Jobs at Novo Nordisk

Distribution Quality Coordinator

- Supply Chain and Logistics
- Denmark - Bagsværd

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

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

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

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

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

At Novo Nordisk, your skills, dedication and ambition help us change lives for the better. In exchange, we offer you an opportunity to work with extraordinary talent and benefit from a range of possibilities for professional and personal development.

Contact
For further information, please contact Christina Grauballe at +45 3075 2053.

Deadline
14 December 2013.

QA Academic for Development Products

- Quality
- Denmark - Gentofte

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

About the department
In Chemistry, Manufacturing & Control (CMC) API QA we assure that each and every Active Pharmaceutical Ingredient (API) activity in our development and support projects live up to the cGMP requirements. The development portfolio is expanding and thus we seeking a new colleague to help us support the growth.

We are 29 colleagues in three teams. You will join the downstream team and have 14 dedicated colleagues. Our mission is to assure that our manufacturing processes, intermediates and finished API (purification and chemical synthesis) meet the internal and external requirements. Furthermore we’re responsible for release of API for all of Novo Nordisk’s clinical trials. The production facilities and the development laboratories are located in Bagsværd, Gentofte and Måløv, and you will move between the different locations and the QA office on a day-to-day basis.

The job
You assure best-in-class quality of our new manufacturing processes and API for clinical trials. Document approval in connection with development, manufacture, stability and release of API for clinical trials as well as maintenance and improvement of the quality system (SOP’s) will constitute some of your daily tasks. In addition, you will participate in our development projects and in close cooperation with your colleagues you identify and contribute to the strengthening our stakeholders’ compliance level and act as a consultant for them.

We operate in a LEAN-dominated environment, and you will have the opportunity to contribute with ideas for improvements and drive the subsequent implementation as well. Working within QA will definitely challenge your professional and individual skills, and you will find that your tasks cover many different clinical stages of the product development.

Qualifications
You hold a Master’s degree in Pharmacy, Chemical Engineering or possess equivalent qualifications besides a strong quality mindset. You have at least 3 years’ experience with GMP, product release, production or quality assurance. As we operate both in a national and an international environment, you must speak and write Danish and English fluently.

You are ambitious and determined on creating world-class results and ensure quality of the highest order. Moreover, you thrive in a role where you use your knowledge and bring your arguments and negotiation skills into play. You are able to adapt but also challenge our way of working so that we constantly improve our methods and processes.

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

Contact
For further information, please contact Tenna Aggerholm Møller at +45 3079 9918 or Peter Søtofte Elten at +45 3079 8453.

Deadline
16 December 2013

Project Assistant to Haemophilia R&D Portfolio

- Project Management
- Denmark - Søborg

We are looking for a Project Assistant to support one of our Project Vice Presidents.If you are well structured and service minded, have a can-do attitude and are ready for an exciting job in an international environment where challenges are a natural part of your daily work then we may have just the right job for you.

About the department
The Haemophilia R&D Portfolio SVP area drives the haemophilia portfolio currently consisting of five projects in clinical development or regulatory submission phase. Haemophilia project management is responsible for planning, optimising and tracking all parts of haemophilia projects, including timelines, key deliverables and financial planning.

The Job
As Project Assistant you will join the project management team and work closely with the Project Vice President (PVP) and the other three project assistants in the area as well as with a broad range of enthusiastic colleagues who are changing the possibilities in haemophilia. You will also be interacting with colleagues from different areas in the organisation.

Your job function will be to support the project management in driving the project activities towards agreed goals. You will be responsible for planning, optimising and tracking a range of project activities including coordination of the budgeting process and keeping the project plan and project website updated. Part of your responsibilities will also be to arrange project team meetings and seminars including preparation of meeting minutes and follow-up on actions. Moreover, you will in collaboration with the PVP prepare material for upper management meetings (e.g. Project Reviews), monthly project reports and communication materials (e.g. slides and pre-reading). In addition, you will provide daily support to the PVP such as booking of travel and travel settlement.

Qualifications
Our ideal candidate has at least 2-3 years relevant experience within the pharmaceutical industry, preferably with project management. Financial understanding and experience in budgeting is a must and knowledge of SAP is preferable. Being part of a multi-cultural team, fluency in oral and written English is a requirement and relevant training within medical terminology is an advantage. You are a skilled user of various IT systems including MS Office.As a person you are enthusiastic, engaged and have a can-do attitude. You are well-structured with a sense of details. You also enjoy working with tight deadlines and multiple and frequently changing priorities using good collaboration skills and a sense of humour. You are flexible, good at problem-solving, working independently and proactively 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 Birgitte Hermansen at +45 3079 6433.

Deadline
9 December 2013.

GMP partner

- Production
- Denmark - Hillerød

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

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

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

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

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

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

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

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

At Novo Nordisk, your skills, dedication and ambition help us change lives for the better. In exchange, we offer you an opportunity to work with extraordinary talent and benefit from a range of possibilities for professional and personal development.

Contact
For further information, please contact Anne Reker Cordt at +45 3079 9308.

