EURES SOC: PROCÉS DE SELECCIÓ EMPRESA DANESA DEL SECTOR BIOFARMACÈUTIC

NOVO NORDISK IS LOOKING FOR HIGHLY QUALIFIED ENGINEERS AND PROFESSIONALS TO SUPPORT PHARMACEUTICAL
MANUFACTURING IN DENMARK. Novo Nordisk is a global healthcare company with more than 90 years of innovation and leadership in
diabetes care employing approximately 41,000 people in 75 countries and markets its products in more than 180 countries. Novo Nordisk
employees share the ambition to continuously make a difference for more than 24 million people living with diabetes and other serious
chronic conditions. You will be in excellent company, working alongside dedicated and highly competent colleagues. We are at the forefront
of development in technology and processes, and we know success depends on dedicated
individuals contributing to every step of the way.
This is where we need you.
WE ARE ESPECIALLY HIRING EMPLOYEES EXPERIENCED IN: Fermentation, CIP / Cleaning, Freeze drying, Aseptic / Clean
room, HPLC, Purification, Injection moulding, Process support, Environmental monitoring, HVAC, Automation, Serialisation,
Utility, IT in manufacturing / IT System Management, Validation, QA and Audit, GMP /or quality management systems,
Compliance and documentation, Project and Management experience from pharma/ food manufacturing.
HOTSPOT IS NOT ONLY A BUZZWORD
- IT IS A PLACE IN DENMARK
Interested in a Life-changing career?
Read more about opportunities at Novo Nordisk
at novonordisk.com/manufacturing
MAKING A MOVE: We are part of an international company with colleagues in all corners of the world. More and more
nationalities join us at Kalundborg, so our work environment is increasingly international and we will help you getting settled in.
“Even though the weather is a bit colder than in Northern Spain I very much enjoy my life in Denmark. I came here because I saw that there
were great opportunities for me to work within the pharmaceutical industry and in an international environment. I got an inspiring job I
would not have gotten in Spain and I am part of a team where there are development opportunities for everyone. Now Denmark feels like
home and I just keep improving my Danish and evolving in my position at Novo Nordisk Manufacturing Kalundborg,”
says Flor Abalde Gil, who moved from Spain to Denmark in 2012.
If you are interested in meeting us please follow the detailed instructions in:
https://www.sepe.es/contenidos/personas/encontrar_empleo/encontrar_empleo_europa/paises/dinamarca/empleo_dinamarca.html
• Meet us in Barcelona 12 May 2016, hours 11.00 – 18.30
• Meet us in Madrid 10 May 2016, hours 11.00 – 18.30 A work life
balanced career
in Denmark?
WE HELP YOU
SETTLE IN

NOVO NORDISK: RECLUTAMIENTO SECTOR FARMACEUTICO Y BIOCIENCIA.
MAYO 2016 Madrid y Barcelona
El servicio público de empleo danés “Workindenmark” y “EURES España” organizan un
proceso de selección para la compañía del sector bio-farmacéutico
El proceso de selección tendrá lugar en Madrid el día 10 de Mayo y en Barcelona el 12 de Mayo.
Novo Nordisk.
Principalmente buscan ingenier@s con alguna experiencia en el sector, pero también especialistas
de Bio-ciencia, Farmacia...etc con experiencia; revise las competencias exigidas en cada uno de
los puestos, no sólo la titulación.
Puede usted consultar la descripción de la oferta y valorar si su perfil se adapta a los requisitos que
demandan.
No está culturalmente aceptado en Dinamarca publicar el salario en las ofertas de empleo, pues se
negocia. En todo caso los salarios en Dinamarca son bastante elevados y están de acuerdo a las
cualificaciones de los candidatos (para cualquier duda sobre este u otros aspectos relacionado con
un puesto en concreto puede solicitar la información en el teléfono que se facilita en cada uno de los
puestos ofertados)
Procedimiento:
Si usted está interesad@ en una o varias ofertas y quiere presentar su solicitud, siga las siguientes
instrucciones:
-Envíe su CV y Carta de presentación en inglés a “eures.nordicos@sepe.es”
-En el asunto del mail escriba el nombre(s) del puesto de trabajo al que se postula seguido
del nombre de la ciudad
-Si la empresa considera su perfil apropiado será usted invitad@ a asistir al evento y la empresa le
hará una entrevista de trabajo.
(Madrid o Barcelona) donde usted estaría dispuesto a asistir a la
entrevista.
La fecha límite para enviar su CV y Carta de presentación es el jueves 5 de Mayo.
Las ayudas TTE-FSE de EURES ofrecen cobertura de gastos de viaje para las entrevistas de trabajo.
Puede consultar si cumple usted los requisitos en el siguiente enlace:
https://www.sepe.es/contenidos/personas/encontrar_empleo/encontrar_empleo_europa/tu_primer_e
mpleo_eures.html

PUESTOS OFRECIDOS:
• Automation Professional in Diabetes Finished Products (Ingeniería)
• QA assistant with great SAP skills (Farmaeconomía, técnico de laboratorio, danés)
• LEAN Partner in Quality Assurance (Formación en LEAN)
• Asset manager (Master en Ingeniería)
• Director for Strategy & Planning (Ingenierías, formación en gestión de lineas de suministro o formación
en finanzas o administración de empresas)
• Business Controller in Diabetes Finished Products (MBA)
• Associate Manager in Device Manufacturing & Sourcing (Título en ciencias, ingeniería o farmacia)
• Process Supporter for Tablet Production (Formación en farmacia, Ingeniería Química o similar)
• Operations Manager for CMO tablet and Packaging (Formación en farmacia, Ingeniería Química o
similar)
• QA Supplier Engineer in DMS Operation QA (Ingeniería Industrial con experiencia en sector pharma)
• Be the Inspiring and Proactive Associate Manager - Global QA Oversight (Master en ingeniería,
farmacia o relacionada)
• Senior QC Professional for Raw Materials (Master en farmacia, ingeniería o ciencias)
• Associate Manager (Master en ciencias, ingeniería o relacionado)
• QA Chemist for Manufacturing Development in Biopharm (Master en ciencias, química, farmacia...etc)
• Structured leader for team in Biopharm Manufacturing Development (Ingeniería, farmacia o similar)
• Aseptic Process Supporter in Diabetes Finished Products (Master en Ingeniería, farmacia o relacionada
con 1 ó 2 años de experiencia)
• QA Professional in Device Manufacturing & Sourcing Process QA (Master en ingeniería industrial,
maquinaria, plásticos o similar)

