesser og levering af HPLC-kolonner og være en del af et team i udvikling med fokus på faglighed, engagement og quality mindset ? Du er positiv, engageret og fleksibel, og du trives med en omskiftelig hverdag, hvor fokus sættes ud fra kundernes behov. Vi har brug for din hjælp i en 9-10 måneders periode. Vi tilbyder en spændende arbejdsplads med skiftende udfordringer, hvor du kan opnå god erfaring med kolonneproduktion/stabilisering af produktionsprocesser. Arbejdet foregår i en uformel atmosfære, hvor vi har fokus på som team at levere i rette kvalitet til vores kunder.

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. Tungt fysisk arbejde kan forekomme. Såvel udvikling som produktion dokumenteres.

Jobbet
Arbejdet vil hovedsagelig bestå i at udføre og dokumentere laboratoriearbejde omkring levering af HPLC-kolonner og stabilisering af produktionsprocesser for kromatografiske geler og kolonnepakning.

Vi producerer, pakker og kvalitetskontrollerer kolonner. Du vil afhængig af erfaring komme til at udføre kemiske udviklingsforsøg med geler og kolonner/arbejde med forskellige produktionsprocesser og i mindre omfang kvalitetskontrol samt indgå i vedligehold og rengøring af udstyr. Du vil have kundekontakt, deltage i planlægning, dokumentere og håndtere ordrer, herunder udføre PC-arbejde.

Du vil opleve, at vi fokuserer på LEAN principper, og du vil kunne bidrage til at optimere vores arbejdsgange omkring kolonner.

Kvalifikationer
Du er uddannet (industri)laborant med erfaring indenfor HPLC-analyse og dokumentation (ISO/GMP). Det er en fordel, hvis du har kendskab til organisk syntese.

Du er god til at planlægge og organisere din arbejdsdag. Som person er du omhyggelig og samvittighedsfuld omkring udførelsen af dine arbejdsopgaver. Det er vigtigt, at du har en god ordenssans. Du skal være indstillet på at lære nye måder at gøre tingene på og være en engageret teamspiller, der gerne viser vejen i samarbejde med kollegerne.

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 er selvstændig og tager styring over egne opgaver, og du trives med at løse opgaverne i tæt samarbejde med dine kolleger. Du tager ansvar for, at vi både som team og individer, når de mål forretningen har brug for. Du kan lide at optimere arbejdsgange og er god til at afslutte opgaver.

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.

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
Vi har brug for din hjælp i en 9-10 måneders periode. Vi tilbyder en spændende arbejdsplads med skiftende udfordringer, hvor du kan opnå god erfaring med kolonneproduktion/stabilisering af produktionsprocesser. Arbejdet foregår i en uformel atmosfære, hvor vi har fokus på som team at levere i rette kvalitet til vores kunder.

Vil du vide mere om stillingen, er du meget velkommen til at kontakte Kirsten Modvig på telefon på +45 2429 4119.

Ansøgningsfrist
6. januar 2014

Process Engineer (Hillerød, Denmark)

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Process Engineer

- Production
- Denmark - Hillerød

Are you ready to use your expertise in securing high quality work within the medical device area of Novo Nordisk? Device Manufacturing Development (DMD) is a project organization comprising nearly 250 engaged employees that strive to make us the best manufacturing development partner of medical devices. Our dedication is to build superior quality into device products. Our challenge is to execute an increasing portfolio of diverse development projects and bring them fast to market.

About the department
Pilot Operations handle all operational activities through the whole supply chain from purchasing of materials to delivery of finished products to our affiliates. Our main task is to support new product introduction by maturing the manufacturing process of new high quality devices. A job is waiting for you in a challenging and developing environment. In our Process Support team in Hillerød, you will join a team of 9 engaged employees. Together we assure quality and compliance in the production of NovoPen® Echo, NovoPen® 5 and execution of new projects.

The job
You will be responsible for continuously improving our manufacturing processes in our moulding, assembly and packaging area. Together with colleagues inside and outside the department, you will be responsible for developing the quality and compliance level, with high focus on corrective and preventive actions. You will be working in a culture of lean thinking and with a high quality mind-set and your technical understanding you will help to optimize our processes. Finally, you will be responsible for qualifying equipment and write GMP documentation. This job will give you the opportunity to join a project organisation where co-operation and flexibility have high priority. You can look forward to a job with ever-changing assignments and a frequent rescheduling of priorities, and as such you will need to take many independent decisions within your area.

Qualifications
You hold a relevant degree in engineering (B.Sc. or M.Sc. level) within, Mechanics, Manufacturing or Medicine and Technology. You are able to drive processes proactively in a complex production environment with many stakeholders. You have knowledge and experience within documentation of quality and compliance in relation to GMP. Your area of interest is within automated processes (PLC, Robot assembly equipment etc.) both on a technical and a theoretical level.

On a personal level, you are known for dedicating yourself to work proactively in order to solve the tasks 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. In addition, you are able to handle complex tasks and deliver in due time to meet our customers’ expectations. You are a team player and a skilled communicator, and you thrive in unfolding your high level of energy and spirit in an international, dynamic environment. You are fluent in spoken and written English and Danish

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.

Please mark your application "18719BR Process engineer".

Contact
For further information, please contact Thomas Bach Nielsen at +45 3075 0052.

Deadline
17 December 2013.

Pharma Field Sales - Diabetes Care Specialist (DCS) Monroe, LA Job (Monroe, MA, US)

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Requisition ID 18601BR
Title Pharma Field Sales - Diabetes Care Specialist (DCS) Monroe, LA
Job Category Field Sales
Job Description Novo Nordisk is a focused healthcare company and a world leader in diabetes care. We are actively working to change the course of the diabetes pandemic, improve the daily lives of people with diabetes, and to expand the possibilities for people with hemophilia.

