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Employer: AGC Biologics

Location: Copenhagen, Denmark

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.

Are you an experienced and passionate specialist in QC equipment, software, and compliance? Do you have a solid understanding of data integrity and enjoy working in a dynamic team where independence and expertise are key? If so, this position in our QC Equipment Department could be the perfect opportunity for you!

About QC & The QC Equipment Department:
The Quality Control (QC) organization is responsible for release testing of clinical and commercial batches, and validation of the analytical methods, as well as analysis of raw materials and stability programs. We are working in an international and customer oriented way to secure fast and reliable manufacturing of medicines to our customers.

QC consists of five departments: QC Bioassay, QC Chemistry, QC Microbiology, QC Support and QC Planning & Systems. The first three mentioned are major analytical areas, and the last two mentioned are support areas.

The current position is located in the QC Planning & Systems area, in the QC Equipment Department. QC Equipment consists of 12 dedicated and skilled professionals, supporting all equipment in QC. The role is based in Søborg, Denmark.

Role & Responsibilities:
You will play a pivotal role in managing the QC equipment and software (i.e. HPLC, CE, Octet, SoloVPE, qPCR, NIR, pipette robots). You will be responsible for ensuring that our equipments meet regulatory requirements and standards while actively contributing to hands-on equipment troubleshooting. This position requires a combination of technical expertise, and a deep understanding of data integrity principles.

Your Key Responsibilities:

• Equipment lifecycle management, including qualification and validation.
• Ensure compliance with cGMP regulations and ALCOA+ principles.
• Configuration of software, and collaborate with the IT department.
• Work with software and computerized QC equipment, including documentation and troubleshooting.
• Actively participate in laboratory troubleshooting
• Contribute to process optimization and the implementation of new technologies.
• Collaborate with team members and cross-functional departments to ensure efficient operations and high-quality outcomes.

Your Profile:

• A relevant scientific degree, within chemistry, biotechnology, engineering or pharmaceutical sciences.
• Documented experience with QC equipment and software, including qualification, validation, and compliance.
• Strong understanding of cGMP regulations and ALCOA+ principles.
• Practical experience with laboratory work and equipment.
• Independent, structured, and proactive in your approach to work.
• Thrive in a dynamic environment and possess excellent collaboration skills.

What We Offer:

• An exciting and challenging position in a dynamic QC Equipment Department.
• Opportunities for professional and personal development.
• A dedicated and skilled team working together to achieve common goals.
• Competitive salary and employment terms.

 

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Employer: H. Lundbeck

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Employer: H. Lundbeck

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Employer: Demant

Location: Smørum

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Employer: FujiFilm

Location: Hillerod

Join Our Growing Team at Fujifilm Diosynth Biotechnologies Denmark.

We are thrilled to share that Fujifilm Diosynth Biotechnologies Denmark is expanding, and so is our QC Compliance Support team. Our team of thirteen dynamic professionals is eager to welcome a new member with a background in GMP, ideally from previous QC or QA roles, or someone with proven experience in change management combined with a deep interest in quality and compliance. Take this opportunity to manage, coordinate and lead Change Controls in QC in a supportive and knowledge-sharing environment.

So, are you looking for an exciting new opportunity with a fast-growing company that values your work-life balance and well-being? Take this opportunity to manage Compliance Support Tasks within QC with a friendly and engaging team, and enjoy a competitive salary, a flexible workspace with remote work options, on-site massage sessions, access to a modern fitness center, and many other employee benefits. We can’t wait to meet you and help you settle in!

About the Quality Control Department

Located in Hillerød, our Quality Control department comprises approximately 260 employees across five testing teams and five support teams. We support onsite manufacturing with testing of drug substance and raw materials used in manufacturing, testing stability samples and testing of drug products and finished goods manufactured external.

