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Ambitiøs og energisk Automatik Supporter (Kalundborg, Danmark)

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Ambitiøs og energisk Automatik Supporter

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

- IT
- Danmark - Kalundborg

Er du et ambitiøst og passioneret menneske med en stor interesse inden for automatik og IT? I så fald er du måske vores nye Automatik Supporter.

Om afdelingen
Vi er en del af Novo Nordisks produktion i den del, der hedder Biopharm API, hvor vi blandt andet producerer NovoSeven. Vores opgave er at dyrke og rense Faktor VII, og du bliver en del af den afdeling, der supporterer produktionen vedrørende autimatik, IT, eksternt miljø, vand og energi.

Jobbet
Du bliver en del af et team på 12, hvor vi er 5 i automatikgruppen. Teamet er meget dedikeret og du vil have svært ved at finde bedre faglige sparringspartnere inden for automatik. Jeres opgave bliver sammen med den øvrige support afdeling at være med til at opjustere og validere procesenhederne i en ældre API linje, så den lever op til GMP kravene. Det giver dig en unik mulighed for at være med til at præge det fremtidige setup.

Dine opgave er overordnet support på automatik, herunder Procos og CTS/BMS. Det indebærer sikring af, at produktionssystemerne er i compliance med gældende regler, håndtering af daglig support, være bindeledet mellem proces og automatik i forbindelse med programændringer og fejlrettelser samt first line support i kontrolrummet, hvor man i samarbejde med kemikere håndterer hændelser for produktionen. Du vil have flextid med en arbejdsuge på 37 timer, som kræver at du er på arbejde i tidsrummet 9.00 til 15.00. Du bestemmer selv, om du møder tidligt og går tidligt eller omvendt. Ud over det vil du være en del af en vagtordning, som kræver, at du højst har 2 timer til sitet i Kalundborg, som også bliver din daglige arbejdsplads.

Læs mere om sitet i Kalundborg her: www.novonordisk.com/kalundborg-careers

For at løse dine opgaver i rette kvalitet og i rette tid kræver det, at du er dygtig til at prioritere og skabe overblik over produktionsprocessen. Den får du dels genne procesanalyse men i høj grad også gennem at skabe gode relationer og dialog med både support-kemikere, operatører, QA og vores eksterne leverandører. Du skal stille de rette spørgsmål, vise interesse og udfordre holdninger og processer.

Kvalifikationer
Du har en høj grad af interesse for automatik og en akademisk uddannelse, som kan være både som ingeniør, pharmaceut eller anden naturvidenskabelig retning. Du taler og skriver engelsk.

Som person er du meget ambitiøs med det du gør og er i det hele taget et passioneret menneske. Du har gennem erfaring – både på og uden for studie – vist, at du nemt skaber dialog med andre mennesker og ikke er bange for både at stille de ’dumme’ og vovede spørgsmål. Du er en team-player, og føler først du er en succes, hvis dit team er en succes.

Du har let ved at forstå processer og skabe dig et overblik, så du er i stand til at finde den gode løsning men også i stand til prioritere. Det gør det ligeledes nemt for dig at navigere i en kompleksorganisation, hvor prioriteterne hele tiden ændres.

Til gengæld tilbyder vi dig mulighed for at arbejde med usædvanligt dygtige kolleger, og vi tilbyder dig en bred vifte af muligheder for udvikling af din karriere.

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 Thomas Grønkjær på +45 3075 3607.

Ansøgningsfrist
1.december 2013

Teamleder til IM1 Multiline (Kalundborg, Danmark)

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Teamleder til IM1 Multiline

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

- Produktion, Teamleder
- Danmark - Kalundborg

Kan du gå forrest og motivere, inspirere og lede driftsoperatører, så har vi dit nye job klar til dig. Du kommer til at udfolde dig i en nyetableret afdeling i rivende udvikling, hvilket giver masser af muligheder og udfordringer. Vi står netop nu foran en større implementering af en ny finrensningslinje, og du kan hermed få muligheden for at spille en central rolle i denne spændende proces.

Om afdelingen
Du bliver en del af afdelingen IM1 Multiline Purification i Kalundborg. Vi har ansvaret for finrensning af diverse nye produkter til kliniske formål, der skal understøtte nye diabetes produkter kommer hurtigt på markedet. Afdelingen består p.t. af ca. 20 medarbejdere – og der mandes i øjeblikket op til at kunne imødekomme fremtidens udfordringer.

Jobbet
Dit overordnede mål er at sikre en stabil og effektiv produktion, hvor vi leverer i rette kvalitet, rette mængde, til rette tid og til lavest mulig omkostning. Skal du lykkes med dette, kræver det meget aktiv og synlig ledelse af de ca. 15 operatører, du får som faste medarbejdere i dit team. Der vil forekomme perioder, hvor der vil være nødvendigt at få flere medarbejdere om bord for at kunne løfte opgaverne. Du skal sørge for at rammerne er på plads ift. bemandingsplaner, opstilling af mål for teamet, ansættelser, eventuelle afskedigelser og oplæringsplaner for nye medarbejdere etc. Her sparrer du bl.a. tæt med din teamlederkollega og kollegerne i ledelsesteamet, og har samarbejde på tværs afdelinger og fabrikker.

Din helt afgørende udfordring er imidlertid, at sikre nødvendige kompetencer og den flexibilitet der skal til, for at kunne gennemføre de opgaver teamet stilles over for. Dette drives især af, at afdelingen løbende skal oprense forskellige nye produkter, og kunne håndtere de forandringer dette fører med sig.

Kvalifikationer
Du har en teknisk eller akademisk uddannelse, og/eller har fået skabt en god all round teknisk forståelse gennem din karriere som leder i et GMP-reguleret farmaceutisk produktionsmiljø. Du kender også til LEAN og har lyst til at arbejde aktivt hermed som del af din hverdag.

Din faglige identitet er først og fremmest som leder, og du trives derfor med at sætte retning og løse de problemer, der dagligt opstår i et højeffektivt produktionsmiljø. Du ved derfor også, at du får brug for dine gode kommunikationsevner, din naturlige empati og din fleksible indstilling ift. at få skabt løsninger, hvor alle involverede føler, at de er blevet hørt. Derudover skal du kunne bruge MS Office samt være god til både dansk og engelsk.