Deadline
10 January 2014

International PostDoc

- Research & Development
- Denmark - Måløv

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

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

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

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

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

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

At Novo Nordisk your skills, dedication, and ambition help us change lives for the better. In exchange we offer you an opportunity to work with extraordinary talent and benefit from a range of possibilities for professional and personal development.

Contact
For further information, please call Bo Wiinberg on+45 3075 3030.

Deadline
18 December 2013

Training Coordinator – temporary position

- Administrative
- Denmark - Søborg

Are you a skilled coordinator who takes pride in supporting and creating a well-structured environment for your colleagues? Do you have a genuine desire to support and collaborate, and do you adapt easily to a changing environment and shifting demands? In this job, you will be a part of the Novo Nordisk worldwide Trial Management organisation; supporting the department in the daily work.

About the department
A temporary, full-time position as Training Coordinator is now vacant in Trial Management Anchor of Trial Execution (TE); start 01-Feb-2014 ending 01-Feb-2015. We are 20 employees of diverse background, responsible for process optimisation within the Trial Management and Medical area and competency development of medical and trial management staff globally. The job is based in Søborg.

The Job
As Training Coordinator your key function will be to support the trainers and coordinate logistics of training activities within Trial Execution. You will be the contact between organisers, participants and external suppliers and venues. Your responsibilities will include budget estimate and follow-up; help with MS Powerpoint presentations as needed, practical assistance during the training sessions as well as administration of course evaluations.

You will also assist the department in organising knowledge sharing meetings, coordinating the arrangement and preparing minutes. You will be the chair of the Training Academy with responsibility for scheduling the meetings, planning the agenda, taking minutes and ensuring follow-up on actions.

In addition, you will be part of a team responsible for support and maintenance of the TE Web on GlobeShare in accordance with company and area principles. You will also be the back-up for the department assistant.

Qualifications
Preferably, you have experience from a similar job. You must have previous experience and interest in administrative tasks and be service-minded. You are proactive with strong organising capabilities. You have a quality mindset, meet your deadlines, communicate effectively, and prioritise your work in a dynamic environment. You are a dedicated team player who inspires trust among colleagues. Fluency in written and spoken English is essential and cross-cultural awareness is important. You have excellent computer skills in MS Office and GlobeShare (Sharepoint).

At Novo Nordisk we use our skills, dedication and ambition to help people with diabetes, haemophilia and other serious diseases change their lives. By working with us you will have the opportunity to contribute to this important mission.

Contact
For further information, please contact Charlene Gudnitz at +45 3079 5181 or Susanne Møller Nissen at +45 3075 6195.

Deadline
15 December 2013.

Training and Competency Advisor

- Regulatory Affairs
- Denmark - Søborg

We are currently seeking a passionate and knowledgeable Training and Competency Advisor to join our internal training function in Regulatory Affairs.

The successful candidate will play a key role in the continuous development and training of Regulatory Affairs employees through the Regulatory Academy.

As a Training and Competency Advisor, you will be responsible for implementing a range of effective training and development initiatives including developing plans and processes to drive performance improvement across the Regulatory Affairs SVP area.

About the department
Regulatory Affairs is responsible for global strategies to obtain and maintain market authorisations worldwide for all Novo Nordisk's new products and for life cycle management activities such as new medical indications, new or changed production methods, or new facilities. Regulatory Affairs also carries responsibility for labelling of Novo Nordisk products. You get the opportunity to join an international, high performing Regulatory Academy team in Søborg, Denmark, responsible for providing contemporary regulatory training and competence development opportunities internally in Novo Nordisk.

The Job
Design effective training aligned with business strategies and other learning and development activities across the organisation .Design and implement effective learning and development programmes for all levels of staff, using a variety of training methods. Analyse training needs and evaluate the effect of implemented training activities. Work with external consultants to ensure excellent and cost effective services. Support the Head of Regulatory Affairs in in co-ordinating leadership development, an effective competence model and in designing an effective training strategy.

Qualifications
A Master’s degree (Adult Education and Training, Psychology, Human Resource or other similar academic degree from e.g. Copenhagen Business School). Experience in design and delivery of training solutions. Knowledge of a wide range of training/learning solutions and how to adapt them to meet business needs (experience from virtual training will be regarded as beneficial). Knowledge of training need analysis, training evaluation, and training methodologies (experience from documenting the effect of training will be regarded as an extra asset). Experience from knowledge management supporting collaboration and sharing of information across an organisation. Strong project management skills. Proficient with the use of the Microsoft Office suit. A good command of the English language and preferably experience from working in a global/international setting.

As a Training and Competency Advisor, you must possess excellent communication, interpersonal, and presentation skills and have a methodical and analytical approach. You should be organized and have the ability to work on your own initiative and build strong working relationships. Flexibility and the ability to work under high time pressure while maintaining a good sense of humour is a must.

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 talented individuals and benefit from a range of professional and personal development possibilities.

Contact
For further information, please contact Lena Munk at +45 3079 6098.

Deadline
11 December 2013

Business Analyst

- Production
- Denmark - Hillerød

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

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

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

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

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

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

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

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

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

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

Deadline
18 December 2013

Studentermedhjælper

- Studerende
- Danmark - Gentofte

Studentermedhjælper på Steno Center for Sundhedsfremme

Interesserer du dig for forskning og sundhedsfremme, og vil du være med til at udvikle nye tilgange til at forebygge diabetes? Har du lyst til at være en del af et konkret forsknings- og udviklingsprojekt med børn og unge i folkeskolen?Så skal du måske være vores studentermedhjælper?!

