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Produktionsplanlægger (Måløv, Danmark)

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Produktionsplanlægger

- Supply Chain & Logistics
- Danmark - Måløv

Er du på udkig efter nye udfordringer inden for klinikproduktion? Clinical Supplies Packaging søger en ny planlægger til vores produktion med ansvar for at sikre den daglige planlægning i pakkeriet. Du vil blive en del af et dedikeret og dynamisk team, der arbejder med etikettering og pakning af nye produkter til klinisk afprøvning i Novo Nordisk.

Om afdelingen
Clinical Supplies Packaging er en del af CMC Supply, og vi er ansvarlige for at pakke og distribuere udviklingsprodukter i høj kvalitet til Novo Nordisks klinikstudier over hele verden. For at kunne imødekomme kravene fra en voksende R&D projekt pipeline arbejder vi fokuseret med at forkorte vores leadtime og samtidig øge kapaciteten og kvaliteten i vores produktion.

Jobbet
Vi kan tilbyde et job med mange udfordringer og forskelligartede arbejdsopgaver i et område, som er i konstant udvikling. I teamet håndterer vi både etiket print, manuel og automatisk pakning af alt fra meget små specialiserede ordrer til store standardiserede ordrer, og du vil som planlægger have ansvaret for den operationelle planlægning af driften i tæt samarbejde med pakkeriteknikere og planlæggere i andre afdelinger.

Dine opgaver vil yderligere omfatte koordinering med vores interne kunder, opfølgning på produktionsmålene, samt kontinuerlig udvikling og optimering af planlægningsværktøjerne til at matche den løbende udvikling i produktionen og efterspørgslen.

Kvalifikationer
Vi søger en medarbejder med en relevant uddannelse som ingeniør eller lignende. Erfaring med farmaceutisk produktion og forståelse for arbejdsgangene ved pakning vil være en klar fordel. Vi arbejder fokuseret med Lean både i afdelingen og tværorganisatorisk gennem diverse projekter. Da du vil være i kontakt med mange forskellige medarbejdere i organisationen, er det vigtigt, at du trives i en udadvendt funktion.

Vores nye planlægger skal have et godt overblik og være vant til at agere før problemerne opstår, være engageret og fleksibel, samt kunne holde hovedet koldt i pressede situationer. Samtidig leder vi efter en team-player, der er åben og nysgerrig over for udfordringer og nye måder at arbejde på, går til opgaverne med god energi og kan bidrage positivt til teamet.

Stillingen ønskes besat snarest.

I Novo Nordisk baseres beslutninger og handlinger på deres indflydelse på samfundet, miljøet og muligheden for at skabe økonomisk overskud. Det skaber tilsammen en ansvarlig kultur med et sundt og engageret arbejdsmiljø.

Kontakt
Vil du vide mere om stillingen, så kontakt Martin Baunø Nielsen +45 3075 1760.

Ansøgningsfrist
4. december 2013

Director (Gentofte, Denmark)

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Director

- Management
- Denmark - Gentofte

Department manager with potential for more.Can you lead and inspire through team leaders and are you able to motivate and set direction? Do you want to ensure quality and stable delivery of analytical results of biopharmaceutical products in Novo Nordisk? Then we have the job for you in the largest Quality Control Department in Biopharm.You will be head of the ‘Biopharm QC Chemistry’ department which is responsible for quality control analyses on Finished Product and APIs as well as stability studies and complaints. The department consists of approximately 75 employees organised in 4 teams each headed by highly competent team leaders.

About the department
Biopharm QC Chemistry is a laboratory with high quality and LEAN standards. We are responsible for chemical analyses on a range of Novo Nordisk product, including Human Growth Hormones, Glucagon and products for Haemostasis. In addition, we analyse new products, not yet on the market, and are involved in transfer of analytical methods to our sister locations abroad. We offer a very exciting job with excellent development opportunities among highly competent colleagues in a positive working environment.

The Job
As department manager you will be the focal point of your department and your team leaders. You will act as an inspiring sparring partner to your team and you coach and empower your team leaders and employees to deliver excellent results and take responsibility for their own professional and personal development. The overriding focus area of this substantial career position is to ensure punctual batch release through delivery of high quality analyses in time in full compliance with the authorities’ expectations. In a dynamic and challenging environment with short deadlines you are able to make prioritisations and take responsibility for understanding and meeting stakeholders’ requirements also when the solution is not obvious.As part of the quality control management team you will have the responsibility to implement the Quality Control Strategy for Biopharm. We have a high focus on continuous improvements of our processes both with regard to simplicity, compliance and delivery and you will be expected to initiate and drive Lean projects aiming at optimising our internal processes in order to be able to meet the increasing demands from authorities and from the growth in our business.

Qualifications
You hold a Master’s degree in Pharmaceutical Sciences, engineering or a related discipline. Most importantly, you have strong managerial experiences, and it is natural for you to set direction and motivate your employees to follow your lead. You are known for your positive attitude as well as your empathy and you know how to win acceptance through direct and clear communication. You have a documented ability able to manoeuvre and prioritise in a dynamic and challenging environment with short deadlines and you thrive in the decision-making role. It is natural for you to take ownership due to your high level of personal drive and a strong sense of initiative and you work proactively to drive processes forward. You are used to driving improvement projects with focus on processes, quality, compliance and lead time. If you have laboratory insight and are familiar with QA/QC and production processes, it will be a major asset. Proficiency in written and spoken English is necessary.

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

Contact
For further information please contact Vivian Fussing at +45 3075 5055.

Deadline
28 November 2013.

Financial Analyst (Bagsværd, Denmark)

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Financial Analyst

- Finance
- Denmark - Bagsværd

We are looking for a talented employee to our Financial Risk Management department in Corporate Treasury. Corporate Treasury is a part of Novo Nordisk Corporate Finance and is responsible for handling Novo Nordisk's financial risk on a group level.

About the department
Corporate Treasury is divided in two departments: The Financial Risk Management department is responsible for managing foreign exchange risk, interest rate risk, financial counterparty risk and capital structure on a group level. The Cash Management department is responsible for financing, financial advisory and capital structure activities of Novo Nordisk's affiliates world wide, global cash management and bank strategies and Novo Nordisk's In House Bank.

