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Specialist, Regulatory Affairs (Temporary Position)

As Regulatory Affairs Specialist, you will be responsible for lifecycle management of products manufactured at Orifarm’s own manufacturing sites. Therefore, you will collaborate closely with colleagues across functions, such as chemists, formulation specialists and co-workers within Quality, Supply Chain, Manufacturing and Sales.

Further, your main responsibilities include to:

• Gather information and documentation for variation applications
• Update dossier sections

Senior Data Manager

The Senior Clinical Data Manager is responsible for leading and overseeing data management activities associated with clinical trials, ensuring data accuracy and consistency, and managing data cleaning and quality control processes.

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

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.

Creative Assistant

Are you inspired to contribute your expertise to a global leading Flavors Organization? Are you passionate in working in a dynamic team with creative and empowered people?

Your Focus will be:

• Always following correct compounding procedures
• Prepare compounded flavors for evaluation, including preparation and running of difference testing if project requires.
• Coordinate with QC to obtain specifications of all experimental recipes within 24 hours of completion of evaluation.

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.

Specialist in Organic Coating Processes and Chemicals, Materials & Processes Engineering Department, Terma Aerostructures A/S.

Your role involves overseeing all organic coating processes, ensuring compliance and quality of materials such as epoxy- and polyurethane-based paints. You will also manage the requirements for consumable chemicals, like solvents for surface cleaning.

The responsibility furthermore entails the overall responsibility for REACH surveillance and chemical substitution activities at our Grenå manufacturing site, in close collaboration with other process owners.

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?

Laboratory technologist / technician - DTU Aqua

The position is affiliated to the section for Marine Living Resources with main tasks related to the research area Fish Biology.

You will be responsible for organising and maintaining our laboratories, ordering and keeping track of chemicals and consumables, and overviewing safe operating procedures. Laboratory tasks include sample registration and preparation for different analyses, conducting analyses, e.g. histology using different staining techniques and digitisation, molecular analyses including RNA/DNA extraction, cDNA synthesis, primer design and qPCR, and assisting in experimental studies of fishes.

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.

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.

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.

Craft Brewer

Er dit drømmejob at lave innovative øl af de bedste råvarer i et lille og dynamisk team, i tæt samarbejde med forskere? Og matcher du de fleste af nedenstående kvalifikationer?

Ansvarsområder

• Brygning, gæring, tørhumling, filtrering og rengøring på semiautomatiske anlæg
• Tapning på dåser og forskellige fustager på semiautomatiske anlæg

HSE Specialist

As an HSE Specialist, you will have the opportunity to develop and implement safety policies and procedures, conduct training sessions, and ensure compliance with local, state, and federal regulations.

In joining our team, you'll have the opportunity to make a significant impact, ensuring the safety and well-being of our workforce while contributing to our continued success at Duferco Danish Steel.

Senior Technical Service Engineer, Global Hydrocracking

This is an opportunity to join a team, where we support the sale of catalysts and technologies that can help our customers world-wide in producing environmentally friendly fuels.

You will be involved in the technical part of the catalyst sales process preparing technical proposals and performance evaluations for our customers’ hydrocracking units. You will participate in internal projects to improve our calculation tools and knowledge creation within the field of upgrading heavy fossil and renewable hydrocarbons into valuable products.

Radiochemistry Research Scientist for Minerva Imaging

The position is in a dynamic and exciting team involving studies researching new radiochemical synthesis methods and developing targeted radionuclide therapies, which necessitates close collaboration with our scientists and technicians across the organisation.

We are an informal organization with a strong focus on open and honest communication. We value humour and a natural care for one another.

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.

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.

Department Manager for Histology

We are seeking a dedicated Department Manager to lead our Histology department. The ideal candidate will possess proven leadership abilities and a passion for managing and developing teams, preferably with a background in Histology. 

The Histology department is committed to delivering high-quality histological data within all Gubra’s research areas, including MASH, obesity, metabolic and fibrotic disorders. Our growing team consists of 7 scientists and 5 laboratory technicians who work collaboratively across Gubra and provides valuable, decision-making data for customer studies as well as internal projects.

Principal DMPK Scientist

Currently, we are looking for a new principal DMPK scientist, who has experience in supporting discovery and development projects in characterization and selection of drug candidates.

Responsibilities

• Design, conduct, and manage in vitro, and in vivo experiments to evaluate the ADME and PK profiles as well as toxicokinetics of drug candidates both in-house and at contract research organizations
• Develop and execute assays for measuring drug concentration and metabolite identification from in vitro and in vivo experiments