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WORKINDENMARK

WORKINDENMARK

 

Workindenmark is a free public service for international jobseekers and Danish companies. Our website www.workindenmark.dk is the official Danish website for international recruitment and job seeking. On the site you’ll find need to know and nice to know information about living and working in Denmark.

On Workindenmark.dk you can find specific information:
In our job bank, you can search for jobs in Denmark with companies looking specifically for international job seekers. Also make sure to follow Workindenmark on Facebook and LinkedIn.
You and your family can find useful information on all aspects related to moving to Denmark for work: 

> Job search in Denmark
> Residence and work
> Corporate culture
> Language etc.

JOB OPPORTUNITIES
Denmark experience lack of highly qualified professionals and skilled workers within Life Science, such as:

> Engineers (ICT, electrical, data, automation or robot)
> Biotech-professionals
> Process Operators (be able to manage industrial equipment/ facilities, ensure technical procedures and quality assurance)
> Msc. in chemistry (bio, protein, physical or analytical) 

WORKING AND LIVING IN DENMARK
Denmark has a lot to offer. The Danish society is characterised by a highly developed welfare system with beneficial childcare, free schools, free healthcare, and more. Danish companies offer good working conditions, modern facilities and high-quality technical equipment. Competence development is highly prioritized and most workplaces regularly offer continuing education to their employees. Previous studies have shown that a majority of foreign national workers in Denmark felt that their quality of life increased while living in Denmark. Although it is a result of several different factors, many highlight the positive balance between family life and career in Denmark.

Foreign nationals who come to Denmark often mention safety and security as the country’s most important characteristics. It is possible to get by easily in Denmark without speaking Danish from the start as nearly all Danes speak English. To learn more about working and living in Denmark, visit our website www.workindenmark.dk

Company
Title

MES Engineer - NNE
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Employer: Novo Nordisk Engineering (NNE)

 Does the idea of being a part of a team of MES (Manufacturing Execution System) engineers, working on Danish production sites with our customers, appeal to you?
Do you thrive on the possibility of creating new solutions in our MES system running in a complex production environment? Then you’ll fit right in!

We are experts in end-to-end pharma engineering, and we design and build pharma facilities that are essential for millions of patients all over the world. Our success is built on our relationships, both with our colleagues and our customers. If you are passionate about working for a noble cause on projects shaping the future of sustainable and intelligent pharma facilities, NNE is the place to be. 

Locations: Kalundborg

The Role & Department
In our department we work with Manufacturing Execution Systems (MES), and our team of multidisciplinary IT engineers are working on both upstream and downstream processes within pharma and biotechnology. All our work is project-based, which means that with every new project, you’ll develop your competencies further.
Please notice, that this role requires you to mostly be on location at our customers in Denmark, Kalundborg.

Responsabilities
As a MES Engineer, you’ll be:

  • Working side by side with innovative colleagues.
  • Advising clients on how to maximize the benefits of our MES System.
  • Gathering technical requirements through a variety of techniques (e.g., facilitated workshops, work sessions, interviews and technical analysis).
  • Ensuring that workflows / recipes are successfully designed and developed in line with site business processes and technical standards.
  • Commissioning and undertaking test and qualification of IT systems in manufacturing environments.
  • Estimating and coordinating own tasks.
  • Working closely with our customers on site.

Requirements
We care about who you are as a person. In the end, how you work, and your energy, is what impacts the results we achieve as a team.

As a person, you are:

  • A team-oriented person, curious and eager to learn.
  • Understanding of your colleagues’ individual and cultural differences.
  • Aware of your surroundings and able to flag any concerns.
  • Agile and able to prioritize urgent tasks.
  • Excited to build on the NNE culture of innovation.

We believe these qualifications are needed for you to do well in this role:

  • Either an engineering, computer scientist or similar degree or having pharmaceutical production experience.
  • Experience with MES systems like Körber PAS-X, Emerson Syncade or NNE LMES.
  • Experience from Pharma/Regulated business (not a requirement).
  • You speak and write Danish and English (Danish not a requirement but recommended).

If you do not check all the boxes, you are welcome to offer alternative experience that you think would be valuable in this role.

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C&Q Engineer for Pharma Projects - NNE
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Employer: Novo Nordisk Engineering (NNE)

Does the idea of being at the forefront of commissioning and qualification for cutting-edge pharma facilities excite you? Are you passionate about ensuring the smooth and safe installation and qualification of high-tech equipment in a dynamic project-based environment? If so, we have a job opportunity for you!

We are experts in end-to-end pharma engineering, and we design and build pharma facilities that are essential for millions of patients all over the world. Our success is built on our relationships, both with our colleagues and our customers. If you are passionate about working for a noble cause on projects shaping the future of sustainable and intelligent pharma facilities, NNE is the place to be. 

Locations: Virum

The Role & Department
We are looking for a Commissioning & Qualification (C&Q) Engineer to join our team, focusing on ensuring the successful installation, commissioning, and qualification of equipment and systems. As a C&Q Engineer at NNE, you will be involved in the critical stages of site commissioning where you will plan, coordinate, and execute work related to the installation and testing of equipment and systems.

Our team ensures high-quality project execution in a collaborative and safe working environment. We are dedicated to helping our customers automate their facilities and implement state-of-the-art technology.

Responsabilities
As a C&Q Engineer, you’ll:

  • Review and follow-up on detailed plans from the installation of equipment and systems to mechanical completion and through the first dynamic testing and commissioning activities.
  • Systemize and mark up P&IDs for various pre-commissioning activities (boundary drawings).
  • Ensure smooth communication and planning between stakeholders on-site through regular meetings.
  • Follow up on outstanding issues and monitor the progress and quality of C&Q activities.
  • Provide guidance and support related to C&Q to colleagues, management, and other stakeholders.
  • Maintain a high focus on Health, Safety, and Environmental (HSE) aspects to ensure a safe working environment for yourself and your colleagues.

Requirements
We care about who you are as a person. In the end, how you work, and your energy, is what impacts the results we achieve as a team.

As a person, you are:

  • Are agile and able to prioritize urgent tasks while maintaining quality standards.
  • Have a solution-oriented mindset and are always keen to improve processes.
  • Are a good listener and respectful of individual and cultural differences among colleagues.
  • Take initiative and actively work towards improving C&Q processes based on your experience.
  • Are highly collaborative and enjoy working in team-based environments.
  • Are mindful of your surroundings and able to flag concerns when necessary.

We believe these qualifications are needed for you to do well in this role:

  • A degree in engineering (mechanical, process, or related field) or marine engineering ("maskinmester").
  • Knowledge of project management, risk assessment, and quality assurance.
  • Fluent in both Danish and English (written and spoken).

If you do not check all the boxes, you are welcome to offer alternative experience that you think would be valuable in this role.

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Business Intelligence (BI) Data Analyst - NNE
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Employer: Novo Nordisk Engineering (NNE)

 Does the idea of developing business-critical data solutions excite you? Do you thrive on building cloud-based BI solutions and developing reports in Power BI and Excel? Then you’ll fit right in!

We are experts in end-to-end pharma engineering, and we design and build pharma facilities that are essential for millions of patients all over the world. Our success is built on our relationships, both with our colleagues and our customers. If you are passionate about working for a noble cause on projects shaping the future of sustainable and intelligent pharma facilities, NNE is the place to be. 

Locations: Virum

The Role & Department
We are looking for a Data Analyst to join our team of in our department for Financial Systems. As a team, we are developing and maintaining applications within the Finance Domain. Furthermore, you will be a part of the cross organizational ERP project.
As our new Data Analyst, you will play a pivotal role in developing business critical data solutions for NNE, as you will participate in building our cloud-based data reporting solution while also ensuring a smooth transition from our current reporting environment.

Responsabilities
As Data Analyst, you’ll:

  • Participate in project activities building a cloud-based Business Intelligence (BI) solution that integrates with Dynamics 365 ERP system.
  • Develop new reports in the cloud, together with a dedicated and strong team of data analysts.
  • In general build, change, and deploy reports in Power BI or Excel based on user Interpret and reconcile data from multiple sources.
  • Handle ad hoc data requests from end users.
  • Provide backend support for other applications within the Finance domain, e.g., Planning and Consolidation application as well as other systems.

Requirements
We care about who you are as a person. In the end, how you work, and your energy, is what impacts the results we achieve as a team.

As a person, you are:

  • Excellent problem-solving and collaboration skills.
  • A curious mindset and are a great team player.
  • A strong understanding of business processes and the ability to translate user requirements into technical specifications
  • Agility and the ability to prioritize urgent tasks.
  • Excitement to build on the NNE culture of innovation.

We believe these qualifications are needed for you to do well in this role:

  • Prior experience working as a Data Analyst with advanced skills in data analysis, pivot tables, and complex formulas.
  • Strong knowledge of SQL, Power BI and ETL development with ability to write and optimize queries for data extraction and manipulation.
  • Familiarity with Azure Synapse Analytics and knowledge of Microsoft Fabric are an advantage.
  • Bachelor’s degree in business, Computer science, Engineering, or related fields.

If you do not check all the boxes, you are welcome to offer alternative experience that you think would be valuable in this role.

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GMP Consultant - NNE
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Employer: Novo Nordisk Engineering (NNE)

Are you experienced working with Good Manufacturing Practice (GMP) in projects or operations? Would you like to be part of a team of skilled colleagues, ensuring GMP compliance in engineering projects shaping the pharma facilities of the future? And do you thrive on engaging with customers? Then you’ll fit right in!

We are experts in end-to-end pharma engineering, and we design and build pharma facilities that are essential for millions of patients all over the world. Our success is built on our relationships, both with our colleagues and our customers. If you are passionate about working for a noble cause on projects shaping the future of sustainable and intelligent pharma facilities, NNE is the place to be. 

Locations: Kalundborg and/or Virum

The Role & Department
We are seeking GMP Consultants to join our GMP Design & Support department. Our team tackles innovative and complex projects that will challenge and engage you. Why do we need you? Our mission is to help our customers bring well-designed GMP facilities into operation quickly and predictably. Your role will be pivotal in delivering the best possible service to our clients, making your broad knowledge and expertise in GMP regulations and compliance essential.

Responsabilities
As a GMP Consultant, you’ll be:

  • Supporting our customers in setting the GMP design strategy for engineering projects, and verifying compliance with the strategy throughout the project.
  • Facilitating the interpretation of cGMP to ensure that the solutions delivered to our customers are GMP compliant.
  • Focusing on customer needs for an innovative and efficient pharma business operation, without compromising GMP compliance.

Requirements
We care about who you are as a person. In the end, how you work, and your energy, is what impacts the results we achieve as a team.

As a person, you are:

  • Passionate about bringing well-designed GMP facilities into operation.
  • Enthusiastic, results-oriented, and have a desire to learn and act as a mentor to others.
  • Enjoying variation and flexibility in your projects.
  • Demonstrating technical curiosity as well as a sense of quality and service.
  • Responsible when solving tasks, and you thrive in a dynamic and global work environment where you can work independently as well as in teams.
  • Approaching projects and customers with a can-do attitude, and you can listen and ask questions to understand their needs.
  • Understanding and respectful of your colleagues’ individual and cultural differences.

We believe these qualifications are needed for you to do well in this role:

  • You have experience working in a GMP-regulated environment.
  • You are knowledgeable about GMP regulations and how to apply them in your work.
  • You are familiar with terminologies like Quality Risk Management, Room Classifications, and Science and Risk-based approaches to validation
  • You value having fruitful dialogues with colleagues and customers.
  • You speak and write fluent English.
  • You have a diploma or master’s degree in life sciences or other relevant education.