Stillingen

På Steno Center for Sundhedsfremme, som er et forskningscenter på Steno Diabetes Center, har vi brug for en studentermedhjælper til projekterne Imove på folkeskoler i Københavns Kommune og EU projektet HEPCOM.

Steno Center for Sundhedsfremme udvikler ny viden, metoder og tilgange til sundhedsprofessionelle og andre aktører som kan skabe bæredygtig social forandring til fremme for folkesundheden. Centeret integrerer social- og humanvidenskabelig forskning, for at skabe nye tilgange på et område, som i den grad trænger til at blive videnskabeligt fornyet. Centerets ambition er at udvikle et nationalt og internationalt kraftcenter med fokus på social forandring.

Din profil

• Du studerer et relevant fag, fx folkesundhedsvidenskab, sundhedsfremme, pædagogik, sociologi, antropologi, idræt eller psykologi.

• Du mestrer til fulde dansk og engelsk i tale og skrift.

• Du har erfaring med brug af teorier og metoder i relation til fysisk aktivitet, sundhedsfremme, pædagogik og læring.

• Du er dygtig, ambitiøs, motiveret, selvstændig, kreativ, engageret, resultatorienteret og en god kollega.

• Du har faglig og menneskelig modenhed og kan både arbejde selvstændigt og i et tæt samarbejde i en tværfaglig gruppe, hvor en positiv indstilling og humoristisk sans er afgørende.

• Du er tolerant og kan kommunikere med folk med forskellig baggrund.

Det er desuden en klar fordel, hvis du har erfaring med at:

• arbejde på forskningsprojekter.

• skrive videnskabelige tekster.

• arbejde i tværfaglige miljøer.

• arbejde med børn, unge og sundhedsfremme.

Ansøgning

Ansættelsen er to dage /ugen i hele 2014 ved forebyggelsesgruppen ved Steno Center for Sundhedsfremme på Steno Diabetes Center. Dele af arbejdet vil foregå i de udvalgte skoler.

Din ansøgning, på dansk eller engelsk, skal indeholde:

• Din motivation og baggrund for at søge stillingen (max 1 side)

• CV (max 2 sider)

Ansøgningsfrist fredag 13. december 2013, kl. 12.00.

Samtaler afholdes i uge 1. Stillingen ønskes besat snarest og senest 1. februar 2014.

Kontakt

Yderligere information

Kontakt Maria Bruselius-Jensen (mbuj@steno.dk).

Læs også om Steno på http://www.stenodiabetescenter.com

Om Steno Diabetes Center A/S

Steno Diabetes Center er en af verdens førende institutioner inden for diabetesbehandling og forebyggelse. Steno ejes af Novo Nordisk A/S og er en 'not for profit' virksomhed, der arbejder i partnerskab med det danske sundhedssystem. Steno står for behandlingen af ca. 5.600 mennesker med diabetes.

Lean Consultant

- LEAN
- Denmark - Hillerød

Do you strive for developing a LEAN culture among leaders and employees in an exciting organisation? Is the LEAN mindset a natural part of your working behaviour? Are you strong at facilitation, coaching, process optimization, problem solving and eager to create continuous improvements in an organisation dealing with development projects and pilot production?

About the department
You will support the whole Device Manufacturing Development (DMD) organisation and have a key role in implementing the LEAN strategy and plans. DMD is a young project organisation comprising more than 250 dedicated employees striving to make us the best manufacturing development partner of medical devices. Our goal 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. The position is a part of our LEAN team anchored in the Business Support department. We are a small team supporting the management group in the LEAN journey.

The Job
You will be responsible for teaching, supporting, and coaching leaders and employees in LEAN together with the rest of our LEAN team. The main tasks will be coaching of leaders with regards to performance board meetings and systematic problem solving. The challenge is to make the LEAN concepts meaningful in a project organisation as well as in a flexible pilot production. In addition to LEAN implementation you will also be expected to facilitate and take the lead when critical problem solving is taking place.

An important part of the position is to build a strong relationship to the management group and to the project managers in DMD in order to ensure and support a LEAN approach in all business areas - a LEAN approach which should create both short and long-term results anchored appropriately in the organisation.

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

Qualifications
You have an academic degree in business administration, engineering or similar, and you have at least a couple of years of experience with LEAN implementation.

We expect you to have large experience within facilitation, coaching, performance board meetings and systematic problem solving and you have built up strong project- and stakeholder management skills. You have a good understanding of the Supply Chain and experience with LEAN in pharmaceutical production is an advantage. A technical background is an advantage; otherwise you should be fast at gaining the necessary understanding of the technical details to be able to facilitate problem solving or other processes.

As a person you are responsible, pro-active and co-operate easily at all levels. You work independently, have a strong drive with focus on execution and results and you are keen at taking initiatives.

You are analytical and good at seeing potential improvements while being able to coach leaders and employees to see the potential themselves. Last but not least, you have excellent communication skills and are fluent in written and spoken English.