Site Kalundborg er en by i byen, kun 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.

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 Erik Nielsen Schmidt på +45 3075 2149

Ansøgningsfrist
17 november 2013

Team Leader for Oral Analytical Development (Måløv, Denmark)

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Team Leader for Oral Analytical Development

- Research & Development
- Denmark - Måløv

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

About the department
We are 42 colleagues, who will be organised in three teams, and are responsible for development and validation of analytical methods for oral protein products for preclinical and clinical trials. The department covers a broad range of analytical technologies (e.g. U/HPLC and dissolution).

The Job
You will spearhead a team of 4 analytical scientists and 6 technicians who carry out development and validation of analytical methods for phase 1, 2 and 3 of oral formulations of proteins. You have responsibility for the team’s performance and for ensuring that the objectives of the projects and the organisation are met or even exceeded. You make sure that we have the right resources and competences at hand at all times and urge your team to undergo both personal and professional development. You focus on creating a work environment that fosters job enthusiasm and you encourage and facilitate professional discussions. You seek to establish good collaboration with your stakeholders and participate in cross organisational projects and collaborations. You will lead a LEAN supporting culture where continuous improvement is a natural part of everyday work.

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

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

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

Deadline
20 November 2013.

Analysekemiker med QC-erfaring (Gentofte, Danmark)

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Analysekemiker med QC-erfaring

- Produktion
- Danmark - Gentofte

Er du den nye kemiker i New Product Support teamet i Novo Nordisk i Gentofte?

Vi er en afdeling i rivende udvikling. Vi arbejder med kvalitetskontrol af Biopharm’s brede portefølje af hæmofili produkter. Derfor har vi brug for straks at ansætte en medarbejder med solid QC-erfaring.

Om afdelingen
Teamets funktion er at udarbejde dokumenter til registreringsfiles samt overførsel af analysemetoder til datterselskaber i udlandet. I teamet sidder også afdelingens analyse- koordinatorer, som har ansvaret for projektledelse på tværs af organisationen. Afdelingen validerer analysemetoder til nye hæmofili produkter. Derudover supporterer vi de tre kemiske site QC laboratorier i Biopharm, hvor vi gør brug af vores tekniske viden kombineret med systematisk problemløsning.

Vi er en velfungerende afdeling med mange spændende opgaver, faglige udfordringer, mulighed for udvikling og stor kontaktflade ud af afdelingen. Her er en uhøjtidelig og god stemning med vidensdeling på tværs af teams og faggrupper. Selvom vi har mange opgaver, har vi en god balance mellem arbejde og fritid. Der er ca. 40 medarbejdere i afdelingen, organiseret i tre teams samt en stabsfunktion, som varetager tværgående aktiviteter.

Jobbet
Du og dine kolleger i teamet er ansvarlige for at overføre analysemetoder for de nye produkter i forhold til gældende myndighedskrav til vores datterselskaber. Du skal udarbejde protokoller, rapporter samt registreringsdokumenter.

Endvidere kan der være supportopgaver til site QC eller andre teams i afdelingen, hvorfor fleksibilitet og problemløsning også bliver en del af hverdagen. Alt i alt er det et udfordrende og udviklende job, der kræver energi, dynamik og fleksibilitet.

Kvalifikationer
Du er uddannet farmaceut, cand. Scient., eller lignende og har en solid QC-baggrund fra flere år i et miljø med GMP-kontrol. Her har du også arbejdet i et travlt miljø, og du trives med en uforudsigelig arbejdsdag. Du har for eksempel erfaring med godkendelse af analysemetoder, validering og standardisering af HPLC-analyser, og du er god til at skabe et klart overblik og prioritere dine opgaver; også når deadline nærmer sig. Du går aldrig på kompromis med kvalitet, og er samtidig god til at afslutte dine opgaver til tiden, og derefter gå videre til næste opgave med entusiasme og energi. Du er åben og engageret og kan inspirere og motivere dine kolleger. Du bruger dine LEAN-evner til at forny vores arbejdsprocesser og du arbejder systematisk og analytisk for at være i stand til at møde deadlines. Du taler og skriver både 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 Mette Riskjær Bell på +45 3075 7680

Ansøgningsfrist
20. december 2013

Senior Project Manager (Bagsværd, Denmark)

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Senior Project Manager

- Project Management
- Denmark - Bagsværd

Are you looking for an opportunity to leave your mark on the organisation and work with stakeholders on an international scale? This could very well be your chance to be part of a truly global workplace where passion and engagement are met with opportunities for professional and personal development.

About the department
Contract & Local Manufacturing, CMO Local Markets is responsible for establishing, monitoring and supporting our partners within licence and contract manufacturing worldwide. Our main office is located in Bagsværd, Denmark, but you can reside in a relevant country and work from here.

The Job
You develop and improve how we work with partners with the aim to securing stable processes and timely delivery of quality products. Specifically, you will deal with development and manufacturing at a Contract Manufacturing Organisation (CMO) located in for example Bangladesh, Cuba and Mexico. In other words, you head projects that aim at establishing and supporting our production activities. The projects vary in duration and content, and typically, you will focus on technology transfer, preparing gap analyses, and developing GMP and production documents. Moreover, you will work out the project plans and secure correct and timely execution. To guarantee proper follow-up, you monitor and report on the projects’ progression and pursue any changes to the project scope, schedule or cost. You will play an important role facilitating smooth and effective collaboration with our local manufacturers ensuring that they operate in compliance with corporate requirements. The position will require stays of short and medium length abroad, typically 1 week, 8-12 times per year.

Qualifications
You hold an MSc e.g. in Pharmacy or Engineering, or you have a comparable technical background. Irrespectively, you have experience with QMS systems and aseptic production of insulin, in particular formulation, filling and corresponding support functions. Alternatively, you have experience from QC/QA departments or project management knowhow within production, equipment or utilities. Either way, you have worked in an international environment and obtained technical knowledge as well as solid business understanding. You are dynamic, structured and persistent and have a technical, analytical approach to project/CMO management. You use your excellent communication skills to transmit project status to many different stakeholders, and you can deliver results in collaboration with a team as well as independently. Finally, you are proficient in English besides French, Arabic or Spanish.