About the QC Compliance Support Team

The QC Compliance Support Team is integral to our GMP compliance efforts and handles a variety of tasks including:

• Managing and writing QC Change Controls for both internal and customer-initiated changes.
• Coordinating, writing and documenting lab exceptions (OOS/OOT) and QC Deviation Investigations
• Preparing quality data for metric analysis and review meetings.
• Supporting customer contacts, supporting internal audits and inspections, and providing assistance across the QC organization and other departments onsite.

About the Role

• Drive and coordinate change controls with relevant stakeholders and experts.
• Maintain GMP documentation in collaboration with stakeholders and QA.
• Prepare and present performance KPI data in review meetings.
• Identify and execute process optimization opportunities.
• Take on new tasks linked to our site’s expansion in the coming years.

Preferred Qualifications:

• Experience in cGMP and pharmaceutical manufacturing.
• Proficient in managing Change Control records.
• Prior roles in CMO/CDMO/CLO or QC/QA.
• Academic degree or relevant training/experience.
• Self-motivated and systematic, with a strong aptitude for process improvement.
• Adaptable, with a focus on personal and professional growth.
• Excellent communication and collaboration skills.
• Familiarity with QC data systems (e.g., LIMS) and metrics tools (e.g., Tableau) is a plus.
• Proficiency in English; Danish proficiency is a plus but not required.

We Offer

• A competitive salary and bonus package.
• Benefits including health insurance, massage and physiotherapy, health checks, and a fitness center.
• Remote work options.
• Recently added amenities like a mobile barista coffee van.
• Canteen services including Friday brunch and monthly afternoon cake.
• A commitment to creating the best workplace environment, focusing on health and well-being.

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Employer: FujiFilm

Location: Hillerod
Time type: Full time

Manufacturing Associates (Operators) for the Drug Substance Manufacturing at FUJIFILM Diosynth Biotechnologies

For the Drug Substance Manufacturing Unit in Hillerød, FUJIFILM Diosynth Biotechnologies is looking for Manufacturing Associates (Operators) to support the biopharmaceutical production operations. 

FUJIFILM Diosynth Biotechnologies is currently expanding its capacity to support the large-scale production by adding 14 x 20,000L bioreactors and three downstream processing lines in Hillerød. The additional production capacity will make the facility the largest end-to-end Contract Development and Manufacturing Organization (CDMO) in Europe, offering a total of 20 x 20,000L bioreactors for drug substance production complemented by comprehensive drug product and finished goods services.

This is an excellent opportunity to join our company at a pivotal time of growth and be part of an exciting journey.

We are currently looking for candidates within our Drug Substance Manufacturing (DSM) for the two departments; Upstream and Downstream. These are covering different steps in the biopharmaceutical production such as Media/Buffer preparation, CIP, SIP of equipment, expansion of cell cultures, and purification via multiple column steps.

The common denominator of the departments is the acknowledgement and development of each employee. The teams consist of 10-20 Manufacturing Associates with different experience and educational backgrounds that collaborate closely on getting our medicine safely and quickly to the market, while staying true to our core values; Genki, gemba, delighting our customers and trust.

You will work on a day or night shift, 7 days during a 14-day period, including every other weekend. 

Please add in your application which shift or shifts you prefer.

The work schedule is as follows:
Week 1: Monday, Tuesday, Friday, Saturday and Sunday
Week 2: Wednesday and Thursday

The shifts are as follows:
Day 1: 06:00 – 17:04
Day 2: 07:45 – 18:49
Night 1: 18:30 – 04:43
Night 2: 20:05 – 06:18

Please be aware that your first 6 weeks will consist of a training period, both onsite and offsite.

