Jobs at Novo Nordisk

Quality Assurance Professional

- Quality
- Denmark - Hillerød

Do you have a mind for quality assurance? Then join Novo Nordisk’s Device Manufacturing Development (DMD) as our new Quality Assurance Professional and contribute to defeating diabetes worldwide

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

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

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

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

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

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

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

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

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

Deadline
15 January 2014.

Requisition ID 13847BR
Title SR DIRECTOR - COMMERCIAL CHANNEL MANAGED MARKETS
Job Category Marketing
Job Description PURPOSE:
Develop over-arching commercial strategy (Managed Care; Pharmacy Benefit Managers; mail order) for Novo Nordisk US to optimize profitable access. Manage the performance of commercial channel, including accountability for tracking and improving Channel share and profit performance, key account prioritization, and development of marketing strategies, messages and tactics that will optimize business within that Channel for Diabetes, Biopharmaceuticals, & pipeline brands – e.g. Managed Markets Execution. Provide support and guidance to the field sales force and the Managed Markets Sales (MMS) team in the execution of these programs. Lead the effort to collaborate with brand marketing to help develop brand-optimizing managed care strategies and tactics for key products across managed market channels. Translate brand strategies for managed care into product portfolio strategies, value propositions, and promotion programs tailored for the retail market. Develop supporting contracting strategy for the commercial channel. Stays abreast of market dynamics as well as changes. Ability to create and articulate a vision for navigation through an ever changing healthcare environment.

RELATIONSHIPS:
Reports directly to the Vice President, Managed Markets. Works in strong collaboration with Pricing and Contract Operations; Brand Marketing, MMSales, Sr. Directors for Institutions and Government with MM leadership to ensure excellent coordination across all retail markets. Interacts with many levels and departments at Novo Nordisk and NNAS especially: Extended Brand Teams including Brand leadership across Diabetes, Biopharmaceuticals, & Pipeline; Pricing Committee, Sales Management and Operations, and Health Policy (Washington Office). External relationships include key executives and customers, associations, and a host of related vendors and consultants. NNI Executive Team.

ESSENTIAL FUNCTIONS:

Customer Channel Strategic Planning:
• Collaborates with internal and external stakeholders to leverage and implement knowledge of reimbursement, managed care and healthcare policy.
• Collaborates with Pricing group and develops pricing strategy consistent with customer and market indicators and overall portfolio strategy targeting long-term market share growth.
• Develop and implement corporate and brand strategies in conjunction with the Novo Nordisk Brand Teams and MMS, that result in increased market share of Novo Nordisk products within managed care customer Channels and specific accounts.
• Develop plans and execute key programs that will drive long-term profitable relationships with key accounts and the managed market Channel overall.
• Develops and maintains relationships with key organizations in targeted customer Channels.
• Identifies emerging customer Channels and evaluates the business opportunity for any or all Novo Nordisk Inc. products.
• Leads the managed care channel strategic planning process for all marketed products and ensures cross-functional support for strategic direction.
• Provide managed markets insights and act as an integral part of the brand planning process, through membership on one or more Extended Brand Teams, thereby taking accountability for the quality of the managed markets portion of brand marketing plans.
• Uses and leverages understanding of the competitive landscape to anticipate and pre-empt future competitor moves to create strategic opportunities for enhancing portfolio performance through the development of innovative plans and strategies.
• Uses industry, reimbursement, and disease area expertise to provide strategic direction and planning in ways that reveal new opportunities, potential threats and mitigating actions.

Product And Service Investment:
• Develops and maintains relationships with key customer executives.
• Develops and oversees implementation of key metrics. Regularly reviews current program progress to ensure profitability goals are on track.
• Develops relationships with and commitment from relevant NNI and NNAS departments to ensure successful execution of promotional strategies.
• Maximizes revenue and profitability and understands return on investment (ROI) concepts to ensure program effectiveness. Ensures short-term sales and market share objectives are met.

Product Promotions:
• Close collaboration with Extended Brand Teams, to ensure plans and programs are consistent with brand messages and positioning.
• Direct interaction with customers to understand their business objectives and needs. Use diabetes and business acumen to develop and implement collaborative programs that meet both the customers and Novo Nordisk's business objectives.
• Generates understanding and commitment throughout the organization regarding business strategies, through communication and collaboration with NNAS and NNI departments.
• Leads development of programs to improve product reimbursement, product pull through and product awareness. Directs activities of external suppliers and agencies to ensure completion of projects on time and within budget. Leads and coordinates program implementation efforts between Account Executives, Field Sales and in-house personnel.

PHYSICAL REQUIREMENTS:
Approximately 25% overnight travel.

DEVELOPMENT OF PEOPLE:
• Ensure that reporting personnel have 3P forms with annual goals and measurements that are consistent with the priorities of the business, and that interim reviews are held so that their work is focused on those priorities, and they understand their level of accountability for results and the measurement process.
• Ensure that the IDP forms include completed Learning and Aspiration plans and are in place for all reporting personnel to enable the achievement of goals and capability to assume increased levels of responsibility.
• Manage the application and communication of all Novo Nordisk policies, procedures, and Novo Nordisk Way of Management.

KEY SUCCESS FACTORS: EDUCATION, EXPERIENCE, KNOWLEDGE AND SKILLS
• A Bachelor’s Degree required; solid, relevant experience may be substituted for degree, when appropriate ; advanced degree preferred.
• A minimum of 15 years of progressively responsible experience within sales, marketing, or managed markets related functions required.
• Ability to manage complexity.
• Anticipates problems and roadblocks to avoid crisis management.
• Demonstrated ability to develop team members.
• Demonstrated experience in diverse functions required.
• Develops accurate short and long term plans, and business analysis.
• Effectively prioritizes and spends his/her time and the time of others on what is important.
• Ensures timely execution and follow-up to meet deadlines.
• Knowledge of diabetes, managed care, trade and government marketplace required.
• Pharmaceutical industry experience required.
• Proven success in developing strategy through expert understanding of market and industry.
• Relationships with Managed Care, Trade, Government executives and KOLs required.
• Supervisory experience required.
Department DM - CUSTOMER CHANNEL MKTG (MCO)
Position Location US - Princeton, NJ
City Princeton, NJ
State/Provinces US - NJ
Degree Required Bachelor's Degree Required
Percent Travel 20 - 30%