At Novo Nordisk, you will have the opportunity to build a life-changing career in a global business environment. From research and development, to manufacturing, marketing and sales, we strive to improve quality of life for more than 366 million people living with diabetes.

Contact
For further information, please contact Kim Steffensen at +45 3079 70 08.

Deadline
28 November 2013.

IT Governance Manager (Bagsværd, Denmark)

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IT Governance Manager

- IT
- Denmark - Bagsværd

We are looking for an IT Governance Manager in Product Supply IT – a central unit responsible for setting direction and ensuring effective IT strategy execution globally. Are you experienced with IT in a complex and global environment? And are you motivated to facilitate central IT governance processes in Product Supply? Then this might be the job for you.

About the department
You will be part of the IT Strategy & Planning department. We Set direction and align ambitions for IT in Product Supply worldwide, and we govern the strategic project portfolio leading to fulfilment of ambitions. We have recently reorganised the function, which gives you a unique opportunity to put your personal finger print on a new team at an ambitious mission.

The Job
As IT Governance Manager you are responsible for maintaining IT governance standards and flows in Product Supply. A key responsibility in the job is facilitation of the Product Supply IT Council (PS-ITC), consisting of senior business leaders. IT projects above 5 MDKK worldwide are governed here, and you provide decision material, facilitate and document the meetings.

As a prerequisite to get PS-ITC acceptance to start implementing a new IT solution, projects need to attend one or more solution challenges with a group of central IT architects. The IT Governance Manager ensures planning and coordination of solution challenge sessions.

On top of these primary governance tasks you will drive ad hoc assignments in Strategy & Planning, such as KPI developments, balanced scorecards and stakeholder management tasks.

Qualifications
It is important that you work independently and can extract key information from a complex environment. You have most likely worked as IT consultant, IT project manager, or in a management governance function. Preferably you hold a master degree in a relevant field like Engineering, Computer Science or Business Administration combined with 3-5 years of working experience. Alternatively you have a shorter academic background, but bring more years of relevant working experience. Experiences with production IT and/or GxP environments are considered a strong advantage, but not a prerequisite.

As you will operate in multi-stakeholder environment, you need strong interpersonal skills and proven communication capabilities – particularly in writing. As a person you are reliable, structured, proactive and team oriented.As Product Supply is a global organisation you must speak and write English at negotiation level.

At Novo Nordisk, you will have the opportunity to build a life-changing career in a global business environment. From research and development to manufacturing, marketing and sales, we strive to improve quality of life for more than 366 million people living with diabetes. And 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 Anders Johansen at +45 3079 2794.

Deadline
17 November 2013.

IT Project Portfolio Manager (Bagsværd, Denmark)

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IT Project Portfolio Manager

- IT
- Denmark - Bagsværd

We are looking for an IT Project Portfolio Manager in Product Supply IT – a central unit responsible for setting direction and ensuring effective IT strategy execution on all larger IT projects globally. Do you have solid experiences with IT in a complex and global environment? And are you motivated to develop and mature project portfolio management as a leaver for strategy realisation? Then this might be the job for you.

About the department
The Project Portfolio Manager will be part of the Strategy & Planning department. We Set direction and align ambitions for IT in Product Supply worldwide, and we govern the strategic project portfolio leading to fulfilment of ambitions. We have recently reorganised the function, which gives you a unique opportunity to put your personal finger print on a new team on an ambitious mission.

The Job
A key responsibility in the job is development of strong business cases in order to optimise strategic roadmaps. As projects get prioritised and initiated, you will interact with the Project Managers on an on-going basis to monitor progress according to agreed timeline, scope, and cost. But also to maximise realisation of planned business benefits across the entire portfolio in line with the overall strategy.

The position contains a large amount of independency. You must seek influence on individual projects to apply standards and best practices. But as Project Portfolio Manager you are also obliged to report unsatisfactory progress according to the agreed master plan to the Product Supply IT Council in due time for proper mitigations.

Qualifications
It is important that you work independently and have solid experience with IT projects. You have most likely worked as IT Project Manager and/or Project Portfolio Manager and you have a relevant academic background within Engineering, Computer Science, Business Administration or the like.

Experience with production IT and GxP environments are considered a strong advantage.

You will operate in a multi-stakeholder environment. Hence you need strong interpersonal skills and proven change management capabilities. As a person you are reliable, structured, proactive, team oriented and you have a strategic mind-set.

As Product Supply is a global organisation you must speak and write English on negotiation level.

At Novo Nordisk, you will have the opportunity to build a life-changing career in a global business environment. From research and development to manufacturing, marketing and sales, we strive to improve quality of life for more than 366 million people living with diabetes. And 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 Anders Johansen at +45 3079 2794.

Deadline
17 November 2013.

Teamleder til IM1 Multiline Purification Support (Kalundborg, Danmark)

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Teamleder til IM1 Multiline Purification Support

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

- Produktion, Teamleder
- Danmark - Kalundborg

Kan du gå forrest og motivere, inspirere og lede driftssupportere bestående af akademikere og teknikere, så har vi dit nye job klar til dig. Du kommer til at udfolde dig i en nyetableret afdeling i rivende udvikling, hvilket giver masser af muligheder og udfordringer. Vi står netop nu foran en større implementering af en ny finrensningslinje, og du kan hermed få muligheden for at spille en central rolle i denne spændende proces.

Om afdelingen
Du bliver en del af afdelingen IM1 Multiline Purification i Kalundborg. Vi har ansvaret for finrensning af flere forskellige nye produkter til kliniske formål, der understøtter, nye diabetes produkter kommer hurtigt på markedet. Afdelingen består p.t. af ca. 20 medarbejdere – og der mandes i øjeblikket op til at kunne imødekomme fremtidens udfordringer.

Jobbet
Dit overordnede mål er at sikre en stabil og effektiv produktion, hvor vi leverer i rette kvalitet, rette mængde, til rette tid og til lavest mulig omkostning. Du står i spidsen for de ca. 12 driftssupportere, der er tilknyttet afdelingen. Du skal sørge for at sikre tilpasning af produktionslinjen til nye produkter, sikre kapacitetsoptimering, opstilling af mål for teamet, ansættelser, eventuelle afskedigelser og oplæringsplaner for nye medarbejdere etc. Her sparrer du bl.a. tæt med din teamlederkollega for operatører og kollegerne i ledelsesteamet. I fabrikken arbejder vi tæt sammen på tværs af afdelinger, og samarbejder tæt med de andre produktionsenheder i Kalundborg.