Pharma Field Sales - Diabetes Care Specialist (DCS) Monroe, LA

This position represents Novo Nordisk within an assigned territory with the goal of maximizing sales and positioning Novo Nordisk as the leading company in diabetes care. The DCS must assume responsibility for achieving sales goals by implementing marketing and sales strategies aimed at effectively selling and promoting Novo Nordisk’s portfolio of diabetes products to physicians, pharmacists, nurses, and other paramedical customers and current co-promotion partners who make or are involved in purchasing and prescribing decisions. This position also determines and recommends the most appropriate Novo Nordisk product and approved usage for the needs of the customers.

The DCS reports to the District Business Manager of the specific sales territory and interacts regularly with territory partners. The DCS sells and promotes Novo Nordisk’s portfolio of diabetes products with a focus on targeted and non-targeted primary care physicians, pharmacists, nurses, and other members of patients’ primary care team.

KEY SUCCESS FACTORS: EDUCATION, EXPERIENCE, KNOWLEDGE AND SKILLS
•At least one year pharmaceutical sales experience OR at least one year business-to-business (B2B) sales required.
•Bachelor’s Degree from college or university accredited by an organization recognized by the US Department of Education required. Advanced degree preferred.
•Top 20% sales ranking for 1 out of last 2 years in a sales role, documented (regionally or nationally) or equivalent documentation for B2B candidates
•Proven leadership and decision-making ability.
•Solid understanding of diabetes disease state and Novo Nordisk’s products, coupled with aptitude for learning and ability to communicate technical and scientific product and disease management information.
•Must have a consistent proven track record of winning sales results
•Must be a self-starter and be able to evaluate options and make decisions with minimal supervision.
•Intermediate computer skills required (Windows, Word, Excel)
•Prior computer experience using sales data/call reporting software ideal
•Must maintain a valid driver’s license and obey all applicable traffic laws.
•Approximately 15% overnight travel

A winning attitude and passion for making a real difference in the lives of our patients ensures the right fit for you and the team at Novo Nordisk. Our passion for helping people live better lives and our award-winning product pipeline can only be as effective as our ability to provide life-changing information to physicians and customers. Our Sales professionals ensure that the latest therapies and products reach the people who need them most, by listening to their needs and advocating for even greater enhancements.
Department SALES - NORTHERN LOUISIANA
Position Location US - Field Based - Across US
City Monroe
State/Provinces US - MA
Degree Required Bachelor's Degree Required
Percent Travel 10 - 20%

NC Handling FlexPen-PLP (Hillerød, Denmark)

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NC Handling FlexPen/PLP

- Project Management
- Denmark - Hillerød

Are you eager to deliver the best prefilled devices to the market? Now you have the chance to become Process Supporter in Device Manufacturing Development.

Anticipate a key role where you will consolidate our compliance and product quality for the patient and our production sites and contribute to the efficiency of the assembly processes.

This job invites you to collaborate with a variety of functions from Device R&D to the production sites globally in PS: DMS, DFP and Biopharm. You should anticipate up to 45 yearly travel days to various sites.

You ensure the performance of the prefilled devices and assembly processes in terms of quality, delivery and efficiency

As Process Supporter you will be responsible for supporting the production sites in delivering an increasingly high product quality. You will provide expertise on the product quality IC and NC from production and actively contribute or drive product and process improvements.

About the department
You will join a dedicated and highly competent team of 10 product and process experts and be at the crossroad between DRD, Quality and Production.

The job
Your primary goal is to ensure that the production sites deliver consistently a high quality product in compliance with internal quality requirements and cGMP. Specifically, you will handle product quality IC’s and NC’s from the prefilled devices assembly sites and in collaboration with the product experts in DRD and DMD, you will assess the severity of the defects and contribute to the elimination of the root causes. As such you will be a major player in the continuous improvement of the product quality, process stability and efficiency.

Furthermore you will ensure the compliance to and update of our standards such as the QFS, pFMEA and other quality rationales.

You mission will lead you to the shop floor around the world to support the production sites in preventing and correcting the potential quality and performance issues and where you will actively use our growing product and process expertise to train and educate our colleagues from production.

Quality oriented with insight into Prefilled Product and Processes

Qualifications
You have combined your Master’s degree in pharmaceutical, mechanical engineering or similar with 2 years of experience in quality or process support.

From previous employment in PS or DRD, you have gained insight into our devices and assembly processes and know what it means to operate in a cGMP-regulated environment. To be a success, you will also need your experience with product quality, manufacturing processes, cLEAN® and project management skills.

On a personal level, you have a patient centred approach and never compromise on quality. You have a global mind set, and you enjoy building relations across organisational levels and geography. Impeccable communication skills are a must as well as the ability to prepare high quality presentation material. It goes without saying that you need fluency in written and spoken Danish and English.

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

Contact
For further information, please contact Yannick Segonne +45 3079 2318.

Deadline
18 December 2013

Safety Medical Writer (Bagsværd, Denmark)

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Safety Medical Writer

- Quality
- Denmark - Bagsværd

Are you interested in drug safety and pharmacovigilance writing?” Do you want to be part of a department that keeps patients safe? Then we definitely want to hear from you!