Tasks:
In the position as Manufacturing Associate, you will e.g., work on the following tasks: 

• Execution and revision of cGMP documents
• Handling and completion of batch documentation
• In-process sampling and analytical measurements
• Execution of validation protocols
• Read and understand work instructions (in English)
• Training new colleagues
• Reporting deviations
• Possibility of being a part of different projects such as, process optimization, red lining SOPs, 5S and continuous improvements

Qualifications:

• We are looking for operators, preferable with experience from a similar pharmaceutical production company or similar regulated businesses OR a Life Sciences Graduate who have recently finalized their Bachelor or Master degree relevant for Biologics Manufacturing and are keen on starting their career in a manufacturing and international environment where things move fast.
• It is a plus if you have experience with cGMP and/or SOPs or knowledge of chromatography and filtration processes.
• You will get the opportunity to customize your development plan in agreement with your manager based on your wishes and qualifications.

We are hiring for attitude, so we are looking for people who have a lot of drive and proven interest with working under GMP and enjoy working with numbers, math and IT tools. You are very quality-oriented and thorough. You are proactive, responsible, organized and able to take ownership of tasks. Furthermore, you are a good team player who thrives on setting a good example.

You must be keen on learning new things, and the first period will of course include thorough training.

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• Distributed Control Systems (DCS)
• 800xA
• S88 - batch
• Delta V
• SattLine

For the right candidates, who are serious about moving to Denmark, we offer an extensive relocation/mobility package.

What do we do at NNE?

Location: Kalundborg
Department: Process Automation
Employment Type: Full Time

How you might spend your days
As a DCS Process Automation Engineer, you’ll be working with a diverse team where you’ll be:

• Design developing, programming, commissioning, qualifying, FAT, SAT, UAT and Handover of application for Distributed Control Systems (DCS)
  
• Interacting with process experts and colleagues with expertise in surrounding systems and equipment like MES, Historian systems, instruments, production equipment etc.
  
• Supporting developing and optimizing automation methods and strategies to meet our customers’ needs and sharing working knowledge with colleagues and partners
  
• Supporting automation strategies and architectures to support our sister departments internationally and expand NNE’s Process Automation engagement

Who you are
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:

• Understand your colleagues’ individual and cultural difference
  
• Are aware of your surroundings and able to flag any concerns
  
• Are agile and able to prioritize urgent tasks
  
• Are team-oriented and able to collaborate on team projects
  
• Are reliable, curious and eager to learn
  
• Are appreciative of feedback, because it contributes to your growth

The miles you’ve walked
In all positions, there are some things that are preferred, and others, a bonus. If you do not meet all the qualifications listed below, you are welcome to offer alternative experience that you think would be valuable 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

Do you feel like the right person for this position?
📩 To apply for this position, you have two options:

1. Online, during the week from May 5th to 11th

2. By visiting the stand in Milan and handing your CV to the HRs.

Remember, you can use both methods to make an impact!

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What do we do at NNE?
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.

Location: Kalundborg
Department: Mechanical Team
Employment Type: Full Time

How you might spend your days
Your role will depend on your educational background and technical skills. In the mechanical department you'll be working with some or more of the following topics:

• Dimensioning and specifying pipes, components and equipment
• Specifying and designing tanks
• Handling purchase and supplier contracts
• Executing projects in the construction phase using supervision and supervise of contractors and suppliers 
• Controlling of FAT/SAT activities
• Conducting tendering work
  

Who you are
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:

• Thrive in a workday that can bring both varied and complex tasks, which can sometimes be unpredictable when working on projects
• Can communicate information in a transparent and precise manner to your manager and colleagues as well as customers and other relevant stakeholders
• Can organise tasks in a structured way
• Are curious and open-minded to learn new things
• Have a positive approach and can be persistent when facing challenges
• Should be willing to relocate to Denmark if currently living abroad
• If Danish isn’t your native language, don’t worry. We have 35 different nationalities, and our corporate language is English. 

The miles you’ve walked
In all positions, there are some things that are preferred, and others, a bonus. If you do not meet all the qualifications listed below, you are welcome to offer alternative experience that you think would be valuable in this role. 