If you do not check all the boxes, you are welcome to offer alternative experience that you think would be valuable in this role.

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Project Manager in large, complex project within Pharma - NNE
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Employer: Novo Nordisk Engineering (NNE)

Do you want to work with a highly skilled project team in a complex setting, and does the idea of making an impact for patients all over the world excite you? Then you’ll fit right in!

We are experts in end-to-end pharma engineering, and we design and build pharma facilities that are essential for millions of patients all over the world. Our success is built on our relationships, both with our colleagues and our customers. If you are passionate about working for a noble cause on projects shaping the future of sustainable and intelligent pharma facilities, NNE is the place to be. 

Locations: Kalundborg

The Role & Department
We are looking to expand our team of almost 50 highly skilled, cross-disciplinary project managers. We are currently leading some of the most exciting and interesting engineering projects within pharma and biotech projects. All activities are project-based, and you will be playing a key role in a successful delivery.

Your role in the project will be either as a work package owner with responsibility for one or several work packages or as an assisting PM to one of our more senior project managers.

Responsabilities
As Project Manager, you’ll be with a multi-disciplinary team, where you’ll be:

  • Taking leadership to ensure project objectives are met within scope, budget, and timeline.
  • Developing and maintaining detailed project plans, including milestones, resources, and risk management.
  • Serving as a key liaison between clients, stakeholders, and internal teams to facilitate communication and ensure project alignment with organizational goals.
  • Motivate and inspire the project team.
  • Identifying potential risks and implementing proactive strategies to mitigate challenges.
  • Supporting the continuous improvement of project management processes within the organization.

Requirements
We care about who you are as a person. In the end, how you work, and your energy, is what impacts the results we achieve as a team.

As a person, you are:

  • understanding of your colleagues’ individual and cultural differences.
  • a good listener who always comes with solutions.
  • aware of your surroundings and able to flag any concerns.
  • agile and able to prioritize urgent tasks.
  • able to collaborate on team projects.
  • excited to build on the NNE culture of innovation.

In all positions there are some things that are needed, and others a bonus. We believe these qualifications are needed for you to do well in this role:

  • You have a M.Sc. or B.Sc. within engineering, chemistry, biotechnology, pharmaceutical production or similar
  • You have proven project management skills.
  • You communicate well in English, both in writing and orally.
  • Familiarity with the pharmaceutical and biotech industries is an advantage.
  • If you do not check all the boxes, you are welcome to offer alternative experience that you think would be valuable in this role.
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IT Validation Engineer - NNE
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Employer: Novo Nordisk Engineering (NNE)

Does the idea of working with validation of complex data engineering solutions excite you? And do you thrive on close collaboration with great colleagues? Then you’ll fit right in!

We are experts in end-to-end pharma engineering, and we design and build pharma facilities that are essential for millions of patients all over the world. Our success is built on our relationships, both with our colleagues and our customers. If you are passionate about working for a noble cause on projects shaping the future of sustainable and intelligent pharma facilities, NNE is the place to be. 

Locations: Virum or Kalundborg

The Role 

We are looking for a Validation Engineer to join our team of highly skilled colleagues in Manufacturing Intelligence. As a team, we are working on providing full-service intelligence solutions for pharma manufacturing, covering all aspects of data engineering and science, including cloud deployment, app development, data implementation, data management, GxP validation, and advanced analytics.

We specializes in data connectivity solutions that enable data-driven decision-making, process automation, and faster access to critical production data.

Why do we need you? Our goal is to grow our Danish team providing our customers with skilled resources for their projects and strategic challenges. Your role will be key in developing solutions for customers, ensuring proper testing and documentation of solutions, and continuously give input to our department’s skillset and delivery models.

Responsabilities
As an IT Validation Engineer, you’ll be:

  • Part of setting the standard for testing and qualification of the developed solutions
  • Coordinating with engineers across disciplines in close collaboration with our customers
  • Participate in IT risk assessments and requirement setting
  • Monitoring the quality of the validation work and supporting engineers during test activities
  • Working with Science and Risk based validation with high focus on quality of data and data integrity

Requirements
We care about who you are as a person. In the end, how you work, and your energy, is what impacts the results we achieve as a team.

As a person, you are:

  • Enthusiastic about IT and data quality and interested in learning
  • Outgoing who actively seek advice and share knowledge among colleagues and peers
  • Result-oriented and have a well-structured work ethic
  • Efficient and keep your promises and deadlines
  • Comfortable with direct Customer interaction and relationship building


In all positions there are some things that are needed, and others a bonus. We believe these qualifications are needed for you to do well in this role:

  • Experience in the Lifesciences and/or Biotech Industry preferably particularly in Commissioning, Qualification and Validation of automation systems, software, or IT
  • Have worked with GAMP5, SRV, IT risk assessments and GMP test documentation is an advantage
  • Knowledge of/or experience working with MS Azure DevOps or eTIMS (HP ALM)
  • Knowledge of/or experience in basic coding languages, markdown editing etc
  • You have a degree in engineering or other relevant work experience
  • You speak and write English fluently and optionally Danish

If you do not check all the boxes, you are welcome to offer alternative experience that you think would be valuable in this role.

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Process Automation Engineer - NNE
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Employer: Novo Nordisk Engineering (NNE)

Does the idea of being a part of NNE’s all-time largest Process Automation team excite you? And do you thrive on solving complex challenges and driving innovation? Then you’ll fit right in!

We are experts in end-to-end pharma engineering, and we design and build pharma facilities that are essential for millions of patients all over the world. Our success is built on our relationships, both with our colleagues and our customers. If you are passionate about working for a noble cause on projects shaping the future of sustainable and intelligent pharma facilities, NNE is the place to be. 

Locations: Kalundborg

The Role & Department
We are looking for curious and experienced colleagues seeking the opportunity to join a fantastic company, where we together have the aspiration of becoming best in class within Automation Solutions for Pharmaceutical Engineering.

The Process Automation teamwork with consultancy, design & development, implementation, and validation of Automation solutions for the Pharma and Biotech industries. We work in projects and base our solutions on a deep understanding of our customers’ production processes – and if standard components can’t do the job, we develop our own. We are skilled in a broad range of process areas within API production, e.g. fermentation, recovery and purification, utility, and cleaning systems. We are right now looking into a long, exciting pipeline of large data driven, greenfield plants with modular/scalable designs.

You will be working in an enthusiastic and exciting team with more than 60 colleagues. Furthermore, you will become part of a global Process Automation team with more than 125 motivated employees. You will discover that your future colleagues are highly professional and forthcoming in welcoming you to the team.

Responsabilities

  • Advising customers on their selection of automation solutions
  • Designing, developing, implementing, qualifying and supporting Process Control Systems (PCS/DCS)
  • Interacting with process experts and colleagues with expertise in surrounding systems and equipment like MES, Historian systems, instruments, production equipment etc.
  • Developing and optimizing automation methods and strategies to meet our customers’ needs and sharing working knowledge with colleagues and partners
  • Forming the basis of automation strategies and architectures to support our sister departments internationally and expand NNE’s Process Automation engagement

Requirements
We care about who you are as a person. In the end, how you work, and your energy, is what impacts the results we achieve as a team.

As a person, you are:

  • Understand your colleagues’ individual and cultural differences.
  • A good listener who always comes with solutions.
  • Able to prioritize urgent tasks, flag concerns, and collaborate effectively.
  • Eager to learn and are excited to build on the NNE culture of innovation.
  • Reliable and committed to contributing positively to the team.
  • Appreciative of feedback because it contributes to your growth.

In all positions there are some things that are needed, and others a bonus.
We believe these qualifications are needed for you to do well in this role:

  • You have 3 years or more of working experience and hold a degree as an engineer, ideally within electrical, automation, process or marine engineering.
  • You have 2 years or more of working experience with PCS/DCS Application development (for example 800xA or SattLine), working in GMP/GAMP environment or with execution of Automation projects
    Knowledge of batch production is valued.
  • You have an interest of working with PCS/DCS Application development (800xA or SattLine).
  • You find the GMP/GAMP environment exciting.
  • If you do not check all the boxes, you are welcome to offer alternative experience that you think would be valuable in this role.
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Data Partner
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Employer: Ferrosan Medical Devices

The Role & Department
Do you want to be part of an innovative IT-team within a company making a global impact on healthcare? Join us at Ferrosan Medical Devices, where you can shape the future of surgical care while developing your skills in a fast-paced environment. Every other second our products help surgeons and nurses control bleedings and avoid complications in surgical procedures. We make seconds count in surgical care! And we need you on our team!

We expand our team with a Data Partner role that will serve as a strategic link between our data science team and our business units. This role is crucial in driving the integration of data insights into business decisions, enhancing data literacy, and fostering a data-centric culture. Your role will be to ensure that our data-driven initiatives support our overall business objectives and generate measurable value.

Responsibilities
Your role will amongst other be to:

  • Collaborate with our business units to identify data needs, drive data initiatives, and deliver actionable insights for strategic decisions.
  • Translate complex data analytics into clear, actionable business recommendations.
  • Lead the implementation of data governance standards to ensure data quality and integrity across the organization.
  • Manage data-related projects, including coordinating with stakeholders to ensure successful execution and alignment with business goals.
  • Drive the development of data literacy within the organization, empowering business units to make data-informed decisions.
  • Communicate findings and strategies effectively to diverse stakeholders through reports, dashboards, and presentations.

Your profile
A passion for data is an absolute must and an insight into how to use the data for management insights, too, and other than that you can probably tick off all or some of the below requirements:

  • A bachelor’s or master’s degree in data science, business analytics, information technology, or a related field.
  • Proven experience in a data-focused role, ideally within a business environment delivering strategic insights.
  • Proficiency in data analysis and visualization tools (e.g., SQL, Python, R) and experience with business intelligence platforms (e.g., Power BI).
  • Strong project management skills, with the ability to drive data initiatives from concept through execution.
  • Excellent communication and stakeholder management skills, with the ability to translate data concepts into business terms.
  • A proactive, analytical mindset with a passion for using data to drive business success.

We offer
We offer a truly purpose driven workplace with strong roots in values. What exactly this means is quickly visible to our new colleagues. We are driven by improving patient outcomes and we take our values to work every day – we care about each other, our environment and our customers and we win for patients with innovative high-quality solutions.  
 
We offer an inclusive workplace with the opportunity to have real impact and a development curve, that you can steepen in the pace, that is suitable to you. You will meet a DK rooted company growing in number of international colleagues and a way of working, where hybrid, digital, learning and innovation are key words. And we take pride in having fun😊. 

 

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IT/OT Engineer
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Employer: Ferrosan Medical Devices

Introduction
Do you want to be a part of the IT department in a company with a unique impact on global healthcare? Grab this opportunity to join a rapidly growing company, where we are ready to invest in you. Here you will not only get to impact the production and development of our products; you will also have every opportunity to develop your skills further.

Every 2nd second Ferrosan Medical Devices’ products help surgeons and nurses control bleedings and avoid complications in surgical procedures. We make seconds count in surgical care! And we need you on our team!

About Ferrosan Medical Devices A/S
Ferrosan Medical Devices develops and produces a portfolio of medical devices used in surgical care. Our portfolio consists of various hemostatic products to minimize bleeding challenges in surgery and electromechanical medical devices to perform breast biopsies. We are an international company with products registered in more than 100 countries. Our products are marketed in collaboration with global MedTech partners. Innovative ideas are developed and matured from the first thought to finished implementation in production. And we manage the business with an uncompromising focus on quality based on current GMP requirements.

