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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.

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.

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.

Laborant til mikrobiologisk team

Har du lyst til at være med til at sikre vacciner til forebyggelse af infektionssygdomme?

Bavarian Nordic er i en rivende udvikling og derfor søger vi en laborant til det mikrobiologiske team i Kvistgaard. Du vil i stillingen bidrage til test og frigivelse af vacciner mod kritiske sygdomme. QC-mikrobiologi har ansvaret for at udføre analyser af rutine prøver og valideringer af nye produkter. Desuden yder vi support til vores produktion.

Dedikeret farmakoepidemiolog til Lægemiddelstyrelsens Dataanalysecenter

Lægemiddelstyrelsen er en helt unik arbejdsplads, i at vi er Danmarks eneste regulatoriske myndighed for lægemidler og medicinsk udstyr. Med denne position følger et helt særligt ansvar, som vi er meget stolte af og bevidste om i vores arbejde.

Dine primære arbejdsopgaver i Lægemiddelstyrelsens Dataanalysecenter er bl.a.:

• Designe, planlægge og udføre farmakoepidemiologiske analyser på sundhedsdata bl.a. vedr. forbrug, effekt og sikkerhed
• Udarbejdelse af rapporter, notater og præsentationer til forskellige målgrupper

Prøvemodtagelse på natholdet

Kunne du godt tænke dig at prøve kræfter med arbejdet i et laboratorie og har du interesse for naturvidenskab?

Som en vital del af vores nathold vil du være en nøglespiller i vores laboratorieproces. Du vil være ansvarlig for modtagelse af prøver, håndtering af asbestanalyser og registrering heraf. Du vil arbejde i et mindre team, der sørger for, at alle prøver bliver korrekt modtaget og behandlet for at opretholde et effektivt arbejdsflow gennem natten.

Fleksibel og nysgerrig QA-koordinator med lederpotentiale

Kan du se dig selv stå i spidsen for at sikre høj kvalitet for mere end 1500 forskellige produkter årligt?

For Persano Group søger vi en QA-medarbejder, som kan se sig selv vokse ind i en ledende funktion, og som har den rette mængde af drive, nysgerrighed og ejerskab til at bidrage i en familiedrevet virksomhed, hvor stor passion er den kultur, der gennemsyrer virksomheden.

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.

PhD scholarship in amino acid optimization of fish feed - DTU Aqua

Is fish nutrition and aquaculture your future carrier? Do you want to contribute to making aquaculture more sustainable and reduce its environmental impact? Here is your chance.

DTU Aqua offers a 3-year PhD position in fish nutrition. Your overall focus will be on dietary nutrient optimization including amino acid uptake and utilization aiming at optimizing diets and reducing discharge of nitrogen from aquaculture.

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.

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

PhD scholarship: Computational Prediction of Nuclear Fission Products Behavior in a Molten Salt Reactor – DTU Chemistry

A 3-year PhD scholarship concerned with the use of computer simulation for predicting fission products (FP) behavior – such as solubility – in a Molten Salt Reactor (MSR) is available.

In the SolveMSR project – funded by the Independent Research Fund Denmark – we will work towards creating a computational framework for predicting FP behavior in the fuel salt matrix of MSRs. We will benchmark the framework against experimental data.

Site QEHS

Brænder du for at arbejder med QEHS, kan du godt lide at arbejde i et overskueligt team – så er du måske vores nye Site QEHS på vores site i Aabenraa? Du vil være tovholder på at implementere og opretholde kvalitets- og EHS standarder.

Dine ansvarsområder bliver udvikling og implementering af QEHS-strategier, -politikker og -mål i overensstemmelse med virksomhedens overordnede mål.

Senior 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.

You will become a process owner of one or more of our production processes in SFI. This means that you will be responsible for, among other things, validation documentation, revalidations, and risk assessments for the specific process.

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.

Senior Technical Writer - Regulatory (CMC)

You will join the Technical Writing team within Global Regulatory Affairs. We are responsible for global regulatory CMC writing of regulatory documents in applications for new approvals, worldwide market expansions, and product lifecycle activities. We work with a variety of pharmaceutical products, including small molecules, peptides, biologicals, recombinant products, and gene therapy.

Stepping into an informal and collaborative environment, you will have close interfaces with many different disciplines, including Global Pharmaceutical R&D, manufacturing sites, Product Supply, Quality Assurance, Ferring affiliates, and development sites around the world.

Formulation Scientist

As a Formulation Scientist at our European Innovation Center in Hørsholm, Denmark, you will play a crucial role in researching formulation technologies for pheromone line of products.

Responsibilities:

• Research new formulation approaches and innovative new technologies for pheromones.
• Design and execute experiments to develop robust formulations for various products, with a special emphasis on pheromones.

Laborant til Incoming QC

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

I Incoming Quality Control (IQC) foretager vi kvalitetskontrol af råvarer og Outsourced supplier materials, hvor vi sikrer at den korrekte dokumentation er tilstede, før vi godkender råvarerne til produktion. Desuden foretager vi test af nogle råvarer, ELISA tests, Bioburden og analyser af vandprøver.

Hverdagen består hovedsageligt af grundig kvalitetskontrol af dokumentation og reviews samt laboratoriearbejde, men vi prioriterer også tid til løbende forbedringer af vores arbejdsgange og processer.

Supervisor til Trikinlaboratoriet

Er du motiveret og kvalitetsbevidst? Har du interesse i at arbejde som Supervisor i en gruppe på 7 personer, så er du måske den nye medarbejder vi søger til vores nathold!

Vi er på udkig efter en ansvarsbevidst kollega, som har lyst til at varetage driften af laboratoriet på vores nathold i samarbejde med vores Manager på dagholdet.

Din hverdag vil bestå i at lede og fordele arbejdet i laboratoriet, samtidig med at du indgår i det forefaldende analysearbejde. Du vil blive en del af et team bestående af 7 kollegaer, som har et solidt kendskab til at udføre analysen efter beskrevne procedurer.

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.