The job
The Financial Analyst will join the Financial Risk Management department and together with your colleagues you will manage exchange rate and interest rate exposure, handle daily liquidity management and conduct financial analysis. You will provide information and make recommendations to senior management, including analysis and recommendations on Novo Nordisk capital structure. You will closely follow developments in financial markets, and you will be in frequent contact with our international banks and you are going to trade on behalf of Novo Nordisk.

You are offered a challenging opportunity to develop your professional competencies in a highly professional and dynamic organisation, being part of a dedicated team.

We invest a lot in both professional and personal development and have a thorough individualised development plan for each employee. It is an important objective for us to continuously develop employees to take on in-creased responsibilities. Consequently, the candidate must be open for rotation and development across Corporate Treasury.

Qualifications
To enter this position you have preferably 2-5 years of relevant experience within the financial risk management area and a strong academic background, e.g. an MSc in Economics or Finance. You feel confident in making complexities understandable and approachable. You are also ambitious and a team player. It is important that you possess strong collaboration skills as you will cooperate closely with your colleagues, including staff func-tions within Finance, Legal and IT. You excel in written and spoken English. Finally, you are also a strong user of technology e.g. Excel and Visual Basic.

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 Henning Klemmensen +45 3075 5205.

Deadline
1 December 2013.

Financial Analyst (Bagsværd, Denmark)

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Financial Analyst

- Finance
- Denmark - Bagsværd

We are looking for a talented employee to our Cash Management department in Corporate Treasury. Corporate Treasury is a part of Novo Nordisk Corporate Finance and is responsible for handling Novo Nordisk's financial risk on a group level.

About the department
Corporate Treasury is divided in two departments: The Financial Risk Management department is responsible for managing foreign exchange risk, interest rate risk, financial counterparty risk and capital structure on a group level. The Cash Management department is responsible for financing, financial advisory and capital structure activities of Novo Nordisk's affiliates world wide, global cash management and bank strategies and Novo Nordisk's In House Bank.

The Job
The Financial Analyst will join the Cash Management department and will get an important role in capital struc-ture decisions and in providing financial advisory and analysis within the treasury area towards our affiliates in Emerging Markets. Together with your colleagues you will further develop our global cash management and IT structures and you engage in bank tenders and banking strategies.

You are offered a challenging opportunity to develop your professional competencies in a highly professional and dynamic organisation, being part of a dedicated team. You can look forward to a broad and international contact base and you ensure professional cooperation with our affiliates in Emerging Markets and the banking sector as well as staff functions within Finance, Legal and IT.

We invest a lot in both professional and personal development and have a thorough individualised development plan for each employee. It is an important objective for us to continuously develop employees to take on in-creased responsibilities. Consequently, the candidate must be open for rotation and development across Corporate Treasury.

Qualifications
To enter this position you need solid analytical skills and a strong academic background, e.g. an MSc in Eco-nomics or Finance and you have 0-2 years of relevant experience. You feel confident in making complexities understandable and approachable. You are also a team player, ambitious and work efficiently across functions and geographical boarders. Finally, you excel 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 Mads Jæger at +45 3079 5991.

Deadline
1 December 2013

Contract Professional (Måløv, Denmark)

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Contract Professional

- Research & Development
- Denmark - Måløv

If you excel in contract negotiation, relation management with academic institutions and execution, you have just the right foundation for this challenging and exciting job.

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 the R&D organisation. Our objective is to facilitate talent attraction and competence development in Novo Nordisk R&D. As such, one of our core responsibilities is the management of the Novo Nordisk PhD and post.doc programme (STAR), which currently employs 80 fellows.

The job
You will have two main focus areas. On the one hand, you negotiate and execute collaboration agreements with international universities and research institutes in relation to the STAR programme and other talent attraction activities in R&D. On the other hand, you manage a portfolio of R&D-related sponsorship agreements, donations and the like aiming to build a centre of excellence within the regulatory framework for industry/university interactions. As such, you will become the R&D organisations’ first line adviser regarding issues on how to address Health Care Professionals (HCPs). This area is undergoing a great many changes internationally, which calls for insight, sound judgement and impeccable personal integrity.

You will also be responsible for the administration of contracts, and accordingly you contribute to ongoing optimisations of templates, systems and processes. Across your tasks, you will work closely together with colleagues, e.g. in Corporate Legal, Corporate Patents, and Business Development.

Qualifications
You hold a university degree, preferably in law, business law or a related field, and your CV mirrors successful contract negotiation and execution experience as well as an understanding of the underlying legal aspects. You have experience in drafting, negotiating and establishing industry/university research collaborations, which has provided you with knowledge within contractual, legal, Intellectual Property Right, HCP and business-related issues. To succeed, you will need all of your networking, stakeholder management and relation building skills in combination with your resilience. Lastly, you are used to working with English as your primary language, and you know that the best results are generated through close collaboration with other people.

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 for the benefit of patients.

Contact
For further information, please contact Palle Høy Jakobsen, at +45 3079 6287.

Deadline
2 December 2013.

Area Training support (Hillerød, Denmark)

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Area Training support

- Production
- Denmark - Hillerød

Are you our new colleague working with development and implementation of a training system in a production environment? We are right now looking for competent supporter to strengthen our performance in relation to the quality of our training and documentation in our production.

Do you want to play a central role in a department with tasks involving contact with many people daily? Do you like to teach and follow up on the achieved results? Then we have an exciting new position as Area Training Supporter.

About the department
The department consists of approximately 80 employees who ensures the assembly of millions of FlexPen® for diabetics around the world. The department is comprised of 2 production teams, 1 technical support team and 1 support team responsible for the quality. The environment is characterized by fast pace and frequent prioritizations daily to ensure timely delivery of quality products to many different customers. There is an open and honest atmosphere in which we aim to utilize and develop your competencies and skills.

The Job
You will be responsible for training employees in the operational standards as well as ensuring the quality of the training. Furthermore you will assist the leaders in coordinating the training. You will also assist in the development and quality assurance of Competence Matrix, Job Training Plans, Training Materials and in structuring the department's training activities. You collaborate with the department’s shop floor trainers and coach them in the use of training methods. You will function as a role model in terms of living the standards of training. Your focus will be the department's training structure and the quality assurance of this. You will join a training network across the departments in SDK, a network where professional development experiences are exchanged and better practices shared.

