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Business Developer with a background in Science

Do you want to be at the forefront of Targeted Radiopharmaceuticals and Molecular Imaging?

We are looking for a professional Business Developer with a background in life sciences and the ambition to contribute to further strengthening Minerva Imaging as the trusted partner for targeted radiopharmaceuticals and molecular imaging.

What truly matters is your passion for the advancement and know-how of our scientific studies and your ability to foster long-term relationships with our collaborators.

Vil du være med til at tegne fremtidens IT-løsninger indenfor Patologi og Genetik?

Du får en spændende rolle på tværs af vores produkter i hele Health Divisionen, men i særdeleshed med fokus på løsninger i patologiafdelingen.

Med din baggrund fra laboratorieområdet vil du i høj grad skulle konsultere og rådgive vores kunder, ligesom du bliver ansigtet udadtil på fysiske kundemøder, både opsøgende samt opfølgende. Med din viden vil du være i stand til at analysere kundebehov, for efterfølgende af levere input til en løsningsbeskrivelse.

Sales Manager

Are you seeking to make a difference in an innovative, fast growing medtech company with a cutting-edge technology? We're currently seeking a dedicated individual to fill a position as Sales Manager.

Your main responsibilities

• Lead generation
• Develop and execute sales strategies
• Customer relationship management

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.

QEHS Manager

Unique opportunity to join an innovative biotech company with a proven and sustainable technology on the edge of global expansion.

Do you want to help develop the protein of the future, which will make it possible to feed the world's growing population without damaging our ecosystems?

You will be leading a small team responsible for managing and coordinating all QEHS activities, including certifications, audits, and training. You will ensure that operations are conducted in a safe and efficient manner and in conformance with safety regulations.

QC Laboratorie Supporter (Barselsvikariat 12 måneder)

Vi søger en person med det rette servicegen og energi, og som forstår kravene i et cGMP QC-laboratorium. Som vores kommende kollega er det vigtigt at du har forståelse for arbejdet i et laboratorie, er indforstået på en travl hverdag med skiftende prioriteringer.

Er det lige dig vi står og mangler, så kan vi tilbyde dig et spændende og udfordrende job i en virksomhed der går en spændende fremtid i møde med mange nye kunder og produkter og store muligheder for personlig udvikling og ansvar. Dette er en tidsbegrænset stilling, men vi udvider og vækster hele tiden så hvem ved hvad fremtiden bringer?

Senior Test Engineer

Join GE HealthCare to help perform transducer integration on our next-generation ultrasound scanners and further develop our test tools and laboratories.

As our new Senior Test Engineer, your typical tasks will include measurements of sound pressure, acoustic power, thermal characteristics, image performance and other transducer properties.

You will take part in hands-on work while also playing a key role in maintaining and further developing our transducer integration processes and two laboratories.

Forbrugerklagenævnet søger sagkyndige til teknisk bistand til forbrugerklagesager til området for planter

Er du teknisk uddannet eller besidder anden særlig fagkundskab, og vil du bidrage til retssikkerhed for forbruger og erhvervsdrivende, er du måske den sagkyndige ekspert, som vi søger til Forbrugerklagenævnet?

Opgaverne består som udgangspunkt i at:

• Foretage tekniske undersøgelser af varer/ydelser.
• Formidle undersøgelsernes resultat i skriftlig udtalelse, som skal være skrevet i et klart og letforståeligt sprog.

Det betyder konkret at du skal kunne vurdere, hvad fejlen på den omhandlede vare skyldes, herunder om det kan være en materiale- eller fabrikationsfejl, almindeligt brug eller forbrugerens uhensigtsmæssige brug mv.

Test, kvalitet og overvågning – laborant til skiftehold

Kunne du tænke dig at arbejde i en global produktionsvirksomhed, hvor kvalitet er altafgørende? Trives du med både selvstændige opgaver og samarbejde med kolleger?

Du udfører en del af dine opgaver i vores moderne laboratorium, men har også din gang i produktionen. Her udtager du prøver, giver tilbagemeldinger og har generelt et tæt samarbede med operatørerne.

Du vil opleve at ansvar, troværdighed og kvalitet er styrende værdier hos os. Vi udnytter hinandens kompetencer og giver både plads til og forventer initiativ og involvering. Vores omgangstone er afslappet og præget af tillid og respekt.

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.

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

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.

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!

Clinical Evidence Lead

Do you want to:

• Lead the clinical development and clinical data strategy across application areas
• Lead the wording, substantiation, and documentation of clinical claims for regulatory compliance and commercial utilization
• Contribute to the clinical evidence activities in development projects and give input to PMCF

The main responsibilities of your new team are to drive the clinical strategies to ensure timely execution on clinical deliverables to support regulatory submissions and commercial strategies.

Senior Clinical Scientist

Do you want to:

• Execute clinical evaluation and documentation activities, including clinical input to PMCF and PMS.
• Provide clinical support to global registrations.
• Support and drive ad hoc clinical activities and problem solving

The main responsibilities of our Clinical Development team are to drive the clinical strategies to ensure timely execution on clinical deliverables to support regulatory submissions and commercial strategies.