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Clinical Supply Manager

The Clinical Supply Manager will be managing outsourcing of packaging, labelling, and distribution of clinical trial supplies for all clinical trials.

You must have extensive knowledge of cGMP and have a focus on the level of quality in work performed.

We strongly endorse a flexible working environment around its core working hours of 09:00-15:00 and endorses fair and equal pay practices.

Application Specialist – Beverages

Are you passionate about product development within all types of beverages from premium organic CSD's to flavored spirits?

You will work in a high-paced, collaborative and energetic environment optimizing key elements of beverage applications such as taste, stability, preservation and appearance with the goal to design the perfect balance between these elements.

Biocompatibility Specialist

We are looking for a Biocompatibility Specialist to join the Reprocessing and Biocompatibility team for a 12-month project position.

This is a great opportunity if you would like to gain experience with biocompatibility for advanced reusable medical devices, as you will be part of a cross-functional effort on documenting the safety and performance through the lifetime of our ultrasound scanners, transducers, and accessories.

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.

QC Laboratory Technician

Har du lyst til en hverdag fyldt med spændende opgaver, fokus på høj produktkvalitet og med en stor grad af ansvar? Synes du, det er sjovt at arbejde med ingredienser til en bred vifte af fødevarer?

Primære arbejdsopgaver:

• Analyser af råvarer, mellemvarer og færdigvarer, herunder kemiske og sensoriske analyser
• Frigivelse af råvarer, mellemvarer og færdigvarer
• Udarbejdelse af analysecertifikater til vores kunder

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

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.

Technical Writer to GE HealthCare Denmark

Join GE HealthCare to help develop high quality instructions for use for our ultrasound scanners, transducers, and reprocessing methods in compliance with rules and legislation in various countries. This is your opportunity to become part of an innovative team where your work has a real impact on people’s lives around the world.

Our Technical Documentation team consists of six dedicated and passionate specialists with a mix of seniority, educational backgrounds, and nationalities. Our Technical Writers develop and maintain the user documentation for our high-performance equipment.

QA Specialist

You will be responsible for ensuring safe, reliable, and compliant products during new product development and maintenance of existing product platforms.

You will have the opportunity to:

• Provide Design Control guidance for QMS and regulatory compliance in an FDA regulated and ISO compliant environment.
• Represent Quality Assurance in design and development projects and in cross-functional teams supporting new product development.

Senior QA / Systemansvarlig

Som systemansvarlig for kvalitetssystemet vil du have en bred funktion, hvor du vil blive involveret i alle aspekter i virksomhedens kvalitetsarbejde.

Arbejdsopgavernes karakter spænder fra det strategiske til det operationelle, og deres udførelse kræver en vekslen mellem at sidde ved skrivebordet og at være ude på gulvet.

Både de faglige og de personlige udviklingsmuligheder ligger lige for i en rolle, som skal varetages med både selvstændighed og løbende sparring med virksomhedens erfarne kvalitetschef.

Continuous Improvement Partner

As a Continuous Improvement Partner in Drug Substance Manufacturing, you will be part of a team of Improvement Partners who develops and sustains systems and tools that enables the organization to consistently increase the level of operational excellence in manufacturing.

Your primary tasks will include but not be limited to:

• Develop and sustain CI systems and tools.
• Coach on ideal behaviour that drives a proactive improvement culture.

Engineering Project Manager

Har du en passion for at drive teknologisk udvikling og bruge dine kompetencer i den grønne industrielle omstilling?

Den succesfulde kandidat vil have en ledende rolle i ALGIECEL's full-scale demonstrationsprojekt, der transformerer CO2-emissionerne på Novonesis' faciliteter i Kalundborg til bæredygtige algebaserede produkter gennem en yderst effektiv og kompakt fotobioreaktor.

Tiden for forandring er nu, og dette er din chance for at blive en del af vores højt motiverede team!

PhD scholarship in Fish Bacteriology and Prophylaxis with specific Emphasis on Bacteriophages as a Control Method – DTU Aqua

Join us on our mission to monitor and promote health of fish and shellfish, with special focus on sustainable aquaculture.

You will be working within bacteriology and microbiology with emphasis on host-pathogen interactions and disease prophylaxis in fish. The focus will be the fish pathogen Flavobacterium psychrophilum and bacteriophages as a prophylactic control measure against disease outbreaks with this important pathogen in aquaculture.

Your work will be part of externally funded research projects, among them the IFD Grand Solutions project AQUAPHAGE Towards a sustainable aquaculture: Phage-based solutions for disease prevention in rainbow aquaculture.