Jobs at Novo Nordisk

Strategy Consultant

- Supply Chain and Logistics
- Denmark - Bagsværd

This is your chance for an exciting career within Supply Chain Management. A position as strategy consultant in Strategic Planning is currently open for replacement. This is an opportunity to join a competent and dedicated team responsible for global planning activities in our production unit, Product Supply.

About the department
Strategic Planning is part of the Supply Chain Planning function, responsible for optimizing and aligning our end-to-end supply chain.

Strategic Planning is responsible for the long term planning and overview of production capacity for all marketed products as well as products in the development pipeline.

During the coming years, Novo Nordisk will be launching more products than ever before, with the need for faster production ramp up and with a continued volume growth in a more globalised production footprint. This added complexity requires robust strategic planning processes for Product Supply.

The Job
In Strategic Planning, we have close cooperation with the business units and our approach is to act as strategic partners based on strong planning competencies combined with a good understanding of the business in which we operate.

In this position you will get an excellent opportunity for gaining valuable experience within the Novo Nordisk supply chain, building unique business knowledge and gaining insights into the strategic considerations of the company. You will become familiar with current and future supply and demand challenges and you will have an opportunity to make a significant difference in terms of proposals and recommendations to senior management. You will participate in, and drive, various activities and projects to continuously improve our end-to-end supply chain management, risk management and scenario building processes.

Qualifications
You hold a master’s degree within a relevant business education, and you have a minimum of 3 years relevant working experience. You have a solid business understanding with strategic insight and are able to identify scenarios and make recommendations in a complex decision-making environment. You have experience with demand planning and/or capacity planning either from a support function or from a more operational unit. You have high analytical skills and are very confident with data retrieval, analysis and management presentations. However, analyses and details never make you forget the big picture.

You are ambitious, result-oriented and can structure your own work. You are comfortable working both independently with responsibility for your own tasks, and as part of a team. In general, you collaborate and navigate easily with all levels in the organisation. You work independently, take responsibility and are respected for the results you create. You thrive in a competent and dedicated team with an informal working environment. You write and speak English fluently.

You work strategically, as well as tactically and are willing to invest significantly in the development of the strategic planning processes in Product Supply as well as your own individual development.

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 Linnet at + 45 3079 9039.

Deadline
24 November 2013

Standard Supporter

- Research & Development
- Denmark - Søborg

Are you interested in working with clinical standards and data? Do you want to be an important partner in the drug development process? Do you like to work with cutting edge knowledge and processes? Do you like a challenging and rewarding workplace?

About the department
Data Management Standards & Support (DMSS) is situated in Søborg and currently employs 22 people working in various roles to support standard ways of handling data across Novo Nordisk clinical trials. You will be part of a team that supports the use and governance of our clinical data standards across multiple systems used for data collection and reporting of our clinical trials. We work closely with multi-functional and international teams on a variety of clinical and technical projects in a pleasant and informal atmosphere.

The job
The Standards Supporter’s work is focused on supporting system integration between the three systems used for handling data for Novo Nordisk’s clinical trials: Electronic Data Capture (EDC), Oracle Clinical (OC), and our Clinical Data Warehouse (CDW). We facilitate flow of data through these systems in a standardised way, working closely with Data Managers, Biostatisticians, Statistical Programmers, Trial Managers and others within clinical development. The overall goal is to ensure standardised, GCP compliant, quality clinical trial data across our systems to enable reporting to regulatory authorities on a global basis.

Primary challenges will be to handle requests for new objects in Oracle Clinical, ensuring an optimal integration with both EDC and CDW, and to review documentation, including Case Report Forms (CRFs) to ensure compliance with standards.

Within the department, there is another team primarily focused on mapping clinical data from source systems to CDW in close collaboration with trial teams, including data base annotations to ensuring conformance with CDW standards, as well as participating in data cleaning meetings and support to trial teams with ad hoc data inquiries. Processes are continually being developed and optimised, and it would also be possible to participate in this work in the long-term.

In addition to supporting trial teams, we also expect you to take part in developing, enhancing, and maintaining documentation and processes related to our clinical systems and standards. As we are continuously initiating new improvements, including a new initiative to implement CDSIC controlled terminology, there will be also be opportunities to develop project management skills and participate in training and communication.

Qualifications
You have a B.Sc. or M.Sc. within IT or another relevant degree and extensive knowledge and experience with clinical data in the pharmaceutical industry, and preferably knowledge of Oracle Clinical and SQL programming. You are technically strong, have a demonstrated ability to understand data structures, and possess knowledge of relational databases. You have excellent overview and coordination skills. You have high attention to detail, and you thrive doing careful meticulous work.

Furthermore, you are comfortable working in English on a daily basis (both spoken and written) in a global organisation. You have strong cooperative and analytical skills. You are capable of working independently, taking responsibility, and showing initiative. We expect you to be able to maintain an overview several tasks in parallel without compromising the quality of your work and that you remain high spirited, also when things are moving fast.