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

Contact
For further information, please contact Camilla Damsgård Robertsen at +45 3079 5280.

Deadline
16 December 2013

Supporter til Mikrobiologisk laboratorium

- Produktion
- Danmark - Bagsværd

Vil du være med til at supportere vores mikrobiologiske laboratorium? Er du kvalitetsbevidst og har masser af drive og selvstændighed, og vil du være med til at sikre at vores laboratorium er i compliance med gældende GMP og ISO krav? Har du erfaring med arbejde i et mikrobiologisk GMP laboratorium? Så er du måske vores nye kollega.

Om afdelingen
QC Mikrobiologisk Laboratorium, QCM består af ca. 40 medarbejdere fordelt på 2 teams. Vi udfører mikrobiologisk analyse på vand og insulinprodukter, og vi har en stor kontaktflade til vores samarbejdspartnere i produktionen. Du bliver en del af support teamet som består af 5 kemikere, 9 laboranter/speciallaboranter og 3 operatører.

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

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

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

Stillingen er et 2-årigt vikariat.

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

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

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

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

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

Kontakt
Vil du vide mere om stillingen, så er du meget velkommen til at kontakte Marianne Foss Hansen på + 45 3075 9846.

Ansøgningsfrist
15 december 2013

Operatør til produktionen i Kalundborg

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

- Produktions operatør
- Danmark - Kalundborg

Tør du udfordre dig selv i en af vores højteknologiske færdigvarefabrikker i Kalundborg? Vil du spille en vigtig rolle i produktionen af livsvigtige lægemidler? Kan du bevare overblikket og holde fast, når hverdagen ikke forløber lige efter planen?

Så er et job som operatør i Novo Nordisk, Product Supply, måske noget for dig. Her får du mulighed for at gøre en forskel for patienter med diabetes. Samtidig giver vi dig chancen for at udnytte dit potentiale, da vi har fokus på personlig og faglig udvikling. Du kan se frem til et job med stort ansvar, hvor du skaber resultater i samarbejde med dine kolleger.

Product Supply er ansvarlig for produktionen af alle produkter, der sælges af Novo Nordisk. Det er vores opgave at sørge for, at produkterne er tilgængelige, når kunderne skal bruge dem. Vi sikrer også, at alle produkter lever op til de aktuelle kvalitetsstandarder. Product Supply beskæftiger ca. 9.500 medarbejdere.

Vi søger nu operatører primært til vores aseptiske produktion i Kalundborg. Der er tale om både faste og midlertidige stillinger. De ledige job formidles gennem Operatørernes Rekrutteringscenter (ORC), og der vil derfor også være mulighed for at komme i betragtning til andre operatørjobs på Novo Nordisk i Kalundborg.

I din ansøgning bedes du venligst angive tydeligt, hvorvidt du er interesseret i vikariater og/eller faste stillinger. Da det meste af vores produktion kører i døgndrift året rundt, arbejder vi på skiftehold med skiftevis dag-, aften- og nattevagter både på hverdage og i weekenderne.

Vi er ambitiøse med kvalitet og hygiejne
Du kan se frem til en hverdag med mange og varierede arbejdsopgaver, men hovedvægten i jobbet ligger på betjening af vores procesudstyr. Du skal bl.a. varetage påfyldningen og sikre, at produktionen kører gnidningsfrit. Ofte vil rengøring af produktionsfaciliteterne og udstyret også være dit ansvar.

Arbejdet i steril produktion stiller meget store krav til hygiejne og kvalitet. Derfor arbejder vi hele tiden med at sikre et højt kvalitetsniveau og udfører således løbende dokumentation af vores arbejde. Det bliver også din opgave at sørge for, at produkterne lever op til kvalitets- og myndighedskrav herunder GMP, som er en forudsætning for vores produktion.

Kvalitetssans og teknisk indsigt
Du har erfaring fra et produktionsmiljø og gerne kendskab til fyldning i sterilt område. Det er også en fordel, hvis du tidligere har arbejdet i aseptisk produktion og kender til GMP.

Du skal være klar til at håndtere de udfordringer og forandringer, som ligger foran dig og 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.

Da udstyret kræver en del teknisk indsigt, skal du have interesse og flair for teknik og være fortrolig med brug af IT. Du har dansk, matematik og engelsk på mindst 9. klasses niveau, og måske har du også en uddannelse som for eksempel industrioperatør, procesoperatør, håndværker eller lignende. For at komme i betragtning til jobbet, er det et krav, at du vedhæfter alle dine eksamensbeviser ved fremsendelse af ansøgningen via vores hjemmeside.

Kontakt
Vil du vide mere om stillingen, så kontakt Operatørernes Rekrutteringscenter (ORC) på +45 3079 7626 i telefontiden, som er fra den 5. - 12- dec. kl. 13.00 til 15.00 (lørdag og søndag eksklusiv).

Deadline
12. december 2013

Tekniske ingeniører til stærkt produktions-setup

- Produktion
- Storkøbenhavn

Finder du din faglige motivation i tekniske udfordringer, og vil du se din indsats skabe synlige resultater i et verdensklasse produktions-setup, så er det nu, du har muligheden. Vi mangler tekniske ingeniører/tekniske profiler i Hillerød, Gentofte og Måløv, og vi er helt klar til at byde dig velkommen.