• Solid experience in design of tanks, pressure equipment, installations and relatable engineering challenges
• Experience in the process-, pharmaceutical or life science industry
• Hold a degree within mechanical engineering, machinist or similar technical capabilities that can be used for specifying components, installations and the like on construction sites

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

Do you feel like the right person for this position?
📩 To apply for this position, you have two options:

1. Online, during the week from May 5th to 11th

2. By visiting the stand in Milan and handing your CV to the HRs.

Remember, you can use both methods to make an impact!

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Employer: Novo Nordisk

To drive growth, Novo Nordisk is pioneering the use of modern technologies to improve processes and increase efficiency across our pharmaceutical manufacturing facilities, and you can be part of this journey! Join us to help shape and enable world-class manufacturing processes for our life-saving treatments.

By applying for the Talent Pipeline, you will be considered as a potential match for open positions in Denmark related to automation and manufacturing execution. We will match your profile continuously against all suitable positions to ensure you do not miss out on a life-changing career. 

Locations: You can apply for our talent pipelines in Hillerød, Kalundborg or Greater Copenhagen, which covers on-site positions in: Bagsværd, Gentofte, Søborg, Lyngby, Måløv, and Kirke Værløse.

 

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Employer: Novo Nordisk

Attention all Process Engineers and Scientists! We are seeking experienced candidates as well as newly graduated professionals to join our team. Are you a Process Engineer or Scientist looking for a new challenge? Do you want to work for a fast-growing pharmaceutical company dedicated to improving the lives of millions of patients worldwide? If so, we want to hear from you!

 Whether you are an experienced professional or a newly graduated candidate, if you have skills and experience in data analysis, process systems, descriptive and prescriptive analytics, we encourage you to apply to be considered for multiple Process Engineer or Scientist positions. Join one of our production teams in Kalundborg and be a part of our mission to improve the lives of millions of patients worldwide.

The Position
We are looking for Process Engineers & Scientists who have an interest in understanding pharmaceutical processes, developing monitoring tools and analysing data for recommendations for improvements and development. Furthermore, you have an interest in business impact and understanding how interconnected decisions play a crucial role when manufacturing pharmaceuticals.

Location: Kalundborg, Denmark
Job category: Engineering & Technical

Specifically, you will:

• Analyse large amounts of data for extracting correlation and causation for process understanding.
• Examine and understand data from quality control (QC) analyses.
• Develop, maintain, and recommend statistical process control charts for process monitoring.
• Use a science, data-based approach for quantifying process deviations.
• Utilize a team-based approach for recommending process improvements-optimizations.
• Handle deviations when processes do not operate as intended.
• Write and execute change requests to implement improvements including validation when required.
• Develop maintenance strategies to optimize running time.
• Coordinate with other process owners in the department to ensure optimal production capacity at all times.
• Take part in cross-functional meetings to align and further develop processes across the production site.

These positions give you a great opportunity to play a part in shaping the future of manufacturing across the organization, in close collaboration with teach-transfer in Novo Nordisk. We will match your profile with relevant roles depending on your level of experience and professional background. We work with positions that range from entry-level to senior process engineers and scientists.

Qualifications for Process Engineer & Scientist roles

• Bachelor’s or master’s degree in chemistry, natural science, mechanical engineering, production engineering or a related field.
• Solid experience in manufacturing, with GMP experience being an advantage.
• Ability to independently understand scientific principles required for manufacturing pharmaceutical substances related to the interaction of chemistry and equipment.
• Ability to monitor data and extract information.
• An appetite for connecting the understanding of process science to product quality.
• Professional proficiency in written and spoken English. Knowledge of Danish or other languages is considered a plus.

For both Process Scientist & Engineer roles it is key that you understand how to convey complex information to varying audiences and thereby, explain the purpose to get everyone onboard. 

Do you feel like the right person for this position?
📩 To apply for this position, you have two options:

1. Online, during the week from May 5th to 11th

2. By visiting the stand in Milan and handing your CV to the HRs.

Remember, you can use both methods to make an impact!