Additional desirable skills are experience with CDISC, project management, training and communication, CRF design, OC set-up, clinical data warehouse, SAS programming, statistical analysis, and knowledge of laboratory or genetic data in clinical trials.

In return we offer an interesting and challenging job with a high degree of individual responsibility and good personal development opportunities in an international atmosphere.

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 call Dorte Straarup +45 3079 5986 or Heather Brage +45 3075 0076.

Deadline
26 November 2013.

QA for Qualification/Validation in Pilot fac.

- Research & Development
- 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 and facility. The department is recently established to support the development of oral protein formulations in our stakeholder departments.

The Job
In close cooperation with your colleagues in QA, you act as a consultant for our pilot. You contribute to finding solutions for ad hoc questions and challenges within compliance of the facilities.The job is related to qualification/validation of equipment in the pilot facilities. You will assure that the documentation for implementation and maintenance of equipment is compliant with internal and external requirements.Furthermore, you will approve facility related documentation needed for the operation of the plant eg. change request, non-conformities, SOP’s, environmental monitoring and utilities.

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, Chemical Eng. or corresponding qualifications and at least 1-2 years of experience within the pharmaceutical industry. You have thorough knowledge within more of the following areas: GMP, validation/qualification, equipment used in tablet and/or aseptic production.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 at+45 3075 7333.

Deadline
5 December 2013.

Sr. QA for Qualification/Validation in Pilot fac.,

- Research & Development
- 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 and facility. The department is recently established to support the development of oral protein formulations in our stakeholder departments.

The Job
In close cooperation with your colleagues in QA, you act as a consultant for our pilot. You contribute to finding solutions for ad hoc questions and challenges within compliance of the facilities.The job is related to qualification/validation of equipment in the pilot facilities. You will assure that the documentation for implementation and maintenance of equipment is compliant with internal and external requirements.Furthermore, you will approve facility related documentation needed for the operation of the plant eg. change request, non-conformities, SOP’s, environmental monitoring and utilities.

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, Chemical Eng. or corresponding qualifications and at least 5 years of experience within the pharmaceutical industry. You have thorough knowledge within more of the following areas: GMP, validation/qualification, equipment used in tablet and/or aseptic production.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 at +45 3075 7333.

Deadline
5 December 2013.

cLean consultant

- LEAN
- Denmark - Hillerød

Do you strive for simplicity and clarity? Then this could be your chance to play a key role in an organisation where management in both word and action paves the way, and where LEAN has top priority. 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 Novo Nordisk’s cLEAN and Strategy department in Device R&D, which is responsible for driving and supporting LEAN activities as well as for the strategy and devices projects portfolio management. You will be working with a dedicated team of colleagues at the forefront of LEAN implementation in an R&D environment.

The job
As LEAN consultant your main priority will be to facilitate workshops supporting the planning of development projects with the aim to make the development process more robust. Additionally you will identify and drive cross-organisational improvement projects and you will act as a sparring partner for the Team Leaders and Project Managers in Device R&D supporting them in executing effective board meetings and address problems in a systematic way. Across all activities you will ensure that relevant stakeholders are taken into account in goal setting, and you drive the projects forward by continuous follow up, communication and goal attainment. You can anticipate a very independent job where you actively contribute to lasting and measurable process improvements.

Qualifications
You have a relevant academic degree and you are among the best within your field. You have 1-3 years’ experience with process optimisation projects, practical experience as workshop facilitator and teaching and good LEAN, change management and project management skills. You have an analytical and structured approach to the problem-solving processes. Having many contacts from employees to senior management, across all kinds of professional backgrounds, requires excellent stakeholder management and communication skills including the ability to explain complex subjects in an easy understandable way – in English written and spoken.

On a personal level, you are known for your positive, energetic and open-minded attitude when dealing with challenges and you find it is easy to associate with colleagues at all levels in the organisation. To succeed in your work across the organisation you need to be emphatic and yet display a decisive approach.

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 Davide Ricci at +45 3075 2179. For more details about Device R&D please see www.novonordisk.com/Device-RD.

Deadline
4 December 2013.

Business Analyst

- Research & Development
- Denmark - Hillerød

Are you looking for a highly independent job where you can make an impact on Novo Nordisk’s strategy development and sourcing of new technologies within Device R&D? Then you could be the ambitious Business Analyst we are looking for.

About the department
As a part of the Device Research & Development we are responsible for coordinating and supporting cLEAN activities, for the internal strategic analyses and strategic planning processes and for the devices projects portfolio management. Additionally we support technology scouting and sourcing activities. Your new department consists of 7 people and you can look forward to 20-30 travelling days per year and to becoming part of an international setup where you will work with utterly skilled colleagues and external partners.