Din helt afgørende udfordring er at sikre den nødvendige balance mellem den daglige produktion og klargøring til de kommende kampagner.

Dette stiller store krav til teamets kompetencer og den flexibilitet, der skal til, for at kunne gennemføre de opgaver, teamet stilles over for. Dette drives især af, at afdelingen løbende skal oprense forskellige nye produkter, og dermed kunne håndtere de mange forandringer, dette fører med sig.

Kvalifikationer
Du har en akademisk uddannelse, og har erfaring som leder/projektleder i et GMP-reguleret farmaceutisk produktionsmiljø. Din viden ligger særligt i spændet mellem produktion, procesoptimering og projekter. Du kender også til LEAN, og har lyst til at arbejde aktivt hermed som del af din hverdag.

Din dagligdag er som faglig leder, hvor du trives med at sætte retning og løse de problemer, der dagligt opstår i et højeffektivt produktionsmiljø. Du ved derfor også, at du får brug for dine gode kommunikationsevner, din naturlige empati og din fleksible indstilling ift. at få skabt løsninger, hvor alle involverede føler, at de er blevet hørt. Derudover skal du kunne bruge MS Office og særligt Excel samt være god til både dansk og engelsk.

Site Kalundborg er en by i byen, kun 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.

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 Erik Nielsen Schmidt på +45 3075 2149

Ansøgningsfrist
17. november 2013

Internship in Global Environment, Health & Safety (Bagsværd, Denmark)

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Internship in Global Environment, Health & Safety

- Student and Internships
- 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 internships provide exciting learning opportunities for students who bring new ways of thinking to our company.

About the department
You will join 24 highly skilled colleagues in the department Global EHS, situated in Bagsværd. Here we focus our efforts on supporting the Novo Nordisk organisation in (Environmental, Health & Safety) matters. A part of our responsibility is to ensure EHS training of the organisation and to operate and develop procedures and tools to support our EHS Management System for the ISO14001 and OHSAS18001 certified areas in Novo Nordisk. Besides this, the department works with Novo Nordisk EHS Management System, EHS Strategies and EHS compliance issues.

The Job
Approximately ½ of your time you will become part of a small group of people in the department developing APB´s (“ArbejdspladsBrugsanvisninger”). The other ½ of the time you will be involved in different tasks and projects that matches specific competencies you may have as well as your preferences for development.

Qualifications
You have a good understanding within the area of chemistry. This understanding probably comes from your studies within chemistry, pharmacy or engineering. Due to the fact that a major part of the job is developing APB´s in Danish language, fluency in Danish is a pre-requisite. As a person you have a natural talent for collaboration and you have a quality mind-set. You are capable of working on very specific tasks that requires patience and your full attention as well as tasks and projects that draws upon your ability of being flexible and ready to become involved on an AD-HOC basis.

Practicalities
Requirement: Students who have conducted more than two years of their study.

Period: The internship position is a full-time position for 4-6 months.

Start date: 3. February 2014.

Contact
For further information, please contact Sif Press-Kristensen +45 3079 4509 or Tomas Schou Winther +45 3075 1458.

Deadline
20 November 2013.

Internship in Sales and Marketing Excellence, Novo Nordisk (Søborg, Denmark)

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Internship in Sales and Marketing Excellence, Novo Nordisk

- Student and Internships
- Denmark - Søborg

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 internships provide exciting learning opportunities for students who bring new ways of thinking to our company.

About the department
In Sales and Marketing Excellence we work to advance the way we most effectively bring the value of our innovative medicines to patients. We operate in a global cross-functional environment - across countries, product teams and functions - to ensure stronger processes and capabilities. We service the global marketing organisation with concepts such as the Novo Nordisk Marketing Academy for Excellence (G-MAX) and manage key governance functions such as the Global Sales Forum, PMComm (Lifecycle Management Committee) and the Biosimilar Commercial Group. Finally, we drive a wide array of commercial excellence projects, including development of innovative ways to strengthen the link between Marketing and Sales.

The Job
By joining the Sales and Marketing Excellence team you will get a unique opportunity to dive into novel ways of doing global marketing and sales. By supporting the establishment and implementation of key projects and offers you will learn about overall commercial processes and methods. You will be an integral part of our core team and tasks will vary from strategic and longer term to ad hoc practical support.

Qualifications
We are looking for an intern who is passionate about marketing and sales. You can drive projects independently taking a methodical approach to your work and tasks, but demonstrating flexibility when priorities change. In addition, you enjoy being busy and maintain a can-do positive spirit through times of pressure.

You are currently in your first or second year of studying on your master degree in business, or a related field. You already have some experience with cross-functional project management either in a work or academic setting. You have excellent interpersonal and communication skills. You must be fluent in both oral and written English.

Practicalities
Currently studying a Masters degree in business or a related field.

Period:The internship is a full time position for 4-6 months.

Start date: First week of Feb 2014

Contact
For further information, please contact Asger Jacobsen +45 3079 0161 or Mette Flinch Bertelsen +45 3079 5783.

Deadline
20 November 2013.

Tekniker til teknisk produktionssupport - Solid Dosage Forms (Måløv, Danmark)

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Tekniker til teknisk produktionssupport - Solid Dosage Forms

- Forskning og Udvikling
- Danmark - Måløv

Søger du nye udfordringer indenfor formulering eller analytisk metode udvikling af solid dosage forms? Vores Orale Protein Formulerings Enhed (OPF) i Måløv udvides I øjeblikket og derfor søger vi nye kollegaer til at dele vores dedikation og entusiasme mod vores ultimative mål. Novo Nordisk har sat sig det ambitiøse mål at være på markedet med en fast doseringsform af vores insulin og GLP-1 baserede lægemidler. I jobbet som tekniker vil du være involveret i CMC aktiviteter omhandlende produktion og analyse af fast doserede lægemidler i klinisk afprøvning. Dette involverer proces udvikling, opskalering, pilot produktion samt proces kontrol.

Om afdelingen
Vi er 31 medarbejdere i afdelingen, som vil blive organiseret i 2 teams og er ansvarlig for udvikling og fremstilling af orale protein produkter til prækliniske og kliniske studier. Afdelingen dækker over et bredt interval af procesteknologier til solid dosage forms, teknisk support samt projektledelse og eksekvering relateret til kvalificering af udstyr, utilities og facilitet.