About the department
Safety Surveillance Reporting is responsible for aggregate safety reporting on the surveillance of adverse reactions reported for marketed products and products under development at Novo Nordisk A/S. We are a dynamic, well-functioning, international team of 10 Safety Medical Writers and 6 Safety Publishers. We work together to coordinate, prepare, and electronically publish all key safety surveillance reporting documents. As we work in a rapidly changing regulatory landscape, where the global requirements for reporting on pharmacovigilance activities are still evolving, change-readiness and out-of-the-box thinking are both invaluable assets.

The Job
This is a permanent job as a Safety Medical Writer in Safety Surveillance Reporting at Novo Nordisk A/S. In this role, you will be responsible for planning and managing the process for document preparation in a cross-functional environment, soliciting relevant information from stakeholders for different areas across Novo Nordisk A/S, and being overall responsible for writing high quality documents. You will typically work in close collaboration with Safety Surveillance Advisors, Medical Specialists from Global Development, Medical Advisors from Medical Affairs, Project Managers from Regulatory Affairs, and Safety Publishers. While your key responsibilities will include preparing the key safety reporting documents (including Development Safety Update Reports, Periodic Safety Update Reports, and Clinical Risk Management Plans), you will also be expected to actively contribute to continual process improvements and other improvements projects.

Qualifications
You have a university degree (MD, PhD, MSc or equivalent) with a demonstrated a flair for, and genuine interest in scientific communication in English (publications or equivalent). Experience from the pharmaceutical industry and pharmacovigilance in particular, are a major advantage, but not a must. Strong project management and inter-personal skills are a pre-requisite for the role as Safety Medical Writer as co-ordinator and writer in the multi-disciplinary teams. You must be good at planning, coordinating, and reaching consensus. You are able to work independently, but at the same time you are a strong team player who adapts easily to a changing environment and tight deadlines. As all our documents are written in English, you must be fluent in both written and spoken English. Good attention to detail is important for reviewing documents, and for spotting important details amongst large volumes of data. You are thorough, structured and conscientious, and you have a good sense of humour. Experience with LEAN or similar is an advantage for contributing to continuous process improvement.

At Novo Nordisk A/S, 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 Samuel Ramsden +45 3075 5727 or Terrie Ramirez +45 3079 7385.

Deadline
6 January 2014.

Building responsible (Kalundborg, Denmark)

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Building responsible

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

- Production
- Denmark - Kalundborg

Are you passionate about building requirements and building security?

We are seeking a Building Responsible. As our plant is now more than 10 years old and the external requirements from authorities are increasing, we are looking for an ambitious and professionally building engineer for the largest insulin plant in the world.

About the department
In Insulin Manufacturing I, Support, in Kalundborg you will be part of a dynamic department with 40 competent employees. Your building responsibilities will influence more than 450 people across the plant. This job will give you the opportunity to join a world leader within diabetes care. Main objective of the department is to support the world´s largest insulin plant, within disciplines of Business support, Process automation, Authority-coordination, and Project Management.

The job
You will be part of the Business Support Team consisting of 10 colleagues working with finance, logistics, document control and raw materials. You will have the responsible for building requirements, building- security and safety, as well as the strategic plan for the building. You will coordinate the activities and have the day to day management within the building area.

Qualifications
Ideally you hold a Building and Civil Engineer degree, or you have a Bachelor of Architectural Technology and Construction Management. To this you have added 3 years’ practical experience as responsible for building within the pharmaceutical production environment.

With your interpersonal skills, you are able to communicate with people at many organisational levels. Moreover, you possess a natural drive and the ability to inspire and motivate people.

Finally, you have a good business understanding which you combine with your knowledge within building requirements and comprehend the values of a large production site. Your IT skills include at least MS Office and building access security control.

Novo Nordisk in Kalundborg is a city within the city. The area is situated a about one hour from Copenhagen and covers 1,350,000 m2, including a private road grid. We produce more than 50 % of the insulin in the world. We are at the front edge of the development within technology, systems, methods and processes. If you are our new colleague, we can guarantee opportunities that you will have a hard time finding anywhere else.

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 Mette Krogh at +45 3075 6166.

Deadline
15 December 2013

Erfarne produktionskemikere- -ingeniører (Kalundborg, Danmark)

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Erfarne produktionskemikere/ -ingeniører

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

- Produktion
- Danmark - Kalundborg

Brug dine GMP-evner i verdens største insulinproduktion i Kalundborg

Novo Nordisk er verdens førende virksomhed inden for diabetesbehandling. Vores ambitioner og dygtige medarbejdere har bragt os meget langt. Og vi er slet ikke færdige. Derfor investerer vi massivt i hele vores værdikæde. Det gælder globalt og ikke mindst i vores produktions-setup. Vores fabrikker i Kalundborg er en hjørnesten. Og det er her, du kommer ind i billedet. Lige nu mangler vi erfarne produktions­kemikere.

Om afdelingen
Vores succes gør, at vi mangler dygtige specialister med GMP-erfaring i en hel række produktionsteams i Kalundborg. Jobbene spænder bredt, og vi har derfor brug for profiler med forskellig erfaring og specialisering. Produktionen består af gæring, grovrens og finrens. Resultatet bliver en bred vifte af innovative insuliner til gavn for patienter over hele kloden.

Jobbet
Vi mangler produktionskemikere/-supportere, der kan bruge deres viden og erfaring til at gøre vores produktion så effektiv som overhovedet muligt, fordi den hviler på gennemtænkte og standardiserede processer og systemer. Procesoptimering baseret på vores LEAN-værktøjer løber således som en rød tråd på tværs af disse stillinger, hvor stort ansvar og indflydelse går hånd i hånd. Som kemiker/kemiingeniør/farmaceut kan du fx komme til at arbejde med at håndtere afvigelser, supportere og vejlede vores driftsoperatører, udføre kontrolanalyser, validering, systematisk problemløsning, dokumentation, projektarbejde m.m.