Automation Professional in Diabetes Finished Products
Department: Production
Place: Denmark - Bagsværd
Are you looking for an excellent opportunity to apply your knowledge within automation to support the local insulin production at Novo
Nordisk? Do you know what it means to set the standards of tomorrow? Then you may be our new Automation Professional to our filling
process at Diabetes Finished Products(DFP).
About the department
You will be part of the Technical Support Team, at Line 29. We are experienced and highly engaged Specialists, Technicians and
Professionals, all responsible for their various fields of expertise and to support the insulin production filling of 3 ml cartridge. You will be
working closely together with Specialists, Technicians, Professionals and Operators to secure technical support, systematic problem
solving and optimization of our processes, Standard Operating Procedures(SOP’s) and different systems. We are highly engaged in
using Lean tools and are striving to deliver best in class support to our line filler.
The position
The filling lines are a vital part of the aseptic production. As an automation professional you will provide support, guidance and active
make validation, design/modifications and failure investigations related to automation issues together with your colleagues. You will be
the key person in securing correct automation system requirements are maintained and adjusted, to ensure that relevant automation
requirements are preserved. You will also participate in developing the future technology within the filling area in Site Bagsværd (BA).
In addition to this you will play an active role in the identification and sharing of best practises, together with your colleagues from sites
globally.
Qualifications (Ingeniería)
You have a relevant academic background as an engineer, automation technology or similar education.
You have some experience from aseptic production and project execution, but this is not a demand.
You have experience with pharmaceutical processes and equipment from an automation perspective, as well as knowledge about Good
Manufacturin Practise(GMP), 21CFR Part11 and other relevant regulatory requirements. We also expect you to be familiar with
validation aspects from an automation perspective. Basic understanding of Programmable Logic Controllers(PLC) code, Supervisory
Control and Data Acquisition (SCADA) and Manufacturing Execution System(MES) is needed. You will primarily work in S7
Programmable Logic Controllers(PLC) technology.
You are a team player, yet capable of delivering results independently when required. You have good networking skills and a well-
developed understanding of other cultures. As the job requires interacting with many different people, at different levels within the
organisation, good communication skills as well as a service minded and professional approach is required.
Working at Novo Nordisk
At Novo Nordisk, we use our skills, dedication and ambition to help people with diabetes. We offer the chance to be part of a truly global
workplace, where passion and engagement are met with opportunities for professional and personal development
Contact
For further information, please contact Michael Tanggaard Staunstrup on +45 3075 1832

QA assistant with great SAP skills
Department: Quality
Do you want to work with Quality Assurance and secure quality mind set in a complete supply chain? Do you like to cooperate with our
internal stakeholders all over the world and secure the quality of master data for all Novo Nordisk packaging sites worldwide? Then we
have the right job for you in Sourcing QA.
Sourcing QA, Team Printed Packaging Materials is responsible for Quality Assurance of Printed Packaging Materials for Novo Nordisk
A/S Products. The team is responsible for release and approval of Printed Packaging Materials for all our Danish packaging sites, and
for approving master data for packaging orders for all Novo Nordisk packaging sites. Furthermore we have a global QA responsibility for
setting direction regarding incoming QC test methods and approval of specifications for Printed Packaging Materials worldwide.
In the years to come we are facing challenges regarding increased amount of new launches, squeezed deadlines and new demands for
unique identification of all packed products. The team currently consist of 5 QA assistants and 7 QA professionals.
The position
You will work closely together with the 5 other QA assistants. Your primary responsibility will be approval and maintenance of master
data and packaging orders in our electronic IT-systems. You will participate in projects when new demands for master data and
packaging materials must be implemented, and you will meet with stakeholders, whenever challenges needs a solution that calls for
collaboration across departments. Furthermore you will support the team in other daily tasks, such as updating relevant QMS
documents, data trend analysis and archiving GMP documentation.
We work in a dynamic and challenging environment with short deadlines, so you must be able to make prioritisations and take
responsibility for customer requirements also when the solution is not obvious. You must be capable of working independently and
support the team in the daily tasks. We have a high focus on launches and short lead times in order to secure a high level of quality and
compliance in the entire supply-chain from our suppliers to release of products.
Qualifications
You are educated as administrative assistant, laboratory technician, pharmaconomist or another similar education. You must have
a flair for IT-systems and data handling, and you are an experienced SAP user. If you have knowledge of excel and PRISM it will also
be an advantage. You must have a strong quality mind-set, and good knowledge of GMP rules and quality assurance from the
pharmaceutical industry will be preferred. As we are cooperating broadly with many stakeholders (Quality Control, Regulatory
department, R&D), good collaboration and communication skills are needed and if you have experience with batch documentation
review it is a positive asset. You must be fluent in Danish and English, both written and spoken. We offer a very exciting job with
excellent development opportunities among highly competent colleagues in a positive working environment.
We will review the applications on a daily basis, and start the interview and hiring process as soon as possible, so please do not hesitate
to send your application.
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 Signe Munkholm Hoeck +45 3079 7854.

LEAN Partner in Quality Assurance
Department: Quality
Place: Denmark - Kalundborg
Are you strong at facilitation, coaching, process optimization, problem solving and eager to create continuous improvements in a
dynamic organisation?
Then you might be our new dynamic LEAN partner in QA, Novo Nordisk. You will be in charge of continuously implementing and
improving our work in a Lean way in the Diabetes API QA area and you will influence the business results in the QA area.
Be a part of an important QA department with a big foot prin. We are supporting a variety of areas e.g. QA responsible for QC
laboratories, qualification/validation projects, manufacturing development and business support to the entire QA area in Diabetes API
this includes running the BSC process, risk process, LEAN strategy and analysing areas to improve. Furthermore you will get a chance
to be part of one of our major global quality improvement projects.
The position
You will be responsible for driving the LEAN thinking way and you will be a forerunner for systematic problem solving, performance
boards and other LEAN tools. You will have the opportunity to coach and spare with the leaders and employees and thus helping them
to reach and sustain their LEAN leadership maturity levels.
You will be heading projects which will give you the opportunity to influence on results in QA and you will follow up on processes and
ensure anchoring so we reach our ambitious process optimisation goals. In this way you will ensure that the solutions are anchored
within the QA area. We expect you to be our ambassador for management regarding the LEAN mindset and to be a coach and a
challenger for the management group.
Qualifications (Formación en LEAN)
The person we are looking for has a relevant background and education. You are comfortable in working independent but are a team
player. You are able to translate complicated issues to commonly understandable language and to communicate to stakeholders,
colleagues and management at all levels in a clear manner. You have an involving and proactive style and can work with people at all
levels of the organisation. You are known as an inspiring person with many ideas and a strong drive.
You have experience with LEAN doing facilitation, coaching, workshops, project and performance board meetings and systematic
problem solving, and know how to motivate colleagues and hereby secure their involvement to create a LEAN culture where everybody
contributes.
Your solid experience with change management makes you comfortable working with many different personalities in a changeable
environment. You have a structured approach to problem solving and the ability to keep your head straight when challenging
management on the way things are done. To be able to prepare and visualise data, it is necessary that you are familiar with IT-systems
as e.g. Word and PowerPoint and have good knowledge of Excel.
You are fluent in written and spoken English as our corporate language is English.
Novo Nordisk in Kalundborg
Novo Nordisk in Kalundborg is a city within the city. The area is situated a good hour from Copenhagen and covers 1,350,000 m2. We
produce some 50 % of the insulin in the world.
At Novo Nordisk, your skills, dedication and ambition help us change lives for the better for patients around the world. In exchange, we
offer you an opportunity to work with extraordinary talent and to benefit from a range of possibilities for professional and personal
development.
Contact
For further information, please contact Jesper Bønnelykke at +45 3079 1823

