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Research Analyst

Are you in the right job? Do you want a challenge out of the ordinary?

The Primary Research Analyst has the responsibility of identifying, developing, and maintaining a network of contacts and relationships in the pharmaceutical and biotech industry and organizations.

An academic background in pharmacy or in biotechnology is an advantage but not a necessity as extensive internal training will be provided.

Process Engineer

Are you an experienced process engineer with solid experience from process engineering, technology, or a production company? Do you have technical knowledge within thermodynamics, fluid dynamics, compressible flow, and process design?

Do you want to join us in accelerating the global energy transition? Then you might be the Process Engineer we are looking for to join our team at Green Hydrogen Systems.

(Senior) Drug Substance Specialist

We are currently seeking a (Senior) Drug Substance Specialist who is energized by collaborative and fun teamwork, excels in handling complex tasks, and enjoys continuous learning.

Your responsibilities will include late-stage drug substance development, up-scaling and process validation as well as support in the commercial phase. Effective coordination with external partners is a significant aspect of this role.

Laboratory Technician

Are you looking for an exciting and challenging job in a laboratory with great opportunity for personal development and responsibility? Do you have experience with biodegradability, environmental or ecotoxicological studies?

If your answer is yes, we can offer you a challenging position in an informal and truly international environment in a company that helps solve the world’s challenges in water environments.

Regulatory Affairs Clinical Specialist

Due to many activities in our exciting clinical development projects, we are seeking two new colleagues to our Regulatory Affairs function.

Your key responsibilities will be to contribute with regulatory expertise to global strategies and execution within your assigned project(s). You will be the regulatory responsible in the clinical trial teams and provide regulatory guidance and support for the planning, execution, and reporting of clinical trials worldwide.

Graduate – Software Automation Program

Cognizant Denmark is currently seeking applications from Graduate Engineers for our Graduate Program in 2024 based in Hillerød, Denmark.

Successful candidates will be part of the Global Graduate Program.

This Program is an intensive 8-week Training Program that consists of Classroom Training, Workshops, Theory, Practical Training, and a Simulation Project.

Sustainability Advisor

Hvad har lufthavnen (en af Danmarks største virksomheder), en mellemstor dansk kommune og et stort parkeringshus til fælles?

De har alle et stort energiforbrug, og derfor arbejder vi i Københavns Lufthavne med at sætte en dagsorden for bæredygtighedsområdet. For eksempel har vi siden 2022 opsat over 400 el-ladestandere omkring lufthavnen, til at oplade både passagerers, partneres og egne el-køretøjer.

Vi er med til at udvikle nye teknologiske løsninger for luftfartsbranchen. Det bidrager til, at vi i 2030 når vores mål om at være net zero for vores egen drift, som omfatter vores energi- og brændstofforbrug. I 2050 udvides målet til at være net zero for hele vores drift og værdikæde.

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

Senior Specialist til QC hos Xellia Pharmaceuticals

Drømmer du om mere ansvar, med forskelligartede opgaver, og har du en passion for mikrobiologi? Vil du spille en central rolle i Xellias produktionen af livsvigtig antibiotika?

Som senior specialist vil du blive faglig ansvarlig for vores count release-laboratorie, som bl.a. udfører TVC- og LAL-analyser. Derudover vil du indgå i tæt samarbejde med vores sterile produktioner angående EM, hvor de nye Annex 1-krav stiller øgede krav til vores compliance, som du vil spille en vigtig rolle i.

Scientist (maternity leave temp), cell-based immunotherapies

Are you enthusiastic about developing next generation cell-based immunotherapies that bring new hope to late-stage cancer patients?

You will help the R&D team in a 6-months temporary position as one of our coworkers is on maternity leave, and will help the team with a possibility for further extension.

We are looking for a person experienced in immune oncology or related area with documented practical experience in cell culture and flow cytometry.

Sales Trader

We are looking for a Sales Trader who will play a vital role in ensuring BioCirc’s ambitious growth plans.

The successful candidate will together with the Portfolio Manager be responsible for the short-term sale of Certificates, optimizing the portfolio, gather market intelligence, and ensuring value added through the whole supply chain of biomethane production, but also new renewable products stemming from our energy clusters.

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.

Laborant

Har du øje for detaljen og fokus på kvalitet? Henter du samtidig energi via samarbejde, og kunne du tænke dig at blive vores 6. medlem i vores kvalitetslaboratorium?

Opgaverne omfatter blandt andet:

• Analyser og kontroller jf. vores kvalitetskontrolplan
• Support og samarbejde med produktionen
• Dokumentation og sikring af sporbarhed

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.

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

Project Leader – process/hydrogen safety

Do you want to apply your skills to promote a fast and safe transition of the energy and transportation sectors away from carbon-based fuels?

You will be leading diverse teams of experts to deliver state-of-the-art results to our partners in the hydrogen sector, working on some of our largest fire safety projects.

We have great offices and facilities, and you get good staffing conditions, such as pension scheme, dental insurance, and health insurance. We have an active staff and art association, and our chefs cook delicious food for us daily.

Battery specialist

Do you want to apply your skills to promote a fast and safe transition of the energy and transportation sectors away from carbon-based fuels? Do you have experience working with or developing battery technologies?

As our new Battery Fire Specialist, you will provide expertise on Li-ion batteries and other upcoming technologies to the team. You will be part of projects performing risk analyses, battery fire tests, and fire safety design for clients and in R&D contexts.

Senior Environmental Impact Specialist

Are you passionate about making a difference in the apparel and textiles industry by measuring and communicating environmental impacts?

As a Senior Environmental Impact Specialist you act as the internal go-to specialist and it is expected that you engage with various stakeholders internally and externally to provide specialised knowledge.

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.