Jobbet
Som en af vores teknikere bliver du ansat i et produktionsområde i vækst med afvekslende opgaver. Du bliver involveret i den daglige tekniske support til GMP produktion af tabletter til oral administration. Du vil få en bred vifte af ansvarsområder og opgaver i forbindelse med den daglige support. Da du bliver en del af det team, der supportere produktion af stabile doseringsformer baseret på peptider og proteiner, kan du glæde dig til en stilling med højt tempo, hvor quality/compliance er en vigtigt del af at sikre kvaliteten af vores GMP produktioner.

Dit primære ansvarsområde vil være teknisk support på følgende udstyr herunder koordinere implementering og test af nyt udstyr: Sigte, blander, rullekompaktor, tabletmaskiner (Korsch, Fette), coatere samt planlægge og udføre løbende forbedringsprojekt på produktionslinjerne. Dette indebærer at skrive ændringssager, afvigelsesrapporter, trendrapporter, instruktioner, systemevalueringer samt godkende kalibreringsdokumentation, indkøbe småudstyr og have kontakt til leverandører. Du vil også få mulighed for at deltage i projekter og vil her få ansvar for opdatering af dokumentation og ændringer i procedurer.

I det daglige samarbejde du med en lang rækker af vores kollegaer, for at sikre kvalificering af udstyr. Du er erfaren i brugen af IT systemer der understøtte den daglige GMP produktion ift. den supporterende del, som dokumentation og kvalitet. Du er bekendt med Lean metodik, kvalitetsbevidst og er en person der trives med løbende forandringer.

Kvalifikationer
Du er uddannet procesteknolog, farmakonom, laborant eller tilsvarende og har mindst et par års praktisk erfaring fra den farmaceutiske industri. På det personlige plan trives du med en høj grad af fleksibilitet – og med din evne til at omstille dig befinder du dig rigtig godt i en stilling, hvor dagene ikke ligner hinanden. Du er struktureret, en god planlægger og har stort fokus på kvalitet i dit arbejde. Samtidig sætter du pris på en uformel tone og tæt samarbejde i teamet. Du er engageret tager initiativ og søger selv udfordringer, du har et ”can do mind-set”.

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
For yderligere information kontakt Claus Juul-Mortensen +45 3075 9732 eller Jeanette Marcussen +45 3079 0529.

Ansøgningsfrist
17. november 2013.

Associate manager IM2 purification (Kalundborg, Danmark)

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Associate manager IM2 purification

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

- Produktion, Teamleder
- Danmark - Kalundborg

Kan du gå forrest og motivere, inspirere og lede akademikere og teknikere der supporterer produktionen af livsvigtig Insulin, så kan dette være dit nye job. Du kommer til at udfolde dig i en succesrig afdeling i rivende udvikling, hvilket giver masser af muligheder og udfordringer. Vi står netop nu foran en større opskalering og forbedring af produktionen, og du spiller en central rolle i den spændende proces. Du har dermed muligheden for at blive leder i en af de mest profilerede fabrikker i Novo Nordisk.

Om afdelingen
Du bliver en del af afdelingen Insulin Purification IM2. Vi står for finrensning, der er sidste del af API produktionen af Novo Nordisk’s verdensklasse insulinprodukter. Kulturen i afdelingen er præget af historien, de gentagne gange har vist at vi kan hvad vi vil, og vi npr de mål vi sætter os. Afdelingen består p.t. af ca 150 medarbejdere – og der mandes i øjeblikket op til at kunne øge produktionskapaciteten.

Jobbet
Dit overordnede mål er at sikre en stabil og effektiv produktion, hvor vi leverer i rette kvalitet, rette mængde til rette tid og lavest mulig omkostning. Skal du lykkes, kræver det meget aktiv og synlig ledelse af de medarbejdere, du får i dit team. Du skal selvfølgelig sørge for, at rammerne er på plads ift. bemandingsplaner, opstilling af mål på både team- og medarbejderniveau, ansættelser, eventuelle afskedigelser og oplæringsplaner for nye medarbejdere etc. Her sparrer du bl.a. tæt med dine teamlederkollegaer og kollegerne i ledelsesteamet, ikke mindst på det strategiske område, som også omfatter samarbejde på tværs af afdelinger og fabrikker.

Din helt afgørende udfordring er at få teamet til at spille aktivt og positivt med i forhold til de udfordringer og forandringer de møder i deres hverdag. Du skal på daglig basis og i mange sammenhænge forklare, hvorfor det er rigtigt og nødvendigt at ændre rutiner, arbejdsgange, roller og strukturer i organisationen. Samtidig skal du kunne træffe og gennemføre de nødvendige beslutninger i en kompleks hverdag.

Du referer til afdelingslederen og indgår i afdelingens ledelsesteam.

Kvalifikationer
Du har en akademisk uddannelse (f.eks. cand. scient., ingeniør eller farmaceut)og har eventuelt en god allround teknisk forståelse. Du har erfaring fra et GMP-reguleret farmaceutisk produktionsmiljø og har et godt kendskab til LEAN. Du forstår hvorfor Kvalitet og Compliance er meget vigtige parametre for Novo Nordisk, og hvordan disse parametre er med til at skabe værdi for patienten.

Din faglige identitet er først og fremmest som leder, og du trives med at sætte retning og løse de problemer, der dagligt opstår i et højeffektivt produktionsmiljø. Du bruger dine gode kommunikationsevner, din naturlige empati og din fleksible indstilling ift. at få skabt løsninger, hvor alle involverede føler, at de er hørt.

I Novo Nordisk er det dine evner, dit engagement og dine ambitioner, der hjælper os med at forbedre mange menneskers liv. Du får chancen for at arbejde sammen med usædvanligt talentfulde kolleger og mulighed for at udvikle dig fagligt som personligt.

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 Peter Sørensen på +45 3079 2718.

Ansøgningsfrist
27. november 2013

Internship in Biopharm, Mammalian Cell Banking (Hillerød, Denmark)

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Internship in Biopharm, Mammalian Cell Banking

- Student and Internships
- Denmark - Hillerød

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 internships provide exciting learning opportunities for students who bring new ways of thinking to our company.