Oversee all assigned projects/products/processes. Assist the Director/Sr. Director/VP in assuring Novo Nordisk compliance with internal SOPs and Federal and State regulations, including compilation and submission of any required documents to regulatory agencies. Act as liaison with FDA for assigned projects. Supervises designated personnel.RELATIONSHIPS:Report to the Director/Sr. Director Regulatory Affairs. Interact with key company personnel both within and outside of Novo Nordisk-US as related to assigned projects. Develop and maintain positive rapport and working relationships with other personnel in Regulatory Affairs, CMR, and other local and headquarter departments in support of initiatives and to accomplish company goals. FDA liaison for designated projects or as requested by supervisor. Supervises junior Regulatory Affairs staff.ESSENTIAL FUNCTIONS:* Act as liaison with NNI and NNAS departments for preparation of documentation necessary for submission of applications.* Approve specified regulatory submissions.* Assist senior Regulatory Affairs personnel in assuring compliance.* Coordinate and supervise the development of regulatory strategies for new or modified pharmaceutical products, 510(k) devices and medical device/pharmaceutical combination products under development or license for assigned projects.* Facilitate and organize the compilation of applications (IND, NDA, Biologics, Devices, combination products) to government agencies in support of investigational and marketed products. Maintain up-to-date knowledge of the data, information, and formats required for inclusion in these applications.* FDA liaison on key matters.* Identify the need for and provide input into development of systems for assigned projects for the efficient operation of the department.* Lead FDA meetings.* Lead major label negotiations.* Major labeling negotiation.* Manage complex projects.* May act as FDA liaison for all project issues.* May act as GRT member.* Participate in and/or coordinate all negotiations and interacts with FDA personnel as assigned.* Provide information and training for NNAS in areas of US IND, NDA, 501(k) and combination product processes. Disseminate information on proposed and new FDA regulations and guidelines for assigned products/projects, including CDRH human factors engineering guidances.* Provide input as requested for device design and process verification and validation activities; review and collate documentation required for 510(k) and medical device/pharmaceutical combination product FDA submissions.* Provide input into development of regulatory and quality systems.* Provide input into development of SOPs for the efficient operation of the department and inter-department activities.* Provide training to the regulatory staff and Sales Reps as needed.* Responsible for development of regulatory submission strategies.* Review data from contributing departments (including NNAS) and provide comments to assure accurate and complete documents for inclusion in these applications.* Submit all types of applications to FDA.* Supervise and advise staff members.* Supervise and coordinate all regulatory activities relating to regulatory compliance for assigned marketed and investigational products.* Supervise and coordinate the planning of FDA submissions for assigned products/projects to ensure most efficient use of resources.* Supervise the review and sign-off on all labeling for marketed products prior to use for assigned products/projects.* Supervise the review and sign off on instructions for use and other product labeling as necessary to comply with FDA requirements for investigational and marketed device and combination products.PHYSICAL REQUIREMENTS:Some overnight travelDEVELOPMENT OF PEOPLE:* Contribute to development of Associates and Managers.* Ensure that reporting personnel have timely performance evaluation forms with annual goals and measurements that are consistent with the priorities of the business, and that interim reviews are held so that their work is focused on those priorities, and they understand their level of accountability for results and the measurement process.* Ensure that the IDP forms include completed Learning and Aspiration plans and are in place for all reporting personnel to enable the achievement of goals and capability to assume increased levels of responsibility.* For global projects, advise members of the global regulatory team and provide input to goal setting and performance appraisal for team members in head quarters within assigned projects.* Manage assigned junior to more experienced personnel and their simple projects or portions of projects as direct report(s).* Manage the application and communication of all Novo Nordisk policies, procedures, and Novo Nordisk Way of Management.KEY SUCCESS FACTORS: EDUCATION, EXPERIENCE, KNOWLEDGE AND SKILLS* A Bachelor's degree in life science or related area required; advanced degree may be substituted for relevant experience when appropriate.* Ability to establish sound working relationships.* Ability to work independently.* Detail & deadline oriented; well organized.* Excellent verbal and written communication skills essential.* Experience and knowledge of the relevant current requirements of FDA required.* For global projects, prior interaction or exposure with other key regulatory authorities e.g. EMEA, EU national authorities, PMDA* Good interpersonal skills; ability to interact with staff on all levels.* A minimum of 10 years related experience required (i.e. pharmaceutical, medical device/pharmaceutical combination product, clinical research, or laboratory exp.). At least 6 years direct regulatory experience required..* For managers of people, some supervisory experience required.Department CMR - THERAPEUTIC AREA (1)Position Location US - Princeton, NJCity PrincetonState/Provinces US - NJDegree Required Bachelor's Degree RequiredPercent Travel 20 - 30%

Requisition ID 5691BR
Title Executive Director - Hemostasis
Job Category Medical
Job Description To provide medical leadership including the assessment and support of product development and extension, and professional services for Biopharmaceutical marketed products.

RELATIONSHIPS:

This position reports to the Vice President, Clinical Development & Medical Affairs, BioPharm and manages the Clinical Development and Medical Affairs, Hemostasis Team. It is accountable for managing multiple internal relationships within NNI and NNAS. External relationships include working with the medical community and customers.

ESSENTIAL FUNCTIONS:

PROTOCOL DEVELOPMENT
•Conduct needs assessment for therapeutics in healthcare, the risks of intervention and the potential market for intervention.
•Review, refine, prioritize and manage the Hemostasis Clinical Trials Program.
•Develop medical affairs capabilities.
•Manage core project teams between NNI and NNAS to integrate clinical /medical core programs.
PRODUCT SUPPORT AND SAFETY
•Evaluate reports of adverse outcomes, apply clinical medical acumen and interpret regulatory guidelines and directives to judge risk and causality.
•Participate in meetings and the Promotional Review Board (PRB).
•Assure the ongoing safety and adequacy of labeling of NNI's marketed products from a medical perspective.

SALES AND MARKETING
•Provide medical input to marketing plans, promotional campaigns and new product launch platforms.

PRODUCT DISCOVERY AND DEVELOPMENT
•Coordinate Medical Department strategic review of in-licensing candidates and external development projects for NNI’s existing in-line product franchises.

MEDICAL AND PATIENT COMMUNITY
•Must have (and continue to build) relationships with key thought leaders in the hemophilia community.

•Develop educational curricula to effectively teach.
•Serve as an expert in hematology.
•Maintain necessary credentials and remains in good standing within the medical community and medical ethics boards.

DEVELOPMENT OF PEOPLE:
•Ensure that reporting personnel have 3P forms with annual goals and measurements that are consistent with the priorities of the business, and that interim reviews are held so that their work is focused on those priorities, and they understand their level of accountability for results and the measurement process.
•Manage the application and communication of all Novo Nordisk policies, procedures, and Novo Nordisk Way •Ensure that the IDP forms include completed Learning and Aspiration plans and are in place for all reporting personnel to enable the achievement of goals and capability to assume increased levels of responsibility.