You will participate in the preparation and presentation of training documentation for both Danish and foreign authorities in relation to audits and inspections.

Qualifications
You hold a relevant MSc. or equivalent e.g. within pharmaceuticals, psychology, communication, education or training. You are able to drive processes proactively in a complex production environment with many stakeholders, and you enjoy building relations across organisational areas and levels. And you have the desire to learn and grow within the training activities in a pharmaceutical support environment.

You are familiar with working in a GMP regulated environment. You know the language of LEAN and have experience with change management. In addition to Danish, you must be able to speak and write English. Your personal qualities define you as robust and a self-starter with a high level of energy. You can safely navigate in an environment of change and are able to establish relations to and cooperate with a wide variety of colleagues.

Feel free to submit your CV & application in either English or Danish.

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 Christian Rank: at +45 3075 4929 or Morten Lundgren at +45 3079 0957.

Deadline
01 December 2013.

novoGloW design configuration adviser (Bagsværd, Denmark)

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novoGloW design configuration adviser

- IT
- Denmark - Bagsværd

Corporate Quality Operations is looking for a person who can take active part in establishing the new novoGloW support function. novoGloW is a workflow-based IT system, based on the EtQ Reliance platform. The Change Control application in novoGloW is configured to handle Novo Nordisk Change Requests.

About the department
The position as novoGloW design configuration adviser is based in the newly formed novoGloW Operations team which focuses on improvements and support to the Change Control process. The team is currently anchored in the novoGloW project, which goes live in March 2014, and consists of a dynamic mix of process and system competencies.

The job
We need a person who can:

Provide functional system support to experts and super users

Facilitate Change Advisory Board (CAB) meetings

Test changes and upgrades, including preparation of UAT (User Acceptance Test) and PQ (Performance Qualification) test cases

Agree on solutions with tech roles and vendors

Give input to specification changes, for example to URS (User Requirement Specification) and TDS (Technical Design Specification)

Maintain validated lists and alerts in novoGloW

Train super users and business configuration advisers in system changes and updates of related documents

Give input to procedures and instructions for the Change Control process

Mature user requests to meaningful requirements (elaborate change)

Specify new requirements

Qualifications
You have a relevant university degree combined with good English skills. You can document experience with design configuration and you will need to become EtQ Reliance Engine certified. You master teaching and giving presentations. It is an advantage if your experience includes work within: the pharmaceutical industry or other regulated industry, quality management processes in general and Change Control in particular, workflow-based IT system, IT system specification, test and validation.

Strong team working abilities, a good sense of humour, being pro-active and confidence in handling tight deadlines are all pre-requisites!

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 Charlotte R. Winther at +45 3079 0508.

Deadline
1 December 2013.

Supportkemiker (Køge, Danmark)

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Supportkemiker

- Produktion
- Danmark - Køge

Da vi udvider vores Produktionssupport team søger vi en kemiker med teknisk interesse, hvis primære ansvar bliver support til vores klassificerede renrumsfacilitet.

Om afdelingen
FeF Chemicals A/S er et aktieselskab 100% ejet af og fuldt integreret i Novo Nordisk.

FeF producerer en række produkter bl.a. specialprodukter til Novo Nordisk produktionen samt kvarternære ammoniumforbindelser (API) og pakning af human insulin til verdensmarkedet. Produktionssupport varetager supporten til disse produktionsområder.

Du bliver en del af et team, hvor vi i forvejen er 3 kemikere og 6 teknikere. Samlet i produktionsområdet er vi godt 60 medarbejdere og på hele FeF ca. 140.

Jobbet
Human Insulin er der, hvor dit primære ansvarsområde vil være. FeF har sluthåndteringen, hvor insulinen afvejes i salgsemballager i klasse C rum. FeF har den direkte kontakt med kunderne og dit job vil derfor også indeholde en væsentlig kundekontakt i forbindelse med kundeaudits.

Du vil således blive Produktansvarlig for Human Insulin med ansvar for daglig support til operatørerne herunder primær drivkraft på afvigelser, ændringssager og forebyggende aktiviteter i dette produktionsområde samt opdatering af dokumenter og udførelse af kvalificeringer/valideringer. Med andre ord bliver du hovedansvarlig for GMP compliance.

Herudover vil der være opgaver på tværs af support og den øvrige produktion, hvor du som en del af supportteamet er med til at problemløse, optimere og forebygge hændelser.

Kvalifikationer
Du har en akademisk baggrund som ingeniør eller tilsvarende gerne med erfaring indenfor produktion i klassificeret renrum, miljømonitorering (EM) og kvalificering/validering. Grundet kundekontakt i forbindelse med audits skal du kunne tale og skrive engelsk.

Som person har du let ved at omgås medarbejdere på alle niveauer i organisationen, kan lytte til dem og absorbere viden, er fleksibel og humoristisk. Du er selvstændigt arbejdende og trives med mange bolde i luften og tager ansvar for, at vi både som team og individer når de mål forretningen har brug for. Du kan lide at optimere arbejdsgange og er god til at afslutte opgaver.

Har du også viljen til at finde en vej og et glimt i øjet kan du blive en del af vores meget velfungerende team, hvor arbejdet foregår i en uformel og humørfyldt atmosfære med fokus på kvalitet og sikkerhed.

Kontakt
Vil du vide mere om stillingen, så er du meget velkommen til at kontakte Vesna Schneider på telefon 3037 0062

Ansøgningsfrist
1. december 2013

Test Coordinator (Hillerød, Denmark)

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Test Coordinator

- Quality
- Denmark - Hillerød

Do you have solid planning and organising skills? Are you looking for a job where you play a key role ensuring the quality of Devices before they reach the hands of millions of people living with diabetes worldwide? Then we encourage you to keep reading as we are looking for a new Test Coordinator.

About the department
You will join a team providing verification tests of devices to support device development projects in Device Manufacturing Development. You will have 12 new colleagues, including Laboratory Technicians, Technicians and Engineers, who are dedicated to deliver test documentation that, ensure the authorities’ approvals of assembled Devices.