Asset manager
Deparment: Project Management
Place: Denmark - Hillerød
Are you passionate about understanding the equipment and preventive maintenance? Are you motivated by building relationships and
achieving ambitious results? And are you ready to join and take responsibility for building the asset management role in the newly
established Project Office? Then you might be the candidate for the job as our asset manager in PPM & Project Support team
responsible for our asset management program.
The job is located in Hillerød in Diabetes Finished Products (DFP). You will be part of our Project Office and join a small team PPM &
Project Support, where we are responsible for Project Portfolio Management, Project Governance, Shutdown and Asset Management
for the whole site. Together with the production you will be responsible for ensuring preventive maintenance and risk analysis of the
equipment.
You will join a dynamic team and ambitious employees with various backgrounds within project portfolio management, finance and
project management all striving for excellence.
The position
As asset manager you will be responsible for driving the development of a local asset management program in DFP HI together with the
management. This includes description of the role, the responsibility and the tasks to be performed. Furthermore you will be responsible
for implementing the local asset management program and ensure participation in the DFP Process Group, where alignment of the
asset management strategy will be done across the DFP sites.
The tasks include among others risk assessment of equipment and parts, identification of end of life of equipment, general Life Cycle
Management and tasks related to the asset management program. You will cover the site meaning equipment in Aseptic Production,
Assembly and Packaging together with our Material Handling system.
Qualifications (Master en Ingeniería)
You have an MSc in Engineering or similar, supplemented with a minimum of 5 years’ experience as a mechanical/maintenance
engineer or equivalent. You have experience within maintenance, preventive maintenance programs in production or similar. It will be
an advantage if you have some experience within project management, but it is not a requirement. Preferable, you know what it means
to operate in a GMP-regulated environment.
On a personal level you are very structured and able to make detailed plans. You are able to keep the overview in a large and complex
organisation with many stakeholders and ongoing changes. You are pro-active and thrive with driving tasks independently to the finish
line. You have a global mind-set and enjoy building relations across organisational levels. Good communication skills are a must
including the ability to create good cooperation with directors as well as employees in the production.
Contact
For further information, please contact Gitte Brynningsen on +45 3079 3675.

Director for Strategy & Planning
Deparment: Strategic Planning
Grasp a golden opportunity for joining Diabetes Finished Products (DFP) and taking on the exciting position as Director for Strategy &
Planning. We want to maintain the position as the world leader in diabetes care by ensuring DFP in reaching our strategic goal and to
plan for the future. We have an engaged and people focused culture, which is strongly founded on the Novo Nordisk Way.
Strategy & Planning’s role is to ensure an optimal utilisation of the DFP network with seven production sites across the world (France,
US, China, Brazil and Denmark) through DFP Business Plan, DFP Supply Landscape strategy, Business Reviews and volume target
setting.
Through tactical supply chain planning the department ensures DFP can always deliver and continuously are improving the DFP
production unit cost.
The department is furthermore responsible for managing and providing transparency on performance across DFP. Governing the
Balanced Score Card process, facilitating Key Performance Indicator(KPI) management reports and through trend analysis setting
direction for the organisation of 6.000 employees.
The department is as well providing logistic support on operational and tactical matters ensuring optimal conditions for the DFP
production sites to focus on producing according to plans.
The position
In this position, a high degree of independence is needed, as the position holder should be able to drive the strategic processes of DFP
including involvement of key stakeholders, setting direction and capability to challenge top management in both DFP and Product
Supply. You have the ability to solve problems quickly in a complex environment involving all areas of DFP including production,
warehouse, shipping, Supply Chain Planning, QA etc. You will also be involved in spotting and working with talents for the global DFP
organisation.
You will be managing 3 teams in Strategy & Planning. You can succeed in the position by being able to network, collaborate and work at
a high professional level with Management, Project managers and key stakeholders; as well as maintain a reputation for fulfilling
expectations and delivering results. You will be responsible for obtaining buy-in from key stakeholders on various initiatives and projects.
With a global operation and supplier network some travel activities must be expected.
Qualifications
You hold a degree in Engineering, Supply Chain Management, Finance or Business Administration combined with around 3-5
years of experience as Site Business Support Director or FLIT Director at one of the affiliates.
You also have proven people management experience with the ability to inspire and motivate the team to deliver high quality results.
You characterise yourself as a flexible person with strong leadership skills combined with the ability to challenge and set direction at all
levels within Product Supply from head of PS to operators in production areas. You also have an extrovert attitude and solid networking
skills, enabling you to navigate among various stakeholders. Last but not least, you have solid English language skills in both speaking
and writing.
At Novo Nordisk we use our skills, dedication and ambition to help people with diabetes and change their lives. By working with us you
will have the opportunity to do the same in a global business environment.
Contact
For further information, please call Bjørn R. Mogensen at +45 3075 1999 or Irene Yu at +45 3075 8018.

