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Student Assistants for NBCD A/S within Clinical Operations

Do you dream of working with pharma and research? Are you curious, service-minded, and envision yourself thriving in a dynamic research environment with varied tasks?

Then come join us as a student assistant and become part of a company, that operate at the forefront of international drug development research, where you'll have the opportunity to broaden your skillset, shape your own day and contribute to various projects.

Senior Project Manager

Are you motivated by being the driver of the implementation of new equipment/facilities or complex upgrading projects) up to EUR 15 million?

You will be responsible for and ensure project execution of all phases in your projects including scope definition, identifying the solution, and mitigating risks, time, budget, and quality. We primarily work with the stage gate model for our larger projects.

Project Account Manager - Pharmaceutical kundesegment

Som Project Account Manager i Hilti får du en spændende hverdag, hvor din vigtigste opgave bliver at udvikle relationer til kunder igennem byggeriets faser på projekterne. Der er tale om en rådgivende salgsrolle, hvor du får stor frihed til selv at påvirke og planlægge din hverdag.

I Hilti arbejder vi struktureret med medarbejderudvikling. Hvert år vil du blive præsenteret for en detaljeret udviklingsplan, der sikrer, at du vokser i din rolle, og støttes og guides, så du kan realisere dine karrieredrømme.

Regulatory Affairs Specialist

The RA Specialist for Radiometer is responsible for ensuring coordination of regulatory activities for a few of our Blood Gas products manufactured in California to help ensure continued compliance in all markets.

In this role, you will have the opportunity to:

• Facilitate coordination of regulatory activities between California and Denmark for design control activities and international registrations for a few of the instruments/consumables manufactured in our California site.
• Ensure compliance with EU regulations.
• Generate STED files, international submissions & assess design changes.
• Plan and execute projects for new regulatory requirements.

Senior Regulatory Specialist

The Senior Regulatory Affairs Specialist at Radiometer is responsible for collecting and generating documentation for product submissions to ensure compliance with international regulations. This role is critical for ensuring that Radiometer's products can be sold in markets around the world.

If you thrive in a fast-paced environment, are used to playing a critical supporting role and want to work in a world-class efficient team that is part of a Global RA department and have interactions and stakeholders to connect with in a global scale - read on.

Procesingeniør

Har du lyst til at starte din karriere med at arbejde inden for farmaceutisk produktion? Og har du mod på at bevæge dig ud i tværfaglige udfordringer, der ligger lidt uden for din uddannelse?

Vi er en virksomhed i vækst, og produktionsvolumenerne vokser – så derfor har vi et stort behov for at styrke vores ingeniørgruppe med et nyt medlem, der kan medvirke til, at vi får moderniseret vores udstyr, som produktionen vil få stor gavn af.

QC-laborant med varierende opgaver

Har du lyst til at sikre kvaliteten af vores API’er i en QC-funktion, hvor du får lov at løse en palet af forskellige opgaver? Har du lyst til at blive en del af en velfungerende gruppe, hvor du løbende bliver trænet i nye opgaver af dine erfarne kolleger?

Så er det måske dig, der er vores kommende QC-laborant. Vi er i en proces, hvor vi vokser, og derfor søger vi en laborant, der trives med fleksibilitet og gerne vil udvikle sig.

Vi vil altid være lydhøre over for den enkelte laborant. Hvis du har interesse for en opgave, så lytter vi og sørger for, at du bliver trænet i den og får lov til at løse den

IT Administrator

Are you specialized in IT system administration?

Would you like to optimize and maintain our data centers, VMware setup as well as our backup services such as Veeam and Data Domain, and more? Are you process-minded with good attention to detail? Would you like to be a part of a dedicated IT Operations team in development?

Then you might be the IT Administrator we are looking for!

Laborant/Senior Laborant

I jobbet som Laborant/Senior Laborant i Translational Pharmacology vil du være ansvarlig for planlægning, koordinering og gennemførelse af in vivo / ex vivo farmakologiske eksperimenter som bidrag til vores prækliniske forskningsprojekter.

Ansvarsområderne omfatter bl.a.:

• Gennemførelse af in vivo-undersøgelser af høj kvalitet i gnavere, herunder bidrag til protokoller, planlægning, udførelse og dokumentation.
• Udførelse af grundlæggende kirurgi hos gnavere, herunder anæstesi og analgesi.
• Prøvetagning og håndtering af blod- og vævsprøver af høj kvalitet.

IT Administrator (Cloud)

Are you specialized in IT system administration of Microsoft cloud solutions? Would you like to optimize and maintain our Azure datacenter, as well as our Microsoft 365 services such as Exchange, Teams, SharePoint and more? Are you process-minded with a good attention to detail?