Dit mål er at bidrage til en stabil produktion i absolut topkvalitet og altid i overensstemmelse med gældende kvalitets- og GMP-regler. En helt afgørende del af dette er en standardiseret proces, og her spiller du en nøglerolle. Grundlæggende deler du din indsats mellem at håndtere afvigelser og arbejde på optimeringsprojekter. I begge roller bruger du meget tid på gulvet i produktionen for så at tage dine iagttagelser med til skrivebordet, hvor du udarbejder dokumentation. Jobbet giver dig et stærkt fundament for at fortsætte din karriere som fx projektleder på bl.a. optimeringsprojekter eller som leder – hvis du ønsker det.

Kvalifikationer
Du er kemiker, ingeniør, farmaceut eller lignende, og du har solid erfaring med procesanlæg og processtyring. Du er således vant til at arbejde efter systematiske kvalitetssystemer, og du er selv bannerfører for høj kvalitet. Det er helt naturligt for dig at tage ansvar for dine opgaver og nå dine deadlines. Samtidig er det afgørende, at du trives i et travlt miljø, der er i stadig forandring. Du kan derfor både prioritere mellem mange sideløbende opgaver og være med til at drive forandringer, der forbedrer. Da vi er mange involveret i processen på tværs af faggrupper, afhænger din succes i høj grad af din evne til at skabe og pleje relationer med mange forskellige mennesker – samt selvfølgelig din lyst til at arbejde målrettet for, at vi lykkes som et hold. Derudover skal du kunne begå dig på engelsk i skrift og tale.

I Novo Nordisk er det dine evner, dit engagement og dine ambitioner, der forbedrer mange menneskers liv – i samspil med usædvanligt talentfulde og passionerede kolleger.

Novo Nordisk i Kalundborg

Novo Nordisk PS Kalundborg er i sig selv en by i byen, kun godt en times kørsel fra København. Området er på størrelse med 270 fodboldbaner. Vi er 2.700 mennesker i alt fordelt på 15 fabrikker, og vi producerer ca. 50 % af verdens insulin. PS i Kalundborg kan helt kort sammenfattes til: udviklingsmuligheder uden ende. Skulle du have lyst til at flytte til Kalundborg, kommer du til en by tæt på skov og vand, med gode skoler, sports- og fritidsfaciliteter og meget mere. Har du brug for det, har vi gode erfaringer med at hjælpe tilflyttere med at finde ny bolig. Besøg vores hjemmeside og læs mere om de forskellige job og PS Kalundborg.

Vi glæder os til at høre fra dig: novonordisk.com/kalundborg-careers

Kontakt
Vil du vide mere om stillingen, så kontakt Jacob Dahl Nielsen på +45 3075 5486.

Ansøgningsfrist
31. januar 2014

Tekniske ingeniører (Kalundborg, Danmark)

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Tekniske ingeniører

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

- Produktion
- Danmark - Kalundborg

Brug dine GMP-evner i verdens største insulinproduktion i Kalundborg

Novo Nordisk er verdens førende virksomhed inden for diabetesbehandling. Vores ambitioner og dygtige medarbejdere har bragt os meget langt. Og vi er slet ikke færdige. Derfor investerer vi massivt i hele vores værdikæde. Det gælder globalt og ikke mindst i vores produktions-setup. Vores fabrikker i Kalundborg er en hjørnesten i dette. Og det er her, du kommer ind i billedet.

Om afdelingen
Vores succes gør, at vi mangler dygtige tekniske ingeniører i en række teams i Kalundborg. Du bliver del af et team, der har ansvar for den tekniske support til en produktionsenhed. Dit og kollegernes fokus er, at udstyret altid er i topform og compliance. Teamet er således en helt uundværlig del af arbejdet med at sikre en stabil og sikker produktion. Videndeling og stærkt teamwork er en naturlig del af vores hverdag, og vi kan love spændende udfordringer og masser af udvikling for dig personligt.

Jobbet
Dit grundlæggende fokus bliver at sikre compliance på vores produktions- og/eller utility-udstyr og herunder at bidrage til, at vi hele tiden forbedrer udstyret rent teknisk og dermed også gør det mere effektivt. Du kommer både til at arbejde med kravspecificering , kvalificering og eksekvering af forretningskritiske tekniske projekter. I dagligdagen vil nogle af dine vigtige opgaver blive systematisk problemløsning baseret på vores LEAN-værktøjer, håndtering af hændelser/afvigelser og ændringssager og udarbejdelse af operationelle dokumenter. Du spiller også en vigtig rolle i arbejdet med at sikre det rette vedligeholdelsesomfang. Som teknisk ekspert får du derudover ansvar for at håndtere kontrakter med både interne og eksterne leverandører.

Kvalifikationer
Du har teknisk baggrund som ingeniør eller tilsvarende suppleret med viden inden for fermentering, oprensning, utility og/eller autoklaver. Skal du have succes, skal du arbejde systematisk og analytisk og kunne bevare overblikket, når du arbejder på flere sideløbende opgaver/projekter samtidigt – og dermed også levere inden for de aftalte deadlines. Det er ligeledes vigtigt, at du trives med at arbejde i et super dynamisk miljø, der er i stadig forandring. Det kræver evnen til at møde kollegerne og opgaverne med en positiv indstilling og tro på, at bag ethvert problem gemmer sig en løsning, som du nok skal finde. Det er en forudsætning for at søge, at du er god til dansk i skrift og tale. Derudover skal du være god til engelsk.