About the department
The department works with production of mammalian cell banks and the development of cultivation processes for mammalian cells. The Mammalian Cell Banking team works with the production of cell banks for both internal use in the department and development business area as well as for our production business area.

In the Bioreactor team we are working with different process types - batch, fed-batch and continuous processes - and strive for constant optimization of these processes right from the start of the inoculation train to the last step in the production bioreactor. This work is performed across scales from shaker flask experiments up to pilot scale bioreactors. In close collaboration with key internal stakeholders in our Research Unit as well as other business areas we work on establishing robust and reliable processes.

The job
You get the opportunity to join a high performing team in Hillerød, Denmark, responsible for the production of mammalian cell banks. The cell banks are used within whole NN for production of API for TOX and clinical studies as well as in late stage projects. This means that you have the opportunity to work with a variety of stakeholder with different mindsets. You will support the team and will gain insight into Good Manufacturing Practice (GMP), which is the key for development and production of drugs. Be a part of our team in day-to-day business processes and tasks – preparation and review of documents as well as hands-on experience in e.g. lab work and environmental monitoring. In this role you will perform experiments, help to develop/ensure timely delivery of our products, work with team members on writing and reviewing documents, and assist with optimizing our daily procedures.

Qualifications
We are looking for an intern who is curious and passionate about biology. You are currently studying on your master’s degree in pharmacy, biology, bioengineering or other relevant field. General knowledge of cell biology and key methodologies (database analysis, practical experiments in the lab and microbiology) is preferred. We expect candidates to be service minded, curious to learn something and bring a can-do attitude. Fluency in both oral and written English, sound personal judgment and excellent interpersonal skills are required.

You are an outgoing person with a personal drive and dedication. You have professional and personal impact that is reflected in your desire to take initiative and delivery the right quality. In addition, you thrive in a busy environment and bring a can-do attitude and a healthy sense of humour to your work – even when the pressure is on. Finally, you must have strong work ethic and willingness to take responsibility for your own learning.

At Novo Nordisk we use our skills, dedication and ambition to help people with Diabetes and Haemophilia and change their lives. By working with us you will have the opportunity to do the same in a global business environment.

Practicalities
Requirement: Students in their first or second year of their master studies.

Period: The internship position is a full-time position for 4-6 months.

Start date: 01 feb 2014

Contact
For further information, please contact Christiane Wiendahl; +45 3079 4862.

Deadline
30 November 2013

Senior Supply Chain Project Manager (Hillerød, Denmark)

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Senior Supply Chain Project Manager

- Supply Chain and Logistics
- Denmark - Hillerød

Do you want a position with great influence and responsibility where you help ensure that our patients get their product on time? Then you have the possibility to become Senior Supply Chain Project Manager for Logistics in Novo Nordisk, Diabetes Finished Products (DFP).

About the department
Site Denmark Logistics is, among other things, responsible for the long and short term planning, coordination and prioritization of activities within the Novo Nordisk’s production of diabetes products. The goal for the department is to support a stable and ambitious supply chain organization, which is ensured through a close cooperation with the production, top performance on delivery and a proactive communication with our customers. We work with a large network of stakeholders within Novo Nordisk, from production to launch coordination and sales offices all over the world. We have a great focus on getting our products fast to market both in regards to a stable flow in our existing production, but also when launching new products. LEAN is therefore a natural part of the way we operate.

The Job
You will be part of a team of supply chain project managers and supply chain analysts. The main focus of the team is to support and develop logistics in Site Denmark. You will be project manager for a wide range of projects spanning from short term one-man projects to major cross functional projects across Site Denmark Logistics and Manufacturing. Specific tasks would be launch coordination of major launches and scrap analysis. You can look forward to a position with a high degree of influence and you will have the chance to work with continuously improving our logistics processes. You have a possibility to utilize your project management, analytical and communicative skills. You will be appreciated for your ability to present complex issues in a simple and understandable fashion for managers and give your suggestions to actions.

Qualifications
You are passionate about logistics, project management, data analysis and process optimization. You probably hold a degree as cand.merc, engineer or similar and you are fluent in English. You are motivated by ambitious goals and you can make things happen. Your strategic and analytical mindset enables you to challenge our processes and will make you a good sparring partner. You are super user in MS Excel and preferably you have experience with MS projects, SAP, SAP APO and SAP BW.

Feel free to submit your application/CV in either Danish or English,

At Novonordisk, 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 Jens Frost at +45 3075 6439.

Deadline
24 November 2013

Udstyrstekniker (Bagsværd, Danmark)

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Udstyrstekniker

- Forskning og Udvikling
- Danmark - Bagsværd

Har du flair for udstyr og styr på kvaliteten? Vi søger en selvstændig og dygtig tekniker med erfaring fra anlægs- og udstyrs kvalificering og med flair GMP og dokumentationsarbejde.

Om afdelingen
Afdelingen er Downstream Pilot Plants, afd. 201 i Bagsværd. Afdelingen består af 3 teams, heraf to kampagne teams der oprenser proteiner til toksikologiske og kliniske studier og et supporterende team, der understøtter driften i tæt samarbejde med pilot anlæggene, Technical Support samt QA funktioner. Den ledige stilling hører til i Supportteamet, der består af 5 teknikere og 2 kemikere. Vi løser en lang række opgaver i forbindelse med drift og vedligehold af eksisterende anlæg og udstyr, kvalificering og implementering af nyt udstyr, monitorering af forsyninger og utility, prøvekoordinering samt vedligeholdelse og udvikling af kvalitetssystemer og processer. Du vil i teamet få en flok højt engagerede og hjælpsomme kolleger, der oftest har et lunt glimt i øjet.

Jobbet
Dit hovedansvar vil blive udarbejdelse af dokumentation, der bidrager til at holde pilotanlæggene i compliance. Du kommer til at stå for at udarbejde og styre ændringssager på udstyr samt at udarbejde dokumentation til kvalificering og commisioning. Herudover er opgaverne behandling af afvigelser, opdatering af instruktioner der beskriver arbejdsgange i afdelingen, rapporteringer m.m. Din hverdag vil veksle mellem undersøgende arbejde med at finde de rigtige løsninger og dokumentationsarbejde med input og sparring fra kollegaer med forskellig faglig baggrund.