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Employer: Novo Nordisk

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 skilled and innovative automation engineers 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.

We’ll match your profile proactively with relevant positions. Once a Hiring Manager shows interest in your profile, the Hiring Manager Team will reach out to you and tell you more about the current position and invite you for the 1st Interview.

About the positions
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. 

Location: Kalundborg, Denmark
Job category: Digital & IT

Qualifications
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.

In addition, you have the following qualifications:

• Bachelor’s or master’s degree in Automation, IT, Autonomous systems, Robotics, or another related field
• Strong knowledge of IT/OT
• A technical background and/or experience within engineering, IT/OT, digitalization and automation
• Fluent in English both oral and written. Danish is a great advantage.

Technical skills/knowledge:

• Advanced automation e.g.: (PLC, SCADA, DeltaV, ABB SattLine/800xA)
• Manufacturing Execution Systems e.g.: (PAS-X or Syncade)
• Collaborative- and mobile robotics e.g.: (Universal Robots, Kuka, MIR, Omron, Nipper).

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.
We also welcome and encourage early talent to apply for our pipelines, as we are committed to fostering growth and development in our employees and providing opportunities for long-term career success.

Do you feel like the right person for this position?
📩 To apply for this position, you have two options:

1. Online, during the week from May 5th to 11th

2. By visiting the stand in Milan and handing your CV to the HRs.

Remember, you can use both methods to make an impact!

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Employer: Ferrosan

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.   

Role summary 
We are in search of a proficient Data Engineer to become a valuable member of our dynamic team. As a Data Engineer, you will understand the data products and pipelines we have on the platform and deliver new data products together with different business domains and the team. You will continuously improve how we implement new products most efficiently. Being a true team player with a focus on creating an open, inclusive, and collaborative work environment and establishing transparency in the team is fundamental.

The ideal candidate should excel in utilizing Azure cloud solutions, be proficient in C# and python programming, and have a robust ability in documentation, which is crucial for meeting regulatory requirements in the medical devices sector. In this role, you will have the chance to shape and build the future data platform for Ferrosan Medical Devices. 

Your responsibilities 

• Develop and maintain ingestion pipelines from various data sources such as databases, APIs, logs, and external datasets in Microsoft Azure and Microsoft Fabric.
• Cleanse, preprocess, and transform raw data into structured formats suitable for analysis and storage.
• Integrate data from multiple sources, ensuring data consistency and accuracy across various data repositories.
• Design, manage, monitor and optimize data pipelines and databases for scalability, improved performance, responsiveness, and resource efficiency.
• Document data engineering processes, workflows, and data models for team members and stakeholders. Collaborate with data scientists, analysts, and other teams to understand their data requirements and provide them with the necessary data assets.
• Stay on top of industry trends in AI and data science, incorporating cutting-edge methodologies and technologies into our projects.

Your profile 

• You hold a relevant educational background in Computer Science, Data Engineering, Information Technology or a related field (master’s degree may be preferred or considered a plus).
• You have proven experienced in data integration, data modelling, data governance, and data quality best practices using modern data technologies.
• You are diligent to details and have a knack for troubleshooting, researching and working through sophisticated data-related problems to develop innovative solutions.
• You are proficient in programming languages such as C# and Python as well as experience with scripting languages like SQL.
• You have profound knowledge of database management systems and experience working with Microsoft Fabric
• You enjoy cultivating a strong engineering culture in an agile and DevOps environment.
• You are fluently speaking and writing English

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 haemostatic 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. 

Do you feel like the right person for this position?
📩 To apply for this position, you have two options:

1. Online, during the week from May 5th to 11th

2. By visiting the stand in Milan and handing your CV to the HRs.

Remember, you can use both methods to make an impact!