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

Novo Nordisk i Kalundborg

Novo Nordisk PS Kalundborg er i sig selv en by i byen, kun godt en times kørsel fra København. Området er på størrelse med 270 fodboldbaner. Vi er 2.700 mennesker i alt fordelt på 15 fabrikker, og vi producerer ca. 50 % af verdens insulin. PS i Kalundborg kan helt kort sammenfattes til: udviklingsmuligheder uden ende. Skulle du have lyst til at flytte til Kalundborg, kommer du til en by tæt på skov og vand, med gode skoler, sports- og fritidsfaciliteter og meget mere. Har du brug for det, har vi gode erfaringer med at hjælpe tilflyttere med at finde ny bolig. Besøg vores hjemmeside og læs mere om de forskellige job og PS Kalundborg.

Vi glæder os til at høre fra dig: novonordisk.com/kalundborg-careers

Kontakt
Vil du vide mere om stillingen, så kontakt Jacob Dahl Nielsen på +45 3075 5486.

Ansøgningsfrist
31. januar 2014

Programmers for clinical development (Søborg, Denmark)

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Programmers for clinical development

- Research & Development
- Denmark - Søborg

Are you interested in working with biological data and would you like to be part of a future with a strong pipeline of products, which ensures huge variety of tasks, great opportunities for individual development and influence on decision making?

Do you wish to work in a highly professional, engaged and global environment, where you can use your programming skills and quality mindset bringing clinical projects to registration and market? You may be one of our new statistical programmers.

About the department
The Biostatistics function is growing and consists currently of 150 statisticians and statistical programmers globally in our R&D clinical development organisation. Biostatistics is a dynamic department which cooperates with many different areas in the organisation both within Denmark and across borders with our affiliates in the US, India, China and Japan, as well as our outsourcing partners in India. Biostatistics provides a strong scientific community and we are organised in smaller units for each clinical project to ensure close collaboration with our various stakeholders.

The job
As statistical programmer your primary responsibility is to develop SAS programs based on clinical data for reporting of clinical trials, preparing summary documents and publications as well as supporting regulatory commitments. You handle many assignments concurrently and will work in close collaboration with a team of statisticians and statistical programmers.

You will be involved in coordinating and supervising the work of contract houses around the world performing outsourced programming tasks. Therefore we expect you to communicate programming/technical problems and ideas both internally and externally, as well as coach more junior colleagues. You must take responsibility for both standard tasks and more complex and time critical tasks.

Development of methods and processes, as well as knowledge sharing is continuously on-going in Novo Nordisk, especially based on the initiative of the employees. We expect you to take part in the maintenance of Biostatistics as a good and challenging place to work. In exchange we of course offer great opportunities for on-going training to ensure the continued competency development of our employees.

Qualifications
You have a B.Sc. or M.Sc. within science, IT or other relevant degree, extensive knowledge and experience with the SAS programming language, as well as preferably experience within clinical research. You are able to write efficient, well documented and standardised computer programs. Furthermore, strong cooperation and analytical skills as well as an understanding for data structure are a necessity. You are capable of working independently, take on responsibility and show initiative.

We expect you to be independent and that you are flexible and efficient. In addition we expect you to be able to overview several challenging tasks in parallel without compromising the quality of your work and that you remain high spirited, also when things are moving fast. Experience with project management will be an advantage.

Good collaboration and communication skills are necessary characteristics. You are also 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 in a global business environment.

Contact
For further information, please contact Lise Voss Skotner at +45 3079 4474 or Trine Næstoft at +45 3075 2135.

Deadline
12 January 2014.

Programmers for clinical development (Aalborg, Denmark)

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Programmers for clinical development

- Research & Development
- Denmark - Aalborg

Are you interested in working with biological data and would you like to be part of a future with a strong pipeline of products, which ensures huge variety of tasks, great opportunities for individual development and influence on decision making?

Do you wish to work in a highly professional, engaged and global environment, where you can use your programming skills and quality mindset bringing clinical projects to registration and market? You may be one of our new statistical programmers.

About the department
The Biostatistics function is growing and consists currently of 150 statisticians and statistical programmers globally in our R&D clinical development organisation. Biostatistics is a dynamic department which cooperates with many different areas in the organisation both within Denmark and across borders with our affiliates in the US, India, China and Japan, as well as our outsourcing partners in India. Biostatistics provides a strong scientific community and we are organised in smaller units for each clinical project to ensure close collaboration with our various stakeholders.

The job
As statistical programmer your primary responsibility is to develop SAS programs based on clinical data for reporting of clinical trials, preparing summary documents and publications as well as supporting regulatory commitments. You handle many assignments concurrently and will work in close collaboration with a team of statisticians and statistical programmers.

You will be involved in coordinating and supervising the work of contract houses around the world performing outsourced programming tasks. Therefore we expect you to communicate programming/technical problems and ideas both internally and externally, as well as coach more junior colleagues. You must take responsibility for both standard tasks and more complex and time critical tasks.

Development of methods and processes, as well as knowledge sharing is continuously on-going in Novo Nordisk, especially based on the initiative of the employees. We expect you to take part in the maintenance of Biostatistics as a good and challenging place to work. In exchange we of course offer great opportunities for on-going training to ensure the continued competency development of our employees.

Qualifications
You have a B.Sc. or M.Sc. within science, IT or other relevant degree, extensive knowledge and experience with the SAS programming language, as well as preferably experience within clinical research. You are able to write efficient, well documented and standardised computer programs. Furthermore, strong cooperation and analytical skills as well as an understanding for data structure are a necessity. You are capable of working independently, take on responsibility and show initiative.