The Job
Your objective is to support the Device R&D management team with project portfolio management activities and with the strategic definition of innovation directions for the portfolio of research projects. It is also your task to participate to business strategy development and perform ad-hoc business analyses for the SVP of Device R&D. You will also have a relevant role in our technology scouting and licensing efforts supporting the Device R&D Sourcing Director. You can look forward to operating with a wide-ranging surface of contacts, which also includes a string of stakeholders at upper management level within e.g. Product Supply and Global Marketing.

By driving successful technology scouting activities and by taking our project portfolio management initiatives and early innovation direction to the next level, you will achieve success in this position. Moreover, your success will be measured by your ability to develop new models and tools for strategic analyses and project portfolio management.

Qualifications
You hold an MSc e.g. in Engineering, Physics, Chemistry or similar disciplines preferably supported by some business education (MBA, HDD etc …). Irrespectively, you have 1-2 years’ experience from a medical tech or high tech industry, which could derive from a consultancy, pre-sales function, R&D or business development area. In your career you have acquired skills for stakeholder management, and you are confident conducting business analyses, developing strategies and managing project portfolios.

On a personal level, you are known for your positive and energetic attitude when dealing with challenges. You can think outside the box when needed, and with your ambitious attitude and high level of drive you get things done. Moreover, you have sound analytical and communication skills and a structured and practical approach to your tasks enabling you to deliver in due time. Finally, you have fluency in English.

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

Contact
For further information, please contact Davide Ricci at +45 3075 2179. For more details on Device R&D please look at www.novonordisk.com/Device-RD.

Deadline
4 December 2013.

Senior specialist R&D Academic Relations

- Research & Development
- Denmark - Måløv

If you have a strong combination of business understanding, pharmaceutical research & development experience, and relationship management competencies, this is a rare opportunity to play a key role in enabling the long-term success of the Novo Nordisk R&D organisation.

About the department
You will join R&D Academic Relations located in Måløv. We are responsible for developing and maintaining a consolidated and strategic approach to the collaboration with selected academic institutions across R&D. Our objective is to facilitate talent attraction and competency building in Novo Nordisk R&D. As such, one of our core responsibilities is the management of Novo Nordisk’s PhD and PostDoc program (STAR) that is currently employing app. 80 fellows.

The job
Your focus will be to support our outreach to selected Danish and international universities in order to facilitate strategic collaboration with these universities. As such, you will drive fellowship activities from proposal to implementation to ensure identification, attraction and recruitment of international talents to our global R&D organisation. You will handle optimisation, coordination and integration of fellowship programs across R&D including the STAR, PhD school and Scholarship programs. Another vital task will be to plan and carry out ongoing development, implementation and optimisation of processes that can reduce the administrative workload related to the main tasks in the job. You must establish a close collaboration with the R&D Line of Business and other units with an external focus including sourcing units and HR. Hence, your ability to coordinate internally and externally is crucial for your success.

Qualifications
To succeed in this job, you will need to have a solid academic background – you probably have a PhD degree within Natural Sciences or similar. This has provided you with knowledge about the dynamics of the academic community and made you capable of working with English as your primary language. Your previous career has given you at least five years of experience from one or more jobs where you have worked with external relations in academia or in the pharmaceutical industry – ideally with an international scope. You are an experienced project manager who can steer processes and projects all the way from initial analyses through strategy development to final implementation. You have solid networking and communication skills, and at the same time, you know the value of creating results based on true teamwork. Furthermore, you rely on your resilience and will to push through. Finally, as you will be acting as our ambassador, high personal integrity and impeccable values must constitute your personality.

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 Palle Høy Jakobsen at +45 3079 6287.

Deadline
2 December 2013.

New Product Coordinator

- Production
- Denmark - Gentofte

Do you thrive in a fast paced environment, juggling many challenges at the same time? Do you have a can-do attitude, continuously seeking improvements? And do you enjoy interacting with a diverse set of stakeholders? If you can answer yes to these questions, you may be the New Product Coordinator we are looking for in Biopharm QC New Haemophilia.

About the department
Novo Nordisk, Biopharm QC New Haemophilia is a newly established laboratory with high quality and LEAN standards. We are responsible for chemical and biological analyses on finished products and API of Novo Nordisk new haemophilia products not yet on the market. In addition we have one marketed Haemophilia product. Because of this wide range of products, Biopharm QC New Haemophilia interacts with many internal stakeholders every day. Stakeholders are from both R&D, CMC and production. This requires a single point of contact for both our customers, but also for the organisation in Biopharm QC New Haemophilia. We offer a very exciting job with development opportunities among high competent colleagues in a positive working environment.

The job
As New Product Coordinator you communicate openly and honestly securing the interests of both Biopharm QC New Haemophilia and our stakeholders. You will be the link between Biopharm QC New Haemophilia and the rest of of Biopharm, through recurrent stakeholder meetings and management of our Service Level Agreements with these stakeholders. You will be involved in follow-up activities to ensure Biopharm QC New Haemophilia delivers as agreed. This is a position in which you will work closely together with the departments' local logistic planners and you will also enjoy a high degree of influence on the flow of incoming samples and their deadlines in Biopharm QC New Haemophilia. The responsibility for maintaining forecasts for sample flow related to existing and new facilities/products in Biopharm QC New Haemophilia will also be yours.