Business Controller in Diabetes Finished Products
Deparment: Finance & Auditing
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. Is the combination of financial controlling as well as being a valued finance partner to management a strong motivation
factor for you?
If so, you may be our new colleague! A position as Business Controller in Diabetes Finished Products (DFP) Finance for Site Bagsværd
is open.
The DFP Controlling & Planning team is a global team, based in Denmark, responsible for driving key finance controlling processes,
such as monthly reporting, quarterly reporting, Rolling Estimates (REs) and Anchor Budgets (AB). In addition, the team is identifying and
driving opportunities to ensure operational excellence within DFP Finance. In this job your primary contacts will be within the Danish
production organization and you will also get the opportunity to build a global network through your collaboration with colleagues
worldwide, running various financial processes globally.
The position
Together with colleagues, you will participate in and be responsible for various financial planning and reporting processes to
management. The tasks include preparation and follow up of the monthly reporting, budgeting and controlling and various improvement
projects. In this job it is expected that you built a strong relationship with Site Bagsværd management. It is expected that you spend
approximately 2 days a week on the shop-floor where it all happens and where you will gain valuable information on what issues should
be prioritised.
Qualifications (MBA)
You hold a Master’s degree in business administration or similar with excellent results and you must have a flair for numbers and
systems. You have several years of experience with controlling and planning tasks, preferably from within Product Supply. You have the
ability to think and act strategically but you are also motivated by the daily follow up.
As a person, you are ambitious and a team-player and you know how to balance meeting both deadline and quality of your work. You
have good communication skills and can easily interact with employees at all levels in the organization. Your tasks will also require that
you can work independently and are able to structure and prioritise your own time and tasks. You have lots of energy and a winning
mentality and attitude. Lastly, you speak and write English fluently.
Please submit your application and CV in English.
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. As an employee at Novo Nordisk, you will have the
opportunity for supplementary training, professional growth and personal development together with inspiring, deeply committed
colleagues. You will be part of a company that believes in making a difference to patients, to the medical profession and to society.
Contact
For further information, please contact Cristina Sima at +45 3079 7978.

Associate Manager in Device Manufacturing & Sourcing
Department: Quality
Can you lead and inspire a team of highly competent and independent employees responsible for Quality Assurance of validation of
components world-wide? Do you have a high quality mindset? Do you feel motivated by challenges requiring a high level of professional
competency and leadership experience then you might be the right leader for the Validation Quality Assurance Team in Device
Manufacturing & Sourcing(DMS).
In Device Manufacturing & Sourcing(DMS) Validation Quality Assurance we are looking for a dedicated Associate Manager. The
Associate Manager will be responsible for the quality of validation of our manufacturing of components at our suppliers as well as
internally at Novo Nordisk A/S. The components are delivered to our medical devices worldwide.
DMS Validation Quality Assurance(QA) consists of 9 highly qualified Quality Assurance(QA) engineers that are responsible for Quality
Assurance of the validation of injection moulding and pre-assembly equipment of our production internally and externally. Part of our
daily task is Validations, change control, ensure the quality of moulded and pre-assembled components internally in Device
Manufacturing & Sourcing (DMS) and by Novo Nordisk suppliers.
The position
You will head up the Device Manufacturing & Sourcing(DMS) Validation team consisting of 9 employees. The Validation team is
responsible for world-wide Quality Assurance(QA) approval of validations for Novo Nordisk injection moulding and pre-assembly
equipment for all Novo Nordisk prefilled devices. You will act as the Quality Assurance(QA) line of defence in securing that all
components produced both internal in Novo Nordisk and at suppliers are using validated equipment which have been Quality
Assurance(QA) approved. Activities are coordinated in close cooperation with our many stakeholders both internally in Device
Manufacturing & Sourcing(DMS) and in other parts of Novo Nordisk. It will be your responsibility to proactively ensure the development
of the team in a quality and LEAN perspective. You will be responsible for the compliance, standards and safety instructions including
GMP and ISO to ensure the components are in compliance with Novo Nordisk regulation. Quality mind-set is an incorporated concept of
our daily work.
You continuously follow up on the team’s performance and manage board meetings to provide a complete overview and coordinate your
team tasks. The tasks include solving daily challenges, optimizing core processes and improving the daily performance. You work with
personal development and competencies, in which systematic training and systematic problem solving play a crucial role. Your
leadership supports a LEAN culture where continuous improvement is a natural part of everyday work.
We offer you a managerial position with many exciting challenges giving you the possibility for individual development. You will be
supported in your career path and together we will make plans for your further education. We prioritise a good work life balance. We are
located in Hillerød approx. 30 km. north of Copenhagen.
Qualifications
You are goal-oriented, responsible and show great empowerment. As the position requires contact to different stakeholders you have to
be service-minded and to have excellent communication, prioritisation and decision-making skills.
You have at least 3-5 years of leadership experience. You are able to solve complex tasks by constructive communication based on
your professional knowledge without compromising quality and patient safety. Preferably you have academic background in science
(e.g. engineer, pharmaceuticals etc) or extensive experience from relevant business a requirement an education in science,
supplemented with experience from production in Good X Practice(GxP) regulated companies. The ideal candidate has experience in
ISO13485, cGMP, validation, Quality oversight and Lean. You must be energetic and be able to set ambitious but realistic goals and to
achieve them.
On a personal level you are ambitious and have a great interest in developing yourself. You make a difference and by your dedicated
and determined quality approach you complete your tasks in a satisfactory way. You are independent and not afraid to take the initiative.
You have a good sense of humour.
At Novo Nordisk, your skills, dedication and ambition help us change lives for the better for patients around the world. In exchange, we
offer you an opportunity to work with extraordinary talent and to benefit from a range of possibilities for professional and personal
development.
Contact
For further information, please call Lene Cletus Petersen on +45 30790412.

Process Supporter for Tablet Production
Department: Production Support
Place: Denmark - Måløv
Are you ready to make a difference? And are you committed to support a GMP production in Novo Nordisk? Right now we are looking
for a production chemist with a high quality mindset and GMP experience to join us in the HRT bulk production, a part of Biopharm
Finished Products.
The job is located in Biopharm Finished Products MA&VA, HRT Bulk production, which is a tablet production producing Hormone
Replacement Therapy (HRT) products including the processes; granulation, compression and coating. The department consists of 55
employees and is based in Måløv, Denmark and consists of three teams; a Production team, a Technical Support team and a Process
Support team. The vacancy is in the Process Support Team that consists of 12 dedicated supporters.
The position
The primary responsibilities of this position will be to support the operators in the daily production and secure that we live the
requirements of our quality management system and that we work systematically according to the LEAN principles implemented in the
department. Furthermore, you will handle deviations from standard procedures, implement corrective actions, handle change requests,
review batch documentations, write protocols, reports and various documentations related to the HRT bulk production. In this job, you
will be in close contact with professional colleagues both in the department as well as in QA, QC and Product Support departments. This
means you will have a various working day in cooperation with professional and dedicated colleagues.
Our department is highly motivated and this position offers you a unique opportunity to strengthen your experience in a GMP production
environment, realise personal as well as department goals and see the benefits of your work. You will experience an enthusiastic
working climate where we take a personal responsibility for quality, delivery and each other.
Qualifications
You hold an academic degree (Cand. Pharm, chemical engineer or the equivalent). You have experience from the pharmaceutical
industry and knows how to perform in a GMP environment. Experience with tablet production is in your favour. Preferable you have
knowledge of the LEAN principles. On a personal level you have a positive can-do attitude, you are engaged, systematic and take
responsibility to ensure deadlines are met. You enjoy working with major challenges and can maintain an overview in a busy work day
while complying with the requirements for manufacturing of drug products.
Contact
For further information, please contact Maj-Britt Buch at +45 3075 7662