The Job
Your goal will be to carefully coordinate the work of your team ensuring that we deliver verification test reports of high standard on time. You will coordinate the testing of products before they are launched to market as well as marketed products subjected to changes or problem solving. As a key figure managing the contacts for your team, you can foresee close collaboration with colleagues in R&D, Product Maintenance and Regulatory Affairs. You will also attend to board meetings to secure participation from key stakeholders, as well as you plan workshops and communicate the role of the department to other stakeholders. At all times, you make sure to follow up on planning issues and challenges, just as you ensure smooth communication between your team, customers and stakeholders. You can look forward to a challenging position where you will gain vast insight into our testing environment and work with colleagues in Denmark and other parts of the global organisation.

Qualifications
Your background covers a degree in Engineering or similar and solid experience managing or coordinating projects. If you are familiar with different testing standards or equipment or have acquired experience from a GMP regulated environment it will be an advantage. On a personal level, you demonstrate sound interpersonal and communication skills. Colleagues know you as a person with a proactive mindset who enjoys building relations and collaborating across interdisciplinary boundaries. It goes without saying that you must have strong planning skills and a structured approach in order to keep focus on many tasks simultaneously. It shows that you have drive and that you get your energy from working in a high-paced environment with many deadlines. At the same time, you know how to support and motivate others to make them deliver on their targets. Lastly, you have proficiency in written and spoken English.

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

Contact
For further information, please contact Lars Aagaard +45 3079 2095.

Deadline
8 December 2013

Clinical Trial Administrator (Søborg, Denmark)

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Clinical Trial Administrator

- Administrative
- Denmark - Søborg

Do you want to be part of a dynamic team driving clinical trial activities worldwide, developing novel therapy for Type 1 diabetes?

About the department
Clinical Operations, Insulin and Devices-1 in Global Development is looking for a colleague to join us working as Clinical Trial Administrator. We have a team of experienced and enthusiastic International Trial Managers and Clinical Trial Administrators who are responsible for planning and conducting clinical trials within the area of diabetes and medical devices.

We offer a dynamic work place with dedicated colleagues who seek an atmosphere of trust and transparency.

The Job
As Clinical Trial Administrator you will assist one or more International Trial Managers, who are responsible for conducting clinical trials. As Clinical Trial Administrator you will have a significant role in supporting the trial planning and execution by conducting trial related tasks.

Your main responsibility will be to manage the administrative tasks for the clinical team; take meeting minutes, help create presentations, coordinate website and newsletters, prepare and monitor clinical trial budgets, and establish and maintain trial master files. In addition you will be involved in the preparation and conduct of Monitor and Investigator meetings.

Qualifications
You have a BA in business administration or equivalent. You have 2-3 years of administrative experience from working in large and/or complex projects or line functions within the pharmaceutical industry. This will include experience with budgeting, accounting and project planning. You are proficient with both written and spoken English, and you have flair and interest for IT and technical solutions including the Microsoft Office Package.

Our ideal candidate has a structured approach to tasks, an analytical mind set and a proactive behaviour. Good communication skill, cross cultural understanding and ability to work in a complex and busy environment with a service minded attitude is a must.

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

Contact
For further information, please contact Birgitte Berg +45 3075 8445.

Deadline
2 December 2013

Senior International Trial Manager (Søborg, Denmark)

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Senior International Trial Manager

- Research & Development, Trial Manager
- Denmark - Søborg

Do you want to be part of a dynamic team driving clinical trials activities worldwide, developing novel therapy for Type 1 diabetes?

About the department
Clinical Operations, Insulin & Devices-1 in Global Development is looking for an experienced colleague to join us in a position as Senior International Trial Manager. We are a team of experienced and enthusiastic International Trial Managers and Clinical Trial Administrators, who are responsible for planning, conducting and finalising clinical trials within the area of medical devices and diabetes. We offer a dynamic work place with dedicated colleagues who enjoy an atmosphere of trust and transparency.

Our working environment is characterised by interesting and demanding assignments and continuous professional development opportunities.

The Job
You will function as the global project manager and your main responsibilities will be to plan, coordinate and manage the clinical trial activities from preparation of the study protocol to reporting. You will develop relevant trial documents, including protocols, recruitment strategies, communication plans and trial budgets.

You will chair the trial related international study group, for which you will plan and conduct team meetings, that ensures information sharing and engagement. You will cooperate closely with Novo Nordisk affiliates worldwide as well as other stakeholders involved in the daily management of the clinical trial. In addition you will be responsible for the preparation and conduct of Investigator and Monitors meetings prior to trial start.

As Senior International Trial Manager you will mentor other staff in executing trial management tasks.

Qualifications
You have a relevant educational background, preferably a university degree in Natural Science or equivalent with a minimum of 5 years of experience in trial management related positions. You have a broad knowledge of clinical trial methodology and experience from working in a project organisation.

You have a strong quality mind-set, communicate effectively with high impact, meet deadlines, approach tasks in a structured way and you are able to work with multiple and frequently changing priorities in a dynamic environment. Furthermore, you have the ability to work independently.

You are a dedicated team player who inspires trust amongst colleagues and partners. You have excellent cross cultural awareness and are fluent in written and spoken English.

In Novo Nordisk it is your skills, your commitment and your ambition, which helps us to improve many people’s 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 Birgitte Berg at +45 3075 8445.

Deadline
2 December 2013

International Trial Manager (Søborg, Denmark)

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International Trial Manager

- Research & Development, Trial Manager
- Denmark - Søborg

Do you want to be part of a dynamic team driving clinical trials activities worldwide, developing novel therapy for Type 1 diabetes.

About the department
Clinical Operations, Insulin & Devices-1 in Global Development is looking for an experienced colleague to join us in a position as International Trial Manager. We are a team of experienced and enthusiastic International Trial Managers and Clinical Trial Administrators, who are responsible for planning, conducting and finalising clinical trials within the area of medical devices and diabetes. We offer a dynamic work place with dedicated colleagues who enjoy an atmosphere of trust and transparency.Our working environment is characterised by interesting and demanding assignments, flexible working conditions and continuous professional development opportunities.