Additionally, you will be responsible for the departments' project/investment portfolio and act as a project manager on selected projects. Support to the performance boards, including update of KPIs will also be part of the job description. Project portfolio includes both internal improvement projects and cross-organisational projects.

You will work with all parts of the Biopharm QC organisation, and broadly with Biopharm CMC Production sites, providing you with the opportunity to thoroughly getting to know the supply chain with Biopharm. The position will provide you with indirect management experiences, and hence could be a stepping stone towards a leader position in Novo Nordisk.

Qualifications
You hold an MSC in pharmacy, biology, engineering or similar, supplemented with a minimum of 3 years' experience as a project manager. You are confident working in a GMP regulated environment. It will be an advantage if you have experience with laboratory or logistics.

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 call Lissi Falch on +45 3075 1015.

Deadline
23 November 2013.

Requisition ID 18132BR
Title Pharma Field Sales-Diabetes Care Specialist (DCS)-Bronx S, NY
Job Category Field Sales
Job Description Pharma Field Sales - Diabetes Care Specialist (DCS) - Bronx S, NY

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.

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 10% 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 - BRONX NY
Position Location US - Field Based - Across US
City BRONX
State/Provinces US - NY
Degree Required Bachelor's Degree Required
Percent Travel 0 - 10%

Projektleder til udvikling af international E-learnings program

- Forskning og Udvikling
- Danmark - Gentofte

Steno Diabetes Center søger Projektleder til udvikling af international E-learning program til REACH projektet

Har du projektlederegenskaber, erfaring med E-learning og udvikling af web-baseret undervisning, er du måske den vi søger.

Om projektet

Steno Education Center er en afdeling i rivende udvikling. Vi fokuserer på at udbrede kendskabet til diabetesbehandling i de områder i verden, der har størst behov. Vi udvikler og afholder nationale og internationale kurser og programmer målrettet sundhedsprofessionelle.

Som et led i et nyt spændende projekt om uddannelse af sundhedsprofessionelle i udviklingslande har Steno Education Center fået en større bevilling fra Novo Nordisk Fonden til at starte en satellit i Asien og udvikle et E-learning program målrettet sundhedspersonale i udviklingslande. Steno ønsker at udvikle E-learning programmer, som dels skal underbygge vores allerede etablerede kurser med blended learning samt udvikle et internationalt E-learnings koncept fokuseret på diabetes. Programmet retter sig mod sundhedsprofessionelle i udviklingslande og skal udvikles med fokus på interaktivitet og inddragelse af deltagerne.

Om stillingen

Du vil blive ansvarlig for at organisere og koordinere programudviklingen, identificere leverandører til mere tekniske løsninger, være ansvarlig for den overordnede struktur og pædagogiske linie, implementering og evaluering af programmet. Programmet udvikles på engelsk, men vil skulle oversættes til lokale sprog afhængigt af brugerfladen. Udviklingen skal ske i samarbejde med engagerede forskere og klinisk arbejdede læger og sygeplejersker på tværs af Steno Diabetes Center og i samarbejde med vores internationale kolleger. Du vil komme til at arbejde i et udfordrende miljø med engagerede og inspirerende kolleger. Der vil kunne forekomme rejseaktivitet

Kvalifikationer

Du har en relevant kandidatgrad med fokus på f.eks, instructional design, kommunikation eller lignende samt dokumenteret erfaring med projektarbejde og undervisningsudvikling. Du har praktisk erfaring med IT, digitale medier og læring, har et godt overblik over de digitale læringsteknologier og en veludviklet teknologiforståelse. Vi forventer, at du taler og skriver engelsk og har erfaring med internationale relationer og en udpræget kulturel forståelse. Projektets succes afhænger i høj grad af, hvor godt du er i stand til at inddrage de relevante parter både internt og eksternt.

Du skal kunne arbejde selvstændigt, og være den, der driver projektet fremad. Du skal kunne skabe struktur og overblik, også over projektets økonomi og milepæle. Du skal være komfortabel med at rapportere fremdrift til styregruppen løbende, og derfor også have gode forhandlings- og kommunikationsevner.

Vi forventer, at du er samarbejdsorienteret og en positiv kollega. Det er en fordel at du også er udfarende, nysgerrig og initiativrig.

Løn og Ansættelsesvilkår

Løn og ansættelsesvilkår i henhold til gældende overenskomster indenfor området.

Ansøgning

Ansøgningsfrist 29 november. Stillingen ønskes besat snarest. Ansættelsessamtaler forventes afholdt uge 50 og 51.

Mere info

Spørgsmål vedrørende stillingen bedes rettet til Chef for Steno Education center, Ulla Bjerre-Christensen tlf: 30756264. Stillingebeskrivelse kan rekvireres ved henvendelse til Nina Meier: NME@steno.dk

Om Steno Diabetes Center

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.