Operations Manager for CMO tablet and Packaging
Do you have a background as Chemist, Engineer, Pharmacist or similar and are looking for a chance to work in an international setting
where you can influence and initiate actions to improve existing manufacturing conditions and processes at Chemistry, Manufacturing
and Controls (CMOs) ? Do you thrive in a dynamic setting where you are subjected to changes on a daily basis? Then we might have
the right job for you.
Contract and Local Manufacturing Operations (CLMO) is part of Novo Nordisk’s Product Supply organisation and responsible for all
Novo Nordisk contracts and licence manufacturing of semi-finished and finished drug products to local and global markets. Our main
office is located in Bagsværd, Denmark. The primary role of Contract and Local Manufacturing Operations is to monitor and control the
production handled by Contract Manufacturing Organisations (CMOs) ensuring delivery of products from the Chemistry, Manufacturing
and Controls (CMOs) to our respective customers. Our Contract and Local Manufacturing Operations are located in Central Europe,
Iran, Egypt, India, Bangladesh and Algeria.
The position
As Operations Manager in Contract and Local Manufacturing Operations you will be responsible for the daily operation of selected
Contract Manufacturing Organisations ensuring our products are delivered to our customers timely along with the right level of quality.
Therefore Good Manufacturing Practice (GMP) understanding and knowledge is a key competence. Furthermore, you will also ensure
business compliance e.g. business ethics and responsible sourcing. You will be the main point of contact coordinating communication
between Novo Nordisk and the Contract and Local Manufacturing Operations to the greatest extent possible. The role includes timely
follow up on delivery performance, quality performance and ensuring products are delivered to our customers. Furthermore the role
involves working with and providing input to other functions in Novo Nordisk regarding the Contract Manufacturing Organisations e.g.
Business review meetings, Quality review meetings, audits etc. You will contribute to securing that internal performance management
boards are updated with relevant information.
A recurrent task will be to organize and call for monthly meetings with relevant stakeholders to ensure business is running as expected.
This can be teleconferences or on-site meetings where you will act as meeting owner and host. In addition, you will host on-site
business and quality review meetings at least once a year. As Operations manager you will have a substantial impact on the Contract
and Local Manufacturing Operations with regards to strategy input, prioritizing and follow-up on agreed actions and improvements. You
will also be expected to address delivery issues if necessary and together with the Contract and Local Manufacturing Operations and
Novo Nordisk internal specialists agree on restoration plans when necessary. You will join a dedicated team of highly skilled colleagues
with deep insights and experiences within the area Tablet and packaging. The job has a main focus on packaging operations at Contract
and Local Manufacturing Operations , why experience within this area is a merit. You have experience with handling deviations/Non-
Conformities, Change Requests and Customer Complaints.
The activities are primarily located in Germany, Sweden, Belarus, Iran and Egypt.
Qualifications
You hold a Master’s Degree within e.g. Pharmacy, Engineering or similar. Ideally your theoretical background is combined with at
least four years of practical experience within the pharmaceutical business and manufacturing of pharmaceutical finished goods.
Experience with oral formulations and tablet and packaging is a merit and Good Manufacturing Practice(GMP) knowledge within these
areas is required.
You will be part of several teams – both formally and informally – hence the ability to work across boundaries is critical for your success.
We expect you to make procedural or process suggestions for achieving team goals or performing team functions; providing necessary
resources and help to remove obstacles ensuring the team accomplishing goals. As a person you are good at building trust with
stakeholders and you naturally share important and relevant information with your team. You have an analytical mind-set with the ability
to work in a structured way and an ability to support multiple activities. Preferably you have experience from an international
environment. Furthermore, you have strong communication skills in the English language. Working location will be in Bagsværd and
travelling is an integrated part of your job to some extent, around 15 days per year.
At Novo Nordisk, we create value by putting patients first. Every ten seconds two people are diagnosed with diabetes, and more than
371 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 call Thomas Lindblad at +45 3075 5179.

QA Supplier Engineer in DMS Operation QA
Department: Quality
Would you like to work in an international environment and be responsible for the Quality Assurance of the components to Novo Nordisk
most sold prefilled insulin products? Are you ready to take decisions regarding right level of product quality to ensure patient safety and
compliance? Then you might be the person we are looking for.
In Developing Management Skills ( DMS) Operation Quality assurance (QA)we are looking for an independent and dedicated
mechanic/polymer/machine engineer or similar who will be responsible for the quality assurance of the components for our high volume
medical devices production worldwide. Your job area will be within the fields of advanced injection moulding and springs for medical
devices. The department’s suppliers are located in Europe, USA and Brazil.
The DMS Operation Quality assurance (QA) consists of app 33 highly qualified Quality assurance engineers that are responsible for
Quality assurance of our production internally and externally. The team Supplier Quality assurance (QA) comprises of 13 highly qualified
Quality assurance (QA)Professionals and Technicians who are responsible for the quality of spring and plastic components produced by
our suppliers. The team has a broad background in regard to knowledge/background and diversity which mirrors our ability to
understand our customers and suppliers worldwide.
The position
With support from your colleagues and in close dialogue with the Process Owners you will independently be responsible for the quality
assurance for one of our prefilled devices and be a part of Quality oversight assuring that your supplier is working in compliance.
You will also participate in Operational Business Reviews 2-3 times/year and promote sharing better practice across all moulding
suppliers together with your colleagues. A part of your role is also to be a part of nonconformity investigations and challenge systematic
problem solving, approve nonconformities and change requests. We expect you to have a yearly travel frequency of about 20-30 days.
Quality Mindset and winning culture are incorporated concepts of our daily work. We offer you a position in an international company
with many exiting challenges giving you the possibility for individual development. Together we will make plans for your further
education. We prioritise a good work life balance. We are located in Hillerød in nice surroundings and new facilities approx. 30 km. north
of Copenhagen.
Qualifications
You are independent, have empowerment and take responsibility for your tasks. You are known for thinking systematically and it is
natural for you to work according to standards. You are able to solve complex tasks by constructive communication based on your
professional knowledge and understanding of quality without compromising patient safety. You have at least 5 years of experience
within Medical Device production, quality assurance. You have a strong interpersonal competency and are a good communicator and
hold an understanding of cultural differences.
You hold an academic degree in engineering within mechanic/machine/polymer or similar. You master English on a high business
communication level (oral/written). The ideal candidate has experience in The International Organization for Standardization (ISO)3485,
Current Good Manufacturing Practice (cGMP) and Lean. On a personal level you are ambitious and have a great interest in developing
yourself. You make a difference and by your dedicated and determined approach you complete your tasks in close cooperation with your
colleagues. You are independent and not afraid to take initiatives. You have a good sense of humour.
Contact
For further information, please call Gert Petersen +45 3075 7597.