Om afdelingen
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 dig spændende udfordringer og masser af udvikling for dig personligt. Det gælder uanset, om du vil arbejde med biopharm API-produktion i Hillerød eller Gentofte eller med tabletproduktion i Måløv.

Jobbet
Dit grundlæggende fokus bliver at sikre compliance på vores produktions- og/eller utility-udstyr og herunder at bidrage til, at vi hele tiden gør udstyret bedre rent teknisk og dermed også 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. Har du særlig viden/kompetencer inden for tabletproduktion, så kunne vores site i Måløv blive dit fremtidige arbejdssted. 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.

Kontakt
Vil du vide mere om jobbene i Hillerød, så kontakt Majbrit Kronholm Flenø på 3075 7444. Er Gentofte din favorit, så kontakt Søren Dissing Millgaard på 3075 2721. Vil du til Måløv, så kontakt Lars Grønborg på +45 3079 9839.

Ansøgningsfrist
31 December 2013

Ambitiøs leder med GMP erfaring

- Produktion, Teamleder
- Storkøbenhavn

Danmark – Kalundborg, Hillerød, Gentofte, Måløv, Kirke Værløse og Bagsværd.Novo Nordisk er verdens førende virksomhed inden for diabetesbehandling. Samtidig er vi godt på vej til at få en solid position inden for behandling af blødninger samt behandling med væksthormon og hormonterapi. Vores ambitioner og dygtige medarbejdere har bragt os meget langt, men vi er slet ikke færdige. Derfor investerer vi massivt i hele vores værdikæde globalt, ikke mindst i vores produktions-setup. Og det er her, du kommer ind i billedet.

Om afdelingen
Vores succes gør, at vi mangler ambitiøse teamledere med GMP erfaring på en række af vores danske produktions-sites. Du vil sætte retning for et team, der typisk består af 10-20 højt motiverede og fagligt kompetente akademiske medarbejdere og teknikere. Teamet kan fx være en processupportfunktion eller en QA/QC funktion, hvis fornemmeste opgave er at sikre høj kvalitet i både processer og produkter. Via problemløsning, optimering og dokumentation er du og dit team med til at levere medicin der hjælper mennesker til at leve det liv de ønsker. I Novo Nordisk stræber vi efter at være de bedste.

Jobbet
Som teamleder er det dig, der går forrest, sætter retningen og sikrer, at der er topmotivation og energi i dit team. Vores verden er i stadig forandring mod endnu mere moderne systemer, processer og ledelse. Du spiller derfor en nøglerolle i at sikre, at alle er med og klar på nye ideer og metoder, ligesom du er den, der driver kontinuerlig optimering af processer og systemer gennem LEAN. Samtidig sikrer du selvfølgelig, at dit team når de aftalte mål for produktionsvolumen, kvalitet og leveringstid. Det kræver synlig ledelse, hvor du aktivt kommunikerer klart, så alle kender målene og deres egen rolle i at nå disse. Løbende coaching og udvikling af dit team og de enkelte medarbejdere er ligeledes en hjørnesten i dit job. Opgaverne har generelt høj kompleksitet og kræver at du er sparringspartner for dine medarbejdere og er i tæt dialog med dine teamlederkolleger både i din og andre afdelinger. Uanset hvor du bliver ansat, refererer du til en erfaren afdelingsleder, og du indgår i afdelingens lederteam. 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
Din baggrund er en videregående uddannelse som fx produktionsingeniør, kemiingeniør, farmaceut eller biokemiker. Du har konkret erfaring med GMP enten fra et job i et produktionsmiljø eller fra QA. Herudover har du minimum 2 års erfaring som leder. Du ved derfor, hvordan man coacher, motiverer og engagerer et team. Du kommunikerer klart, så komplekse problemstillinger fremstår logisk og sammenhængende – på dansk og engelsk. Derudover er det vigtigt, at du trives med at arbejde i en foranderlig hverdag, hvor tempoet er højt, og der skal træffes mange beslutninger hver eneste dag. Har du ikke allerede erfaring med LEAN, kender du de grundlæggende principper, og du er klar til at lære mere.

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 Lili Behjat Kristensen på +45 3079 4143. Søger du job i Kalundborg, kan du læse mere om vores største produktionssite ved at bruge linket www.novonordisk.com/kalundborg-careers.

Ansøgningsfrist
12. januar 2014

Ambitiøs leder med teknisk baggrund

- Produktion, Teamleder
- Storkøbenhavn

Novo Nordisk er verdens førende virksomhed inden for diabetesbehandling. Samtidig er vi godt på vej til at få en solid position inden for behandling af blødninger samt behandling med væksthormon og hormonterapi. Vores ambitioner og dygtige medarbejdere har bragt os meget langt, men vi er slet ikke færdige. Derfor investerer vi massivt i hele vores værdikæde globalt, ikke mindst i vores produktions-setup. Og det er her, du kommer ind i billedet.