International Medical Manager/International Medical Director

- Research & Development, Medical Doctor
- Denmark - Søborg

In this job, 366 million people worldwide depend on you to develop the world’s best medicine. If you find challenges like this exciting and inspiring, you may be our new medical specialist within diabetes drug development.

About the department
Medical & Science, Degludec I, at Novo Nordisk A/S headquarter is looking for a medical doctor to take on a position as International Medical Manager/International Medical Director (Medical Specialist). The department is part of Global Development and medically responsible for development strategies of diabetes drugs within development phase 1-4. There are two key focus areas; titration surveillance/treatment guidelines and planning/execution of clinical studies. The department consists of 10 Medical Specialists, a Clinical coordinator, a team administrator and 2 students.

The job
Key responsibilities of the successful candidate will be to take up a role as Medical Specialist within The Insulin Titration Group. This includes being instrumental in developing treatment guidelines applicable on a global scale for various insulins under development. The job entails training activities and external presentations at investigator meetings, congresses etc. A specific focus will be to monitor titration performance and interact with local affiliates and sites around to world to ensure optimal glycaemic control of patients in treat-to-target trials. The candidate will be involved in these activities closely interacting and collaborating across the NN organization. The job is globally oriented and will require strong interaction with highly skilled colleagues and external stakeholders including treating physicians and therapeutic experts. At times, you may expect travel activities at a high level, up to 50% of your time.

Qualifications
We are looking for a medical doctor with documented clinical and scientific knowledge about diabetes. A candidate with experience from clinical development work within the pharmaceutical industry will be preferred. You have a medical degree including scientific training (research activities, PhD, DMSc or equivalent). You are a reliable, open-minded and dedicated team player, who thrives in a global environment of continuous development, and focuses on innovation, quality and results. Interaction with internal and external global experts require proficiency in English, high communication, coordination and planning capacities, and good stakeholder management skills.

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

Contact
For further information, please contact Henriette Mersebach on +45 3075 2108.

Deadline
30 November 2013.

Part-time VP Assistant (maternity leave replacement)

- Administrative
- Denmark - Bagsværd

The position is a part-time, temporary (12 months) maternity leave replacement consisting of 20-25 hours a week with a flexible start date in early 2014.

About the department
Competitive Intelligence monitors, analyses, and communicates key competitor activities to a broad set of stakeholders within Novo Nordisk, including executive management. The area has approximately 15 employees divided into two functional areas and is a part of Corporate Development.

The job
The position is a part-time, temporary (12 months) maternity leave replacement consisting of 20-25 hours a week with a flexible start date in early 2014. As VP Assistant, you will be part of a dynamic team and have daily interactions with many different people. You will be responsible for a number of activities in the area, for example issuing our weekly newsletter, as well as daily administrative tasks. These include meeting coordination, expense reporting, purchasing of supplies and services, booking of travel, budget preparation and follow-up on spending, people administration, etc. In addition, you will be responsible for maintaining our departmental intranet, indexing congress reports, and acting as the delegate in various IT systems. You will also function as the VP’s personal assistant.

Qualifications
We are looking for a person with an open and positive attitude and who is very proactive by nature. It is important that you work in a structured manner and show attention to detail. You must be proficient in written and spoken English at a native level. In addition, IT literacy with Microsoft Office is a must and experience with SharePoint and SAP tools is a strong advantage. You must be able to handle matters of confidentiality. Furthermore, we expect you to be familiar with and to take ownership of various management processes, such as budgeting and cost control.

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 Hans Rommer at +45 3079 4025.

Deadline
1 December 2013.

Requisition ID 18073BR
Title Pharma Field Sales-Diabetes Care Specialist (DCS)-Marine Park, NY
Job Category Field Sales
Job Description Pharma Field Sales - Diabetes Care Specialist (DCS) - Marine Park, NY

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.

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 10% 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 - SOUTH BROOKLYN NY
Position Location US - Field Based - Across US
City MARINE PARK
State/Provinces US - NY
Degree Required Bachelor's Degree Required
Percent Travel 0 - 10%

SVP Training Partner in Product Supply Quality

- Human Resources
- Denmark - Bagsværd

Can you ensure that training is effective and in compliance in the newly established PS Quality organization? Then you could be our new SVP Training Partner.

About the department
In Product Supply (PS) PS Quality consists of the QA units in each of the SVP-areas in Product Supply and acts as the organisational anchor for all QA staff in PS. It is the responsibility of PS Quality to ensure that Novo Nordisk requirements to quality are efficiently met - securing patient safety, product quality, and compliance. Right now we are looking for an experienced Training Partner for PS Quality.As SVP Training Partner, you will report to the Director of People & Communication in PS Quality. You will be a part of a highly dedicated and professional team of 4 HR Partners and a communication Partner. You will be working in an environment of strong values and high standards. Your base will be with the People & Communications team in Bagsværd, though a significant part of your time will be spent across PS production sites in Denmark.