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Location: Virum
Department: Health, Safety & Environment 
Employment Type: Full Time

How you might spend your days
As a Safety Engineer, you'll be working in cross-disciplinary teams all dedicated to creating a safe working environment in the pharma industry. Here you’ll be working with areas such as:

• Safety of machinery and process equipment
  
• Risk assessment including hazardous areas with flammables liquids and dust
  
• Hazardous area classification (ATEX) and explosion protection documents
  
• Safety legislation and regulatory aspects
  
• Safety and risk management processes
  
• Safety solutions in complex installations with explosive atmospheres
  
• Commissioning of Machinery and Process Equipment

Who you are
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 persistent and take responsibility
  
• Have a customer understanding and consultant mindset
  
• Can think positive and take an optimistic approach when facing challenges
  
• Are agile and able to prioritize urgent tasks
  
• Can collaborate on team projects
  

The miles you’ve walked
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 technical or academic background
  
• Experience from the life science manufacturing industry or other similar industries
  
• You possess in-depth knowledge of the current local and global safety legislation and standards
  
• You speak and write Danish and English fluently
  

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

Do you feel like the right person for this position?
📩 To apply for this position, you have two options:

1. Online, during the week from May 5th to 11th

2. By visiting the stand in Milan and handing your CV to the HRs.

Remember, you can use both methods to make an impact!

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What do we do at NNE?
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.

Location: Kalundborg
Department: LMES & Software Engineering
Employment Type: Full Time

How you might spend your days
As a MES IT engineer, you’ll be:

• Working side by side with creative colleagues.
• Advising clients on how to maximize the benefits of our MES System.
• Gathering technical knowledge through a variety of methods (e.g., facilitated workshops, work sessions, interviews and technical analysis).
• Implementing approved solutions in cooperation across different disciplines/systems.
• Commissioning and undertaking test and qualification of IT systems in manufacturing environments.
• Working on site at our customers production sites.

Who you are
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.

The miles you’ve walked
In all positions, there are some things that are preferred, and others, a bonus. If you do not meet all the qualifications listed below, you are welcome to offer alternative experience that you think would be valuable 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.
• You speak and write English fluently (Danish is recommended).
• Experience from Pharma/Regulated business is considered a plus.

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

Do you feel like the right person for this position?
📩 To apply for this position, you have two options:

1. Online, during the week from May 5th to 11th

2. By visiting the stand in Milan and handing your CV to the HRs.

Remember, you can use both methods to make an impact!

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Does the idea of assisting in enhancing global IT infrastructure excite you? And do you thrive on supporting digital transformation? Then you’ll fit right in!

What do we do at NNE?
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.

About the role
We are looking for a motivated and talented Associate IT Infrastructure Consultant join our team in Global IT. As a team, we are working on delivering solutions to the business through IT operations and infrastructure.

Why do we need you? Our goal is to enhance our global IT infrastructure and support NNE's digital transformation. Your role will be key in bridging gaps and supporting the continuous improvement of our IT systems assisting in maintaining and enhancing our global IT infrastructure, ensuring seamless integration between on-premise and cloud environments

Location: Virum
Department: Global IT
Employment Type: Full Time

How you might spend your days
As an Associate IT Infrastructure Consultant, you’ll be:

• Assisting in the management and maintenance of on-premises and cloud-based IT infrastructure
  
• Supporting the implementation and integration of new technologies and systems
  
• Monitoring and troubleshooting network, server, and cloud-related issues
  
• Collaborating with senior IT staff to develop and execute infrastructure improvement plans
  
• Providing technical support and guidance to end-users
  
• Documenting and maintaining IT procedures and policies

Who you are
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:

• Possessing strong problem-solving skills and attention to detail
  
• Good at communicating with a broad variety of people and value teamwork
  
• Eager to learn and adapt to new technologies
  
• Understanding of your colleagues' individual and cultural differences
  
• Aware of your surroundings and able to flag any concerns

The miles you’ve walked
In all positions, there are some things that are preferred, and others, a bonus. If you do not meet all the qualifications listed below, you are welcome to offer alternative experience that you think would be valuable in this role. 