KEY SUCCESS FACTORS: EDUCATION, EXPERIENCE, KNOWLEDGE AND SKILLS:
•MD and 5 plus years Industry experience. Pharmaceutical development or
research experience, including expertise in clinical trial methodology and medical product support, and medical affairs.
•Hematology experience specializing in bleeding disorders is required.

•Experience in development and regulatory areas required.
•Previous supervisory experience required.
•Administrative responsibilities in an institutionalized setting required.
•Must maintain necessary credentials and remain in good standing within the medical community and medical ethics boards.
•Previous Phase I-IIIB and IV clinical trials experience required.
•Some clinical and previous patient care experience required.
•Strategic/Tactical planning experience within a pharmaceutical environment is required.
•Able to assess a clinical outcome and relate it to a drug.
Department CMR - HEMOSTASIS
Position Location US - Princeton, NJ
City Princeton
State/Provinces US - NJ
Degree Required Doctorate Degree Required
Percent Travel 30 - 40%

At Novo Nordisk, our winning culture is focused on cross-functional and cross-cultural teamwork. We combine clinical research to develop new products, regulatory efforts to work with the FDA to bring these products to market, and sales and marketing to convey a strong, clear message to patients and physicians. We encourage employee involvement at all levels, which in turn helps to nourish development and innovation. When employees become involved, the result is a rich exchange of ideas and concepts. And that helps us give more to our customers, to our community and to society as a whole.

In an effort to match your background and experience with our potential future openings, we invite you to upload your resume by clicking on the apply button. Please note your resume will be kept confidential.

We look forward to continuing to provide you with information on Novo Nordisk career opportunities.

Pharmaceutical Sales Opportunities

We look forward to continuing to provide you with information on Novo Nordisk career opportunities.

Requisition ID 19137BR
Title Hemophilia Care Specialist (HCS) - Upstate NY
Job Description Hemophilia Care Specialist - Upstate NY

PURPOSE:
•Represents Novo Nordisk to the Hemophilia patient community and patient organizations (e.g., local hemophilia chapters) with the goal of increasing patient awareness of and engagement with Novo Nordisk’s hemophilia products, support offerings and services in an assigned territory
•Cultivates relationships with patients, caregivers and other community stakeholders by participating in and assisting with community events on behalf of Novo Nordisk
•Establishes and manages relationships with key patient organizations, including local chapters of the National Hemophilia Foundation and, Hemophilia Federation of America chapters etc.
•Attends, and when possible assists with planning events held by patient organizations in his/her territory, and represents Novo Nordisk at selected national events hosted by those patient organizations. Events may include fundraising/volunteering efforts along with representation at educational meetings.
•Serves as the center of coordination for patient-related activities across patient community, Novo Nordisk HTSMs and the broader Novo Nordisk organization (both within BioPharm and relevant functions outside of Biopharm) to ensure that learnings from patients, caregivers and other stakeholders are incorporated into the BioPharm strategy and business decisions
•Collaborates with Market Access and Government Affairs teams when advocacy issues arise and as appropriate.
•Regularly communicates perspectives, findings and insights to BioPharm leadership and the BRD/HTSM population through informal and formal (e.g., oral and written presentations) mechanisms Includes sharing insights and competitive intelligence within the hemophilia area.

RELATIONSHIPS:
•Reports directly to BRD and interacts with other Community Advocates, HTSMs, BioPharm AEs and other relevant NNI functions including Government Affairs
•Member of the Hemophilia Field Force and has h interaction with hemophilia marketing to provide feedback on development and value of direct-to-patient materials, tools and programs.
•Works closely with HTSMs in overlapping territories to share information and insights, and ensure 100% coverage of community events
•Helps identify when home office support and presence is needed at larger community based events such as chapter meetings and other functions.

ESSENTIAL FUNCTIONS:
•Represents Novo Nordisk at local and national hemophilia events
•Develops direct relationships with patients/caregivers and other hemophilia community members including hemophilia organizations and chapters, state and local advocacy groups
•Follows all company policies and remains compliant with patient interactions including completing training and compliance programs throughout the year. Ensures all communications are HIPPA compliant.
•Plans and conducts meetings with state and local chapters with the goal of educating patients, caregivers, and other stakeholders on Novo Nordisk’s products and services
•Executes patient and caregiver educational meetings / exhibits at chapter events, home care meetings, patient conventions, patient dinners, support at community events/camps, etc. about hemophilia and Novo Nordisk products and services
•Supports planning efforts for community fundraising activities as needed (e.g. golf tournaments)
•Proactively works to continually deepen Novo Nordisk’s relationship with State and local advocacy organizations (e.g. local chapters of NHF, HFA, etc.), engaging with Government Affairs when necessary
•Identifies for home office, opportunities for increased levels of presence, support and engagement.
•When necessary, directs questions from the community to the appropriate Novo Nordisk channel (e.g., HTSMs, ePIR,SevenSECURE, etc.)
•Works directly with NNI government affairs group to support efforts for better care of hemophilia patients
•Continually communicates and coordinates with Novo Nordisk HTSMs, BRDs, AEs, SAEs and Marketing team, regularly sharing insights on how NNI can continue to improve its offering to the hemophilia community
•Coordinates with other Community Advocates to prepare internal communications to the BioPharm team, keeping internal stakeholders attuned to the pulse of the community
•Demonstrates high ethical and professional standards at all times

PHYSICAL REQUIREMENTS:
•Approximately 50-70% overnight travel (including evenings & weekends)

KEY SUCCESS FACTORS:
EDUCATION, EXPERIENCE, KNOWLEDGE AND SKILLS
•5+ years of experience in hemophilia care, treatment or advocacy
•Bachelor’s degree required, advanced scientific degree or clinical experience preferred
•Must excel in multitasking, leadership, community building, networking, strategic thinking, project management and problem solving
•Must have exceptional public speaking skills and be comfortable with small and large audiences of patients, clinicians and other members of the hemophilia community
•Proven track record of project management, marketing and/or sales experience
•Should have an aptitude for learning and communicating technical and scientific product and service information
•Excellent written and verbal communication and interpersonal skills are required
•Willingness to work at times that correspond to community events most frequently (e.g., evenings, weekends)
•Intermediate computer skills required (Windows, Word, Excel, Power Point)
•English required, fluency in Spanish is desirable

OTHER:
•Works within Novo Nordisk’s established policies and procedures and ensures alignment of their work to Novo Nordisk fundamentals.
•Embraces Novo Nordisk Values in spirit and actions.
Department BIO - SALES NORTHEAST (H)
Position Location US - Field Based - Across US
City Upstate
State/Provinces US - NY
Degree Required Bachelor's Degree Required
Percent Travel 50 - 60%

Teamleder, Proces Support

- Produktion, Teamleder
- Danmark - Værløse

Har du ledererfaring fra medicinalbranchen og en rigtig god GMP-forståelse? Og har du samtidig lyst til at blive en integreret del af en dynamisk og ambitiøs ledergruppe? Så kan du meget vel være vores nye lederkollega. I Biopharm Tablets & Finished Products (T&FP) har vi nu en ledig stilling som teamleder for et proces-support team i Værløse.