The Job
Drive global implementation of training standards.As SVP Training Partner your overall goal is to ensure that training is effective and in compliance in the new PS Quality organization. You will play a key role in defining the right training set-up for PS Quality. You will be Process Responsible for Training in PS Quality and as such responsible for driving the implementation of Competence Management and the Product Supply Operational Training Standard across PS Quality. In this position you will have two key responsibilities: First, you will be the driver of a professional group of Training Partners. Your job in this regard is to motivate and empower the team to succeed in implementing standards locally and involve the CVP Training Partners in continuous improvement of methods, processes and tools for training effectiveness. This includes driving the development of the QA Training Partner role, following up on implementation status at sites and reporting to management.

Secondly, you will work closely with other support functions such as the Product Supply University and cLEAN® organization in order to co-create concepts and ensure consistency with our management system.

Qualifications
Personal drive and dedication . You have a strong background working with training systems preferably in a large organization. You have a relevant academic degree (i.e. psychologist, cand. merc. or similar) and several years of successful experience working in a global and complex organization. Qualifications and experience with LEAN management in a production environment is highly valued. It is absolutely essential that you are an excellent trainer and coach and able to set a clear direction for functions and sites. And you are able to drive processes proactively and independently in a complex environment with many stakeholders. Experience with change management processes as well as project management is a must.You must speak and write English fluently.

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 Sten Mainz Rode at +45 3079 6356.

Apply online: Mark your application “SVP Training Partner PS Quality”

Deadline
24 November 2013.

Team Leader Oral DP Early Phase Analysis

- Research & Development
- Denmark - Måløv

Are you looking for new challenges within formulation, process or analytical method development of solid dosage forms and do you want to make a difference? Our Oral Protein Formulation Unit (OPF) in Måløv is expanding therefore we are looking for several dedicated, professional and enthusiastic new colleagues. Novo Nordisk is on a voyage towards the development and production of oral formulations of proteins. Our ambition is to develop break-through products based on orally available versions of insulin and GLP-1. You will be involved in CMC activities for formulation/process development, pilot production, scale-up and analysis of solid protein dosage forms towards clinical trials.

About the department
We belong to Novo Nordisk’s R&D organization. The department consists of 49 specialists, academics and technicians, who are organized in three teams. The department is responsible for analytical support to research unit and development and validation of analytical methods for oral protein products for preclinical and clinical trials. The department covers a broad range of analytical technologies (e.g. U/HPLC and dissolution).

The Job
As Team Leader you will be responsible for a team of 12, 4 analytical scientists and 8 technicians. The main tasks of the team are analytical and characterization support to our research unit, early development of analytical methods and GLP responsibilities.You have responsibility for the team’s performance and for ensuring that the objectives of the projects and the organization are met or even exceeded. You make sure that we have the right resources and competences at hand at all times and urge your team to undergo both personal and professional development.You focus on creating a work environment that fosters job enthusiasm and you encourage and facilitate professional discussions. You seek to establish good collaboration with your stakeholders and participate in cross organizational projects and collaborations. You will lead a LEAN supporting culture where continuous improvement is a natural part of everyday work.

Qualifications
You are a passionate people manager with strong analytical skills. You have an educational background as MSc (possibly combined with a PhD) in Analytical Chemistry, Biochemistry or similar relevant scientific discipline. Experience within analytical development for oral solid dosage forms in the pharmaceutical industry and experience with analysis of tablet/capsules and/or proteins will be an advantage.You have proven leadership experience and strong leadership is a connecting thread in all of your work and you use LEAN as a natural element in your leadership. Your professional background has furnished you with a large portion of credibility and respect enabling you to make yourself understood and realize your decisions. As you are the firm basis for your team, you must have an involving and appreciative managerial style and set an example for your colleagues.

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

Application in Danish or English.

Contact
For further information please contact Birthe Ross at +45 3079 2831.

Deadline
29 November 2013.

Material Management Specialist

- Business Support
- Denmark - Måløv

In this job, you can make a true difference and play an important role in Novo Nordisk Clinical Trials Supply Chain. You will build the foundation for the professionalization of material management in Clinical Supplies. Important decisions which can impact the success of our clinical trials will be made based on your analysis and tools. If you find a challenge like this exciting and inspiring, you may be the person we are looking for as a Material Management Specialist in Clinical Supplies.

About the department
CMC Clinical Supplies (CS) is responsible for planning, packing and delivering supplies for the clinical trials in Novo Nordisk. CS Business Support (CSBS) is a small department of highly skilled people who work across CS.CSBS carry out strategic projects and tasks that aim at increasing the efficiency of the clinical supply chain. We work analytically and data based and support CS Management with high quality decision support and solutions.You will report to the CSBS Department manager and be a part of a department, which consists of 5 colleagues besides you. You will be located at Novo Nordisk’s site in Måløv.