We expect you to be independent and that you are flexible and efficient. In addition we expect you to be able to overview several challenging tasks in parallel without compromising the quality of your work and that you remain high spirited, also when things are moving fast. Experience with project management will be an advantage.

Good collaboration and communication skills are necessary characteristics. You are also 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 in a global business environment.

Contact
For further information, please contact Malene Højbjerre at +45 3079 6209.

Deadline
12 January 2014

Statisticians for clinical development (Aalborg, Denmark)

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Statisticians for clinical development

- Research & Development
- Denmark - Aalborg

Are you interested in working with biological data and would you like to be part of a future with a strong pipeline of products, which ensures huge variety of tasks, great opportunities for individual development and influence on decision making?

Do you wish to work in a highly professional, engaged and global environment where you can use your statistical skills and quality mindset bringing clinical projects to registration and market? You may be one of our new statisticians.

About the department
The Biostatistics function is growing and consists currently of 150 statisticians and statistical programmers globally in our R&D clinical development organisation. Biostatistics is a dynamic department which cooperates with many different areas in the organisation both within Denmark and across borders with our affiliates in the US, India, China and Japan, as well as our outsourcing partners in India.

Novo Nordisk has a broad R&D pipeline and most of our statistical work is done in-house, thus we offer a wide variety of statistical challenges. Biostatistics provides a strong scientific community and we are organised in smaller units for each clinical project to ensure close collaboration with our various stakeholders.

The job
As statistician you are responsible for planning and coordinating time critical statistical tasks. You can be involved in a wide range of statistical assignments, such as providing input to clinical development plans, clinical trial protocols, summary documents and publications. Furthermore, you present and provide statistical interpretation of results, both internally and externally. You handle many assignments concurrently and will work in close collaboration with a team of statisticians and statistical programmers.

You will interact in cross disciplinary development teams across country borders and communicate statistical issues and ideas to non-statisticians. You can be involved in coaching of more junior colleagues and be responsible for coordinating and supervising the work of contract houses around the world performing outsourced tasks. Therefore we expect you to be able to communicate statistical problems and ideas clearly.

Development of methods and processes, as well as knowledge sharing is continuously on-going in Novo Nordisk, especially based on the initiative of the employees. We expect you to take part in the maintenance of Biostatistics as a good and challenging place to work. In exchange we of course offer great opportunities for on-going training to ensure the continued competency development of our employees.

Qualifications
You have a solid theoretical background in statistics corresponding to MSc level and experience within clinical research. You have experience with practical applications of biostatistical methodology and statistical software including SAS.

You work independently, take on responsibility and show initiative. You are flexible and efficient and able to handle several challenging tasks in parallel without compromising the quality of your work. We expect that you remain high spirited, also when things are moving fast. Experience with project management is an advantage.

You have good collaboration and communication skills and are fluent in English.

At Novo Nordisk we use our skills, dedication and ambition to improve treatment outcomes for people with diabetes and other chronic diseases. By working with us you will have the opportunity to do the same in a global business environment.

Contact
For further information, please contact Malene Højbjerre at +45 3079 6209.

Deadline
12 January 2014.

Statisticians for clinical development (Søborg, Denmark)

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Statisticians for clinical development

- Research & Development
- Denmark - Søborg

Are you interested in working with biological data and would you like to be part of a future with a strong pipeline of products, which ensures huge variety of tasks, great opportunities for individual development and influence on decision making?

Do you wish to work in a highly professional, engaged and global environment where you can use your statistical skills and quality mindset bringing clinical projects to registration and market? You may be one of our new statisticians.

About the department
The Biostatistics function is growing and consists currently of 150 statisticians and statistical programmers globally in our R&D clinical development organisation. Biostatistics is a dynamic department which cooperates with many different areas in the organisation both within Denmark and across borders with our affiliates in the US, India, China and Japan, as well as our outsourcing partners in India.

Novo Nordisk has a broad R&D pipeline and most of our statistical work is done in-house, thus we offer a wide variety of statistical challenges. Biostatistics provides a strong scientific community and we are organised in smaller units for each clinical project to ensure close collaboration with our various stakeholders.

The job
As statistician you are responsible for planning and coordinating time critical statistical tasks. You can be involved in a wide range of statistical assignments, such as providing input to clinical development plans, clinical trial protocols, summary documents and publications. Furthermore, you present and provide statistical interpretation of results, both internally and externally. You handle many assignments concurrently and will work in close collaboration with a team of statisticians and statistical programmers.

You will interact in cross disciplinary development teams across country borders and communicate statistical issues and ideas to non-statisticians. You can be involved in coaching of more junior colleagues and be responsible for coordinating and supervising the work of contract houses around the world performing outsourced tasks. Therefore we expect you to be able to communicate statistical problems and ideas clearly.

Development of methods and processes, as well as knowledge sharing is continuously on-going in Novo Nordisk, especially based on the initiative of the employees. We expect you to take part in the maintenance of Biostatistics as a good and challenging place to work. In exchange we of course offer great opportunities for on-going training to ensure the continued competency development of our employees.

Qualifications
You have a solid theoretical background in statistics corresponding to MSc level and experience within clinical research. You have experience with practical applications of biostatistical methodology and statistical software including SAS.

You work independently, take on responsibility and show initiative. You are flexible and efficient and able to handle several challenging tasks in parallel without compromising the quality of your work. We expect that you remain high spirited, also when things are moving fast. Experience with project management is an advantage.

You have good collaboration and communication skills and are fluent in English.

At Novo Nordisk we use our skills, dedication and ambition to improve treatment outcomes for people with diabetes and other chronic diseases. By working with us you will have the opportunity to do the same in a global business environment.