Om afdelingen
I Biopharm T&FPs afdeling i Værløse monterer og pakker vi penne og vi er i gang med at udvide antallet af montage og pakkelinjer med flere semi- og fuldautomatiske anlæg. Vi er ca. 100 engagerede medarbejdere, der i fællesskab sikrer, at vi leverer færdigpakkede produkter af højeste kvalitet og til rette tid til patienter i hele verden. I ledergruppen er vi en afdelingsleder, 4 teamledere, en GMP-koordinator og en controller, der stræber efter et tæt og velfungerende samarbejde imellem alle teams på tværs af afdelingen. Vi har en travl og udfordrende hverdag, hvor vi lægger vægt på ligeværdig kommunikation og respekt for alles bidrag til fællesskabet.

Jobbet
Som teamleder for proces-support teamet bliver du ansvarlig for et team på ca. 10 medarbejdere, både akademikere og timelønnede. Det er dit teams ansvar at sikre, at alle ordrer der sendes ud af huset lever op til vores høje kvalitetskrav og cGMP-krav. Teamet bidrager ligeledes til at produktions- og frigivelses-aftaler overholdes. Det er også en del af dit job at sikre, at vi fastholder og videreudvikler en kultur, hvor vi løbende forbedrer os. Det sker igennem daglige tavlemøder, brug af systematisk problemløsning og proceskonfirmering i hverdagen. Du skal sikre, at dine medarbejdere kender forventningerne til dem og har en løbende dialog med dig om deres opgaver og kompetenceudvikling. Vi har en dynamisk hverdag med mange forandringer og du kommer til at træffe vigtige beslutninger i højt tempo.

Kvalifikationer
Med en længerevarende uddannelse har du opnået en evne til at forstå komplekse, kvalitetsmæssige problemstillinger. Derudover har du erfaring fra produktion i GxP regulerede virksomheder eller andre, der er underlagt høje kvalitetskrav. Du brænder for ledelse og har meget gerne erfaring med lederrollen. Det er vigtigt, at du udstråler energi og vindervilje samt har et højt socialt engagement. Du skal kunne udstikke retning og forklare, hvorfor og hvordan, dit team når målene. Samtidig kan du navigere sikkert i en kompleks organisation, hvor du skal koordinere aktiviteter med mange forskellige interessenter på alle niveauer. Vi lægger stor vægt på at være en ansvarlig virksomhed og går aldrig på kompromis med kvalitet og forretningsetik, og de krav stiller vi også til dig.

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

Kontakt
Vil du vide mere om stillingen, så kontakt teamleder Maria Hastrup Jensen på +45 3075 2536.

Ansøgningsfrist
20 January 2014

Vicevært

- Områdedrift og service
- Danmark - Bagsværd

Vil du være med til at skabe de allerbedste fysiske rammer for dine kolleger, så de kan koncentrere sig om påfyldning af insulin til behandling af diabetes over hele verden? Så læs endelig videre, for vi har brug for en ansvarlig og omhyggelig vicevært til at sørge for, at vores bygninger og installationer er i topform og fungerer upåklageligt.

Om afdelingen
Teamet Facility & Utility beskæftiger 10 personer og er en del af Aseptisk Produktion på fabrikken i Bagsværd. Vi er ca. 500 personer, der arbejder med at påfylde insulin, og vores anlæg kører 24/7 hele året rundt.

Jobbet
Din opgave går ud på at holde vores bygninger i god form både inde og ude. Det betyder, at du holder et vågent øje med, at alt fungerer som det skal, og hvis ikke, så tilkalder du hurtig assistance til de opgaver, du ikke selv kan klare på stedet.

Du sørger også for at give besked til de relevante personer, så alle medarbejderne på fabrikken føler, at de er i trygge hænder, når de beder dig om at udføre en opgave. Du refererer til teamlederen og bliver en del af et team, hvor der også indgår procesansvarlige ingeniører og håndværkere. Du får rigtig mange henvendelser på en arbejdsdag, og du har mulighed for at skabe rigtig gode relationer til kolleger overalt i fabrikken.

Stillingen er kategoriseret som F2

Kvalifikationer
Du har en håndværksmæssig uddannelse og erfaring fra et lignende job. Hvis du har kendskab til farmaceutisk produktion og har arbejdet med GMP, så er det helt klart en fordel. Du er grundig og ærekær, så når du påtager dig en opgave, så slipper du den ikke, før den er løst tilfredsstillende. Du ved, at selv korte afbrydelser i produktionen kan koste dyrt for virksomheden, så du skal have en høj grad af forståelse for situationens alvor. Det betyder samtidig, at du skal trives godt i service-rollen, hvor du med din positive tilgang og gode humør er med til at skabe de allerbedste betingelser for dine kolleger.

I Novo Nordisk skaber vi værdi ved sætte patienterne først. Hvert tiende sekund bliver to personer diagnosticeret med diabetes, og næsten 366 millioner mennesker i hele verden har brug for os. At arbejde her handler ikke bare om at tjene til føden, men om at gøre en forskel.

Kontakt
Vil du vide mere om stillingen så kontakt Henrik Vidstrup på +45 3079 8511 på hverdage fra kl 12-14.

Kontakt
2. januar 2014

QA chemist

- Quality
- Denmark - Gentofte

Would you like to be part of Quality Assurance in Biopharm QA for QC?

Biopharm QA is looking for a talented and ambitious QA Chemist with talent for analytical chemistry. You will be a part of quality assurance of the Quality Control laboratories in Gentofte, Måløv and Kalundborg.

About the Department
Biopharm QA QC & Support is responsible for quality assurance of chemical and microbiology analysis of all drug substance and drug product in Biopharm. The department key tasks are to review and approve all sorts of GMP documentation such as validation reports, change requests and non-conformities in order to be able to deliver analytical results for release of products.

As QA Chemist in Biopharm QA QC & Support you will join a group of 23 highly skilled and competent colleagues working in two teams lead by separate Associate Managers. By joining us you will get the chance to obtain professional and personal development and you will get an excellent and unique overview of current authority expectations and demands in the pharmaceutical industry.

