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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.

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.

Laboratory Technician, Colour Anodizing

Are you driven by the challenge of mastering the art and science behind colour anodizing processes to shape the visual appeal and functionality across our wide product range?

Key responsibilities

• Identify and evaluate new technologies, tools, and methods within aluminium production.
• Lead and support implementation of special aluminium colour series.

With approximately 1100 employees, Bang & Olufsen is an agile company that gives room for individual flexibility and decision-making.

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.

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.

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.

Kontorchef til Arter og Naturbeskyttelse

Vil du være med til at løse biodiversitetskrisen? Har du mod på spændende ledelsesmæssige udfordringer?

De konkrete faglige områder, du vil skulle have ansvaret for, er opgaver i forbindelse med biodiversitet og natur, særligt EU-naturbeskyttede Natura 2000-områder i Danmark både til land og på havet, spørgsmål relateret til forslag om en EU-naturgenopretningsforordning, internationale havmiljøopgaver og marin naturgenopretning, herunder etableringen af stenrev og arbejdet med at udpege naturbeskyttede områder til havs.

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.

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.

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

Zacco søger Patent attorney trainees til vores hovedkvarter i Ørestaden eller vores kontor i Århus

Som patent attorney trainee hos Zacco vil du få lagt et program, særligt tilpasset dig og din tekniske baggrund, og en eller flere erfarne kolleger som mentor. Her vil du blandt andet lære at:

• rådgive om beskyttelse af kunders produktudvikling
• udarbejde patentansøgninger, herunder analysere patenterbarhed
• forberede forsvar/anklage i patentkrænkelsessager

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

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.

External Lecturer – “Medical Biotechnology and Drug Development” – DIS Copenhagen

The teaching position is for the fall semester, which will begin in August. You will teach highly motivated undergraduate students from North American universities who are spending a semester studying in Copenhagen.

Why teach at DIS?

• Work in an international, informal and enthusiastic environment with an emphasis on cross-cultural understanding, teamwork, innovation, and adaptability
• Develop interactive and experiential teaching skills and teaching experience in English

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

Department Manager for Molecular Pharmacology

Gubra is seeking a dedicated and experienced Department Manager to lead our Molecular Pharmacology department. The ideal candidate will possess proven leadership abilities and a passion for managing and developing teams, along with a background in molecular pharmacology and drug discovery.

Your tasks include

• Daily management of a team of scientists and lab technicians to ensure high performance, personal development, well-being and engagement.
• Guide the team to accomplish department goals and objectives.
• Oversee the planning, execution, and analysis of experiments to support Gubra’s internal and partnered drug discovery projects.