Role summary
As our IT/OT Engineer, you will be responsible for managing and optimizing our hybrid IT/OT-environment. This role involves maintaining the stability, security, and performance of IT/OT-systems, ensuring seamless integration and operational efficiency.

Responsibilities

  • Ensure continued compliance with GxP-regulations, guidelines and internal procedures
  • Manage and maintain IT/OT-infrastructure, including servers, networks, and storage systems across multiple sites
  • Implement measures to protect IT/OT-systems
  • Troubleshoot and resolve system issues in a timely manner
  • Collaborate with cross-functional teams to ensure IT/OT alignment and integration
  • Develop and maintain system documentation and standard operating procedures
  • Conduct system performance tuning and capacity planning
  • Participate in IT/OT projects e.g. implementation of SCADA-solutions
  • Participate in disaster recovery planning and execution

Your profile

  • Preferably a Bachelor’s degree in Computer Science, Information Technology, or related field
  • A minimum of 5 years of experience in IT/OT system administration in a regulated industry
  • Proficiency in managing Windows and Linux servers
  • Strong understanding of network protocols, firewalls, and security measures
  • Experience with virtualization technologies such as VMware or Hyper-V
  • Knowledge of industrial control systems (ICS) and supervisory control and data acquisition (SCADA) systems
  • Excellent problem-solving skills and attention to detail
  • Strong communication and interpersonal skills

We offer
We offer a truly purpose driven workplace with strong roots in values. What exactly this means is quickly visible to our new colleagues. We are driven by improving patient outcomes and we take our values to work every day – we care about each other, our environment and our customers and we win for patients with innovative high-quality solutions.  
 
We offer an inclusive workplace with the opportunity to have real impact and a development curve, that you can steepen in the pace, that is suitable to you. You will meet a DK rooted company growing in number of international colleagues and a way of working, where hybrid, digital, learning and innovation are key words. And we take pride in having fun😊. 

 

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Senior Project Engineer
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Employer: Ferrosan Medical Devices

The Role & Department
Do you want to be a part of an engineering project team in a company with a unique impact on global healthcare? Grab this opportunity to join a rapidly growing company, ready to invest in you. Here you will not only get to impact the production and development of our products; you will also have every opportunity to develop and grow your own skills.   

Every 2nd second, Ferrosan Medical Devices’ products help surgeons and nurses control bleedings and avoid complications in surgical procedures. We make seconds count in surgical care! And we need you on our team! 

You will become responsible for specifying and implementing next generation manufacturing equipment for internal paste filling processes
We are expanding our production capability in site Søborg as we are approaching new markets with our products. To succeed with this, we are looking for a new colleague to join our department of Technology Innovation, Internal Engineering.

Responsibilities
As our new Senior Project Engineer, you will be responsible for developing and specifying new filling production equipment – both for development purposes and capacity expansion of SURGIFLO®. Here you will be responsible for developing equipment specifications and production equipment to produce within these specifications. You will join a team of project engineers responsible for development of all internal processes and equipment in site Søborg, for the manufacturing of SURGIFLO® and other products.

In collaboration with stakeholders such as team members from Product Innovation and Process Support, you will prepare user requirement specifications, development studies, validation plans, and other documentation needed to ensure that we have effective processes, equipment, and high-quality products. Success in this role will require a structured and data-based approach, where you ensure and verify the correct documentation, and process impact. 

A lot of your work will include close cooperation with both our external machine builders, manufacturing partners and internal stakeholders like Product Innovation, Quality Assurance and Manufacturing. 

Your profile
As a person, you are a team player, and you are skilled in keeping an overview of your tasks. You are quality minded, and you are known for a high commitment to finding constructive solutions as well as taking responsibility for your assignments. You thrive in a high pace environment.

You have a solid data-based approach to your work, and you understand the importance of documentation and processes. At the same time, you thrive when interacting with a range of different people. You have the skills to communicate and convey technical matters into more tangible formulations. Your language proficiency in both written and spoken English is at a professional level as many of your tasks will be executed in collaboration with English speaking colleagues.

Qualifications
Ideally, you hold an Engineering degree or similar and experience with specifying automated manufacturing equipment for manufacturing of medical devices (not a requirement).

Other relevant qualifications are:

  • Experience with filling, assembly, or packaging of pharmaceutical products.
  • Experience with specifying manufacturing equipment for other industries; food, automotive/other.
  • Experience with and understanding of GMP, process risk management, validation, and qualification of production processes.
  • Experience with the design control disciplines.

We offer
We offer a truly purpose driven workplace with strong roots in values. What exactly this means is quickly visible to our new colleagues. We are driven by improving patient outcomes and we take our values to work every day – we care about each other, our environment and our customers and we win for patients with innovative high-quality solutions.  
 
We offer an inclusive workplace with the opportunity to have real impact and a development curve, that you can steepen in the pace, that is suitable to you. You will meet a DK rooted company growing in number of international colleagues and a way of working, where hybrid, digital, learning and innovation are key words. And we take pride in having fun😊. 

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Automation Engineer
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Employer: Ferrosan Medical Devices

Introduction 
Do you want to be a part of Technical Support in a company with a unique impact on global healthcare? Grab this opportunity to join a rapidly growing company, ready to invest in you. Here you will not only get to impact the production and development of our products; you will also have every opportunity to develop and grow your own skills. Every 2nd second, Ferrosan Medical Devices’ products help surgeons and nurses control bleedings and avoid complications in surgical procedures. We make seconds count in surgical care! And we need you on our team!  

Manufacturing at Ferrosan Medical Devices
Manufacturing in Ferrosan Medical Devices consists of approximately 190 people spread across key departments – two production departments, Process Support, EHS and Technical Support, Utility & Facility. These departments work cohesively to ensure the seamless production and delivery of our cutting-edge medical devices, demonstrating a commitment to precision, efficiency, and continuous improvement adhering to Lean methodologies. This position is organized in the “Technical Support, Utility & Facility team” which consists of 24 engineers and technical staff with different technical backgrounds and is led by a Senior Manager and a Manager. You will mainly work together with two other facility colleagues.

Position Overview
Ferrosan Medical Devices is currently investing many resources in their headquarter site in Søborg. So far this has resulted in building a state-of-the-art new factory and updating the utilities, so that daily operations continue to be both energy-efficient and compliant with regulations. Furthermore, the ambition for the Automation area is to become even more robust and thereby more process-oriented through updated system descriptions and renewed processes.

As a result of the investments and renewed ambitions, Ferrosan Medical Devices is now looking to strengthen their department for Technical Support & Utilities by hiring an Automation Engineer, who can help take responsibility for the automated systems used in the manufacturing operations. Your new team consists of 24 highly skilled colleagues who enjoy helping each other and sharing their knowledge.

Your role
As Automation Engineer you will be supporting the Technical Support team with your automation knowledge, and you get to participate in various optimizing projects of production and utility systems to ensure continuous optimization of the technical equipment and machines including setting requirements, testing and documentation. Further you be participating in troubleshooting together with utilities technicians in our production facilities and utilities installations including ensuring the right electrical drawings and machine/system documentation.

During operationally critical situations you provide support to onsite technicians and process owners.

Further tasks could include:

  • Updating electrical documentation
  • Back-up of parameters in VLT/frequency converters, PLCs
  • Troubleshooting and service tasks on existing systems
  • Development tasks in collaboration with colleagues and vendors.
  • Participating in Testing and (re)commissioning of production machines and utility systems.
  • Handling compliance documentation and deviations.

Your profile
First and foremost, it is vital that you are a true team player and a great colleague. You have relevant technical skills, preferably supplemented with experience in automation and GMP production.

  • You have experience with PLC - preferably Siemens software S5, S7, TIA
  • You can read Siemens PLC code
  • Troubleshoot system PLC controller by using PLC code documents.
  • Have a good knowledge of frequency inverters e.g. Danfoss
  • Have good knowledge of machines safety, with various levels of protection
  • Have a good knowledge of automations div. instruments, signals, measuring principles etc.
  • Can read electrical wiring diagrams and use them for troubleshooting
  • Have good knowledge of working within GMP area and compliance.

We offer
We offer a truly purpose driven workplace with strong roots in values. What exactly this means is quickly visible to our new colleagues. We are driven by improving patient outcomes and we take our values to work every day – we care about each other, our environment and our customers and we win for patients with innovative high-quality solutions.  
 
We offer an inclusive workplace with the opportunity to have real impact and a development curve, that you can steepen in the pace, that is suitable to you. You will meet a DK rooted company growing in number of international colleagues and a way of working, where hybrid, digital, learning and innovation are key words. And we take pride in having fun😊. 

 

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Senior Plastic Specialist
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Employer: Ferrosan Medical Devices

The Role & Department
Do you want to be a part of an engineering team in a company with a unique impact on global healthcare? Grab this opportunity to join a rapidly growing company, ready to invest in you. Here you will not only get to impact the production and development of our products, you will also have every opportunity to develop and grow your own skills.   

Every two seconds, products from Ferrosan Medical Devices help surgeons and nurses around the world to control bleedings and avoid complications in surgical procedures. We make seconds count in surgical care! And we need you on our team! 

Joining us at our HQ in Søborg, Denmark, you will become an integral part of our Technology Innovation department, consisting of 20 highly specialized engineers and pharmacists. You will be a part of the Technology Innovation external team dividing your time between operational tasks, ensuring our outsourced production runs smoothly, and play an important role in our development projects. 

Responsibilities
More specifically, you will be spending a great deal of your time working closely with our sub-suppliers of injection moulding, handling the challenges and obstacles that may occur during production.
Doing so, you can look forward to:

  • Supporting our sub-suppliers, ensuring that we can deliver and keep our production running.
  • Participating in projects, design workshops, and cooperating with stakeholders across our organization.
  • Establishing and maintaining documentation packages, and life-cycle management of our components.
  • Overseeing and giving input to validation activities carried out by suppliers.
  • Implementing changes and improvements through our change control system.

Your profile
As a person, you are a team player, and you are skilled in keeping an overview of your tasks. 
You are quality-conscious, and you are known for a high commitment to finding constructive solutions as well as taking responsibility for your assignments.
You thrive in a high pace environment.
You have a solid data-based approach to your work, and you understand the importance of documentation and processes. At the same time, you thrive when interacting with a range of different people.
You have the skills to communicate and convey technical matters into more tangible formulations.
Your language proficiency in both written and spoken English is at a professional level as many of your tasks will be executed in collaboration with English speaking colleagues. 

Qualifications
Ideally, you hold an Engineering degree and experience with injection moulding, plastic production and technical projects.

Other relevant qualifications are:

  • Experience with production – preferably from a similar industry (medtech/pharma/food).
  • Experience with project management.
  • Experience with and understanding of GMP, process risk management, validation, and qualification of production processes.

We offer
We offer a truly purpose driven workplace with strong roots in values. What exactly this means is quickly visible to our new colleagues. We are driven by improving patient outcomes and we take our values to work every day – we care about each other, our environment and our customers and we win for patients with innovative high-quality solutions.  
 
We offer an inclusive workplace with the opportunity to have real impact and a development curve, that you can steepen in the pace, that is suitable to you. You will meet a DK rooted company growing in number of international colleagues and a way of working, where hybrid, digital, learning and innovation are key words. And we take pride in having fun😊. 

 

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User Insights Specialist
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Employer: Ferrosan Medical Devices

The Role & Department
Do you want to be part of the Clinical Insights Department at a company that has a unique impact on global healthcare? Are you ready to influence the future of hemostatic products and accessories? Can you help identify unmet user needs and integrate user experiences into product development? Then join Ferrosan Medical Devices as our User Insights Specialist. Every other second, Ferrosan Medical Devices’ products help surgeons and nurses control bleeding and avoid complications during surgical procedures. We make every second count in surgical care, and we need you on our team! 