You will become part of a team which have a high level of self-governance. The working relations are informal and the team value professional sparring and good humour highly.

The job
The vacant position is situated in Gentofte. The team is responsibles for assuring the microbiological and the chemical control laboratories. The team consists of 12 chemists, where the vacant position is at substitution for a chemist moving to another Biopharm QA department. The job includes QA review of several types of documents related to chemical and microbiological analysis. The analyses performed are for example HPLC, Spectroscopy, Bio and Immunoassay, general pharmacopeia methods, microbiological analysis and Sterility test.

Your main responsibility will be to quality assure the laboratories and thereby contribute to assure, that the products always are of high quality and analysed in full compliance with the current rules and guidelines. On top of that QA is a major player at internal audits and external authority inspections where you are expected to participate.

When started you will undergo an individual and intense training program, where you can expect to be given more responsibility gradually.

Qualifications
You hold an academic degree and preferable you have a shorter or longer work experience from the pharmaceutical business or a company in the food industry.

You must thrive in a role where you are required to take leadership in order to achieve the shared targets in cooperation with your stakeholders. You have a strong quality mind-set, meet your deadlines, and know how to prioritise between different tasks in a dynamic environment. You like and are good at coordinating different tasks for both yourself and other people and you demonstrate an ability to find the right solutions with your colleagues. Your language skills cover proficiency in both Danish and English.

You work independently and make decisions regarding quality tasks and ensure the right balance between quality demands, authority demands and business needs. At the same time, you perform well in a team-oriented environment.

Feel free to submit your job application in either English or Danish, whichever you prefer.

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 Hanne Mørkeberg Torry-Smith on +45 3079 7674 or Ulla Thinggaard on +45 3075 2104

Deadline
3 January 2014

Global Medical Advisor

- Marketing
- Denmark - Søborg

Novo Nordisk, Global Medical Affairs is seeking new a Global Medical Advisor.

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

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

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

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

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

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

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

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

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

Deadline
3 January 2014.

QC Laborant

- Produktion
- Danmark - Hillerød

Vil du være med på holdet af ca. 46 engagerede medarbejdere i det kemiske analyselaboratorium i QCC SDK i Hillerød?

Vikariat 2 årigt.

Om afdelingen
Vi udfører frigivelsesanalyser for Insulin produktionen i Bagsværd, Hillerød, Kalundborg og på prøver fra kontrakt og licensproducenter. Det ledige vikariat er en midlertidig udvidelse og er i ét af afdelingens to teams bestående af 16 laboranter, 1 elev, 2 kemikere og en teamleder.

Teamet udfører kemiske frigivelsesanalyser primært HPLC analyser, men også manuelle analyser på insulin færdigvarer. De daglige opgaver består derudover af review, 2. kontrol af analyser, udarbejdelse af instruktioner, kvalificeringsdokumentation, analyseansvar og apparatansvar.

Vi er et team, som arbejder målrettet og engageret. Vi har det sjovt og kan lide at gå på arbejde og sætter en ære i at udføre kvalitetsarbejde i et hurtigt tempo.

Jobbet
Vi er en del af en afdeling, som står over for mange udfordrende og spændende opgaver, som stiller store krav til vores samarbejdsevne og forandringsparathed. Der stilles store krav til os om at levere frigivelsesanalyser til tiden og arbejde i flow med samme takt som produktionen. Vi arbejder ligeledes meget med cLEAN kultur i laboratoriet og har fokus på målstyring og løbende forbedring af vores arbejde.

Kvalifikationer
Vi søger en engageret og dynamisk laborant/laboratorietekniker, som er i besiddelse af godt humør. Det er vigtigt, at du har erfaring med både udførsel af analyser, HPLC udstyr og de administrative opgaver, der er i et QC laboratorium.

Du skal have kendskab til GMP og har du erfaring med at være ”på” ved inspektioner, er det en fordel. Gode mundtlige og skriftlige dansk og engelsk kundskaber er ligeledes vigtige arbejdsredskaber. Derudover er det vigtigt, at du er god til at samarbejde omkring løsning af opgaver og samtidig er i stand til at løse opgaver selvstændigt til aftalt tid. Fremtiden byder på store udfordringer i laboratoriet, derfor skal du være klar til forandringer og til at bidrage med forbedrende forslag til arbejdsgange.

Som person skal du have drivkraft, være fleksibel og initiativrig samt tænke innovativt og udvise respekt for det omgivende miljø. Det er vigtigt, at du kan tilegne dig ny viden på en hurtig og effektiv måde. Sidst men ikke mindst er det altafgørende, at du kan lide at udføre analysearbejde.

Vi tilbyder et job fyldt med spændende QC opgaver med god mulighed for udvikling inden for det kvalitetsmæssige fagområde. Derudover kan du forvente en høj grad af selvstændighed og indflydelse på eget arbejde. Der er derfor masser af muligheder for at udvikle både personlige og faglige kompetencer for den rette engagerede person.

I Novo Nordisk skaber vi værdi ved sætte patienterne først. Hvert tiende sekund bliver to personer diagnosticeret med diabetes, og næsten 366 millioner mennesker i hele verden har brug for os. At arbejde her handler ikke bare om at tjene til føden, men om at gøre en forskel.

Kontakt
Vil du vide mere om stillingen, så kontakt Lene Vilstrup på + 45 3079 7688 eller Anders Dyrby på + 45 3075 3637.

Ansøgningsfrist
5 January 2014

QC Laborant

- Produktion
- Danmark - Hillerød

Vil du være med på holdet af ca. 46 engagerede medarbejdere i det kemiske analyselaboratorium i QCC SDK i Hillerød?

Om afdelingen
Vi udfører frigivelsesanalyser for Insulin produktionen i Bagsværd, Hillerød, Kalundborg og på prøver fra kontrakt og licensproducenter. Den ledige stilling er en udvidelse og er i ét af afdelingens to teams bestående af 16 laboranter, 1 elev, 2 kemikere og en teamleder.

Teamet udfører kemiske frigivelsesanalyser primært HPLC analyser, men også manuelle analyser på insulin færdigvarer. De daglige opgaver består derudover af review, 2. kontrol af analyser, udarbejdelse af instruktioner, kvalificeringsdokumentation, analyseansvar og apparatansvar.

Vi er et team, som arbejder målrettet og engageret. Vi har det sjovt og kan lide at gå på arbejde og sætter en ære i at udføre kvalitetsarbejde i et hurtigt tempo.