The Job
Our clinical trial activity is steadily increasing in the coming years and to support this development, we are looking for a Material Management Specialist who can support the entire CS supply chain with analysis, new processes and tools to secure inbound materials and trial specific materials are present when needed.

As a Material Management Specialist in CSBS you will be responsible for carrying out analysis of our inbound materials and other trial related materials to decide the proper planning method. You will be responsible for developing and maintaining models that will enable the departments to take appropriate action to meet coming demand. You will act as a sparring partner to the people that work with ordering materials across CS with regards to how to manage them the best way including both order size, stock levels etc. You will also play a vital role in preparing Clinical Supplies for the next step with regards to use of IT for material requirement planning.The role as Material Management Specialist is new and will require that you take ownership and to some extend participate in defining the role and responsibilities yourself based on your previous experience with inventory planning.

Qualifications
You hold a masters degree within production engineering, Cand. merc in supply chain or similar. You have experience with inventory planning and management and material requirements planning, have strong analytical skills, are data minded and have strong IT competencies and use Excel on an advanced level. You are fluent in both written and spoken English and Danish on a professional level.It is essential that your analytical skills are combined with a solid business understanding. You are persistent and are used to communicate with many stakeholders and able to present analysis in an effective way to stakeholders. Your strong communication skills ensure the anchoring of your results in the organisation. On a personal level you work independently, are motivated by optimisation and improvements, deliver high quality output and set pride in keeping deadlines.It is an advantage if you have experience with the pharmaceutical industry or similar production environment.

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 Julie Helsted-Winkel at +45 3075 2790.

Deadline
26 November 2013.

Afdelings LEAN Partner

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

- LEAN
- Danmark - Kalundborg

Afdeling LEAN Partner med ledelsespotentiale

Om Afdelingen
Brænder du for at skabe landets bedste LEAN-kultur gennem succesfuld forandringsledelse, og kan du udfordre Novo Nordisks ledere i LEAN-ledelse? Så bliv den nye afdelings LEAN Partner hos Novo Nordisk i Diabetes Active Pharmaceutical Ingredients (DAPI) i Kalundborg.

Jobbet
Du får en hovedrolle i at implementere og videreudvikle LEAN, og du kan se frem til et udadvendt job med en bred kontaktflade og stor indflydelse på afdelingens og områdets resultater.

Du får ansvaret for at implementere og videreudvikle LEAN i en af vores finrensningsfabrikker, PP IV Detemir i Kalundborg, med 80 dygtige og engagerede medarbejdere. Du kommer tæt på ledelsen som sparringspartner, når du foreslår nye LEAN-tiltag til din afdelingsleder og fabrikkens LEAN-ansvarlige. Du driver projekterne fra start til slut, hvilket indebærer, at du får stor indflydelse på afdelingens resultater. Du følger op på processerne, så du sikrer, at de implementeres ordentligt, og vi dermed når vores ambitiøse effektiviseringsmål. For at sikre at afdelingens LEAN-kompetenceniveau løbende øges, viser du dine kolleger vejen til relevante LEAN-værktøjer, som du træner dem i at anvende. På denne måde sikrer du, at løsningerne bliver solidt forankret i afdelingen. Inden for det første år af din ansættelse vil du blive klædt på i Novo Nordisks cLEAN-uddannelse.

Kvalifikationer
Du har en længerevarende teoretisk uddannelse bag dig, men vi har ikke krav til, hvilken retning du har specialiseret dig i. Din uddannelse har bl.a. givet dig evnen til at nedbryde komplicerede begreber til almindeligt og forståeligt sprog og at kunne formidle det, så det bliver sund fornuft for ledere og kolleger på mange forskellige niveauer. Du har stor erfaring med at implementere og videreudvikle LEAN og ved, hvordan man motiverer og inddrager kolleger og dermed skaber en LEAN-kultur, hvor alle bidrager. Din solide erfaring med forandringsledelse gør, at du trives med at balancere mellem mange forskellige personligheder og holdninger i et foranderligt miljø. Måske har du endda ambitioner om linjeledelse med tiden? Derudover er du i stand til at holde hovedet koldt, når du stiller spørgsmål til vores ledere og den måde, vi gør tingene på. Da du skal kunne bearbejde og visualisere data er det nødvendigt, at du behersker Excel på superbrugerniveau.

Novo Nordisk i Kalundborg er en by i byen. Området ligger ca. en times kørsel fra København og strækker sig over 1.350.000 m2, inklusiv eget vejnet. Vi producerer mere end halvdelen af alt insulin i verden, og vi er helt i front når det kommer til anvendelse af ny teknologi, systemer, metoder og processer. Hvis du er vores nye kollega, så garanterer vi muligheder som du vil få svært ved at finde andre steder.

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 seammen 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 Troels Felding på telefon på +45 3079 4324.

Ansøgningsfrist
24 November 2013.

Business Analyst

- Finance
- Denmark - Bagsværd

In this job, you will be responsible for ensuring financial control of a part of Novo Nordisk’s R&D organisation and impact decision-making based on sound financial insights and a solid business understanding. If you find challenges like these exciting and inspiring, you may be our new Business Analyst.