Become part of our Clinical Insights team
 
At Ferrosan Medical Devices, we develop hemostatic products that surgeons in over 100 countries use to manage bleeding during surgeries. We focus on creating user-friendly solutions that enhance the workflow for operating room nurses. We’ve been developing hemostatic products since 1947, and we take pride in contributing to improved patient outcomes in surgery.
 
Your new team, Clinical Insights, ensures user feedback is integrated throughout the development process—from idea conception to market release. Our deep understanding of user needs and environments guides our development process. We explore unmet user needs and transform them into product features that make a real difference for our users. We leverage usability expertise to bring the best possible products to market—ones that are effective, safe, and easy to use.

Responsibilities
You'll be warmly welcomed into our team of two, where helpfulness and a strong team spirit are key to achieving the best results. Clinical Insights is part of the New Business Development Department, working closely with Device R&D, Product Innovation, Product Development, and Commercial Development.

As part of the early-stage product innovation team, you'll help set the direction for product development based on user needs and market trends.

In this role, you will:

  • Identify and explore unmet user needs within surgery
  • Interpret user and market insights and present recommendations to the innovation team
  • Generate usability engineering documentation and support risk management. 

Your profile

  • You have an educational background in healthcare, life sciences, medical health sciences, or a related field—at least at the Bachelor's level
  • You have a few years of experience in user needs identification and usability/human factors engineering, preferably in the Medtech Industry
  • You know how to gather valuable insights from users using voice of customer and usability engineering methods, and you can translate these insights into product features and design requirements in collaboration with an innovation team
  • You work diligently, in depth, and in a structured manner with multiple usability documents
  • You have knowledge of the IEC 62366 usability engineering standard and FDA guidance for applying human factors and usability engineering to medical devices
  • You have strong collaboration skills
  • You are fluent in English, both written and spoken  

We offer
We offer a truly purpose driven workplace with strong roots in values. What exactly this means is quickly visible to our new colleagues. We are driven by improving patient outcomes and we take our values to work every day – we care about each other, our environment and our customers and we win for patients with innovative high-quality solutions.  
 
We offer an inclusive workplace with the opportunity to have real impact and a development curve, that you can steepen in the pace, that is suitable to you. You will meet a DK rooted company growing in number of international colleagues and a way of working, where hybrid, digital, learning and innovation are key words. And we take pride in having fun😊. 

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Principal Category Manager
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Employer: Ferrosan Medical Devices

The Role & Department
Do you want to be responsible for developing our Sourcing of Plastic suppliers to new heights? Do you want to make a difference for patients undergoing surgery by securing the compliance of the medical devices used by healthcare professionals? 

Here you have the opportunity to get an exciting and challenging job, as Principal Category Manager, in a international company. As Ferrosan Medical Devices is growing, you will be able to shape the job in our Strategic Sourcing Department to a large extent. The position refers to the Senior Manager of Strategic Sourcing.

The department Strategic Sourcing is part of Supply Chain Management, which is a central area in Ferrosan Medical Devices. Strategic Sourcing consists of 6 experienced Category Managers covering direct spend, CMOs and Indirect spend including equipment and machinery. The team is responsible for all aspects of supplier management including supplier selection, negotiation, and collaboration as well as risk mitigation, spend/savings program, and category strategies. 

Responsibilities
You get a central position, with responsibility for the collaboration and development of the company's Plastic Suppliers. There will be a great deal of contact with the suppliers, who are primarily in Europe, as well as a broad contact surface across Ferrosan Medical Devices. Your main tasks will be:

  • Establishment and maintenance of Category strategies.
  • Daily handling and collaboration with our current Suppliers.
  • Negotiations and conclusion of contracts. 
  • Development of the supplier base.
  • Optimizing the processes and structure around the Suppliers.
  • Participate in various product development and optimization projects. 

The overall purpose of the position is to ensure robust cooperation and management of our Plastic suppliers, this to reduce total costs through close cooperation, taking quality, reliability and risk management into account.

To be successful, you must internally work closely together with e.g. Finance, the Development department, the Quality organization and your colleagues in Supply Chain Management and Operations.

Your profile
The ideal candidate for the job holds experience from a similar role managing and leading Categories from a highly regulated industry such as medical devices, pharma, biotech, life science or similar. As a person you have a pragmatic approach, and you find solutions to identified problems:

  • Minimum B.Sc. – ideally a degree at M.Sc. level as an Engineer, Economist or within Supply Chain.
  • Minimum +5 years of experience within purchasing and/or Supply Chain.
  • You have experience with Category Management and supplier handling.
  • Demonstrated track record in finding pragmatic solutions to complex or challenging problems.
  • Highly experienced in stakeholder management.
  • Your work style is involving and impactful.
  • You think in holistic terms and with a business-oriented approach to the solutions.
  • You have created visible results in your current or previous roles.
  • You have experience with GMP.
  • Possess strong oral/written communication skills in English.

We offer
We offer a truly purpose driven workplace with strong roots in values. What exactly this means is quickly visible to our new colleagues. We are driven by improving patient outcomes and we take our values to work every day – we care about each other, our environment and our customers and we win for patients with innovative high-quality solutions.  
 
We offer an inclusive workplace with the opportunity to have real impact and a development curve, that you can steepen in the pace, that is suitable to you. You will meet a DK rooted company growing in number of international colleagues and a way of working, where hybrid, digital, learning and innovation are key words. And we take pride in having fun😊. 
 

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Student opportunities at at Novo Nordisk Engineering
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Employer: Novo Nordisk Engineering (NNE)

As a company NNE value the knowledge that student workers, interns and thesis writers bring to their company. NNE offers specific opportunities for motivated and ambitious students who are eager to pursue careers in the pharmaceutical industry:

  1. Student internships
  2. Student jobs
  3. Master’s thesis projects


1. STUDENT INTERNSHIPS

An internship will provide you with valuable work experience and inside knowledge of the various types of positions and responsibilities at NNE. An internship usually lasts three to six months and assignments vary. Positions are both paid and unpaid and become available throughout the year.

Who can apply?
NNE’s student internship program is designed for students who are enrolled in a degree program (BSc, MSc or MBA degree level) at an accredited college or university.

Engineers
The internships for engineering students are targeted at academic majors in:

  • Automation
  • Architecture and design
  • Structural engineering
  • Civil engineering
  • Mechanical and electrical engineering
  • Chemistry, food, biotechnology, dairy, food science or similar areas

Other areas
We also offer internships in the following areas:

  • Finance/project economy
  • Human resources
  • IT 
  • Purchasing
  • Sales and marketing

2. STUDENT JOBS
Gaining work experience is the perfect way to get a better understanding of roles and assignments you wish to engage in once you finish university. You will obtain valuable industry insight and learn more about yourself, your strengths and your development potential.

We offer between 10-20 hours a week all depending on how you can combine the job with your studies, as we know you need the flexibility, also around holiday and exam periods. Few positions are full-time positions.

Responsibilities
The responsibilities of student staff range from providing customer service and technical support, preparing for and participating in events held by our offices to assisting with various projects as needed.

Who can apply?
Student jobs are designed for students who are enrolled as degree-seeking students at an accredited college or university. Student jobs are available at all our offices worldwide and are posted as needed.

Requirements
You are enrolled in a university or college program.

3. MASTER’S THESIS PROJECTS
A Master’s thesis project is a way for us to get to know you as a student and also to learn about the latest developments in the academic world. Working on a Master’s thesis is your first step into working life and, we hope, a new acquaintance with NNE.

Who can apply?
We invite Master’s degree students to use NNE as a case study in dissertations or major projects within:

  • Automation
  • Architecture and design
  • Structural engineering
  • Civil engineering
  • Mechanical and electrical engineering
  • Chemistry, food, biotechnology, dairy, food science or similar areas

Available case projects
When we have Master’s thesis projects available, we list them on our career site at www.nne.com. If no projects are announced, but you have your own idea that you think could be implemented together with us, you are welcome to contact us.

⚠️ To submit your application, please go to the following site: 
https://www.nne.com/careers/entry-level/

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Graduate Programme - Demant
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Employer: Demant

The Graduate Programme at Demant offers you a unique opportunity to develop your personal and professional skills in a great working environment. You will join us in improving the lives of millions of people worldwide through hearing health.

We offer 10 different tracks:

  1. Commercial Excellence
  2. Global Business
  3. Intellectual Properties
  4. Operations
  5. Finance
  6. Tax
  7. Audiology
  8. Legal 
  9. Engineering 
  10. Commercial 

How it works?
Each track will take you through three or four rotations in a two-year journey. During your rotations, you will get hands-on experience with different challenging projects that allow you to learn and build on your knowledge and skills. We are a global company, so all tracks are designed with an international perspective, in fact, many of our graduates also have the opportunity to go abroad for one rotation. 

After successfully completing the Programme, we offer you a permanent position with Demant - either in Denmark or abroad. However during the Graduate Programme graduates receive a full-time salary from the start.

As a graduate, you will have an introduction week in the beginning, training bootcamps, visits to our business sites, as well as management meetings. Also, we offer you a beneficial health insurance, a wide range of sporting and leisure clubs including offer for massages, a healthy and delicious canteen, and lot of fun activities and events with the other graduates.

When does the Graduate Program start?

For foreign students:
Demant is an international company, and our business language is English. It is possible to apply for the Graduate Programme before you graduate, as long as you complete your studies before the start of the Programme.

Further information: 
https://www.demant.com/jobs-and-career/graduate-programme

⚠️ To submit your application, please go to the following site:
https://www.demant.com/jobs-and-career/graduate-programme

 

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Newly graduated Automation Engineer at Novo Nordisk Engineering
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Employer: Novo Nordisk Engineering (NNE)

Does the idea of learning about Process Control Systems excite you? And do you thrive in gaining knowledge of GMP and pharmaceutical production? Then you’ll fit right in!

We are experts in end-to-end pharma engineering, and we design and build pharma facilities that are essential for millions of patients all over the world. Our success is built on our relationships, both with our colleagues and our customers. If you are passionate about working for a noble cause on projects shaping the future of sustainable and intelligent pharma facilities, NNE is the place to be. 

Locations: Kalundborg

The Role & Department
We are looking for newly graduated Automation Engineers to join our team of Process Automation Engineers. As a team, we are working on the biggest projects in Novo Nordisk history. Our goal is to implement robust and future-proof solutions for our customers. Your role will be key in designing, implementing, and validating automation solutions for the pharmaceutical industries.

Responsabilities

  • Designing, developing, implementing, qualifying, and supporting Process Control Systems /Distributed control system (DCS).
  • Interacting with process experts and colleagues with expertise in surrounding systems and equipment like Manufacturing Execution System (MES), Historian systems, Instruments, Production equipment etc.
  • Developing and optimizing automation methods and strategies to meet our customers’ challenges and sharing state-of-the-art knowledge with colleagues and partners.
  • Advising customers on their selection of automation solutions.
  • Forming the basis of automation strategies and architectures to support our sister departments internationally and expand NNE’s Process Automation engagement.

Requirements
We care about who you are as a person. In the end, how you work, and your energy, is what impacts the results we achieve as a team.

As a person, you are:

  • A team-oriented person, curious and eager to learn.
  • Comfortable with customer relations.
  • Passionate about your work and with a personal drive.
  • Pro-active, cooperative and with a motivated mindset.