Kvalifikationer
Du er uddannet kemotekniker, procesteknolog eller anden teknisk uddannelse. Du er skarp på planlægning, gennemførsel og dokumentation af ændringssager. Vores arbejde udføres i henhold til GMP, og vi forventer derfor at du besidder en systematisk tilgang til at udføre og afslutte dine opgaver og at du har en god ordenssans.

Derudover vil vi meget gerne bringe andre af dine kvalifikationer i spil, så erfaring med SAP-systemer, vedligeholdsplaner eller CRS-relaterede opgaver vil være en fordel. Vi lægger vægt på at du har et godt humør og kan lide at tage fat i opgaverne, også når de ikke bliver lagt tilrette foran dig. Evne til samarbejde og kommunikation er en nødvendighed, da opgaverne bliver løst i fællesskab. Vores hverdag er omskiftelig og derfor er fleksibilitet og omstillingsparathed hos vores kollegaer en vigtig forudsætning.

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 Martin Skarnes på +45 3079 8186, Pia Lavgaard Sørensen på +45 3079 1708 eller Vibeke Bohn Edwards på +45 3079 8463.

Ansøgningsfrist
19. november 2013

Internship in ITS Regulatory Solutions (Bagsværd, Denmark)

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Internship in ITS Regulatory Solutions

- Student and Internships
- 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 internships provide exciting learning opportunities for students who bring new ways of thinking to our company.

About the department
ITS Regulatory Solutions is responsible for System Management of some of Novo Nordisk A/S most important IT systems. We are responsible for Novo Nordisk A/S’s document handling solutions with more than 15,000 users, our global SharePoint solution with more than 30,000 users as well as a portfolio of IT systems within Regulatory Affairs.

You get the opportunity to work with a highly dedicated global team with daily contact to our user communities and vendors throughout the world.

The job
The candidate will work with the daily tasks in a Corporate IT Department and also with management of IT problems, Release and Project Management.

The daily tasks involve contract management, user access management and other administrative tasks that ensure our high compliance level.

Furthermore, the candidate will work on project oriented tasks as part of maintaining our IT Systems. The work involves Project Management, Release Management and Problem Management.

As part of the internship, the candidate will work with and be introduced to important areas of managing IT in the pharmaceutical industry, such as ITIL processes and GXP regulations.

Qualifications
We are looking for an intern with passion for the interplay between business and IT and especially IT System Management in corporate organisations. You are currently studying your master’s degree within IT, engineering or another relevant field. You must have strong general IT and Microsoft Office capabilities. It is a benefit if you have got insight into corporate use of IT, Data Bases and Quality Management with regards to the health industry and Project Management. Coding abilities are not required.

We expect candidates to be service-minded, thrive in a busy environment and bring a can-do attitude. Ability to manage a large volume of tasks (with supervision), fluency in both oral and written English, sound personal judgement and excellent interpersonal skills are required.

You are an outgoing person with a strong personal drive and dedication. You have professional and personal impact that is reflected in your desire to take initiative. In addition, you bring a healthy sense of humour to your work – even when the pressure is on. Finally, you must have strong work ethic and willingness to take responsibility for your own learning.

At Novo Nordisk we use our skills, dedication and ambition to help people with diabetes and change their lives. By working with us you will have the opportunity to do the same in a global business environment.

Practicalities
Requirement: Studying a relevant master degree

Period: The internship position is a full-time position for 6 months.

Start date: 01 February 2014

Contact
For further information, please contact Lars Korsholm Lauridsen; +45 3079 1479.

Deadline
20 November 2013

Internship in IT, Quality & Corp. Development (Bagsværd, Denmark)

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Internship in IT, Quality & Corp. Development

- Student and Internships
- 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 internships provide exciting learning opportunities for students who bring new ways of thinking to our company.

About the department
R&D Solutions is responsible for System Management of critical IT systems used in the clinical trial process in Novo Nordisk A/S. We are 14 employees based in Bagsværd and also have four colleagues working from the Indian part of our organisation. By joining R&D Solutions you will get the opportunity to work with a highly dedicated global team with large contact to our user communities and vendors throughout the world.

The job
You will support the R&D Solutions team in day-to-day business processes and tasks relevant for operating a corporate IT department. This includes system releases, handling IT security issues, contract management, user access management and other administrative tasks. You will also be involved in project oriented tasks as part of maintaining our IT systems, and this will often be in close dialogue with line of business within Clinical Operations. As part of the internship you will gain experience with important areas of managing IT in the pharmaceutical industry and ensuring that IT solutions are implemented and operated effectively in compliance with both external and internal requirements.

Qualifications
We are looking for an intern with passion for the interplay between business and IT and especially IT System Management in corporate organisations. You are currently studying on your master’s degree within IT, Engineering or another relevant field. You must have strong general IT and Microsoft Office capabilities and it is a benefit, but not a requirement, that you have insight into corporate use of IT, data bases and quality management within the health industry. Fluency in both oral and written English, ability to manage a large volume of projects (with supervision), sound personal judgment and excellent interpersonal skills are required.

We expect that you are service service-minded and an outgoing person with a strong personal drive and dedication. You have professional and personal impact that is reflected in your desire to take initiative. In addition, you thrive in a busy environment and bring a can-do attitude and a healthy sense of humour to your work – even when the pressure is on. Finally, you must have strong work ethic and willingness to take responsibility for your own learning.

At Novo Nordisk we use our skills, dedication and ambition to help people with diabetes and change their lives. By working with us you will have the opportunity to do the same in a global business environment.

Practicalities
Requirement: Students in their first or second year of their master studies.

Period: The internship position is a full-time position for 4-6 months.

Start date: 3 Feb 2014

Contact
For further information, please contact Lotte Høeg Juhl Jensen; +45 3079 1002.

Deadline
20 November 2013

Ambitious GMP Partner (Bagsværd, Denmark)

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Ambitious GMP Partner

- Quality, senior position
- Denmark - Bagsværd

Are you ready to take the next step in your career, you now have the opportunity. You will be a key player in ensuring quality and compliance for a specific business area consisting of a number of departments/teams. You will be a member of the Management team and primary sparring partner for the Managers on GMP issues.