About the department
Novo Nordisk is one of the world’s most successful pharmaceutical companies and with a great growth potential. Development Finance is part of Corporate Financial Planning in Corporate Finance and is responsible for the financial management of Novo Nordisk development activities. We have close cooperation and interaction with our business units, and our aim is to act as true business partners based on solid financial competencies, a good understanding of the business in which we operate and strong personal skills.

The Job
You will be part of a young, dynamic and ambitious finance team consisting of 6 dedicated employees. You will be responsible for the financial development of one of the business units in R&D, and hence conduct financial planning and other key financial processes. In order to optimise the financial development within your area of responsibility, you will furthermore be conducting ad hoc analyses and scenarios which you will present to senior management groups for approval.

Besides this you will be involved in various projects aiming at increasing transparency and optimizing processes across both R&D and the Finance organisation.

We invest a lot in both professional and personal development and have a thorough individualised development plan for each employee. Through on-the-job training, projects and courses you will experience a steep learning curve, thus enabling a number of future career opportunities in the global Novo Nordisk organisation.

Qualifications
The right candidate has completed a relevant master's degree (e.g. in finance or economics) with excellent results. You have strong analytical skills, are fluent in written and spoken English, computer literate and ready to invest time and effort in your development and future career. You thrive in a busy environment, bring a can-do attitude, and while being a team player, it is important that you are able to work independently. The atmosphere in Development Finance is informal and humorous. If you can hold on to your good sense of humour at all times, you are the kind of person we are looking for.

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 Kristian Krag Nielsen at +45 3075 3743.

Deadline
22 November 2013

Business Analyst

- Sourcing
- Denmark - Bagsværd

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

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

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

The Job
As Business Analyst you will play a central role in supporting our global users. Further you will apply or develop in-depth configuration competences that make you a subject matter expert transforming business requirements with standard system (Ariba). In addition you will act as system manager and take responsibility for compliance to internal and external requirements. You will be a part of an enthusiastic team that sets high standards and individual targets, but achieves them as a team.You will be based in Denmark however, as part of an increased internationalization some travel activities can be expected.

Qualifications
You are among the best! The person we are looking for have completed a relevant Master's Degree (i.e. Engineering or IT) with excellent results. You have 1-2 years of experience with standard system configuration (ideally Ariba) from a large organization or a consultancy firm.You are motivated by driving change and improvements involving many stakeholders’ at all organisational levels. You have a high level of drive, initiative and persistence and you are result-oriented. Furthermore, you are ambitious and like to be challenged. You are analytical and structure your own work. Good communication and presentation skills are required in English.

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

Contact
For further information, please contact Thomas Munksgaard on + 45 3079 1542.

Deadline
29 November 2013.

QC Microbiologist

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

- Production
- Denmark - Kalundborg

Do you want to use your Microbiology expertise and strong quality mindset to ensure top level quality of hemophilia products? Then we have a position for you.

About the department
Biopharm QC KA performs microbiological and chemical analysis of Novoseven® as well as water and environmental samples from our production plants. The department consists of 47 dedicated employees, divided into 3 teams. We currently have an open position as chemist in the microbiology team. The team consists of four Chemists, twelwe Laboratory technicians and one Associate manager.

The job
You will share the responsibility for daily support and approval of analyses with the other chemists in the team. Further, you will be part of running for instance different improvement projects. The team covers microbiological analyses (Microbial count (TVC), Growth Promotion Test (GPT), Microbial identification) and endotoxin (LAL).

Your tasks will include writing instructions (SOPs), Non Conformity and Change Request reports. You will ensure validation of methods and equipment under strict GMP requirements.

LEAN is an important part of our daily work. You will be involved in systematic problem solving, optimisation and standardisation of processes to bring our products faster to market. We have a high focus on improvement of our processes both with regard to quality, costs and lead time. You will be responsible for running your own projects.

Qualifications
You hold a master degree in Microbiology or a related field. Preferably you have gained a thorough experience in QC working under GMP regulations from previous jobs. Experience with validation of microbiological methods is considered an advantage.

Besides your quality-mindset, you have a winning attitude and focus on achieving your goals. You also have a positive, cooperative spirit and are known for taking action and following through on your tasks.

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 Brian Laursen at +45 3075 1194.

Deadline
25 November 2013

Strategy Consultant (Bagsværd, Denmark)

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Senior specialist R&D Academic Relations (Måløv, Denmark)

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Pharma Field Sales-Diabetes Care Specialist (DCS)-Marine Park, NY Job (MARINE PARK, NY, US)

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Material Management Specialist (Måløv, Denmark)

Afdelings LEAN Partner (Kalundborg, Danmark)

Business Analyst (Bagsværd, Denmark)

Business Analyst (Bagsværd, Denmark)

QC Microbiologist (Kalundborg, Denmark)