We believe these qualifications are needed for you to do well in this role:

  • You have a degree within chemistry, automation, or electrical engineering.
  • You have an interest of working with PCS/DCS Application development such as ABB 800xA or ABB SattLine).
  • You find the GMP/GAMP environment exciting.

If you do not check all the boxes, you are welcome to offer alternative experience that you think would be valuable in this role.

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Vestas Global Graduate Programme
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Employer: Vestas

The Vestas Global Graduate Programme is an important part of our talent strategy. Through the programme, we aim to seek out the future people- and business leaders, specialists, and project managers that can help us reach our ambitious objectives – and make the world a better place while doing so.

The programme is the ideal opportunity for you to embark on an exciting global career while contributing to the solution of one of the most urgent challenges of our time: the climate crisis.

Do you want to play a pivotal part in the green energy transition?

The four areas of interest:

  1. Business, Commercial & Strategy
  2. Digital, IT & Projects
  3. Supply Chain, Service & Logistics
  4. Engineering, R&D & Innovation

How it works?
As a global programme, the Vestas Global Graduate Programme provides you with the opportunity to work in two different areas and locations of our organisation, allowing you to gain a thorough understanding of our purpose, values, and culture. Throughout the two years, you will get two rotations of 12 months each, starting in September. You will be exposed to five modules, each with a different leadership focus. As a Graduate, you will hold a full-time position where you will be equipped with the tools, support, and knowledge you need to succeed. The salary offered is comparable to an entry level position depending on the country in which you are hired.

When does the Graduate Program start?
The recruitment window for the 2025 Vestas Global Graduate Programme will open 1st of December 2024 and close on the 15th of January 2025 at 23.59 CET.

For foreign students:
In order to qualify for the Vestas Global Graduate Programme, you must already have completed either your Bachelor’s or Master’s degree and possess a valid work permit in the country that you are applying for. 

Further information: 
https://www.vestas.com/en/careers/early-careers/graduate-programme

⚠️ To submit your application, please go to the following site:
https://www.vestas.com/en/careers/early-careers/graduate-programme

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Graduate Programs - GN Group
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Employer: GN Group

The GN Group will soon be launching their Graduate Programs which will be open to 15 recent graduates in the fields of Engineering, Finance, Marketing, Information Technology, Supply Chain and Business.

It offers you a unique opportunity to make a true difference in people’s everyday lives. As a GN Graduate you will experience a great network of peers, a steep learning curve, management exposure, and get a unique opportunity to develop personal and professional skills in a global setting.

Our long-term plans include you!

Apply for one of our six tracks:

  1. Engineering
  2. Finance
  3. Marketing
  4. IT
  5. Supply Chain
  6. Business

How it works?
We offer a two-year cross-functional program with 3 rotations of eight months duration. You will spend the 2nd rotation abroad in one of our many subsidiaries around the globe.
You will get included as every other employee in the company and you will work on your own projects during each rotation. As you are considered to be an employee you will be paid a full time salary with pension and other benefits.
During the 2 years that the program lasts, you will be prepared for a career in GN, and we will support you in finding a position in the company during your third rotation.

When does the Graduate Program start?
The recruitment window will open from October 2024, the Graduate Program will start on September 1st 2025.

For foreign students:
We are a multi-cultural and inclusive company, so the only language we require is English.
And even though you are still on your Master, we hope to get an application from you, so you can start your career with us when you finish your education.

Further information: 
https://www.gn.com/Working-with-us/Graduate-Program

⚠️ To submit your application, please go to the following site:
https://www.gn.com/Working-with-us/Graduate-Program

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Staff Scientist in Molecular Palynology at GLOBE Institute
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Employer: Faculty of Health and Medical Sciences University of Copenhagen

Place of employment
The place of work is at the Section for GeoGenetics, Globe Institute, University of Copenhagen. We offer supportive, creative, and stimulating working conditions within a dynamic and international research environment. Our research facilities include a LEAF GOLD certified molecular lab, designed for generating genomic-scale datasets from both modern and ancient specimens, complemented by high-capacity computational servers adept at handling such data.

The Role & Depertement
We invite applications for the position of Staff Scientist in Molecular Palynology. This role is a fixed-term position limited to a period of four years, commencing on 1 January 2025 or as soon as possible thereafter. The position will be based at the Globe Institute, University of Copenhagen.

The successful candidate will join the Conservation Palaeogenetics & Palaeoecology Group at the Section for GeoGenetics, led by Assistant Professor Ana Prohaska. We work at the interface of palaeoecology, ancient genetics, evolutionary biology, and conservation science to understand how species and ecosystems responded to past environmental change and how this understanding can inform conservation decision-making today. Our focus is on identifying and, where possible, recovering genetic diversity relevant to preserving Earth’s contemporary biodiversity into the future. For more information about the group and our research, please see: globe.ku.dk/research/geogenetics/prohaska-group.

Your work will be embedded within the newly awarded Ancient Environmental Genomics Initiative for Sustainability (AEGIS) funded by the Novo Nordisk Foundation. This interdisciplinary research initiative aims to build a more sustainable and secure food production system while also preserving biodiversity in cropping systems under climate change. Its approach is to produce new knowledge and develop innovative methodologies in ancient environmental DNA to identify important organismal associations and genetic adaptations relevant to future food security. The initiative brings together a large international network of researchers with expertise in genetics, ecology, evolutionary biology, plant sciences, computer science, statistics, geology, archaeology, and more.

Responsabilities
The successful candidate will join an exciting new research programme within the AEGIS aimed at advancing the recovery and analysis of ancient pollen DNA using state-of-the-art single-cell sequencing technologies. The main objective of this programme is to develop and employ high-throughput methods for reconstructing ancient plant genomes, which will be applicable to a wide range of plant species worldwide. The selected candidate will contribute to and support (1) the wet lab workflow for sequencing bulk and single pollen DNA in a clean lab setting, and (2) its application to fossil pollen records from various depositional settings, as part of AEGIS’s Data Engine.

The tasks include but are not limited to:

  • Responsibility for the daily operation of the instrumentation for pollen isolation and handling.
  • Responsibility for preparing pollen samples for extraction and library preparation and coordinating their submission to other laboratory pipelines.
  • Participation in the development and implementation of protocols for fossil pollen DNA extraction, library preparation and sequencing.
  • Participation in the establishment of the bioinformatic pipeline for the analysis of ancient pollen DNA data.
  • Technical support in planning and troubleshooting.
  • Participation in the scientific activities of the group and the initiative.
  • Keeping up to date with technological developments.
  • Work in close collaboration with other scientific staff and academics at the section.

Requirements
We are looking for a highly motivated and energetic candidate with the following competencies and experience:

Essential qualifications and skills

  • MSc degree in molecular biology, (paleo)ecology, genetics, evolutionary biology, or a related field.
  • Extensive experience in palynological analysis.
  • Demonstrated experience in molecular biology methods.
  • A genuine interest in developing and advancing wet lab methodologies and protocols.
  • Self-motivation, pragmatic mindset, strong work ethics, and good interpersonal skills.
  • Ability to organise time and work effectively and responsibly, independently and in teams.
  • Strong attention to detail with demonstrated skills in troubleshooting.
  • Enthusiasm to be part of an interdisciplinary research project and work collaboratively with scientists across a wide range of disciplines.
  • Fluency in both written and spoken English (due to the institute's international profile).

Desirable experience and skills

  • PhD in molecular biology, (paleo)ecology, genetics, evolutionary biology, or a related field
  • Knowledge of ancient DNA laboratory techniques.
  • Knowledge of single-cell laboratory techniques.
  • Experience with the production of single-cell and/ or ancient genetic data.
  • Experience with statistical data analysis.

Terms of employment
The average weekly working hours are 37 hours per week.
The position is a fixed-term position limited to a period of four years. The starting date is 1 January 2025 or as soon as possible thereafter.
Employment will be in accordance with the provisions of the collective agreement between the Danish Ministry of Taxation and AC (the Danish Confederation of Professional Associations) as Academic Research Staff.
The monthly salary will be based on the number of years of work experience (seniority) with the possibility to negotiate a salary supplement based on prior experiences and qualifications. The employer will pay an additional 17.1 % to your pension fund.

Further information
For further information regarding the position, please contact Ana Prohaska; 
anaprohaska@sund.ku.dk

 

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Two Laboratory Assistant positions in the Wennerberg Group
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Employer: Copenhagen University

Place of employment
The Wennerberg Group at the Biotech and Research Innovation Center (BRIC), University of Copenhagen, is looking for two Laboratory Assistants for laboratory maintenance with effect from November 15, 2024.

The Wennerberg group at BRIC focuses on identifying new effective precision cancer therapies. This is done with a systems-driven approach where we combine chemical biology, phenotypic profiling, molecular profiling, and informatics to gain an understanding of individual cancers, their drug resistance mechanisms, and how they may be targeted. Our goal is to build the foundation for new types of stratified and individualized curative treatment strategies for cancer patients.

We offer creative and stimulating working conditions in dynamic and international research environment. Our research facilities include modern laboratories, and several core facilities shared between the 24 research groups at BRIC and the neighbouring Finsen Laboratory.

Responsabilities
We are looking for two part-time employees who want to help us with our routine laboratory duties. The jobs entail maintaining our laboratory supplies together with fulfilling weekly cleaning duties. More specifically, your tasks will include:

  • Revising our stocks of general laboratory supplies (i.e., culture plates, pipette tips, PBS, etc.).
  • Filling in order forms for the products that are low in stock.
  • Perform weekly cleaning of our cell lab including incubators, water baths, and LAF benches according to our cleaning guidelines.

Working hours are expected to be divided over 3-4 days/week for a total of 12 h/week.

Requirements
We are looking for a highly motivated and enthusiastic individual to help us out as a laboratory assistant.

  • We expect that you have an ongoing bachelor’s and/or master’s biology education.
  • We also expect that the successful candidate is systematic, detail-oriented, and self-driven.
  • Previous laboratory and research work experience, as part of courses, internships, or employment is a plus.

Terms of employment
Starting date is as soon as possible, with November 15, 2024, being the desired start date. The employment as Laboratory Assistant is a fixed term and part-time position with an average of 12 working hours per week until January 31, 2026.

The employment is made in accordance with the Collective Agreement between the Danish Ministry of Finance and the Organisations of Public Employees – governmental institutions (the OAO-S collective agreement) and the Professional Agreement for clerical employees, laboratory technicians and IT officers in the state.

Further information
For further information please contact Krister Wennerberg, 
krister.wennerberg@bric.ku.dk

 

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Laboratory Manager for reNEW
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Employer: Copenhagen University

Place of employment
The Novo Nordisk Foundation Center for Stem Cell Medicine, reNEW is a worldwide consortium with nodes at the University of Copenhagen, Murdoch Children’s Research Institute, Melbourne, Australia and Leiden University Medical Centre, Netherlands. Researchers within reNEW addresses fundamental questions in stem cell biology and translate research findings to products that will help patients with incurable disorders such as congenital kidney disorders, diabetes, heart defects, neurological conditions, chronic ulcerative conditions, respiratory diseases, bladder defects and infertility.

reNEW Copenhagen is a vibrant, internationally diverse, and ambitious research center with state-of-the-art facilities located at the Faculty of Health and Medical Sciences, University of Copenhagen. The setting is ideally suited for seamless collaboration and access to a large variety of technology platforms within the Copenhagen area as well as within the other reNEW units in Melbourne and Leiden.

The Role
The role of the laboratory manager is to support and enable researchers to perform their work safely and efficiently while ensuring smooth operations within the reNEW laboratories.
The laboratory manager will report directly to the center management and head of staff.