About the department
We are looking for a dynamic GMP Partner to one of our sites on Zealand , where we focus on aseptic production. The GMP Partner and GMP Coordinator setup is a matrix organisation, where you will head the GMP Coordinators across different departments as their Professional Manager.

The Job
As GMP Partner you have the overall responsibility for setting the targets on quality and compliance for your area and for making sure that they will be met. As such, you bring in the latest knowledge within GMP when you challenge our business managers to bring GMP and quality to the top of the agenda. You ensure that the area is in compliance with the authorities’ and Novo Nordisk’s regulations, including ISO9001:2008, and you will become your area’s representative in our cross-organisational GMP group/GMP board. You are also responsible for Quality Management Review (QMR), and you play an active role in audits and inspections, having the GMP Coordinators as your skilled co-workers. You will participate in our GMP network meetings with your peers for sparring, sharing and development of GMP and QMS related topics. The job involves contact and interaction to many different stakeholders in the organisation, from operators, maintenance, LEAN professionals, project managers and to all line management levels.

Qualifications
You hold a degree at minimum master’s level. Your academic background is topped with experience from a pharmaceutical production company where you have gained solid experience within quality, GMP and ISO9001. You are used to create results through projects and know the importance of team collaboration. To succeed, you must thrive in a role where you take leadership, initiate and coordinate a large number of actions and projects. This requires an excellent overview, a structured mind-set and a dedicated way of working as well as very good communication skills. Working cross-organisationally, your networking skills will also be crucial as well as your ability to balance when to compromise and when to stand firm. Finally, you must master English and Danish, written and spoken.

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

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

Contact
For further information, please Contact Søren Karmdal on + 45 3079 1257.

Deadline
18 November 2013.

Enthusiastic GMP Supporter (Gentofte, Denmark)

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Enthusiastic GMP Supporter

- Quality, senior position
- Denmark - Gentofte

Are you ready to take up the challenge to be the one securing and enhancing the quality and compliance level of a production environment? We are looking for a GMP Supporter with the skills, knowledge and overview to secure the department’s GMP and compliance level, making it ready for inspection at all times.

About the department
You will join a high-tech filling factory in Gentofte, where we produce NovoSeven®, GlucaGen® and other Biopharm products. Our responsibilities include: wash and sterilisation of equipment, formulation, sterile filtration, sterile filling, freeze drying and visual inspection.As a GMP Supporter you will join the management team consisting of two team leaders, two specialists and the department manager to whom you will report directly. You will be the primary responsible for the ensuring the compliance level which will be one of the primary focus areas in the department in the coming years.

The Job
Together with the Management team you will be responsible for ensuring that we comply with Novo Nordisk’s quality system. As such, you participate in determining the quality objectives, and through planning and follow-up on quality activity plans and conduction of quality management reviews you ensure that the standards are met. In this respect, you will join the support function, cooperate across the entire area and have close interaction with Quality Assurance. In this way, you provide sparring and consulting on quality and compliance inquires, as well as you interpret processes and come up with quality enhancing initiatives on the problems and improvements that you face in your everyday.In addition, you will drive and coordinate the quality work and secure continuous improvements of audits and inspections, as well as you coordinate and conduct training within GMP.

Qualifications
Besides your relevant education as engineer, pharmacist, cand. scient or similar, it is important that you have a strong sense of quality and experience working with GMP. You have experience working with LEAN tools, preferable in relation to non-conformity investigations.As a person you are a problem solver and you thrive in a dynamic work environment. You are able to make decisions in complex situations. Because quality and precision is essential for the pharmaceutical industry, it is important that you have a high sense of quality. You are able to communicate and be accurate in writing and speaking in both Danish and English. At last but not at least you are out going and enjoy building relations with stakeholders across functional areas and at any organisational 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.

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

Contact
For further information, please Contact Søren Karmdal on + 45 3079 1257.

Deadline
21 November 2013.

Kemikervikar (Gentofte, Danmark)

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Kemikervikar

- Produktion
- Danmark - Gentofte

Vikar for produktionskemiker til fermentering af væksthormon.

Om afdelingen
Til vores processupportteam, der består af 11 kemikere og 3 tekniker og 1 laborant, søger vi en kemiker-vikar i 15 måneder med blik for kvalitet og produktion til at indgå i den daglige support af afdelingens processer. Vores afdeling dækker hele kæden fra fremstilling af produkt i værtscelle til et færdigt, frysetørret produkt, der kan sendes videre til formulering og fyldning. Vores afdeling består af 2 produktionsteams (fermentering og finrens) og af to supportteams: Et med processupport og et med udstyrs- og it-support.

Jobbet
Dit ansvar bliver at supportere den daglige produktion i fabrikken inden for fermentering og recovery. Derudover er det dit job at vurdere data ifm. produktion af vores lægemidler og dermed sikre, at vi altid holder det høje kvalitetsniveau, der kendetegner Novo Nordisk. Du har derfor løbende konstruktiv dialog med dine kolleger og produktionen om, hvordan vi sikrer kvaliteten, forbedrer vores arbejdsmetoder og undgår fejl. Når vi har udfordringer i processen, har du overblikket, tager initiativ og involverer dine kolleger, så problemerne løses hurtigt og effektivt

Kvalifikationer
Du er evt. nyuddannet civilingeniør i kemi/bioteknologi, farmaceut, biolog eller lignende med et godt resultat. Det er et plus, men ikke et krav, hvis du har erfaring med GMP, fremstilling af lægemidler og myndighedskrav til den farmaceutiske industri. Det er derimod vigtigt, at du trives i en hverdag med hovedvægten lagt på dokumentations- og databearbejdning blandet med akutte problemstillinger. Du kan lide at arbejde koncentreret med data, er kendt for at være struktureret og analytisk, og du har tidligere vist, at du kan sammenholde og gennemskue mange data. Du er god til at prioritere dine opgaver og trives i et dynamisk og til tider uforudsigeligt produktionsmiljø. Engagementet hos dig er tydeligt, både når det gælder håndtering af gentagne kendte arbejdsprocesser, og når du står overfor en ny og ukendt problemstilling.

Som person er du energisk og arbejder godt i samspil med andre. Du er desuden god til at skabe en positiv stemning og har en høj grad af ansvars- og kvalitetsbevidsthed.

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 Magnus Erreth på +45 3075 0576.

Ansøgningsfrist
17. november 2013
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