Be the Inspiring and Proactive Associate Manager - Global QA
Oversight
Department: Management
Are you ready to inspire, lead and motivate a team of highly skilled Quality Assurance employees? Are you ready to take on the
responsibility of assuring the basis for the high quality? Do you trust your own ability to navigate a dynamic and challenging environment
and grow as a leader? If yes, then we have an exciting job opportunity as Associate Manager in Sourcing Quality Assurance.
Sourcing QA Raw Materials is responsible for Quality Assurance of Raw Materials, Starting Materials and Process Aids used in the
production of all Novo Nordisk A/S products. We are responsible for Quality Assurance of our suppliers who are located all over the
world. A combination of ensuring the high standard of incoming materials, and involvement in investigations into quality issues by the
use of LEAN tools is part of our daily work to improve and secure robustness in our internal processes. In total we are 27 dedicated
employees divided into 2 teams working in close collaboration with our colleagues in the Quality area and our stakeholders throughout
the global organisation.
The position
You will be responsible for a team which is highly engaged in Quality Assurance of Raw Materials in close contact with our external
suppliers. The team is responsible for approval and release of Good Manufacturing Practice(GMP) Materials for both Active
Pharmaceutical Ingredient(API) and finished product production sites. Furthermore we have global QA responsibility for setting
directions regarding incoming control setup and approval of specifications. We have a high focus on material flow and short lead times
in order to secure a high level of quality and compliance in the entire supply-chain from suppliers to release of products.
The team currently consists of 2 QA Technicians and 8 Quality Assurance professionals.
Your job is to support your staff in their daily efforts to solve quality challenges including problem solving involving external suppliers. We
work in a dynamic and challenging environment with short deadlines, so you must be able to prioritise and take responsibility for
customer requirements also when the solution is not obvious. You must be capable of working independently and support the team by
clearing the way for the delivery of each team member. Furthermore, your team will work in concert with other departments to ensure
that the area is always able to deliver high quality materials in a compliant and timely manner.
As associate manager you lead by example, set the direction, and ensure that your team is highly motivated and engaged. You are
responsible for your team´s performance by, among other things, setting targets and reaching them, and you know how to motivate and
develop your staff. As part of the management team in Quality Assurance , you will be responsible for implementing quality strategies in
your area.
Qualifications
You hold a master’s degree in pharmaceutical science, engineering or related discipline giving you a solid background within
Pharmaceutical science, Biotechnology or Bio-Medicine. Ideally, you have a minimum of 2 years of management experience. Your
quality mindset is well-developed and you have knowledge of Good Manufacturing Practice rules and quality assurance from the
pharmaceutical industry.
Personally, you have a high drive and sense of initiative combined with empathy and the ability to support and engage your team. You
are known for your positive mindset and you enjoy working in a dynamic environment. As we are cooperating broadly with many
stakeholders, the job demands excellent communication and cooperation skills both internally and outside the department. The ability to
give feedback, coach and develop employees is also a focus point for the position. Your language skills include proficiency in English.
work with extraordinarily talented personnel and allow you to benefit from a range of possibilities for professional and personal
development. Your application can be submitted in Danish or English.
Contact
For further information, please call Jeanett Borsdal-Hansen +45 3075 7085 or Asbjørn Vestphal on +45 3075 2812.

Senior QC Professional for Raw Materials
Department: Operations
Do you have a strong Quality Control(QC) background and want to make a difference? And do you enjoy working in an open, dynamic
and social atmosphere with a strong focus on improving and simplifying overall processes? If so, you have the opportunity to play a key
role in our laboratory.
Quality Control Raw Materials is responsible for analytical testing of raw materials and excipients for Novo Nordisk production sites all
over the world. There are currently more than 30 analytical platforms within the laboratory, and more are to be introduced in the future.
We analyse according to several pharmacopoeias European Pharmacopoeia(EP), United States Pharmacopoeia(USP), Japanese
Pharmacopoeia(JP) and
Chinese pharmacopoeia(CP) and other registered methods. The department consists of approx. 65 employees divided into two
operational laboratory teams, a Support team of analytical chemists and the Quality management team where this position is open. We
just moved into our new laboratory in Hillerød.
The position
As our new Sr. Quality Control Professional you will have the opportunity to combine your broad experience from the Quality Control
laboratory and your interest for teaching and guiding others. You will work with and drive improvement projects within the department, as
well as assist our Support team in their daily operation with your knowledge and guidance.
You will be part of the Quality Management team; counting ten enthusiastic peoples either working on improving the processes in the
department or by supporting the overall systems.
The team is based on trust, collaboration and a high degree of delegation within the different areas of responsibilities.
Qualifications
You hold a Master degree in pharmacy, engineering or natural science. You have a strong Good Manufacturing Practice(GMP)
mind-set and minimum 5 years of relevant Quality Control experience from the pharmaceutical industry. You are comfortable in trouble
shooting equipment and analyses, and your experiences include chromatographic platforms, method verification, handling of equipment
qualification and validation. Furthermore you have experiences with handling of deviations, change management, Good Manufacturing
Practice(GMP) inspections and quality management systems.
If possible you have experience with analysis of raw materials, excipients and Active Pharmaceutical Ingredient(APIs).
You have a positive and flexible mind-set and you enjoy being a source of knowledge and to create durable simple solutions to everyday
challenges. You are a team player, and also demonstrate ability to work independently; you take charge, and also ensure stakeholder
involvement and confidence throughout. You have the ability to exchange knowledge. You create structure and overview, have a keen
eye on details and are an example of a strong quality culture. You have a high degree of drive and pro-activeness. You run projects
independently, and consistently ensure timely and high quality deliverables.
Contact
For further information, please contact Siv Sönnichsen Præst at +45 3075 9852.