• Bachelor's degree in Information Technology, Computer Science, or a related field
  
• Basic understanding of network protocols, server management, and cloud computing
  
• Familiarity with IT infrastructure components such as routers, switches, firewalls, and cloud services (e.g., AWS, Azure)
  
• Experience with virtualization technologies (e.g., VMware, Hyper-V)
  
• Knowledge of scripting languages (e.g., PowerShell, Python)
  
• Understanding of cybersecurity principles and practices
  
• You speak and write Danish and English

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

Do you feel like the right person for this position?
📩 To apply for this position, you have two options:

1. Online, during the week from May 5th to 11th

2. By visiting the stand in Milan and handing your CV to the HRs.

Remember, you can use both methods to make an impact!

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Employer: Novo Nordisk

Location: Kalundborg, Denmark

Are you a recent bachelor’s degree graduate within engineering, or have a few years of experience as a Process Engineer? Are you eager to learn, and start a life-changing career within biomanufacturing - specifically within pharmaceutical manufacturing? Then we might have an exciting opportunity for you! Read on and apply today!

At our manufacturing hub in Kalundborg, Denmark, we are looking for talents who are eager to combine education and work experience. This means you can combine pursuing a master’s degree in engineering from the Technical University of Denmark (DTU) in Kalundborg, with gaining valuable industry experience from Novo Nordisk. This is a unique opportunity to graduate with a master’s degree and gain professional experience during 4 exciting years.

About the Industry Master of Science in Engineering within Biomanufacturing 
As a student on the Biomanufacturing study line, you will become part of a fast-expanding industry of chemical and biochemical production in Kalundborg. 

To qualify for the education, you must have graduated recently with a BSc/BEng within chemical engineering, process engineering or similar field of study.

During your time of study, you will become an expert in process thinking and working with chemistry and biochemistry at an industrial scale. Taught by leading experts and professors, you will learn to run a factory and work with all the industrial processes – from development and improvements to embedding new technology and digitalized optimizations. You will gain strong engineering knowledge and an innovative mindset. 

The programme, as a typical MSc Engineering program, consists of 120 ECTS points over a 4-year period. 

Please make sure to apply for the Industry Master of Science in Engineering within Biomanufacturing at DTU, before you apply for the position at Novo Nordisk. To be considered for the part-time job as Process Engineer at Novo Nordisk, you need to have a conditional admission letter from DTU attached to your profile.
 
The Position at Novo Nordisk 
The role as part-time Process Engineer will focus on data analysis, process systems and descriptive and prescriptive analytics. 

You will get to understand pharmaceutical processes, developing monitoring tools and analysing data for recommendation for improvements. Don’t miss this opportunity to learn about business impact and understand how interconnected decisions play a crucial role within manufacturing pharmaceuticals.

Specifically, you will:
•    Analyse large amounts of data for extracting correlation and causation for process understanding.
•    Analyse and understand data from quality control (QC) analyses.
•    Develop, maintain, and recommend statistical process control charts for process monitoring.
•    Use a science, data-based approach for quantifying process deviations.
•    Utilize a team-based approach for recommending process improvements-optimisations.

Qualifications for Process Engineers
Process Engineer candidates should have the following or developing qualifications:
•    Meet the requirements to be enrolled in Biomanufacturing - Industry MSc in Engineering, DTU Kalundborg.
•    Have the ability to analyse data and independently extract information.
•    Have an appetite for solving complex problems applying a systems approach to manage complexity and reach feasible applicable solution. 
•    Be proficient in verbal and written English.

For Process Engineers it is key to understand how to convey complex information to varying audiences and thereby explain the purpose to get everyone on board.

Do you feel like the right person for this position?
📩 To apply for this position, you have two options:

1. Online, during the week from May 5th to 11th

2. By visiting the stand in Milan and handing your CV to the HRs.

Remember, you can use both methods to make an impact!

 

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