Contact
For further information, please contact Lise Voss Skotner at +45 3079 4474 or Trine Næstoft at +45 3075 2135.

Deadline
12 January 2014

Department cLean (Hillerød, Denmark)

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Department cLean

- Production
- Denmark - Hillerød

Device Manufacturing & Sourcing, Moulding Production, Denmark, Hillerød

If you want to play an important role in taking Device Manufacturing and Sourcing’s cLEAN® strategy to the next level, you now have the opportunity. You will support a management team with a strong and very ambitious cLEAN® mindset in Device Manufacturing & Sourcing in Hillerød. Here you can look forward to having personal influence, major challenges and personal as well as professional development.

About the department
You will be part of the Moulding Production Department, who has global responsibility of delivering plastic components for Novo Nordisk injection pens. We value professionalism and responsibility, and have an open and informal team culture. We ensure an environment, where we focus on continuously improving individual and team competences. You will interact in teamwork with your colleagues, and have a broad list of contacts throughout the organization.

The job
Your overall objective is to bring cLEAN® thinking into all our systems, processes and methods. In other words you will contribute to making cLEAN® a natural way of thinking and acting for all employees in Moulding Production Department. You will have the opportunity to work with all aspects of cLEAN®. Two of your key tasks will be the continuous development and implementation of an operational training system and the continuous development and management of project program with focus on manager owned improvement projects.

Qualifications
You have a relevant degree at master’s level, which you have combined with a couple of years’ hands on cLEAN® experience, from a job in which you have created measurable results. As such, you have a strong foundation combining LEAN theory and practical know how and you are fully capable of driving and engaging others in continuous improvement projects from a-z. You can safely navigate in an environment of change and are able to establish relations to and cooperate with a wide variety of colleagues. Your personal qualities define you as robust, empathetic and a self-starter with a high level of energy. Moreover, you have strong communication skills and master the discipline of giving presentations disseminating clear-cut contents. You have experience in planning and facilitating workshops and can create change through others.Last but not least, you have proficiency in written and spoken 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 Rasmus Jørgensen, +45 3075 3047.

Deadline
19 December 2013

Sr. QA Professional (Måløv, Denmark)

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Sr. QA Professional

- Quality
- Denmark - Måløv

Are you looking for new challenges within QA – development of tablets for clinical trials and do you want to make a difference? The project portfolio is increasing, and therefore we are looking for a dedicated, professional and enthusiastic new colleague.

About the department
In CMC OPF QA we have the responsibility for quality assurance of oral formulations and release of investigational medicinal products for clinical trials. We have the QA responsibility of the oral pilot production. The department is recently established to support the development of oral protein formulations in our stakeholder departments.

The job
The job is very varied and challenging. In close cooperation with your 10 colleagues in QA, you act as a consultant for our pilot and formulation departments. You will act as qualified person delegate, and you will have the overview of process within development and production of tablets. The job is a combination of development project and facility related QA tasks in a complex and changing environment. You will approve documentation for development, manufacturing, stability, and QP release of drug product for clinical trials. You will assure that the development documentation is compliant with internal and external requirements.

You will approve facility related documentation needed for the operation of the oral pilot plant.

CMC Supply’s continuing high level of audit and inspection readiness is on top on your agenda.

In CMC Supply QA we work with QA oversight where you proactive together with your colleagues will identify areas where our stakeholders’ compliance can be strengthened.

You have a risk based approach to the development process and product, and you contribute to find the right balance between patient safety, compliance to requirements and effective business conduct.

Qualifications
Ideally, you have a master in Pharmacy or corresponding qualifications and at least 3-5 years of experience within the pharmaceutical industry. You have thorough knowledge within more of the following areas: experience from tablet manufacturing/development, GMP, validation/qualification, requirements for tablet production, and requirements for investigational medicinal products for use in clinical trials.

You enjoy working in a dynamic environment, where teamwork is at the top of the agenda. Also, you are quite adaptable and challenge our way of doing things, so that we will get even better. You focus on results and quality – and contribute to the right level of compliance.

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 Janne Lavritsen +45 3075 7333.

Deadline
5 January 2014

Engineer, Chemist or Pharmacist for primary packaging (Hillerød, Denmark)

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Engineer, Chemist or Pharmacist for primary packaging

- Research & Development
- Denmark - Hillerød

Are you ready for a job where you combine your knowledge of materials, processes, suppliers and regulatory requirements? If so, this position as Primary Packaging Engineer could be your chance to have a key role at Novo Nordisk and build a career among specialists.

About the department
You will be part of the Primary Packaging department in Hillerød. We are part of R&D in Novo Nordisk, and we select primary packaging for direct contact with new pharmaceuticals. Further, we establish and maintain specifications for primary packaging.

The job
You select primary packaging to bring new pharmaceutical products to market. Moreover, you establish and maintain specifications and make sure that we are in regulatory compliance worldwide. In your daily work you will talk to stakeholders and in this way gather requirements to the packaging components. Moreover, you write specifications, ensure testing to verify performance of the components and ensure that everything is correctly documented. You will be in close dialogue with a large number of colleagues in R&D, Quality Assurance, Chemistry, Manufacturing & Control (CMC) and our production units across the world. In addition, you will give advice to device development in Device R&D, handle complaints and non-conformities and deal with day-to-day challenges.

Qualifications
You are a Chemical Engineer, Chemist or Pharmacist by training. Furthermore, you have some years of experience with primary packaging for pharmaceuticals, food or medical devices, or you have experience from a pharmaceutical production. If you have knowledge of GMP, quality assurance as well as plastic, rubber and glass, it will be an asset. You have a curious mindset and are eager to find the best solution. Your written and spoken English is at negotiation level, and there is no question in your mind that correct documentation is an indisputable activity in this job. Lastly, you take ownership of your assignments, secure buy-in from the involved stakeholders and have a structured way of working.

