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Professional, Visual Inspection

Kunne du tænke dig at være med i et spændende eventyr hos en fabrik i rivende udvikling? Har du erfaring med GMP i lægemiddelindustrien?

Du vil blive en del af Production Support og vil være tilknyttet visuel inspektionsprocessen, hvor du vil være med til at sikre proces, procedurer, GMP og generelle forbedringer på vores proces.

QA Specialist

We are seeking a competent new colleague to join our QA team in a dynamic and growing company.

You will be part of our highly dedicated team consisting of 5 colleagues working with a broad range of QA tasks such as batch review, processing of complaints, deviations and change requests as well as validation and ad hoc projects.

Training Partner

Are you passionate about designing high impact training to improve ways of working?

The role will focus on re-designing the training related to onboarding our professionals working directly with our operation, our Operators, and our Laboratory Technicians.

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.

Technical Specialist, Product Quality, Nourish (Maternity cover, 12 months)

Are you an enthusiastic, motivated and detail-oriented professional with a desire to work in a team of colleagues with great technical competencies within production, regulation and processes?

Your core responsibilities:

• Handling deviations for products manufactured at our factories.
• Handling of product quality related complaints.
• Coordinate and implement customer-specific requirements. Maintenance of master data in various IT systems, including SAP.

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.

Project Manager

Trives du med at arbejde sammen med dedikerede og erfarne kollegaer, der brænder for at udvikle og producere medicinske hjælpemidler til børn og unge med funktionsnedsættelse?

Kan du samtidig se dig selv som projektleder i en specialiseret verden, hvor innovativt design, teknik og brugervenlighed skal gå op i en højere enhed, så er det dig, vi søger i vores R&D-afdeling i Gedved ved Horsens.

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

Food Technician - Arhus

Are you passionate about turning ideas into concrete products via your hands-on technical skills?

As Food Technician you will be the prime responsible for running pilot scale trial-production of a wide range of dairy/’plant based’ products. Your work will always happen in close collaboration with product developers/food designers. To be more specific, you will:

• Perform pilot trials within a wide variety of product and technology areas
• Contribute to the preparation of the test proposal and help plan the trials

Head of the Department of Virus & Microbiological Special Diagnostics

Do you have solid management experience and deep insight and experience within virology?

As Head of the Department of Virus & Microbiological Special Diagnostics, you are responsible for the daily management of the department to ensure the diagnostic preparedness for infection in a one-health perspective with synergy between laboratory diagnostics in humans and animals.

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.

Senior LIMS Specialist for Global QC Development

In this role you’ll make an impact by working as a Senior LIMS Specialist in our team, where you will take part in management of projects for LIMS changes across QC laboratories and other stakeholders including implementation, documentation and communication.

Future projects could be introducing and validating LIMS solutions on new equipment or technologies, new LIMS functionalities, improving and aligning existing processes.

Laborant eller procesoperatør til bufferproduktion til cancerdiagnostik

Vil du bidrage til diagnostik af cancer og gøre en forskel for patienter? Bliver du motiveret af laboratoriearbejde i et travlt produktionsmiljø? Er du detaljeorienteret og lægger vægt på korrekt produktion og dokumentation?

Vores hverdag består hovedsagelig af produktioner, grundig dokumentation og reviews men vi prioriterer også tid til løbende forbedringer af vores arbejdsgange og processer.

Der er tale om en fuldtidsstilling på 37 timer per uge. Arbejdstiden ligger i dagtimerne og vi har flextid.

Process Specialist

Do you want to be part of Process Support in a company with a unique impact on global healthcare? Grab this opportunity to be part of a fast-growing company ready to invest in you.

Together with the rest of the team, you will be responsible for the daily support of our production lines. You will learn our processes in detail and gain a good overview of the documentation used in production.

Kickstart your career as a Life Science Business Consultant

Looking for the opportunity to combine your interest in life sciences with the business aspects of consulting?

Then grab this career-building chance to work with and learn from talented colleagues as you help digitalize the clinical landscape for clients across the globe.

Not only will you get to hone the skills that will make you a good consultant, but you’ll also get to see the direct impact of your work as you help pharma companies make a difference in patients’ lives

Product Portfolio Manager, Arla Foods Ingredients - Aarhus

Together with the rest of the team you will make raw material scenario analyses and identify potential challenges to have a fact-based discussion and enable better decision-making.

In short, your responsibilities and tasks include:

• Become a trusted portfolio partner to the commercial organization
• Provide raw material priority recommendation in S&OP and other key-forums

Project Coordinator

Do you have experience managing projects anchored to a GMP facility? Are you eager to contribute to the development of a newly established project team in a production environment?

As a Project Coordinator, you will participate in the successful planning and completion of projects related to the Drug Substance Manufacturing Processes. You will coordinate and follow up on a number of tracks that links to various projects.

Scientist for In Vivo Sales in Boston

Are you passionate about discussing science, identifying opportunities for customer value creation and creating visible results? Do you have excellent analytical skills and a strong commercial mindset? Are you a natural communicator and thrive building relationships? If that is the case, we have a great career opportunity for you.

Your primary area of responsibility will be to partake in day-to-day sales operation, drive the forward-looking dialogues with key customers as well as identifying and following up on new business opportunities. Furthermore, you will be involved preparing sales presentations, market analyses, and marketing materials.

Account Manager – Denmark

Actief Hartmanns is searching for an experienced and enthusiastic candidate for the position of Account Manager.

Are you ready to step out of your comfort zone, excel and redefine the limits of what is possible. That’s just what ZEISS employees are doing every single day – in order to set the pace through innovations and enable outstanding achievements. After all, behind every successful company are many great, fascinating people.

Full training in our products, systems and processes is provided. We offer continuous professional development and the opportunity to work as part of a global team with a wide range of career development opportunities.

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.