Responsabilities
The tasks include:

  • Ensuring optimal usage of instruments and laboratories.
  • Ensuring that the laboratories are following all legal requirements.
  • Communication and training of health and safety rules.
  • Arranging procurement and services of common equipment.
  • Supporting purchase of common laboratory items, including through contact with suppliers, and general organization of stocks, shipment reception and distribution within reNEW.
  • Managing the lab operations team, including task and work assignment
  • Collaboration and communication with the laboratory users.
  • Collaborate and coordinate with reNEW Technology Platform leads to ensure continuous and smooth daily operations.
  • Organisation of laboratory users group meetings.
  • Taking part in various meeting within the university (Chemical coordinator, lab manager, etc.).
  • Budgeting and reporting of common laboratory expenses and handling of internal cost recovery where applicable.
  • Reacting to matters raised by laboratory colleagues and providing guidance and support to address suggestions and incidents.

Requirements

  • You have as a minimum a laboratory or university-based education within the field of life sciences, natural sciences or similar.
  • You have experience in laboratory management (minimum of two to three years) and people management.
  • You have experience in GMO1 laboratory settings, including tissues culture.
  • Experience in Kemibrug, GMO2 laboratory, Sharepoint, booking systems, and/or Lab Guru is desirable.
  • Experience and training in health and safety rules and regulations is desirable.
  • Very good communication skills in Danish and English (written and verbally).
  • You are a friendly and open, yet firm and effective communicator across the broad spectrum of scientific employees within an internationally staffed institution.
  • You have an efficient and self-organised working style and experience of how to effectively communicate in a multifaceted organisation and smaller task-oriented teams.
  • You commit to being physically present and readily available in the lab during working hours.

We offer

  • A stimulating, challenging and multifaceted research environment
  • A combination of active scientific service platforms to interact with, and to develop ideas together to improve our lab for everyone
  • Involvement in cutting-edge research in a diverse and multicultural community
  • Possibility for continued education and training
  • Attractive employment conditions
  • Centrally located workplace.

Terms of employment
Your employment will be at Novo Nordisk Foundation Center for Stem Cell Medicine, University of Copenhagen. The position is full-time (37 hours per week) and for 2 years, and it is open for appointment on 15th of November 2024 or as soon as possible.

Employment as Biomedical Laboratory Scientist will be in accordance with the agreement between the Danish Ministry of Finance and Danske Bioanalytikere
Employment as laboratory technician will be in accordance with the agreement between the Danish Ministry of Finance and OAO/HK STAT. The position is placed in salary group 5.

Depending on qualifications a supplement may be negotiated.

Further information
For further information please contact Associate Professor, Mariaceleste Aragona;
mariaceleste.aragona@sund.ku.dk

 

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Researcher in ex vivo dietary microbiome interventions
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Employer: Copenhagen University

Place of employment
Novo Nordisk Foundation Center for Basic Metabolic Research (CBMR) is an academic research Center that pioneers groundbreaking research towards better cardiometabolic health. Through collaborative interdisciplinary research from single-cell genomics to whole-body systems, CBMR aims to transform the basic understanding of cardiometabolic health and accelerate its translation into prevention and treatment strategies. The Center’s uniquely multi- and interdisciplinary approach combines research in genetics, physiology and pharma­cology, to better understand the complex interplay of the many factors that drive cardiometabolic disease. 

The Role, Project & Departement
We are looking for an experienced and motivated Researcher having extensive experience with ex vivo and in vitro microbiome culture and characterization to work in the Arumugam Group at The Novo Nordisk Foundation Center for Basic Metabolic Research (CBMR). The position is a 2-year position starting December 1, 2024, or after agreement.

The project aims to decipher how dietary components affect specific members of the human gut microbiome using high-throughput dietary interventions on ex-vivo human gut microbiomes.

The Microbiome Systems Biology research group led by Associate Professor Manimozhiyan Arumugam investigates how health and diseases are influenced by our gut microbiome, how the gut microbiome interacts with the host and environmental factors, and how we can therapeutically modulate the gut microbiome to improve metabolic health. The group takes an interdisciplinary approach combining multi-omics microbiome data to study host-microbial cross-talk.

Responsabilities
Your tasks will include:

  • In-vitro culturing and characterizing complex microbial communities; designing and performing dietary/nutrient intervention on these communities; and performing molecular microbiology characterizations.
  • You will work closely together with lab technicians, bioinformaticians and researchers at multiple levels.
  • We expect you to operate and run fed-batch anaerobic fermenters, perform sample collections and extraction of nucleic acids and metabolites.
  • You will be responsible for coordinating the running of multi-omics (metagenomics, metatranscriptomics, meta-proteomics and metabolomics) and data analysis with technicians and bionformaticians.
  • You will also participate in collaborative projects with other research groups at the Center that involves in vitro culturing of gut microbiota.
  • Lastly, you will be expected to actively contribute to creating novel ideas, writing research publications and grant applications, supervising students, and presenting the results at seminars and conferences.

Requirements
We are looking for a highly motivated and enthusiastic Researcher with the following competencies and qualifications:

Essential criteria:

  • PhD in microbiology, molecular biology or a similar field
  • Minimum of three years’ of postdoc experience.
  • Strong project management and coordination skills.
  • Solid experience in operating large volume anaerobic chambers.
  • Solid experience in operating fed-batch fermenters (e.g. SHIME, TIM-2) and maintaining continuous cultures of fecal microbial communities.
  • Strong experience in generating and interpreting metabolomic data from in vitro microbial communities.
  • Strong collaborative skills; ability to share knowledge and expertise, and provide support to a multidisciplinary team.
  • Proven track record showing scientific productivity in peer reviewed journals.
  • Excellent written and oral communication skills in English.
  • Strong interest in learning more about the life science area, particularly metabolic disorders.

Desirable criteria:

  • Experience in culturomics approaches.
  • Experience in setting up defined synthetic microbial communities in vitro.
  • Experience in identifying high-value compounds from microbial world.
  • Insight in the area of health, life science and nutrition research.

Terms of employment
The employment as Researcher is a full time and fixed-term position for 2 years. Starting date is December 1, 2024, or after agreement.
Salary, pension and terms of employment will be in accordance with the agreement between the Ministry of Taxation and AC (Danish Confederation of Professional Associations). Depending on qualifications, a supplement may be negotiated.

Non-Danish and Danish applicants may be eligible for tax reductions, if they hold a PhD degree and have not lived in Denmark the last 10 years.
The position is covered by the “Memorandum on Job Structure for Academic Staff at the Universities” of June 28, 2013.

Further information
For further information please contact Associate Professor Mani Arumugam at 
arumugam@sund.ku.dk. For questions regarding the recruitment procedure, please contact SUND HR CBMR at SUND-HR-CBMR@sund.ku.dk

 

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Junior Automation Engineers Pipeline
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Employer: Novo Nordisk - Denmark

At Novo Nordisk we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives, backgrounds and cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve and communities we operate in. Together, we’re life changing.

Locations: We are looking for candidates to all our locations. This specific pipeline covers on-site positions in Kalundborg.

The Role & Department
Are you ready to take the next step and pursue a life-changing career at Novo Nordisk? Are you driven by automation and digitalization of the Novo Nordisk manufacturing value chain? Look no further!
We are building a talent pipeline for Junior Professionals to join Novo Nordisk in shaping the future through automation.

Joining the Automation Engineers Pipeline

By applying for the pipeline, you will be considered as a potential match for on-site automation related positions, which align with your background, skills, and interests across various areas in Denmark.

 

Due to the expansion of our activities in all business areas and sites, we are currently seeking talents for many different teams across Novo Nordisk, such as Advanced automation, Manufacturing Execution Systems (MES), and Collaborative- and industrial robotics. We encourage you to read more detailed information about the different roles and areas through this link: https://www.novonordisk.com/careers/campaigns/automation-engineer-process-digitalization.html

Requirements
We are looking for someone with an innovative and solution-oriented mindset. As you will be working and collaborating with people from various departments in the organization, it would be preferable that you are ready to take the lead on deploying solutions that bring value.

To apply to our pipeline, we expect that you:

  • Are newly graduated with a bachelor’s or master’s degree within e.g., IT, Automation, or Robotics
  • Would like to build on your skills and experience together with highly dedicated colleagues.
  • Are proactive, solution-oriented, like to share your knowledge and collaborate effectively.
  • Work systematically and with the ability to develop and implement practical actions to deal with issues.
  • Have proficient oral and written communications skills in English. Danish language skills are great advantage.
  • As documentation according to Good Manufacturing Practice (GMP), rules are part of our daily work, it is important that you thrive in ensuring that all your work is well documented.

 

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Junior Automation Engineers Pipeline
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Employer: Novo Nordisk - Denmark

At Novo Nordisk we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives, backgrounds and cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve and communities we operate in. Together, we’re life changing.

Locations: We are looking for candidates to all our locations. This specific pipeline covers on-site positions in Greater Copenhagen area e.g.: Bagsværd, Gentofte, Søborg, Lyngby, Måløv, Kirke Værløse.

The Role & Department
Are you ready to take the next step and pursue a life-changing career at Novo Nordisk? Are you driven by automation and digitalization of the Novo Nordisk manufacturing value chain? Look no further!

Joining the Automation Engineers Pipeline

By applying for the pipeline, you will be considered as a potential match for on-site automation related positions, which align with your background, skills, and interests across various areas in Denmark.

Due to the expansion of our activities in all business areas and sites, we are currently seeking talents for many different teams across Novo Nordisk, such as Advanced automation, Manufacturing Execution Systems (MES), and Collaborative- and industrial robotics. We encourage you to read more detailed information about the different roles and areas through this link: https://www.novonordisk.com/careers/campaigns/automation-engineer-process-digitalization.html

Requirements
We are looking for someone with an innovative and solution-oriented mindset. As you will be working and collaborating with people from various departments in the organization, it would be preferable that you are ready to take the lead on deploying solutions that bring value.

To apply to our pipeline, we expect that you:

  • Are newly graduated with a bachelor’s or master’s degree within e.g., IT, Automation, or Robotics
  • Would like to build on your skills and experience together with highly dedicated colleagues.
  • Are proactive, solution-oriented, like to share your knowledge and collaborate effectively.
  • Work systematically and with the ability to develop and implement practical actions to deal with issues.
  • Have proficient oral and written communications skills in English. Danish language skills are great advantage.
  • As documentation according to Good Manufacturing Practice (GMP), rules are part of our daily work, it is important that you thrive in ensuring that all your work is well documented.

 

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Graduate Programme - Novo Nordisk (in Denmark)
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Employer: Novo Nordisk - Denmark

Turn your master’s degree into a global career​ from September 2025!

‎Our global Graduate Programme is designed to bring together change makers with a diversity of perspectives and equip them with the tools needed to accelerate their personal and professional development. The two-year programme allows you to explore the world while developing your career. You will be taken on three to four rotations around the globe where you will work in a fast-paced environment with plenty of growth opportunities. You will be exposed to different parts of the Novo Nordisk value chain while being challenged to explore your boundaries and reach your full potential. 

After successfully completing the programme, you will be equipped with professional and personal skills to embark on your global career with the guarantee of a position at Novo Nordisk.

We open for applications 1 November 2024 for graduate careers starting 1 September 2025.

What is the Graduate Programme?
The Graduate Programme is a two-year, global career journey with a minimum of three rotations including at least one rotation outside your home country. The destination depends on the specific graduate programme track but it could for instance be in one of the Novo Nordisk sites in Denmark, our International Operations (IO) Strategic Head Office in Zurich, an IO Regional Office or one of our many affiliates globally.