Associate Manager
Are you ready to set direction for a team of 20 highly competent and motivated operators? Then we have the right job for you as
Associate Manager in Device Manufacturing & Sourcing (DMS) Moulding Production.
We are responsible for the supply of moulded plastic components for prefilled devices to DFP and Biopharm. Help us meet our
ambitions to give people with diabetes the opportunity to lead the life they desire.
DMS Moulding Production is a department ensuring high quality and effective output of moulded plastic components for prefilled pen
systems. We are responsible for the moulding production in our internal production facility, covering the main products FlexTouch® and
FlexPro®.
We offer a very exciting job with excellent development opportunities among highly competent colleagues in a positive working
environment.
The position
You and your team’s objectives are to ensure that the production is performed according to plan and in compliance with GMP and
corporate standards. You focus on enabling your team to support our production, and through your leadership and coaching you create
a culture where everyone is ready to perform their outmost, challenge the methods, systems and processes - constantly making them
better, smarter and more efficient. You continuously follow up on the team’s performance and manage board meetings to provide a
complete overview and coordinate the tasks at hand. The tasks include initiation and facilitation of structured problem solving,
minimising scrap level, optimizing core processes and improving the daily performance management. You improve your team’s
performance and work with personal development and competencies, in which systematic training and systematic problem solving play
a crucial role. Your leadership supports a LEAN culture where continuous improvement is a natural part of everyday work. You
collaborate closely with the management team as well as other teams in the department and our closest stakeholders in other
departments. In this job you can make a difference and realise your own leadership potential. You will report to the Director for the
department and be a member of the management team consisting of the Director and 4 other Associate Managers as wells Department
cLEAN and GMP coordinator.
Qualifications
Preferably you hold a Master’s degree in Sciences, engineering or a related education. You have a strong managerial and quality
mindset and are used to drive improvement projects with focus on systems, quality and lead time. If you are familiar with Injection
Moulding and production processes, it will be a major plus. As a person you are known for your positive attitude and for your
documented ability to motivate people. You take ownership and work proactively to drive processes forward, and you are able to
manoeuvre and prioritise in a dynamic and challenging environment with short deadlines. You thrive in the decision-making role where
decisiveness and self-consciousness are crucial key words, and you know how to win acceptance through direct and clear
communication. Proficiency in written and spoken English is necessary.
Contact
For further information, please contact Thomas Iversen at +45 30756219.

QA Chemist for Manufacturing Development in Biopharm
Department: Quality
Place: Denmark - Gentofte
Would you like to be part of Quality Assurance in Biopharm? Biopharm is responsible for the biological products of the Novo Nordisk
product portfolio. Biopharm Quality Assuranceis looking for a talented and ambitious Quality Assurance Chemist to Quality Assurance of
the Manufacturing Development departments in Gentofte and Måløv.
Our department Biopharm Quality Assurance (QC) & Support consists of three teams; two teams responsible for quality assurance of
Quality Control laboratories and one team responsible for quality assurance of development activities. Our key tasks are to review and
approve Good Manufacturing Practice (GMP) documentation such as validation reports, change requests and non-conformities in order
to be able to ensure delivery of high quality products in compliance.
As chemist in Biopharm Quality Assurance (QA) Quality Control (QC) & Support you will join a group of 28 highly skilled and competent
colleagues. 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 team with the vacant position is responsible for quality assurance of 4 support departments in Biopharm. The departments are
supporting Active Pharmaceutical Ingredient (API), Aseptic Production, Process Support and Tablets production. This means that the job
is a unique possibility to have a broad range of stakeholders and specialize in various pharmaceutical disciplines. The Quality
Assuranceteam consists of 9 chemists.
The position
Your main responsibility will be to quality assure the Manufacturing Development and thereby assure, that the products and processes
always are of high quality and in full compliance with the current rules and guidelines.
Your main tasks will be: Quality Assurancereview of documentation of complex cases in production, data to support changes and
deviation, quality assurance of master formula, customer complaints, reference samples and stability studies. Furthermore, the Quality
Assurance team is a major stakeholder at internal audits and external authority inspections, where you are expected to participate. You
will experience an individual and thorough training program facilitated by your skilled colleagues, which will make you able to fulfil your
job and empower you to set the right direction
Qualifications
You hold a scientific academic degree e.g. MSc in Pharmacy and preferable you have a shorter or longer work experience from
the pharmaceutical business. You must thrive in a role where you are required to take the lead 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 are good at coordinating different tasks for both yourself and other people and you enjoy
doing that. You demonstrate an ability to find the right solutions together with your colleagues.You work independently and feel confident
making 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.
Contact
If you want to know more about the position, please contact Anders Bekker-Jeppesen +45 3075 0790.

Structured leader for team in Biopharm Manufacturing Development
Department. Production Support
Place: Denmark - Gentofte
Are you ready to lead and motivate a team of highly qualified colleagues in a team that works with support to Biopharm Finished
Product in Gentofte and Kalundborg? And are you able to ensure consistency between new and marketed products? Can you define a
clear direction for your team and function as an inspiring sounding board for your employees? Can you keep calm and prioritize tasks in
a dynamic and hectic environment? Then we have a good opportunity for you in Biopharm Product Support.
In Biopharm Product Support we are 50 competent employees, organized in three teams.
We are responsible for product support to the productions of finished products in Biopharm and we have product knowledge and
responsibility for all the products in Biopharm. Hence we both have responsibility for the new haemophilia portfolio and for the marketed
products in Biopharm. The department acts as a link between development and production. Therefore we are on top of all the exiting
new products in the pipeline in Biopharm where we ensure that all product knowledge from CMC is embedded in Biopharm.
The position
You will lead a team of 14-16 qualified and competent employees. Your most important tasks will be to ensure the coordination and
prioritisation of support to the productions, to handle and coordinate the product related tasks and to ensure response to questions from
the authorities. You will lead your team by the use of daily board and planning meetings. You will work closely together with QA, the
productions and CMC to ensure progress and the right prioritisation.
You will act a significant part in the continuous creation of improvements through the use of LEAN. This makes us able to optimize our
working processes and to standardise across the products. You can look forward to a working environment on constant move and where
you every day will have to make important decisions in proportion to delivery, prioritisation and fierce deadlines.
Qualifications
You have an educational background as pharmacist, engineer or similar, supplemented with a solid experience from a
pharmaceutical production. You are an experienced leader and your CV shows a minimum of five years of experience with leadership.
You have a good sense of planning, you work in a systematic and structured manner and you are able to keep a sense of perspective. It
is important that you know the value of creating trust and respect from colleagues and employees and that you know how to motivate
your employees in a busy working day. You are able to share knowledge in all organisational levels and with your extrovert and
proactive approach you easily establish a network across the organisation. Finally, you have a high Quality Mindset and are capable of
prioritising your work to fulfil every deadline.
Contact
If you want to know more about the position, please contact Anja Bagger at +45 3075 8044.