The Job
You will function as the global project manager and your main responsibilities will be to plan, coordinate and manage the clinical trial activities from preparation of the study protocol to reporting. You will develop relevant trial documents, including recruitment strategies, communication plans and trial budgets.You will be part of a trial related international study group responsible for planning and conducting team meetings. You will cooperate closely with Novo Nordisk affiliates worldwide as well as other stakeholders involved in the daily management of the clinical trial. In addition you will be part of the preparation and conduct of Investigator and Monitors meetings prior to trial start.

Qualifications
You have a relevant educational background, preferably a university degree in Natural Science or equivalent with a minimum of 2-3 years of experience in trial management related positions. You have a broad knowledge of clinical trial methodology and experience from working in a project organisation.You have a strong quality mind-set, communicate effectively with high impact, meet deadlines, approach tasks in a structured way and you are able to work with multiple and frequently changing priorities in a dynamic environment.You are a dedicated team player who inspires trust amongst colleagues and partners. You have excellent cross cultural awareness and are fluent in written and spoken English.

In Novo Nordisk it is your skills, your commitment and your ambition, which helps us to improve many people’s 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 Birgitte Berg at +45 3075 8445.

Deadline
2 December 2013.

Erfaren ingeniør med talent for projektledelse (Kalundborg, Danmark)

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Erfaren ingeniør med talent for projektledelse

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

- Produktion
- Danmark - Kalundborg

Vil du være med til at sikre Novo Nordisk som foretrukken leverandør af medicin til diabetespatienter over hele verden? Er svaret ja, så har du nu muligheden for at spille en central rolle i vores udvidelse af insulinproduktionen i Kalundborg.

Om afdelingen
Du bliver en del af Insulin Manufacturing II (IM2), som er en af de primære kapaciteter i DAPI’s insulinproduktion i Kalundborg. Du indgår i en projektgruppe, hvis fornemste opgave er at fremtidssikre produktionen og fortsat levering af produkter i højeste kvalitet.

Jobbet
Du får ansvaret for at styre udvalgte projekter, som skal sikre, at vi har den rette kapacitet til at imødekomme behovet i fremtiden. Helt konkret sørger du for, at vi stiller de rigtige krav til processerne, så vi designer løsningerne i høj kvalitet og i henhold til kravene for en insulinproduktion. Efterfølgende sørger du for, at løsningerne bliver implementeret korrekt og rettidigt. Resultatet af din indsats er løsninger, der sikrer en stabil drift. Herudover skal du drive dele af projekter, hvor du er garant for de faglige rigtige løsninger. Alt i alt kan du se frem til et udfordrende job, hvor du kommer til at arbejde sammen med kolleger på tværs af hele organisationen.

Kvalifikationer
Du er uddannet maskiningeniør, mejeriingeniør eller civilingeniør i bioteknologi, og du har både stor interesse for og erfaring med processer og enhedsoperationer. Din erfaring stammer fra et produktionsmiljø, enten fra lægemiddel- eller fødevareindustrien. Solid erfaring med projektarbejde er vigtigt, og du finder stor tilfredsstillelse at få dine projekter sikkert hen over målstregen. Dine kolleger kender dig som en sand holdspiller, der formår at løse udfordringer rettidigt og i konstruktiv dialog med dine interessenter. Desuden er det vigtigt, at du trives med at arbejde i et miljø, hvor du bruger dine evner for at koordinere og prioritere mellem flere opgaver samtidig. Endelig skal du beherske engelsk flydende.

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.

Novo Nordisk i Kalundborg

Site Kalundborg er en by i byen, kun godt en times kørsel fra København. Området er på 1.350.000 m2 med eget vejnet. Vi er 3.500 mennesker i alt fordelt på 16 fabrikker, og vi producerer bl.a. 50 % af verdens insulin. Site Kalundborg kan helt kort sammenfattes til: udviklingsmuligheder uden ende.

Kontakt
Vil du vide mere om stillingen, så kontakt Thomas Olsen på 30 75 08 71. Du kan lære mere om Novo Nordisks største produktionssite ved at bruge linket www.novonordisk.com/kalundborg-careers.

Ansøgningsfrist
1 December 2013

Associate Sourcing Professional (Bagsværd, Denmark)

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Associate Sourcing Professional

- Sourcing
- Denmark - Bagsværd

The Purchasing department within Sourcing Operations as part of Novo Nordisk’s central Supply Chain Management organisation is looking for an Associate Sourcing Professional for the API Purchasing team

About the department
The office is situated in Bagsværd. We are a team of 11 dedicated colleagues, and are responsible for setting up and maintaining effective supply chains for sourcing of production raw materials. We ensure the supply of raw materials for API production together with sourcing of chromatography gels to all Novo Nordisk API manufacturing sites and development departments. We are looking for a highly motivated and result oriented candidate, who takes pride in delivering high quality work in a pro-active way.

The Job
Your main responsibility will be inventory and order management of raw materials from global suppliers including daily operations tasks and optimisation projects. Our ambition is to deliver high quality services to manufacturing sites and their production departments. You will be responsible for specific items, and will ensure deliveries to production in full and on time. To achieve this, you will be in direct contact with our consuming department, production sites and suppliers. You will monitor inventory levels, prioritise needs from production, place purchase orders with international suppliers and coordinate activities with other functions in Sourcing Operations to secure availability of released material. Additionally, you will participate in or drive improvement projects related to processes you are part of and carry out change request assignment within supply to our Running Business and Development production. Internal and external stakeholder management skills are important as a large part of the job requires you to work close together with Quality and other Sourcing departments in Novo Nordisk.

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

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

As a person you are highly engaged, have a positive mind-set and are open towards other people and new ideas. You work independently and you like a dynamic environment with many simultaneous tasks and changing priorities, while managing deadlines. You thrive in an international environment and with people of diverse backgrounds.

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 Peter Eskild Jensen at +45 3079 2516.