The Graduate Programme is Novo Nordisk’s flagship ‘Talent programme’. Many top leaders started their journey in Novo Nordisk as part of the graduate programme, including our CEO Lars Fruergaard Jørgensen.

Is the Graduate Programme paid?
Yes, the Graduate Programme is a full-time position, and we offer a competitive entry level salary. The compensation and benefits package includes components such as pension and health insurance, based on local terms and is applicable to the country you are hired in.

What are the programme track I can apply to?

♦︎ TECHNOLOGY: Revolutionising the pharmaceutical industry through manufacturing technology, digitalisation and data science.

♦︎ PHARMACEUTICAL DEVELOPMENT: Life-changing careers within research and development and trial management.

♦︎ BUSINESS, COMMERCIAL, MARKETING & HR: A range of opportunities across our Global Business functions in HQ as well as in our local affiliates.

♦︎ FINANCE: Developing the next generation of finance leaders across various finance functions

♦︎ PROCUREMENT & SUPPLY CHAIN: Bringing value to Novo Nordisk and making a difference to patients and society while getting to know the core of our business.

♦︎ LEGAL ETHICS & COMPLIANCE: Fostering and strengthening a culture of ethics and compliance while experiencing three jobs in just two years.

Application requirements
Applicants must have a recent and relevant master’s degree* and international experience; for example, working, volunteering or from studying a full semester abroad.

We imagine that you have no more than one year of relevant work experience after graduation, above average academic achievements, and the ability to relocate internationally. In addition, Novo Nordisk’s corporate language is English, so you will be fluent in written and spoken English.

*If you are applying for one of our graduate positions in Latin America the master’s degree criteria is waived. Instead, you have a bachelor’s degree and one to two years of relevant full-time work experience at the time of application. If you have a master’s degree, then you should have a maximum of one year work experience.

Does Novo Nordisk sponsor visas for international students?
Yes, all nationalities can apply to the programme. If selected, Novo Nordisk helps you secure your work visa. 

Do I need to speak Danish in order to apply for the Graduate Programme?
No, our corporate language is English, so speaking Danish is definitely not a requirement. There may be local language requirements for some International Operations (IO) tracks.
 
⚠️ To submit your application, please go to the following site: 
https://www.novonordisk.com/careers/early-career-programmes/graduate.html
 
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Scientist, QA Manufacturing Support
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Employer: AGC Biologics

Our purpose is to bring hope to life by enabling life-changing therapies for patients around the globe, creating a healthier and happier tomorrow. Our mission is to work side by side with our customers in order to improve patients’ lives by bringing new biopharmaceuticals to market.

At AGC Biologics, you will get a unique opportunity working with a variety of different state of the art technologies among +40 different nationalities. This opens many doors for personal development and for you to make a real difference towards both patients, customers and own development. AGC offers an informal and friendly working environment, characterized by the fact that we think it is fun to go to work. We respect each other and our differences. AGC employees are flexible and take pride in working together to achieve goals - as one team.  

The Role & Department
The QA Manufacturing Support Scientist is responsible for quality activities supporting Manufacturing Operations in accordance with procedures and GMP requirements. Functional responsibilities include ensuring manufacturing compliance with applicable procedures, providing real time review of manufacturing records and logbooks, and working with Manufacturing Operations to resolve issues.

Location: Copenhagen, Denmark

Responsibilities

  • Provide an “on-line” Quality presence in the production area during manufacture regarding on the line documents and product checks and quality support for production enquiries. To inform line management of any issues relating to the quality of products or materials.
  • Perform QA sign off after set-up to confirm that the manufacturing line has been set up as per requirements in batch documentation and associated SOPs.
  • Conduct batch record “Stage Approval” as part of batch release process.
  • Participate in Gemba walks of the production area and conduct specific site systems audits in accordance with the agreed schedule.
  • Shipping/ prepacking approval.
  • Manufacturing label management. 
  • Archiving.
  • Review and approval of validation/ qualification documentation.
  • Review all batch documentation, liaising with production management to resolve and clarify any points of issue.
  • Work with manufacturing to drive improvements in GMP compliance across all shifts.
  • Support manufacturing during batch review with Good Documentation Practice related queries.
  • Perform Quality review and approval of deviations (DEVs), change controls (CRs) and CAPAs.
  • Buffer and media MPR review and approval

Requirements  

  • Bachelor's and/or Master’s degree in Natural Sciences.
  • Alternatively, certified laboratory technician with a degree in laboratory science, biotechnology, medical laboratory technology including 3-5 years experience within a GMP environment in the Pharma Industry.
  • Experience with BPR/MPR review will be a plus.
  • Previous biopharma experience is preferred but not a requirement.
  • Strong working knowledge of the principles and guidelines for GMP is a plus.
  • Strong decision maker and ‘can do’ attitude. 
  • Excellent written and verbal communication skills to internal and external stakeholders.
  • Ability to work in a fast paced, matrix environment is essential.
  • Capable of working to deadlines and prioritizing multiple tasks.
  • Flexibility to meet changing needs and priorities of the business.
  • Experience working in a GMP aseptic manufacturing environment will be a plus.  

 

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Scientist, Manufacturing
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Employer: AGC Biologics

Our purpose is to bring hope to life by enabling life-changing therapies for patients around the globe, creating a healthier and happier tomorrow. Our mission is to work side by side with our customers in order to improve patients’ lives by bringing new biopharmaceuticals to market.

At AGC Biologics, you will get a unique opportunity working with a variety of different state of the art technologies among +40 different nationalities. This opens many doors for personal development and for you to make a real difference towards both patients, customers and own development. AGC offers an informal and friendly working environment, characterized by the fact that we think it is fun to go to work. We respect each other and our differences. AGC employees are flexible and take pride in working together to achieve goals - as one team.  

Location: Copenhagen, Denmark

The Role & Department
Do you have experience working in a cGMP environment and are you looking for new opportunities for further growth? Then this position could be something for you.  

As a CDMO, AGC Biologics manufactures drugs for a variety of different customers. Depending on the customer needs, this can be for drugs ranging from development, to clinical and commercial production. Right now, you have the opportunity to join the Mammalian department as a Review and compliance Supporter in Mammalian Production Coordination Team. This position requires high level process and compliance understanding as well as inter-departmental collaboration.  

The Mammalian Production coordination team owns the production process of all products. This includes to support the Production with an error-free and timely production execution and own batch documentation, review and deviation handling. The team has in depth knowledge of the product specific requirements. 

Responsabilities  

  • Responsible for/Consulted during MPR creation on process steps to align production flow and GDocP requirements.
  • Daily review of documentation in production.
  • Accountable for timely batch review according to KPI.
  • Accountable for timely deviation closure (incl. systematic problem-solving during root cause investigation) according to KPI.
  • Responsible for enabling timely batch release.
  • Responsible for data feedback/status on release process. 

Other 

  • Responsible for capturing learnings and align with MPR template owner to continuously improve MPR template.
  • Responsible for sharing knowledge across project groups. 

Requirements  
The ideal candidate holds an Academic degree within science and have previously been working in a manufacturing team operating under cGMP preferably within the pharmaceutical industry. The ideal candidate for the position has several of the below competencies/experiences: 

  • Experience in preferably in commercial/commercial GMP manufacturing. 
  • Have experience with and demonstrated understanding of Good Manufacturing Practices (GMP).
  • Have experience writing, reviewing and approving GMP documentation. 
  • Experienced with operations of single-use technologies and aseptic processing. 
  • Self-motivated, organized and proactive. 
  • Ability to coordinate multi-departmental tasks and deliverables (interaction with Process Transfer, Process Development, Engineering, QA, QC, etc.). 
  • Experience working with multiple projects simultaneously. 
  • Demonstrated experience leading troubleshooting efforts. 
  • Strong communication skills necessary to interact with internal and external stakeholders. 
  • Strong presentation skills.   

 

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Technicians / Service Engineers – DTU Nanolab
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Employer: Technical University of Denmark

At DTU Nanolab, we are expanding our activities within micro- and nanofabrication and therefore need more technicians/service engineers to join us in the development of the technical solutions of tomorrow. DTU Nanolab is one of the world’s best-equipped open access centers within nanofabrication and characterization located at the Technical University of Denmark in Copenhagen. We are seeking curious and dedicated candidates to join our technical support teams in up to four new positions. We encourage both experienced technicians as well as newly educated candidates with a background from vacuum, refrigeration or mechatronics systems to apply.

Our cleanroom facility houses more than 150 highly advanced tools. The tools combine many different areas such as high vacuum technology, RF plasma, gas-handling systems (toxic and non-toxic), pneumatic control systems, and heating/refrigeration systems. This means that you should be able to navigate and troubleshoot in systems with high complexity.

Responsabilities
You will become a member of one of our equipment groups that consist of process specialists and equipment engineers. Here, you will be working together with extremely competent specialized colleagues with a focus on repair and maintenance to ensure that the equipment can meet our quality standards. We expect you to strive to deliver high quality, safe and reliable solutions.

Key tasks include:

  • Take part in the equipment maintenance 
  • Troubleshooting/repair of equipment breakdowns
  • Participate in organizing maintenance and repair tasks
  • Keep focus on safe working environment
  • Maintaining spare parts inventory
  • Carrying out machine upgrades 
  • Documenting breakdowns, repairs and maintenance tasks

Requirements
For these positions, you should have:

  • A minimum of 3 years relevant education within automation, mechatronics or electronics or related technical field relevant work experience may compensate for lack of formal education.
  • Experience of working with vacuum systems, pneumatic controls, electronics, and gas systems would definitely be of benefit but not essential as we are prepared to train the successful candidates.
  • You should be safety minded, self-driven, and pro-active. Since you will be working as part of a team, it is important to have a positive and open-minded attitude.

What we offer
We offer an interesting and challenging job in an international atmosphere with the focus on research, teaching, innovation, and scientific advice for the benefit of the surrounding community. We have an informal and welcoming work atmosphere where commitment is essential, and we keep up a good spirit. Our approach to planning and conducting tasks is team oriented with focus on a well develop social work environment. We offer great flexibility in the position and expect similar flexibility from you.

Terms of employment
Salary and appointment terms are in accordance with either the collective agreement with the Danish Confederation of Professional Associations (AC), or the OAO-S Joint Agreement and the organization agreement for Laboratory Technicians and IT staff (HK/Stat), for Craftsmen and Technicians, for Engineering Assistants and Research Technicians at research institutions, etc., or other relevant agreement.

The position is permanent and full-time (37 hours per week). Starting date as soon as possible (according to mutual agreement). 

The workplace is DTU Lyngby Campus.

Further information
If you would like additional information about the position, please contact Head of Process Engineering Flemming Jensen, 
flje@dtu.dk

 

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PhD Scholarships in Piezoelectric Biopolymer Technology and Devices for Drug Delivery on Demand – DTU Health Tech
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Employer: Technical University of Denmark

If you are establishing your career as a scientist and you have the ambition to develop groundbreaking smart technologies and devices for healthcare, this is the right research project for you.

The aim of the PhD project is to explore and develop new piezoelectric biomaterials and technologies for controlled drug release in smart devices by the application of ultrasound. The focus of the activity will be i) to produce thin films of biomaterials with high piezoelectric properties and loaded with drug molecules, ii) to develop MEMS devices based on piezopolymers, and iii) to develop and optimize a strategy for the remote release of drugs on demand. Within the framework of IDUN, we have extensively explored engineered micro-encapsulated pharmaceutical compounds and more advanced oral drug delivery concepts. In addition, we have expertise on developing piezoelectric materials and device fabrication methods for sensors and actuators for the human body. The PhD candidate will be a part of the IDUN center of excellence, led by Prof. Anja Boisen at DTU Department of Health Technology, and will work under the supervision of Prof. Massimo De Vittorio. IDUN is a highly cross-disciplinary research center with over 40 members, that focuses on development of micro and nanotechnology-based sensors, detection systems and drug delivery devices.