Jobbet
Vi er en del af en afdeling, som står over for mange udfordrende og spændende opgaver, som stiller store krav til vores samarbejdsevne og forandringsparathed. Der stilles store krav til os om at levere frigivelsesanalyser til tiden og arbejde i flow med samme takt som produktionen. Vi arbejder ligeledes meget med cLEAN kultur i laboratoriet og har fokus på målstyring og løbende forbedring af vores arbejde.

Kvalifikationer
Vi søger en engageret og dynamisk laborant/laboratorietekniker, som er i besiddelse af godt humør. Det er vigtigt, at du har erfaring med både udførsel af analyser, HPLC udstyr og de administrative opgaver, der er i et QC laboratorium.

Du skal have kendskab til GMP og har du erfaring med at være ”på” ved inspektioner, er det en fordel. Gode mundtlige og skriftlige dansk og engelsk kundskaber er ligeledes vigtige arbejdsredskaber. Derudover er det vigtigt, at du er god til at samarbejde omkring løsning af opgaver og samtidig er i stand til at løse opgaver selvstændigt til aftalt tid. Fremtiden byder på store udfordringer i laboratoriet, derfor skal du være klar til forandringer og til at bidrage med forbedrende forslag til arbejdsgange.

Som person skal du have drivkraft, være fleksibel og initiativrig samt tænke innovativt og udvise respekt for det omgivende miljø. Det er vigtigt, at du kan tilegne dig ny viden på en hurtig og effektiv måde. Sidst men ikke mindst er det altafgørende, at du kan lide at udføre analysearbejde.

Vi tilbyder et job fyldt med spændende QC opgaver med god mulighed for udvikling inden for det kvalitetsmæssige fagområde. Derudover kan du forvente en høj grad af selvstændighed og indflydelse på eget arbejde. Der er derfor masser af muligheder for at udvikle både personlige og faglige kompetencer for den rette engagerede person.

I Novo Nordisk skaber vi værdi ved sætte patienterne først. Hvert tiende sekund bliver to personer diagnosticeret med diabetes, og næsten 366 millioner mennesker i hele verden har brug for os. At arbejde her handler ikke bare om at tjene til føden, men om at gøre en forskel.

Kontakt
Vil du vide mere om stillingen, så kontakt Lene Vilstrup på + 45 3079 7688 eller Anders Dyrby på + 45 3075 3637.

Ansøgningsfrist
5 January 2014

Quality Engineer for Device R&D (maternity cover)

- Quality
- Denmark - Hillerød

Are you ready to use your QA skills in Device Development projects in Novo Nordisk? As Development Quality Engineer in Device Research & Development, DRD, you will use your knowledge and personality to make DRD develop superior products that help people every day all over the world.

About the department
DRD Quality is newly established from two existing quality departments and we are responsible for quality assurance of development activities from ideas until transfer to production. We are in close cooperation with project managers and Quality Assurance from other parts of Novo Nordisk and external partners.

We also administrate the quality management system of DRD. You will join a group of 12 skilled and engaged Quality Assurance engineers and specialists that work inside the projects to secure compliance to procedures and regulations.

To learn more about Device Research & Development, please visit: www.novonordisk.com/device-rd

The Job
The position is a 14 month maternity cover and we are looking for a skilled and motivated engineer that can support and influence project groups to help them meet the requirements from procedures and regulations. In the projects you will review and approve documentation on requirement engineering, safety risk management, design verification and design validation.

Qualifications
You hold a relevant academic degree in engineering, pharmacy or equivalent and have relevant working experience ideally within combination products (drug/device). You have an up-to-date knowledge of relevant GMP requirements.

You are used to work in a team and are known to deliver according to targets. You make a difference, and by your dedicated and determined approach you complete your tasks in close cooperation with your colleagues. You work in a structured way and you get energized by learning new things. You are robust, can keep focus and you have good communication skills. Quality is essential to you and incorporated in your daily work. On a personal level you are ambitious and have a great interest in developing yourself. You are fluent in both written and spoken English on a professional level.

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 Charlotte Viemose Larsen on +45 3075 5988 or Jørgen Dreier on +45 3075 1482.

Deadline
15 January 2014.

Laborant

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, at vores produkter lever op til de højeste kvalitetskrav og kan du levere svar til tiden? Så er denne stilling som QC laborant måske lige noget for dig.

Vi har en ledig stilling som QC laborant i vores kemiske team i Insulin Manufacturing 1, Diabetes API, Kalundborg.

Om afdelingen
Du vil blive en del af et kemisk analyseteam bestående af 19 engagerede og dygtige laboranter og kemikere med arbejdssted i Kalundborg. Teamet er en del af QC laboratoriet i IM1, hvor der udføres både kemiske og mikrobiologiske analyser af vores produkter i Diabetes API. I afdelingen er vi ca. 40 medarbejdere fordelt i et kemisk og et mikrobiologisk/support team og en stabsfunktion.

Jobbet
Vi kan tilbyde dig et job i et velfungerende team med gode muligheder for udvikling af dine faglige og personlig kompetencer.

Vi søger en erfaren og GMP kyndig laborant til denne en stilling i vores kemiske team. Teamet varetager analyser af insulin fra vores produktionsenhed udført på HPLC, GC, EA og TOC herudover kemiske vandanalyser samt andre mindre analyser.

Som laborant skal du være med til at sikre, at vi driver vores analysearbejde på en god og effektiv måde, herunder at vi i samarbejde med vores kunder i produktionen sikrer, at vi konstant leverer analysesvar i rette mængder, kvalitet og til tiden.

Kvalifikationer
Du er uddannet laborant/laboratorietekniker og har erfaring med udførelse af QC analyser. Kendskab til cGMP og ISO14001/9001 vil være en fordel. Herudover har du måske erfaring med forskellige andre analysemetoder f.eks. TOC, HPLC, GC eller farmakope analyser. Kendskab til LEAN er en fordel, da det er en stor del af vores hverdag.

Vi søger en laborant med et stort engagement samt gode samarbejdsevner. Ligesom der lægges stor vægt på, at du besidder en stor grad af kvalitets- og ansvarsbevidst og kan håndtere flere opgaver parallelt.

Novo Nordisk i Kalundborg er en by i byen. Området er beliggende en god times tid fra København og dækker over 1.350.000 m2 med eget vejnet. Vi producerer ca. 50 % af verdens insulin. Vi arbejder helt på forkant af udviklingen inden for teknologi, systemer, metoder og processer. Er du vores nye kollega, kan vi garantere muligheder, du vil have svært ved at finde andre steder.

Kontakt
Vil du vide mere om stillingen, så kontakt Annette Musiat på +45 3075 0902.