Deadline
2 December 2013

Regional Clinical Research Associate (CRA)- New York, NY Job (New York, NY, US)

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Requisition ID 18062BR
Title Regional Clinical Research Associate (CRA)- New York, NY
Job Category Clinical
Job Description PURPOSE:
Responsible for performing study activities regarding the implementation, monitoring and summarization of clinical trials to ensure patient safety and adherence to protocols, Good Clinical Practice (GCP), ICH Guidelines, federal regulations and SOPs. Close collaboration with other members within Clinical Trial Management (CTM) and with various representatives within CMR.

RELATIONSHIPS:
Reports to a Manager/Senior Manager/Associate Director of Field Management (FM) within CTM. Accountable for actively participating in multiple internal cross-functional teams locally to ensure the effective delivery of assigned project milestones. External relationships are with clinical investigators, and other clinical research vendors as needed to support business objectives for the department and/or function.

ESSENTIAL FUNCTIONS:

COORDINATION / COMMUNICATION, ADMINISTRATION AND PERSONNEL DEVELOPMENT:
- Ensure compliance with the application and communication of all Novo Nordisk® policies, procedures and fundamentals.

FUNCTIONAL SUPPORT:
- May participate in continuous improvement processes for function.

PROJECT SUPPORT:
- Act as primary liaison for assigned study sites while on-site to convey project information, answer questions and in accordance with the CTM escalation pathway to the Lead CRA resolve site related issues.
- Assists the project team in preparation for audits/inspections and is responsible for the quality and completeness of site related performance and documentation. Prepares, collaborates and implements Corrective Action Plans (CAP) with investigative sites with oversight from Lead CRA.
- Attains thorough understanding of study management tasks and responsibilities necessary to implement compliance with protocol/regulatory requirements and NNI SOPs.
- Attends Investigator Meetings and study-specific training for assigned trials.
- Attends site audits according to the CTM Audit Management Plan and executes audit action plans with support from Lead CRA/PM as appropriate.
- Collaborates with the Lead CRA(s) to obtain/share trial specifics issues across all study sites concentrating on areas related to quality, site performance and metrics. Responsible for communicating issues in accordance with the CTM escalation pathway to the Lead CRA(s) and CRAs as appropriate.
- Completes follow up letters from all visit types according to SOPs and completes reports to quality standards within company specified timelines.
- Completes Site Selection, Site Initiation, Routine Monitoring and Close-out Visits according to SOPs and completes reports to quality standards within company specified timelines.
- Develops and maintains collaborative working relationships with clinical investigative sites. Accountable for data integrity, patient safety and regulatory compliance for all assigned sites.
- Monitors recruitment and data quality while on site and remotely through EDC systems/communication with sites.
- Performs on-site drug accountability and reconciliation. Verifies drug storage meets protocol and SOP requirements.
- Responsible for maintaining current Investigator Trial File (ITF) in accordance with NNI SOPs. Performs ongoing reviews of ITF to assure quality of the documentation files and compliance with NNI SOPs, GCP and ICH Guidelines while on site.
- Responsible for assuring adequate and appropriate dissemination of information according to the study specific communication plan between project team members to ensure project success in accordance with the CTM Communication Pathway or Project Specific Communication Plan.
- Understanding of assigned protocol (s) and trial specific manuals/plans to ensure quality and deliverables are met across assigned sites.

STAFF DEVELOPMENT:
- May provide active mentorship of CTM staff to build talent across the department.
- May support in the identification of training gaps, may support the development of training materials to meet that gap and then provision of training as required to improve core competency and skill set of the department.
- May support the maintenance of guidelines, training programs, policies and procedures.

TEAM COORDINATION:
- Accountable for the compliance and quality of CATS reporting.
- Active membership to local project teams.
- Participates in cross-functional teams, locally, to assure timely attainment of project milestones.
- Responsible to conduct oneself in accordance with expectations as a project team member to ensure the success of a matrix management structure.
- Responsible to ensure that the mandatory trial entries are made in IMPACT, NovoDOCs, iSITE, EDC administration, IVRS and updates, and ensure CSIM entries and updates are made.
- Responsible for maintaining focus, locally, for specific project activities within CMR priorities.
- Attend relevant symposia, conferences and scientific meetings, as necessary
- Provide support of training needs across CTM and may support the creation, development and potentially provide training support to meet those needs. This includes any lessons learned sharing across the project team members and/or CTM.

PHYSICAL REQUIREMENTS:
- Approximately 70% overnight travel to visit assigned sites for monitoring and attending trainings/meetings.
- Must live within 50 miles of the regional workload center within assigned region.

KEY SUCCESS FACTORS: EDUCATION, EXPERIENCE, KNOWLEDGE AND SKILLS
- A Bachelors’ degree (science-related discipline preferred) with a minimum of 4 years’ clinical trial experience within the pharmaceutical and/or healthcare setting, of which at least 2 years has been in the role of an on-site monitoring CRA, OR a Registered Nurse (RN) with a minimum of 5 years on-site monitoring experience.
- Demonstrated computer skills (MS Office, MS Project, PowerPoint).
- Demonstrates core understanding of medical terminology and clinical trial activities in relation to execution of a clinical development plan.
- Knowledge of GCP as relates to clinical trial management.
Department CMR - FIELD MGMT NORTHEAST (1)
Position Location US - Field Based - Across US
City New York
State/Provinces US - NY
Degree Required Bachelor's Degree Required
Percent Travel 70 - 80%

Compliancekoordinator (Gentofte, Danmark)

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Compliancekoordinator

- Produktion
- Danmark - Gentofte

Complianceskoordinator til Biopharm Technical Service

Har du lyst til at være en del af en teknisk serviceafdeling med mange processer og leverancer, hvor et højt kvalitets- og compliance niveau skal sikres – så er denne stilling lige noget for dig.

Om afdelingen
Vi er ca. 50 medarbejdere i afdelingen fordelt på 4 teams, hvoraf ”Team Ventilation & køl” repræsenterer 13 medarbejdere. Teamet er ansvarlig for drift og vedligehold af fællesfor-syningerne ventilation, køl og varmedrift, samt bygningsvedligehold på site Gentofte og i Kirke Værløse. Teamets vigtigste mål er forsyningssikkerhed og kvalitet af de leverede ydelser. Med reference til teamlederen søger vi en medarbejder, der med sin viden, erfaring og overblik kan sikre at teamets processer er i kontrol.