Om afdelingen
Vores succes gør, at vi mangler teamledere med teknisk baggrund fra et GxP reguleret miljø på en række af vores danske produktions-sites. Du vil sætte retning for et team, der typisk består af 10-20 højt motiverede og fagligt kompetente ingeniører, teknikere og håndværkere. Dit team er en teknisk supportfunktion, hvis fornemmeste opgave er at sikre at udstyret er i topform, så produktionen kører så problemfrit som muligt. Via problemløsning, optimering og dokumentation er du og dit team med til at levere medicin der hjælper mennesker til at leve det liv de ønsker. I Novo Nordisk stræber vi efter at være de bedste.

Jobbet
Dit job handler om at gå forrest, sætte retning, inspirere og motivere. Din opgave er at få dit team til at spille så godt sammen, at I ikke bare leverer, men leverer bedre end jeres kunder i produktionen tror, er muligt. Både når I udfører her-og-nu problemløsning, og når I udtænker langsigtede optimeringer af produktionsapparatet. Og det er din sprudlende energi og altid optimistiske tilgang til opgaverne, der driver den bevægelse fremad. Samtidig viser du med dit eget eksempel, hvordan man skaber en god og konstruktiv dialog på tværs af roller, opgaver og afdelinger. Tæt og synlig ledelse er således helt afgørende i dette job, så du får skabt et team, hvor alle byder ind med gode ideer, og hvor alle er med på, at forandring og forbedring er to sider af samme sag. Uanset hvor du bliver ansat, refererer du til en erfaren afdelingsleder, og du indgår i afdelingens lederteam. 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 ingeniøruddannelse, og du har en solid teknisk know-how. Du har erfaring fra GxP regulerede produktionsvirksomheder eller andre, der er underlagt høje kvalitetskrav, hvor du eventuelt har fået viden om udstyr og forsyning. Du har flere års erfaring med ledelse og lyst til at tage ansvar for udvikling af dit team både fagligt og personligt. Jobbet som teamleder kræver lige dele fagligt og ledelsesmæssigt fokus, herunder evnen til at træffe mange beslutninger i højt tempo. Samtidig er det vigtigt, at du kan motivere og inddrage dine medarbejdere og bidrage til et positivt samarbejdsklima i afdelingen. Du udstråler ro og overblik, som gør, at dine mange interessenter opfatter dig som professionel og troværdig, og at medarbejderne har lyst til at følge 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 usædvanligt talentfulde kolleger.

Kontakt
Vil du vide mere om stillingen, så kontakt Lili Behjat Kristensen på email lbek@novonordisk.com. Søger du job i Kalundborg, kan du læse mere om vores største produktionssite ved at bruge linket www.novonordisk.com/kalundborg-careers.

Ansøgningsfrist
12 Januar 2014

Ambitiøs leder med produktionserfaring

- Produktion, Teamleder
- Storkøbenhavn

Danmark – Kalundborg, Hillerød, Gentofte, Måløv, Kirke Værløse og Bagsværd.Novo Nordisk er verdens førende virksomhed inden for diabetesbehandling. Samtidig er vi godt på vej til at få en solid position inden for behandling af blødninger samt behandling med væksthormon og hormonterapi. Vores ambitioner og dygtige medarbejdere har bragt os meget langt, men vi er slet ikke færdige. Derfor investerer vi massivt i hele vores værdikæde globalt, ikke mindst i vores produktions-setup. Og det er her, du kommer ind i billedet.

Om afdelingen
Vores succes gør, at vi mangler ambitiøse teamledere med GxP erfaring på en række af vores danske produktionssites. Du vil sætte retning for et team, der typisk består af 10-20 højt motiverede og fagligt kompetente akademiske medarbejdere og teknikere. Teamet kan fx være en teknisk supportfunktion, en processupportfunktion eller en QA/QC funktion, hvis fornemmeste opgave er at sikre høj kvalitet i både processer og produkter. Via problemløsning, optimering og dokumentation er du og dit team med til at levere medicin, der hjælper mennesker til at leve det liv de ønsker. I Novo Nordisk stræber vi efter at være de bedste.

Jobbet
Du får en nøglerolle i Novo Nordisk som leder af 10-20 kompetente medarbejdere med forskellige uddannelsesmæssige baggrunde. Nogle har en teknisk uddannelse, andre en akademisk. Som teamleder er du det fyrtårn, som dit team navigerer efter. Du sætter retningen og levere den positive og smittende energi, der gør, at dit team når et fagligt og socialt niveau i den absolutte top. Med synlig ledelse, sparring og coaching skaber du en kultur, hvor alle er klar til at udfordrer metoder, systemer og processer – løbende gøre dem bedre, smartere og hurtigere. Du refererer til en erfaren afdelingsleder og indgår i afdelingens lederteam. 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 lagt grundstenene til din karriere med en naturvidenskabelig uddannelse på minimum bachelorniveau. Du har erfaring fra produktion i GxP regulerede virksomheder eller andre, der er underlagt høje kvalitetskrav. Hvis ikke du kommer fra den farmaceutiske industri, kan du have fået din erfaring fra fx fødevare- eller kosmetikbranchen. Det betyder, at du er vant til at efterleve de regulativer, som skal sikre, at vores produkter lever op til både kvalitet og sikkerhed. Samtidig har du lært at navigere sikkert i en kompleks organisation med mange interessenter og agendaer.