Ansøgningsfrist
5 January 2014

Clinical Trial Administrator

- Administrative
- Denmark - Søborg

Do you want to assist a dynamic team that drives clinical trial activities in an international setting with the possibility to interact with many different nationalities?

Clinical Operations GLP-1 & Obesity is looking for a Clinical Trial Administrator to join us. As Clinical Trial Administrator you will have a significant role in supporting the trial planning and execution by performing administrative tasks in a pro-active and independent manner.

About the department
Clinical Operations, GLP-1 and Obesity is responsible for the planning and execution of clinical trial activities within diabetes and obesity in very close collaboration with our affiliates. The area include a team of more than 80 highly skilled and very ambitious colleagues.

The job
You will support a team of International Trial Managers who are responsible for the management of our global clinical trials. You will be an essential member of the trial management team, having a significant role in conducting trial related tasks in a proactive and independent manner. You will contribute to successful internal meetings by coordinating and planning the logistics, ensuring availability of applicable equipment, completion of minutes and general support that enables the International Trial Manager to focus on the content and outcome. You will set up and maintain the shared web sites and portals used by the International Study Group for sharing trial related documents as well as contribute to the preparation of newsletters and PowerPoint presentations.

By use of your structured approach and high quality mindset you will be responsible for establishing and maintaining the Trial Master Files in accordance with standard operational procedures. This also includes uploading, updating of information, indexing and QC of trial documents in our different Clinical IT systems as well as IT project tools. You will assist with preparation and updating of the trial budgets by use of our IT budget tools and by supporting the Clinical Project Manager with budget presentations. In addition you will support the trial team with ad hoc tasks as needed.

Qualifications
You have a Bachelor’s degree within an IT or scientific discipline, business administration or communication, Librarian, Medical Secretary, Laboratory Technician or equivalent with experience in an administrative position, preferably within the pharmaceutical industry. You are proficient in both written and spoken English. You have flair for using IT systems and you are highly skilled within MS Office, including Excel. Knowledge of SAP systems is a plus. Our ideal candidate will have a strong customer service mindset, be able to independently organise the work and is well structured with a sense for detail and a good overview at the same time. You like being part of a multi-cultural team. It is important that you can manage deadlines and work with multiple and frequently changing priorities using good collaboration skills and a sense of humour.

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

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

Contact
For further information, please contact Randi Rahbæk at +45 3079 8419.

Deadline
1 January 2014.

GMP koordinator med stor indflydelse på kvalitet

- Kvalitetssikring
- Danmark - Gentofte

Har du lyst til at sætte dit præg på en dynamisk afdeling, hvor din primære rolle bliver at have fokus på kvalitet og compliance? Kunne du tænke dig at blive en integreret del af en engageret og ambitiøs ledergruppe? I Biopharm Tablets & Finished Products (T&FP) har vi nu en ledig stilling som GMP koordinator.

Om afdelingen
I Biopharm T&FPs afdeling i Gentofte pakker vi GlucaGen® og blødermedicinerne NovoSeven® og Tretten®. Vi er ca. 100 engagerede medarbejdere, der i fællesskab sikrer, at vi leverer færdigpakkede produkter af højeste kvalitet og til rette tid til patienter i hele verden. I ledergruppen er vi en afdelingsleder, 5 teamledere, en controller og en GMP-koordinator, der sammen stræber efter et tæt og velfungerende samarbejde imellem alle teams på tværs af afdelingen. Vi har en travl og udfordrende hverdag, hvor vi lægger vægt på ligeværdig kommunikation og respekt for alles bidrag til fællesskabet. Vi er et pakkeri og derfor det sidste led inden vores produkter sendes ud mod patienterne – kvalitet og patientfokus er derfor en integreret del af vores mindset og beslutninger.

Jobbet
Du skal sikre, at afdelingen når og efterlever de gældende kvalitetsmål fastsat af myndigheder, Novo Nordisk og afdelingen selv, og at vi til enhver tid er inspektionsparate til interne audits og inspektioner fra eksterne myndigheder. Du får en vigtig rolle i at sikre, at vi opbygger og vedligeholder de rette kvalitetssystemer og –fora. Du vil, i samarbejde med afdelingens ledelse, arbejde med løbende at løfte kvalitetsniveauet hos afdelingens dygtige og engagerede medarbejdere. Du får et tæt samarbejde med VP-områdets 4 øvrige GMP-koordinatorer, i forhold til faglig sparring og fastsættelse af kvalitetsmål og -retning for hele området. Alt i alt vil du kunne se frem til en spændende og udviklende stilling med gode muligheder for selv at påvirke din dagligdag og på sigt din fremtidige karriere.

Kvalifikationer
Du har solid erfaring med kvalitet og/eller GMP produktion, og du er nu klar til at tage et endnu større ansvar. Du har en relevant naturvidenskabelig uddannelse (farmaceut, kemiingeniør, cand. scient. el. lign.). Dine gode kommunikationsevner og din udadvendte og afslappede personlighed gør, at det falder dig naturligt at skabe tætte relationer til mange mennesker og faggrupper. Det er vigtigt at du har gode kommunikationsevner fordi du som kvalitetskoordinator kommer til at bidrage væsentligt til det gode samarbejde med mange faggrupper. Det er endvidere vigtigt, at du arbejder systematisk og kan prioritere dine opgaver. Du har det store kvalitets- og compliance overblik, når du rådgiver om forretningsmæssige beslutninger, men har også fagligheden med, så du kan dykke ned i helt specifikke kvalitetsmæssige udfordringer. For at få succes i stillingen skal du være engageret og udvise høj grad af selvstændighed. Du trives i en hverdag med høj intensitet og ser det som din fornemmeste opgave at få fulgt opgaverne til dørs.

Hvis du har ambitioner om ledelsesansvar på sigt, så giver denne stilling dig gode muligheder for bedre indsigt i hvad ledelse i Novo Nordisk er.

I Novo Nordisk er det dine evner, dit engagement og dine ambitioner, der hjælper os med at forbedre mange menneskers liv.

Kontakt
Vil du vide mere om stillingen så kontakt Jess Ingemann Theil på +45 3079 8451.

Ansøgningsfrist
10. januar 2014

Project engineer

- Production
- Denmark - Hillerød

Do you want to use your knowledge within injection moulding/automation right in the intersection between R&D and Manufacturing? Then you could be our new Project Engineer in Prefilled Components Manufacturing and Development

About the department
Prefilled Components Manufacturing Development is a part of Device Manufacturing Development (DMD) in Hillerød.