Jobbet
Du bliver sammen med teamets øvrige medarbejdere, ansvarlig for at teamets processer lever op til krav beskrevet i Novo Nordisk ’s kvalitetssikringssystem og cGMP. Du indgår i teamets arbejde med håndtering af afvigelser, systematisk problemløsning, opgavebeskrivelser, udarbejdelse af ændringssager, sikre opdatering af instruktioner og tegningsdokumentation samt opdatering og arkivering af øvrig dokumentation. Du skal samarbejde på tværs af teamet og være i tæt kontakt med afdelingens team for ”Projektledelse, service & vedligehold” samt QA. Dermed sikrer du sparring og rådgivning omkring kvalitets- og compliance spørgsmål, fortolkning af procedurer samt kvalitets-forbedrende løsninger på de problemstillinger og forbedringer, du dagligt involveres i. Desuden driver og koordinerer du kvalitetsarbejdet i teamet, deltager i inspektioner og indgår i teamets vagtordning.

Kvalifikationer
Du er uddannet ingeniør, maskinmester eller tilsvarende teknisk baggrund og har gennem dit arbejde opnået erfaring med kvalitetssikring herunder GMP og compliance i farmaceutisk- eller tilsvarende produktion. Dette har især styrket din evne til at gøre komplekse problem-stillinger forståelige for dig selv og andre, således at du til stadighed sikrer et fælles overblik og fokus. Som person kendetegnes du som en positiv, systematisk og kvalitetsbevidst kollega, der er god til at bevare humor og fleksibilitet i et til tider travlt og omskiftelige miljø. Med dine gode samarbejdsevner og din lyst til at gøre en forskel sikrer du, at tværgående opgaver med en bred vifte af interessenter bliver løst og viser således tydeligt, at du får energi af at interagere med mange forskellige typer af mennesker i løbet af din arbejdsdag. Du vil skulle kommunikere både på dansk og engelsk.

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 Per Knudsen på +45 3079 2669.

Ansøgningsfrist
30. november 2013

Drift- og BMS administrator (Gentofte, Danmark)

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Drift- og BMS administrator

- Produktion
- Danmark - Gentofte

Har du lyst til at være en del af en teknisk serviceafdeling med mange processer og leverancer, hvor et højt kvalitets- og compliance-niveau skal sikres – så er denne stilling noget for dig.

Om afdelingen
Vi er ca. 50 medarbejdere i afdeling 025 fordelt på 4 teams, hvoraf ”Team Ventilation & køl” repræsenterer 13 medarbejdere. Teamet er ansvarlig for drift og vedligehold af fællesforsyningerne Ventilation, Køl og varmedrift, samt bygningsvedligehold på site Gentofte og i Kirke Værløse. Teamets vigtigste mål er forsyningssikkerhed og kvaliteten af de leverede ydelser. Med reference til teamlederen søger vi en drift- og systemadministrator, der med sin viden, erfaring og overblik skal sikre, at teamets processer og BMS-anlæg er i compliance med cGMP.

Jobbet
Du bliver sammen med teamets øvrige medarbejdere ansvarlig for at teamets processer lever op til kravene beskrevet i Novo Nordisk’s kvali-tetssikringssystem. Derudover forventes det, at du deltager i den daglige drift, hvor opgaverne vil være håndtering af alarmer på kritiske anlæg, review af logbøger for kritiske ventilationsanlæg, styre og bistå ved kalibrering af BMS-følere, udarbejde årlig baseline for BMS- og ventilationsanlæg, håndtering af afvigelser, systematisk problemløsning, deltage i tilkaldevagt, deltage i myndighedsinspektioner, oprettelse af udstyrskort, TAG-stamkort, rationalekort o.l., udarbejdelse og opdatering af instruktioner, styring af logbøger, håndtering af ændringssager relateret til BMS-anlæg.

Kvalifikationer
Du er uddannet ingeniør, el-installatør, maskinmester eller tilsvarende teknisk baggrund. Du har gennem dit arbejde opnået solid erfaring med BMS (Siemens Desigo Insight) og har godt kendskab til cGMP i farmaceutisk produktion.

Som person kendetegnes du som en positiv, systematisk og kvalitetsbevidst kollega, der er god til at bevare humor og fleksibilitet i et til tider travlt og omskifteligt miljø.

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 Per Knudsen på +45 3079 2669.

Ansøgningsfrist
30.november 2013

GMP koordinator (Kalundborg, Danmark)

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GMP koordinator

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

- Produktion
- Danmark - Kalundborg

GMP-koordinatorer med sans for kvalitet og compliance søges til Kalundborg. Så hvis du er ambitiøs og har en positiv ’can do’ tilgang, vil du passe perfekt ind hos os.Vil du bruge din viden om kvalitet og compliance i et spændende job med stor indflydelse og tilsvarende ansvar, så har du chancen nu. Du får alle muligheder for at tage egne initiativer og skabe en høj faglighed samt forståelse for vigtigheden af kompromisløs kvalitet og compliance.

Om afdelingen
Vi søger GMP-koordinatorer til Kalundborg, hvor det primære fokus er den aseptiske insulin produktion. Du vil få en bred kontaktflade med Operatører, Teknikere, Teamledere og Afdelingsleder. Derfor får du også brug for din evne til at kommunikere klart og tydeligt, så det giver lige stor mening, uanset hvem du taler med.

Jobbet
Som GMP-koordinator er du ambassadøren for kvalitet og compliance i din afdeling. Du er med til at formulere vores kvalitetsmål som du også følger op på. Sammen med afdelingens ledelse sikre du, at det generelle kvalitetsniveau er i top, og at kvalitetssystemer og processer overholder Novo Nordisks og myndighedernes krav. Det er derfor også dig, der er afdelingens væsentlige spiller for at sikre succesfulde inspektioner og audits i afdelingen. En væsentlig del af dit arbejde handler naturligt om at følge op og løbende optimere relevante processer samt at sikre, at vi er i compliance med gældende lovkrav og egen governance. Sideløbende underviser og vejleder du dine kolleger i regler, systemer og processer. Du får også mulighed for at udfolde din viden ved her-og-nu problemløsning.