Responsibilities
Your overall focus will be on the design, realization, and test of devices such as smart pills or flexible MEMS transducers based on piezoelectric biopolymers such as chitosan and cellulose, the two most abundant biopolymers on earth. You will work with nearby colleagues and with academic, clinical, and industrial partners in Denmark as well as abroad. 

Your primary tasks will be to:

  • Develop biopolymers thin films embedding drugs with high piezoelectric properties.
  • Tailoring the optical, mechanical, piezoelectric and electrical properties of the thin films by advanced and innovative fabrication methods for improving retention and drug delivery on demand. 
  • Design and fabricate piezoelectric devices by advanced micro and nanofabrication methods.
  • Employ ultrasound in order to trigger and speed up the drug release from the piezoelectric biopolymers. Tests will be executed first in vitro and then, after successful validation, in vivo.
  • Teach and supervise BSc and MSc student projects, and be co-supervisor for PhD students

The research activity will be carried out within the framework of the Center of Excellence – IDUN. In IDUN, our motto is ‘bringing science to life’ and we believe in openness, inclusiveness, having ambitions, making a difference and collaboration.

You will play a role mainly in the “Optomechanical Biointerfaces” research group coordinated by prof. Massimo De Vittorio of the IDUN section, and you will interact with several members of IDUN working in different disciplines, such as biology, microfabrication, pharmaceutical science and polymer science. The project is highly interdisciplinary, and we expect that you enjoy teamwork.

Requirements

  • You have a background in materials science, chemistry and/or microfabrication technologies.
  • You are highly independent, self-motivated and enjoy collaboration in a multidisciplinary academic environment.
  • You have the ability to drive the project forward, supervise students and achieve ambitious goals.
  • You must have a two-year master's degree (120 ECTS points) or a similar degree with an academic level equivalent to a two-year master's degree. 

We offer
DTU is a leading technical university globally recognized for the excellence of its research, education, innovation and scientific advice. We offer a rewarding and challenging job in an international environment. We strive for academic excellence in an environment characterized by collegial respect and academic freedom tempered by responsibility.

Terms of employment
The appointment will be based on the collective agreement with the Danish Confederation of Professional Associations. The allowance will be agreed upon with the relevant union. 
The period of employment is 3 years. The expected start date is 1 January 2025 or shortly thereafter.

Further information 
Further information may be obtained from Professor Massimo De Vittorio, 
mdevit@dtu.dk 



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Laboratory Technologist (Laborant) within biology and translational research
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Employer: Aarhus University

The Department of Biomedicine at Faculty of Health at Aarhus University invites applications for a position as a laboratory technologist within biochemistry, medical biology and translational research as per 1 January 2025 or as soon as possible thereafter. The position is a permanent full-time position.

The Department of Biomedicine prioritises diversity and a good work environment, as this is a prerequisite for groundbreaking research. In a diverse and international research environment, dedicated employees are looking to generate new knowledge within biomedical research areas such as infection and inflammation, membranes, neuroscience and personalised medicine. The Department of Biomedicine provides research-based teaching of the highest quality and is responsible for a large part of the medical degree programme. Academic staff contribute to the teaching. English is the preferred language in the laboratory, at meetings and at seminars. The department employs approx. 500 people from all over the world, and they make use of the department's modern laboratory-, core- and animal facilities. The Department of Biomedicine focuses on innovation, entrepreneurship and collaboration with business and industry, and numerous researchers from the department have established companies to develop new medicinal treatments founded in professional scientific basic research. 

Responsibilities

As laboratory technologist, your primary tasks consist in performing multiple biochemical analyses as well as managing samples storage and preparation. You contribute also to the general laboratory operation of the team and the operational and maintenance of laboratory equipment. In your daily work, you have a close interaction with competent colleagues in a stimulating environment.

Your main tasks will consist of:

  • Collection, storage, and preparation of samples from mouse and human origine
  • DNA, RNA, and protein extraction
  • Measure of genes and proteins expression (PCR, Western blotting)
  • Operation and maintenance of laboratory equipment
  • Management of laboratory consumable and procurement

You will report to group leader, Professor Frederic Gachon.

Requirements

  • You have a background as Laboratory technologist (laborant) or Medical Laboratory Technologist (bioanalytiker).
  • Experience and training in animal experimentation.
  • The work language will be English and a reasonable level of understanding, writing, and speaking in English is required.
  • You have good interpersonal skills.
  • Inclusive and team-oriented and able to contribute to a good work environment.

Terms of employment
Terms of employment and pay are regulated by the collective agreement between the Ministry of Taxation and the Organisations of Public Employees, Denmark (OAO) or the Danish Confederation of Public Employees of 2010 (LC/CO10).

 

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Principal Category Manager
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Employer: Ferrosan Medical Devices

The Role & Department
Do you want to be responsible for developing our Sourcing of Plastic suppliers to new heights? Do you want to make a difference for patients undergoing surgery by securing the compliance of the medical devices used by healthcare professionals? 

Here you have the opportunity to get an exciting and challenging job, as Principal Category Manager, in a international company. As Ferrosan Medical Devices is growing, you will be able to shape the job in our Strategic Sourcing Department to a large extent. The position refers to the Senior Manager of Strategic Sourcing.

The department Strategic Sourcing is part of Supply Chain Management, which is a central area in Ferrosan Medical Devices. Strategic Sourcing consists of 6 experienced Category Managers covering direct spend, CMOs and Indirect spend including equipment and machinery. The team is responsible for all aspects of supplier management including supplier selection, negotiation, and collaboration as well as risk mitigation, spend/savings program, and category strategies. 

Responsibilities
You get a central position, with responsibility for the collaboration and development of the company's Plastic Suppliers. There will be a great deal of contact with the suppliers, who are primarily in Europe, as well as a broad contact surface across Ferrosan Medical Devices.

Your main tasks will be:

  • Establishment and maintenance of Category strategies.
  • Daily handling and collaboration with our current Suppliers.
  • Negotiations and conclusion of contracts.
  • Development of the supplier base.
  • Optimizing the processes and structure around the Suppliers.
  • Participate in various product development and optimization projects

The overall purpose of the position is to ensure robust cooperation and management of our Plastic suppliers, this to reduce total costs through close cooperation, taking quality, reliability and risk management into account.

To be successful, you must internally work closely together with e.g. Finance, the Development department, the Quality organization and your colleagues in Supply Chain Management and Operations.

Your profile
The ideal candidate for the job holds experience from a similar role managing and leading Categories from a highly regulated industry such as medical devices, pharma, biotech, life science or similar. As a person you have a pragmatic approach, and you find solutions to identified problems.

  • Minimum B.Sc. – ideally a degree at M.Sc. level as an Engineer, Economist or within Supply Chain.
  • Minimum +5 years of experience within purchasing and/or Supply Chain.
  • You have experience with Category Management and supplier handling.
  • Demonstrated track record in finding pragmatic solutions to complex or challenging problems.
  • Highly experienced in stakeholder management.
  • Your work style is involving and impactful.
  • You think in holistic terms and with a business-oriented approach to the solutions.
  • You have created visible results in your current or previous roles.
  • You have experience with GMP.
  • Possess strong oral/written communication skills in English.

We offer
We offer a truly purpose driven workplace with strong roots in values. What exactly this means is quickly visible to our new colleagues. We are driven by improving patient outcomes and we take our values to work every day – we care about each other, our environment and our customers and we win for patients with innovative high-quality solutions.  
 
We offer an inclusive workplace with the opportunity to have real impact and a development curve, that you can steepen in the pace, that is suitable to you. You will meet a DK rooted company growing in number of international colleagues and a way of working, where hybrid, digital, learning and innovation are key words. And we take pride in having fun😊. 

 

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Clinical Drug Supply Manager
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Employer: GENMAB

At Genmab, we’re committed to building extra[not]ordinary futures together, by developing antibody products and pioneering, knock-your-socks-off therapies that change the lives of patients and the future of cancer treatment and serious diseases. From our people who are caring, candid, and impact-driven to our business, which is innovative and rooted in science, we believe that being proudly unique, determined to be our best, and authentic is essential to fulfilling our purpose.

The Role & Department
Genmab is searching for an experienced Clinical Drug Supply Manager to be part of Global Clinical Drug Supply Operations in Copenhagen, DK or Princeton, NJ in commuting distance to our office locations to work according to our hybrid work arrangement.

Moving forward with many late-stage trials in pipeline, the Clinical Drug Supply Manager will be managing outsourcing of packaging, labelling, and distribution of clinical trial supplies for early as well as late stage Genmab clinical trials. The Clinical Drug Supply Manager will work closely with GMP QA and our CMOs ensuring timely packaging and labelling for our clinical trials as well as IST and PAA for patients with cancer and other serious diseases.

The Clinical Drug Supply Manager must have extensive knowledge of cGMP and have a focus on the level of quality in work performed.

The position reports to the Director of Global Clinical Drug Supply Operations based in Copenhagen.

Responsibilities

  • Manage and coordinate drug supply and to provide IMP for clinical trials, IST, and Pre-Approval Access Programs.
  • Manage and coordinate ancillaries, pre-medication, and comparators for clinical trials.
  • Set-up English Master Label, manage label translation without vendor and approval of label proofs/designs.
  • Manage set-up of distribution framework through service providers.
  • Define appropriate drug supply activities at CMO necessary for providing drug supplies for clinical trials.
  • Contribute to maintenance of SOPs and Work Instructions in the department.
  • Perform training of other team members.
  • Function as Subject Matter Expert within relevant areas.
  • Responsible for being compliant with Genmab’s quality system.

Requirements

  • At least 3 years’ experience in handling clinical drug supply, including setting up label text and handling of ancillaries.
  • Ability to manage stakeholders internally and externally.
  • Experience working with CMO for clinical trial supplies.
  • Training in GDP, GMP and GCP is a requirement.
  • Experience working with IST and PAA from a Sponsor perspective will be an advantage.
  • Excellent communication skills in English - both oral and written.

Moreover, you meet the following Personal Requirements

  • You can structure and organize your work.
  • You are process oriented and contribute to continuous improvements.
  • You have a quality mindset and can prioritize your work in a fast paced and changing environment.
  • You have good interpersonal and communication skills.
  • You can work independently as well as within global teams.
  • You are result- and goal-oriented and committed to contributing to the overall success of Genmab.

About You

  • You are passionate about our purpose and genuinely care about our mission to transform the lives of patients through innovative cancer treatment
  • You bring rigor and excellence to all that you do. You are a fierce believer in our rooted-in-science approach to problem-solving
  • You are a generous collaborator who can work in teams with diverse backgrounds
  • You are determined to do and be your best and take pride in enabling the best work of others on the team
  • You are not afraid to grapple with the unknown and be innovative
  • You have experience working in a fast-growing, dynamic company (or a strong desire to)
  • You work hard and are not afraid to have a little fun while you do so

The Team
You will be part of a highly competent team focused on packaging and labelling of supplies for clinical trials, working closely with the Global Clinical Drug Supply Planning team and our CMOs.
Together with Global Clinical Drug Supply Systems team the three teams make up the Global Clinical Drug Supply department.
We have an international and informal working environment with a high pace while having fun and focus on one team spirit both within and outside the team and department.

 

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