Together with 18 inspiring colleagues, you will define and secure standards for the process development of components, injection moulding and decoration. Anticipate a diversified job where you will collaborate across many functions, from early R&D to manufacturing

The job
A large part of your job will be to drive minor projects on components, tooling and injection moulding. To this end, you focus on achieving the milestones within budget and timeframe. Moreover, you will contribute as an active team player, driving minor parts of large scale projects, together with one or more colleagues in Prefilled Components Manufacturing and Development. To succeed, you must thrive on navigating among an array of stakeholders across geographical and disciplinary boundaries.

Qualifications
For this position we wish to give the less experienced a chance! We do expect that you have finished your degree within Mechanical Engineering, Plastics Engineering or another technical discipline giving you comparable competencies. On a personal level, your colleagues would describe you as an easy-going, self-driven and responsible person. You have a systematic approach to your work and sound overview, which enable you to deliver quality every time – even when the pace is high. Finally, you have good stakeholder management skills and 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 Peter Fredsby at +45 3075 8971.

Deadline
10 January 2014

Ambitious Associate Managers for Novo Nordisk in Kalundborg

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

- Production, Team Leader
- Denmark - Kalundborg

Novo Nordisk is a healthcare company with 90 years of innovation and global leadership in diabetes care. We also have leading positions within haemophilia care, growth hormone therapy and hormone replacement therapy. Our ambitions and skilled employees have brought us far, but we are far from the finish line. This is why we invest massively in our global value chain, especially our production set-up. And this is where you will enter the scene.

About the Department
As a result of our success we are in need of experienced Associate Managers for a series of different teams in Kalundborg. The jobs range widely, which means that we are looking for profiles with different experience and specialisation. Some will have be managing academic teams in business support functions while others will lead the teams in the production. The teams typically consist of 8-20 employees.

The job
The various teams will work with e.g. process support, QA, QC, projects, EHS & IT and maintenance, or logistics, planning, purchase, economy, etc. As Associate Manager you will be an important key player driving your team and hereby Novo Nordisk towards new great results. Relying on your positive and catching energy, you can drive your team to realise their goals – also those exceeding their imagination. You will inspire, guide and set direction for your employees making visible what targets to pursue, why their efforts are so important and how they work efficiently and in compliance with the standards.

In this relation you will initiate continuous optimisations of our systems and processes from a LEAN approach. Changing for the better is a central part of what we do, and as a manager you will take the lead on ensuring innovation and improvement. You will be part of the department’s management team and have close dialogue with team leader across the departments. It is your responsibility to implement Novo Nordisk’s strategy and values within the department. Look forward to a job where you can pursue strong professional, personal and managerial development opportunities.

Qualifications
You have an academic background and managerial experience. As such, you are able to combine your professional knowledge with an open and appreciative managerial style to involve and ensure the dedication of your employees. At the same time, you have strong impact and are able to conduct decisions independently. By extension, you thrive in a changing environment where the goals are ambitious and the complexity is high. If you have no LEAN experience, you still have experience with systematic optimisation and problem-solving. Do you want to work in or support the production, you must have experience with GMP/GxP-regulated environment.

Novo Nordisk PS Kalundborg is a city within the city. The area is situated a good hour from Copenhagen and covers 270 football fields, including a private roadgrid. We are approx. 2.700 people in 15 factories, and we produce some 50% of the insulin in the world. In short PS in Kalundborg kan be summed up to this: endless development opportunities. If you feel like moving to Kalundborg, you will live in a city close to the woods and water, with good schools, sports and leisure time facilities and a lot more. If relevant, we have experience assisting newcomers in finding a new residence here. Visit our website and learn more about the different jobs and PS Kalundborg.

Visit our website and learn more about the different jobs and PS Kalundborg.

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.

We look forward to hearing from you: novonordisk.com/kalundborg-careers

Contact
For further information, please Contact Lili Behjat Kristensen at LBEK@novonordisk.com

Deadline
31 January 2014

Technical Engineers

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

- Production
- Denmark - Kalundborg

Use your GMP skills in the world’s largest insulin production situated in Kalundborg

Novo Nordisk is the world’s largest company within diabetes care. Our ambitions and skilled employees have brought us far, but we are far from the finish line. This is why we invest massively in our global value chain, especially our production set-up. And this is where you will enter the scene.

About the Department
As a result of our success we are in need of skilled Engineers for a series of different teams in Kalundborg. You will be part of a team responsible for providing technical support to one of our production sites. You and your colleagues will focus your efforts on ensuring that the equipment is always top-of-class and operates in compliance with the regulations. The team is, as such, an inevitable part of ensuring steady operations and secure production. Knowledge sharing and strong team work will be a natural part of your everyday, and we promise you exciting challenges that develop you.

The job
You will focus on ensuring compliance of our equipment for either the production or utility area. As part of this, you will contribute to ensuring that we continuously improve the equipment on a technical level and hereby improve efficiency. You will work with demands specifications, qualifications and execution of business imperative projects. During your workday some of your crucial tasks will be to conduct systematic problem-solving based on our LEAN tools, handling of deviations, change requests and preparing operational documentation. You will play a major part in relation to securing a proper level of maintenance. As the technical expert you will be responsible for handling contracts with internal and external suppliers.

Qualifications
You have a technical background as Engineer, supplemented with knowledge of fermentation, purification, utility or autoclaves. To achieve success you will need a systematic and analytical approach and be able to maintain the general view when working on several projects simultaneously and deliver your tasks in due time. It is equally important that you thrive working in a highly dynamic environment of constant change. It calls for an ability to face your colleagues and tasks with a positive attitude and the belief that every problem has a solution for you to find. To apply you must have proficiency in written and spoken Danish. Moreover, you must have good English skills.

Novo Nordisk PS Kalundborg is a city within the city. The area is situated a good hour from Copenhagen and covers 270 football fields, including a private roadgrid. We are approx. 2.700 people in 15 factories, and we produce some 50% of the insulin in the world. In short PS in Kalundborg kan be summed up to this: endless development opportunities. If you feel like moving to Kalundborg, you will live in a city close to the woods and water, with good schools, sports and leisure time facilities and a lot more. If relevant, we have experience assisting newcomers in finding a new residence here. Visit our website and learn more about the different jobs and PS Kalundborg.

We look forward to hearing from you: novonordisk.com/kalundborg-careers

At Novo Nordisk we strive to be the best. We are a world-leader within diabetes care and a major player within the haemostasis treatment as well as growth hormone and hormone therapy. This is why we can offer our employees the opportunity to pursue serious professional development.

Contact
For further information, please Contact Jacob Dahl Nielsen on+45 3075 5486

Deadline
31 January 2014

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