Kvalifikationer
Du er uddannet farmaceut, ingeniør eller lignende, hvor du har fået en god grundlæggende forståelse for kvalitet og compliance. Du kan også have opnået disse kompetencer qua dine erfaringer fra tidligere jobs. Det helt afgørende er imidlertid, at du har flere års erfaring med kvalitets- og compliancearbejde fra en medicinalvirksomhed. Du kender derfor til gældende myndighedskrav, og ved hvad der kræves for at være i compliance. Du har erfaring med projektarbejde, og ved hvor vigtigt det er at skabe resultater gennem andre. Skal du have succes, skal du have lyst til at sætte retning og drive det faglige kvalitets- og compliancearbejde fremad med dine egne initiativer.

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 du får en lang række muligheder for professionel og personlig udvikling.

Kontakt
Vil du vide mere om stillingen så kontakt Thorid Brandt Lassen på +45 3075 9008 eller Iben Bargmann Bjerre på + 45 3075 9487.

Ansøgningsfrist
8. december 2013

Student Assistent (Bagsværd, Denmark)

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Student Assistent

- Human Resources
- Denmark - Bagsværd

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

About the department
We are seeking a student for a part time position (15-20 hours) in our Learning management team which is part of Corporate People & Organisation in Bagsværd, Denmark.

You get the opportunity to join a committed team of 6 HR professionals who are responsible for developing and maintaining standards, processes and tools supporting people development and learning processes across the global organisation. One of our current key projects is to further optimise the Global Onboarding programme to enable fast, effective and engaging onboarding for our new colleagues globally. We seek an engaged student to join our department in order to mainly support project planning, communication and change management activities, whereby you can expect to manage minor projects and act as support to larger projects. Your main role will be to support the onboarding project, where the team is looking forward to welcoming you.

The job
The Global Onboarding project is in the execution phase. You will be working in a dynamic team and will be involved in a variety of different project assignments, including the preparation of communication materials and conduction of change management activities, support to the project manager, ad hoc tasks with respect to training and workshops and support of IT. Overall your main assignment will be to support project roll out and implementation to a diverse group of stakeholders. This means you will be expected to be able to build relations to relevant stakeholders on all levels of the organisation. You can anticipate varied working days with many different tasks and numerous stakeholders.

You will get the opportunity to understand core HR processes and gain hands-on project management experience in in a global organisation.

Qualifications
You are currently studying for your master’s degree in Communication, Human Resource, Organizational Psychology or other relevant field. Please note that we do not accept applications from non-students.

You have sharp analytical skills and knowledge about project management. To drive your projects successfully (with supervision), you need a structured approach, pay attention to details and have a mind focused on quality. You possess excellent communication skills and knowledge within change and stakeholder management. Sound personal judgment and excellent interpersonal skills are required. Good cooperation skills are essential and the ability to work in a global organisation is a prerequisite. Fluency in both oral and written English is required. You have a flair for IT and are an advanced user of MS Office. It is an advantage if you have experience with producing webpages and some knowledge of SharePoint is preferred.

You are an outgoing person with a strong personal drive and dedication. You are motivated by being challenged both professionally and personally. You have a high level of energy, take initiative (proactive thinking) and bring a healthy sense of humour to your work. We expect candidates to be service minded, thrive in a busy environment and bring a can-do attitude. Finally, you must have strong work ethic and willingness to take responsibility for your own learning.

Practicalities

Students in their first or second year of their master studies. The position is a part-time position (15-20 hours) for a minimum of 9 months or longer. Start date as soon as possible.

Contact
For further information, please contact Ulrike Blechschmidt-Neubert on +45 3079 1003.

Deadline
30 November 2013.

HR Business Partner (Kalundborg, Denmark)

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HR Business Partner

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

- Human Resources
- Denmark - Kalundborg

We are looking for an experienced senior HR professional to take up the position as HR Business Partner for the Corporate Vice President for Manufacturing Development and for the Vice President for Business Support in Diabetes API.

About the department
The job is located in Diabetes API, which is part of the manufacturing organisation Product Supply. You will be a part of a highly dedicated HR department with 11 colleagues working with leadership and organisational development. We cover the whole range of HR tasks from organisational communication, leadership development, performance management, training and change processes supporting the business challenges in the organisation.

The job
As HR Business Partner you will report to the HR Director and support the management teams in Manufacturing Development and Business Support located in Kalundborg and Bagsværd. The areas contain 160 employees. You will be a full member of the management teams supporting the leaders on a daily basis within all aspects of leadership, people challenges and organisational development.

The position as HR Business Partner contains a large amount of independence, authority and a chance for you to provide inspiration for our development of HR and communication processes driven by the business demands. Your overall objective is to support the business by developing its leaders and ensuring high level of people performance and development. This is primarily done by supporting and coaching the management teams. In addition, you will be responsible for developing, standardising and improving key cross-organisational processes such as Organisational Review, Performance Management, Talent Management and Employee Engagement. As you grow in this position, you will get very close to the business areas and the complexity and challenges that they hold. Besides executing day to day support, you will also drive strategic P&O activities within Diabetes API.

As HR Business Partner, you can expect a large degree of interaction with Line of Business and with other People & Organisation (P&O) colleagues across the organisation, leaving you with a challenging and inspiring job with great possibilities for the future.

Qualifications
You have a solid professional background in HR which includes a relevant degree and a minimum of five years of working experience within HR and OD – some of these preferably in Novo Nordisk. You understand the organisational mechanisms in a global organisation and you have a proven track record within most or all of the classical disciplines in the HR life cycle. You thrive with developing and improving HR activities that are linked to the overall business purpose and you have extensive experience with what works in practice. You enjoy having the responsibility for both process and outcome and you know by experience that success depends on what your customers think of your deliverables.

As a person you have strong interpersonal skills and are known for building good relations with your stakeholders. You thrive in a working environment that is characterised by cross disciplinary fora, an urge to constantly improve and a willingness to take on new challenges. Your good sense of humour and open mind enables you to contribute to a productive and collaborative 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 contact Lise Ebdrup Lund at +45 3079 7197.

Deadline
29 November 2013
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