We are looking for a skilled IT System Administrator to:

• Help us implement new cloud-based solutions
• Take care of the administration

Analytical Chemist – 12 months position

We seek a highly motivated ANALYTICAL CHEMISTRY scientist, engineer, or technician for our research laboratory in Copenhagen.

The position will give intellectual challenge and rich possibilities to develop your skill sets as well as being part of commercially and scientifically exciting projects.

You will contribute to the development and maintenance of River Stone’s analysis platform, method development as well as routine sample analysis. You will be part of an enthusiastic and strong analytical chemistry team.

Regulatory Affairs Manager

The Regulatory Affairs Manager at Radiometer is responsible for managing the preparation and submission of the required documentation for product registration, approval, and compliance with international regulations.

This role is critical for ensuring that Radiometer's products can be sold in markets around the world. You will have the opportunity to:

• Ensure regulatory compliance to maintain market approvals
• Lead a team of skilled RA associates
• Ensure alignment with relevant stakeholders

Data Engineer for Condition Monitoring and Machine Optimization

Do you want to play a key role in improving performance in the pharmaceutical and industrial manufacturing? Are you passionate about finding patterns in data?

You will implement our CATCH.AI data platform at our customers’ production sites and help them turn data into tangible actions and value.

You are the expert on what makes you happy and efficient. So, whether that entails a 4-day work week or working in the evening or from home that is simply how you will be working.

AFC manager

We offer an exciting and unique opportunity to take on the challenge within a global corporation, engaging with customers and stakeholders worldwide. Daily responsibilities encompass a variety of inspiring and complex tasks overseeing analysis and reporting of economic and financial performance of our Engineering Business Line.

The package includes a pension plan, appealing cafeteria benefits, membership in the staff association and more.

Downstream processing engineer – 12 months position

In this position you will be part of River Stone’s downstream processing (DSP) team, which is responsible for developing purification methods for our biological production processes for pharmaceutical ingredients.

The ideal candidate possesses:

• M.Sc. or Ph.D. degree in chemical engineering, food process engineering, chemistry, or similar
• Experience within down-stream purification processes, like solid-liquid separation, membrane filtration, crystallization and/or drying is a requirement
• Flair and motivation for hands-on laboratory work
• Ability to work in a fast-paced environment with deadlines and sometimes limited time for data analysis

QA Engineer – ensure the quality of our software solutions for pharmaceutical drugs and devices

Do you want to play a key role in delivering software systems that are compliant to the pharmaceutical industry?

As Quality Engineer, you will work together with the project manager, the software developers and the customers validation teams and help secure that our solutions are compliant and lives up to the customers expectation so they can re-use our validation as their own.

You are the expert on what makes you happy and efficient. So, whether that entails a 4-day work week or working in the evening or from home that is simply how you will be working.

Software Developer for commissioning of pharma projects (C#/.NET)

Do you want to play a key role in delivering software solutions for advanced production machines?

As software developer at CIM, you will implement solutions that makes existing machines more intelligent and thereby improves performance and adds functionality leading to better patient safety and a better overall better performance.

You are the expert on what makes you happy and efficient. So, whether that entails a 4-day work week or working in the evening or from home that is simply how you will be working.

Vision Engineer – ensure the quality of pharmaceutical drugs and devices

Do you want to play a key role in delivering vision inspection solutions for advanced production machines?

As Vision Engineer, you will implement inspection solutions that improve patient safety by ensuring the quality of pharmaceutical products and devices.

You are the expert on what makes you happy and efficient. So, whether that entails a 4-day work week or working in the evening or from home that is simply how you will be working.

Senior Specialist Clinical Safety and Pharmacovigilance (CSPV)

At Bavarian Nordic, we aspire to save and improve lives by developing innovative vaccines that are designed to unlock the power of the immune system.

The global team consists of subject matter experts for vaccine safety who work either from our site or remotely in Denmark and globally. Together they constantly collect and assess data for the life cycle benefit risk management across our vaccines whether authorized or still in clinical development.

You would add your clinical safety and pharmacovigilance expertise as your depth knowledge of the PV legislation to the team.

External Lecturer – “Medical Biotechnology and Drug Development” – DIS Copenhagen

The teaching position is for the fall semester, which will begin in August. You will teach highly motivated undergraduate students from North American universities who are spending a semester studying in Copenhagen.

Why teach at DIS?

• Work in an international, informal and enthusiastic environment with an emphasis on cross-cultural understanding, teamwork, innovation, and adaptability
• Develop interactive and experiential teaching skills and teaching experience in English