Du har allerede bevist, at dine inspirerende og motiverende lederevner avler succes, og du er god til at uddelegere ansvar. Du trives i en stilling, hvor du får rig mulighed for at bruge dit store engagement til at motivere andre – og du er selvfølgelig god til at tale med mennesker med mange forskellige baggrunde. Endelig er du handlekraftig og står fast, når det er nødvendigt.

I Novo Nordisk baseres beslutninger og handlinger på deres indflydelse på samfundet, miljøet og muligheden for at skabe økonomisk overskud. Du kommer derfor ind i en virksomhed, hvor din indsats har reel betydning.

Kontakt
Vil du vide mere om stillingen, så kontakt Lili Behjat Kristensen på -45 3079 4143. Søger du job i Kalundborg, kan du læse mere om vores største produktionssite ved at bruge linket www.novonordisk.com/kalundborg-careers.

Ansøgningsfrist
12. januar 2014

Requisition ID 17082BR
Title Entry Level Pharmaceutical Sales Representative – Bradenton, FL
Job Category Sales
Job Description Entry Level Pharmaceutical Sales Representative – Bradenton, FL

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.

PURPOSE:

The position represents Novo Nordisk to Prescribers within an assigned territory with the goal of maximizing sales and positioning Novo Nordisk as the leading company in diabetes care. Provides an in-house talent pool for future Diabetes Care Specialist (DCS) roles.

RELATIONSHIPS:

Externally, the Diabetes Care Associate (DCA) maintains relationships with physicians, nurses, and other paramedical customers. Internally, the DCA reports to a District Business Manager. The DCA also interacts and collaborates on a regular basis with other field-based employees covering the same geographic areas.

ESSENTIAL FUNCTIONS:

• Actively contribute to the overall sales goals of the Company and its Sales/Marketing Departments by:
o Communicating territory activity through timely submission of monthly highlight reports and other appropriate reports
o Contributing to sales and marketing meetings, training programs, conventions and displays as appropriate
o Partnering with the Novo Nordisk Sales/Marketing Departments to maximize appropriate and effectively use selling materials and product information
o Providing recommendations towards sales and marketing solutions based on understanding and evaluation of trends, dynamics, customer needs, and competitors’ products or services
o Recording notes of calls, including products discussed, key issues and concerns addressed, sales aids utilized, samples distributed, and any other information that will ensure maximum effectiveness for future sales calls
• Develop and maintain a mastery of product knowledge and consultative promotion techniques through:
o Continuously promoting and improving knowledge of Novo Nordisk’s products, competitive products, and sales and promotional skills through participation in company sponsored/approved training programs
o Educating physicians, nurses, and other members of patients’ primary care team on diabetes and the use of Novo Nordisk’s products, including the approved uses and benefits of Novo Nordisk’s products for their patients, related disease states, and the Novo Nordisk brand
o Understanding the most up-to-date clinical studies to educate customers and anticipate questions/concerns about Novo Nordisk’s products
• Coordinating with a manager to effectively prioritize time and available resources to achieve maximum sales in the local territory by:
o Evaluating, identifying, and developing order of calls and routes that maximize the opportunity to call on targeted customers
o Developing and implementing the most effective distribution of product samples in territory
o Ensuring maximum customer penetration and sales volume with limited supervision
o Exercising prudent control over samples and other company property in accordance with company policies and procedures and legal requirements
o Managing a discretionary budget to support sales and additional marketing activities
• Identify, develop, maintain, and leverage relationships with physicians, nurses, and other individuals who make or influence purchasing/prescribing decisions by:
o Analyzing and leveraging an understanding of the patient profiles of targeted and non-targeted physicians in the territory and how those profiles impact territory sales
o Evaluating and determining which stakeholders have greatest opportunity to impact sales and use personalized communication techniques to build and maintain effective relationships with those stakeholders
o Identifying and responding to obstacles to use of Novo Nordisk’s products
o Leveraging an understanding of the impact of managed care on physicians’ prescribing decisions and adjusting sales and marketing strategies accordingly
• Sell and promote Novo Nordisk’s portfolio of diabetes products by:
o Developing a customized approach for each call on each customer to assess customer needs and increase sales of Novo Nordisk’s products
o Utilizing available resources to sell and promote Novo Nordisk’s products, including determining which resources to use in any given situation
o Explaining and promoting features and benefits of Novo Nordisk’s portfolio of products, with an emphasis on which products are best suited for particular patient profiles or circumstances
o Coordinating and implementing medical education activities, programs, and special projects to Impact the local retail market share
o Obtaining maximum commitment from customers on every call
o Listening to customers, including anticipating and responding to customers’ questions, objections, and concerns.
o Determining appropriate messages that reading and react to the customer environment to achieve maximum effect on each sales call
• Learn and stays up-to-date with the “Novo Nordisk Way” of selling

PHYSICAL REQUIREMENTS:

• Approximately 20-40% overnight travel (1-2 days)
• Must maintain a valid driver’s license and obey all applicable traffic laws

DEVELOPMENT OF PEOPLE:

• Not Applicable

KEY SUCCESS FACTORS: EDUCATION, EXPERIENCE, KNOWLEDGE AND SKILLS

• Bachelor degree required
• An aptitude for learning and communicating technical and scientific product and disease information
• Basic computer skills (Excel and Word)
• A valid driver’s license required; willing to travel
• Previous experience in retail, Non-Retail/Inside sales or customer service experience preferred.
• Previous formal leadership role in volunteer/community service, military, or organized athletic team/club preferred.
• Must live within the boundaries of the territory or be willing to relocate
Department SALES - DIABETES SALES
Position Location US - Field Based - Across US
City Brandenton
State/Provinces US - FL
Degree Required Bachelor's Degree Required
Percent Travel 30 - 40%

Non-Clinical Project Manager

- Research & Development
- Denmark - Måløv

We have a vacant position as Non-clinical Project Manager in our Non-clinical Project Management department, which comprises 10 Non-clinical Project Managers.

About the department
Non-clinical Project Management are overall responsible for coordination of all Non-clinical activities to ensures optimal project progress from project initiation to regulatory submission and approval. We work in a dynamic and challenging environment integrating all Non-clinical disciplines in order to provide high quality Non-clinical safety assessments across the Novo Nordisk portfolio of drug development projects.

The job
As Non-clinical Project Manager you will be heading Non-clinical project teams and you will be an integrated member of the overall project groups. You will be coordinating complex cross-functional and cross-organisational Non-clinical tasks on one or more development projects. You will ensure a good collaboration environment internally in Non-clinical Development as well as with other stakeholders inside and outside Novo Nordisk, and you will ensure follow up on activities and smooth milestone passing for your projects.

Qualifications
We expect you to have a university degree within the life sciences (DVM, MD, Pharmacist or comparable) and documented professional experience working with Non-clinical development in the pharma industry. PhD degree within a relevant discipline will be an advantage. You are expected to have relevant Non-clinical development knowledge and experience with drug development. You are fluent in oral and written English. You have excellent communication skills, being capable of working in a complex interdisciplinary organization and having the personal power to influence and to retain focus. Engagement and a positive mindset, combined with a willingness to make a difference and walk the extra mile are personal competencies needed in order to be a success in this job.

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 Peter Ravn Brinck at +45 3075 4620.

Deadline
29 December 2013.

Clinical Supplies Coordinator (Temporary)

- Research & Development
- Denmark - Måløv

We are looking for a new colleague in Clinical Supplies Coordination.

Would you like to work in a busy environment with coordination of multiple activities together with a dynamic and dedicated team of colleagues? Can you multitask and are you motivated by the challenge of securing a stable supply chain for clinical trials in new and innovative treatments? If yes, we are looking forward to hearing from you.

About the department
The pipeline of potential new products in Novo Nordisk is continuously growing creating a growing portfolio of clinical trials. Our main and most important task in Clinical Supplies Coordination is to ensure that trial products are available on time and in the right quality and quantity for all clinical trials conducted globally by Novo Nordisk.

In order to meet Novo Nordisk’s ambitious goals within diabetes, haemophilia and other chronic diseases, we are furthermore working with reducing our product waste, to shorten our lead time and optimise the use of resources by means of various LEAN tools.

We are around 50 people in Clinical Supplies Coordination and are located at Novo Nordisk site Måløv. The new candidate will be part of a team of dedicated people working with drug candidates for various treatment groups.

The Job
The job is a temporary position for a duration of 12 months. As Clinical Supplies Coordinator, you will be responsible for the clinical supply chain from contributing to the development of the clinical trial protocols, from a trial supply perspective, and until the product reaches the end user. You will work according to GMP and GCP to ensure that the tight deadlines of the development projects are met.

You will be using project management tools and your main responsibilities are planning and coordination of packaging of clinical trial supplies. You will provide input to our web-based trial supply management system and will be writing trial material manuals. You will conduct training of Clinical Research Associates and study site personnel in trial-specific product handling; hence once or twice yearly you will attend international meetings.

In addition to these trial specific responsibilities, you will take part in projects with focus on optimising our processes.

Qualifications
You hold a university degree in natural sciences, engineering or similar. You have at least 3-5 years of experience from the pharmaceutical industry with clinical trial supplies planning. Alternatively, you have at least 5 years of experience from areas such as drug development or drug manufacturing. Knowledge of GMP/GCP is required.

A significant part of our processes are carried out in various IT systems and it is therefore important that you are able to quickly adapt to such systems.

You are comfortable with taking independent action and manoeuvring in an environment characterised by frequent changes. As Clinical Supplies Coordinator, you are placed in the centre of the clinical supply chain and you need to be robust and a strong communicator. We collaborate with colleagues and partners all over the world; therefore you are fluent in both written and spoken English on a professional level.

We expect you to possess a good sense of humour and to be a team player with a positive attitude to changes and challenges. You have a high level of engagement and flexibility and see continuous improvements as natural part of your job.

In this temporary position, you will be able to further develop your supply chain skills and business understanding, work with many contacts across the organisation, and you will broaden your personal competences and skills.

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 Team Leader Nicolas Omdahl, +45 3079 7114.

Deadline
20 December 2013

Senior system manager to create framework for IT portfolio

- Research & Development
- Denmark - Søborg

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

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

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

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

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

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

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

Deadline
5 January 2014

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