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

Contact
For further information, please contact Lasse Wengel Christoffersen at +45 3075 3567.

Deadline
1 January 2014.

Research Scientist (Gentofte, Denmark)

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Research Scientist

- Research & Development
- Denmark - Gentofte

Would you like to work with formulation development in a team dedicated to developing the next generation of biopharmaceuticals – then we have the job for you!

A challenging position in team Biopharm Formulation Development II is available for a dynamic and skilful scientist within formulation development of biopharmaceuticals.

About the department
Biopharm Formulation Development is part of Injectable Protein Formulation in the R&D area CMC Supply. The department is responsible for formulation development of new biopharmaceutical drug products - primarily soluble and freeze-dried injectables of new therapeutic proteins and monoclonal antibodies. We are involved in development and research projects mainly within haemostasis and inflammation. We are located in Gentofte (Copenhagen, Denmark), and right now we are facing new exiting challenges due to our rapidly increasing project portfolio.

The job
In the team we are 8 Technicians, 6 Scientists/Specialists and a Team Leader. As formulation scientist in team Biopharm Formulation Development II you are responsible for development of stable protein formulations with optimal biopharmaceutical characteristics within our monoclonal antibody and growth hormone portfolio. You work in a team and you will design, interpret and report studies on drug product - hereby generating pharmaceutical documentation for internal and external use. You will interact with a wide variety of internal stakeholders, e.g. Analytical Development, Production Pilot Plant, Quality Assurance and Regulatory affairs.

Qualifications
You hold a Master of Science possibly combined with a PhD in Chemical Engineering, Pharmacy or another relevant scientific discipline. You have working experience within drug product development. It is an advantage if you have working knowledge of the documentation requirements for biopharmaceutical drug products across the development phases. As a person you are result-oriented and flexible. You enjoy working in a team with highly motivated people, dedicated to developing the next generation of biopharmaceuticals. You work systematically, have good collaborative skills and are used to adhering to strict documentation standards. You possess drive and a positive mindset, and you strive to be in a decision-making role. When cooperating you often take the leading role and you enjoy setting direction to others.

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 Anne Mette Beier at + 45 3079 8535.

Deadline
31 December 2013.

Business Koordinator (Bagsværd, Danmark)

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Business Koordinator

- Forskning og Udvikling
- Danmark - Bagsværd

CMC API Development har ca. 350 ansatte. Vi er ansvarlige for API fremstilling og proces-udvikling af nye API kandidater til alle Novo Nordisk udviklingsprodukter. Dette inkluderer områderne gæring, dyrkning, kemisk syntese, grovrens og finrens. Der er stor fokus på en stabil produktion og altid et stort antal spændende projekter i pipelinen. Vi søger derfor en selvstændig og dygtig automatik ingeniør med erfaring fra drift af proceskontrolsystemer, anlægs- og udstyrs kvalificering samt projektdeltagelse på større og mindre investerings-projekter i et GMP miljø.

Om afdelingen
Vi er en teknisk support afdeling og vores primære opgaver er at supportere og sikre stabil drift i vores pilot anlæg. Vi er ca. 40 personer organiseret i tre teams og dækker over mange faggrupper herunder: PCS, projekter og kvalificering, smede, elektrikere, kalibrering, SAP og anlægsteknikere. I teamet Technical Compliance and Automation løser vi en lang række opgaver i forbindelse med drift og vedligehold af automatik-systemer og står også for projektkoordinering af mindre anlægsopgaver.

Jobbet
Du bliver en del af et team på 8, hvor vi er 5 i automatikgruppen. Gruppen er meget dedikeret til at supportere vores kunder på tværs af alle pilot anlæg i Bagsværd. Din opgave er overordnet support på automatik, primært DeltaV. Kendskab til CTS/BMS er et plus. Det indebærer sikring af, at produktionssystemerne er i compliance med gældende regler, håndtering af daglig support, trouble shooting i kontrolrummet, hvor man i samarbejde med kemikere håndterer hændelser opstået i produktionen. Du skal være i stand at gennemføre ændrings- og kvalificeringsopgaver i samarbejde med vores kunder i anlæggene. Derudover kan du fra tid til anden blive involveret i vores investeringsprojekter.

For at løse dine opgaver i rette kvalitet og i rette tid kræver det, at du er dygtig til at prioritere og er i stand til at arbejde selvstændigt. Det forventes at du har evnen til at skabe gode relationer og dialog med både med dine kollegaer i afdelingen, samt operatører og kemikere i anlæggene, QA og vores eksterne leverandører. Du skal kunne stille de rette spørgsmål, vise interesse og udfordre holdninger og processer.

Du kan se frem til en afvekslende og til tider omskiftelig hverdag i et job, hvor det forventes, at du selv kan tage beslutninger og føre dem ud i livet.

Kvalifikationer
Du har gennemført en akademisk eller anden teknisk uddannelse og har en stærk interesse for automatik. Vi er underlagt store kvalitetskrav, så forståelse og kendskab til GMP, GAMP, ISA95/88 er et stort plus. Vi lægger vægt på at du har et godt humør og kan lide at tage fat i opgaverne, også når de ikke bliver lagt tilrette foran dig.

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

Kontakt
Vil du vide mere om stillingen, så kontakt Andreas Heuer på + 45 3079 8595.

Ansøgningsfrist
05. januar 2014
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