Aseptic Process Supporter in Diabetes Finished Products
Department: Production Support
Are you ready to make a difference? Would you like to work at the world’s leading insulin producer? We are looking for a skilled process
supporter with a high quality mind-set and Good Manufacturing Practice experience to join us in the aseptic filling production.
Seize the opportunity to get a job with a lot of development and a varied working day with influence and responsibility in an international
company.
You will be a part of a department where millions of Penfill® is filled for patients all over the world. The department consists of 100
dedicated employees including operators, technicians, engineers, pharmacists and chemists, that all work closely together and across
multiple units. Our primary task is to secure, that our production runs 24/7 and always deliver insulin to our customers, at the right time,
with the right quality. We deliver both existing products to the market but we are also entry point of new products ramping up. The open
position is in the Process Support team, where you will work together with 10 highly engaged colleagues.
The position
In close collaboration with your colleagues in the process support team, you will ensure that the filling processes are in compliance with
all regulations. You will support the operators in the daily production and secure that we live up to the requirements of our quality
management system. As such you will spend time on the production-floor, knowing that being close to the process and the operators will
help you solving problems early and effectively. On an on-going basis, you will handle systematic problem solving, non-conformities,
validations and batch documentation. Additionally you will optimise the production processes in close collaboration with other support
functions and the Qulity Assure functions.
You will also drive compliance improvement projects. As you will be part of the production support team you will be expected, from time
to time, to support production on trouble shooting also outside normal working hours. Therefore you play a key part in the job, of
securing the operations and at the same time secure the release of our products. You can expect a dynamic and varied working day
with an informal atmosphere and good colleagues. Our department is highly motivated and this position offers you a unique opportunity
to strengthen your experience in a GMP production environment realise personal as well as department goals and see the benefits of
your work. You will experience an enthusiastic working atmosphere where we take a personal responsibility for quality, delivery and
each other.
Qualifications
You hold an MSc in Engineering, Pharmacy or other relevant scientific education with a minimum of 1-2 years of relevant
experience preferably within pharmaceutical production. You have a strong mind-set for quality and compliance and like to spend time in
the production. Moreover you have good knowledge of Good Manufacturing Practice/International Organization for Standardization
requirements and have some experience with audits. Furthermore you have a solid knowledge of LEAN and it comes natural to you, to
use problem-solving-tools in your daily work.As a person you can stay focused in a busy working day and you always approach tasks
and colleagues with a positive attitude and energy. You are analytical and work in a structured way and you are used to deliver
according to deadlines.
Working at Novonordisk
Contact
If you have any questions, feel free to contact Savvas Paraskevopoulos at +45 3075 5145.

QA Professional in Device Manufacturing & Sourcing Process QA
Department: Quality
Are you ready to use your expertise to ensure high quality work within the medical device area of Novo Nordisk? Would you like to work
in an international environment and be responsible for the quality assurance of components produced in Device Manufacturing Sourcing
(DMS)? Are you ready to take high impact decisions regarding the right level of quality to ensure patient safety? If so there is a
challenging and exciting position in Device Manufacturing Sourcing Process Quality Assurance (QA).
Device Manufacturing Sourcing is a production organisation located near Copenhagen. Our challenge is to mould, preassemble and
produce high quality components and bring them fast to market. You will be part of our Process Quality Assurance department in
Hillerød where we are 12 engaged and innovative colleagues who strive for a high quality culture and a professional atmosphere. We
are responsible for the quality assurance of the validations which ensure the quality of all components delivered for production of
medical devices worldwide.
The position
As Quality Assurance Professional you are responsible for the quality of our components, including approval of validation
documentation, change requests and instructions. You will be working in cooperation with competent and experienced colleagues. You
are furthermore participating in Quality Assurance related projects. One of your primary objects is to perform review and approval of
validation documents in due time and in full compliance with the ISO and Good Manufacturing Practice (GMP) standards. Good
relations and communication skills are key tools when handling the quality issues in the best possible way. Quality is the key word in this
job and therefore it is natural for you to have an on-going dialogue with your partners regarding how to ensure quality and compliance.
As Quality Assurance Professional quality has your concern which means that you can stand firm when needed in considerations of
patient safety and regulatory requirements. You can look forward to have an exciting job where you have a high degree of responsibility.
We offer this challenging position in a dynamic environment where you have good opportunities for personal and professional
development.
Qualifications
You hold a master degree in engineering within mechanics/machines/plastics or similar academic education. Preferably your
academic background is supplemented with experience from the pharmaceutical industry and/or knowledge regarding moulding and
assembly processes. Based on your experiences within the field you are used to work with ISO and/or Good Manufacturing Practice
and the regulations relevant for medical devices. Furthermore, it is an advantage that you are interested in Information technology
processes. You work systematically and are able to make a perspective view, and you are comfortable with taking decisions. You have a
strong quality mindset and are able to prioritise several tasks in a changing environment. Precise communication is essential and you
must be capable of taking part in a constructive cooperation concerning the various tasks. On a personnel level you are known for your
positivity, flexibility and persistence.
At Novo Nordisk we strive for excellence. 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 Lene Cletus Petersen on +45 3079 0412.

EURES SOC: PROCÉS DE SELECCIÓ EMPRESA DANESA DEL SECTOR BIOFARMACÈUTIC

Recommended

Recommended

More Related Content

Viewers also liked

Viewers also liked (20)

Similar to EURES SOC: PROCÉS DE SELECCIÓ EMPRESA DANESA DEL SECTOR BIOFARMACÈUTIC

Similar to EURES SOC: PROCÉS DE SELECCIÓ EMPRESA DANESA DEL SECTOR BIOFARMACÈUTIC (20)

Recently uploaded

Recently uploaded (20)

EURES SOC: PROCÉS DE SELECCIÓ EMPRESA DANESA DEL SECTOR BIOFARMACÈUTIC