28 jobannoncer matcher din søgning 28 jobannoncer fundet

Com­merci­al Ope­ra­tions Manager (m/f/d)

KWS SAAT SE & Co. KGaA is seeking for a Commercial Operations Manager (m/f/d) to play a vital role in the KWS sugarbeet business in North & South-East Europe (NE/SEE). The position involves planning, organizing, and executing strategic initiatives across crops in these regions. The manager will collaborate closely with country teams and Regional Directors to ensure successful implementation and follow-up of initiatives.

QA Ext. Manufacturing Specialist

Would you like to work in one of the most interesting, complex, and dynamic areas in Bavarian Nordic? Are you ready to engage, support, and mobilize colleagues in a growing international business environment where we focus on saving lives every day?

As a QA Specialist, you will be responsible for daily support, QA oversight, and GMP guidance to Contract Manufacturing Organizations (CMOs) to ensure that our products are manufactured according to current GMP and our marketing authorizations.

Tekniker til et af verdens førende halvleder- og fabrikationslaboratorier

Laboratoriet er et af Europas største, og her får du en helt unik mulighed for at blive en del af et dynamisk og internationalt miljø bestående af forskere, ingeniører og specialister, der forsøger at skabe helt nye og banebrydende teknologier.

Dette forskningsprogram er fordelt på 7 laboratorier på tværs af 3 kontinenter.

Som tekniker kommer du til at spille en afgørende rolle ift. at sikre at laboratoriet er operationelt, og at udstyr altid fungerer efter hensigten.

Lab Maintenance Technician

We are looking for a Lab Maintenance Technician for our client’s brand-new semiconductor and fabrication laboratory in Copenhagen.

The lab is among the largest in Europe and you get to work with cutting edge technology in a highly dynamic environment of scientist, researchers and engineers trying to push the boundaries of computing.

As a Lab Maintenance Technician, you will play a crucial role in making sure that the Lab is operational, and that equipment always is performing accordingly.

Senior Research Technician

Do you want to work with data and HPLC analysis?

You will spend most of your time on HPLC analysis in our modern laboratory, which is designed to provide the best technologies and optimal working conditions.

Collaborating cross-functionally with our research scientists on both daily operations and projects, you will:

• Perform analytical method development in close collaboration with the responsible scientists
• Support formulation development studies with analyses

Manufacturing Process Engineer

Are you a results-driven problem-solver, eager to positively change the world? Do you believe that climate change is the biggest issue facing us today?

You are primarily responsible for primary process tracking, deviation tracking and reporting, as well as process transfer and optimization for our pilot plant and larger manufacturing systems.

Senior Research Technician

Do you want to use your experience and problem-solving skills to work with pharmaceutical product development and early-stage development with a focus on characterization (MFI, DSC, HPLC)?

As a senior research technician, you will spend most of your time in the lab, where your primary role will be to prepare, plan, and perform pharmaceutical development work, including stability studies.

Clinical Project Manager

Do you want impact, freedom to perform, global perspective and super colleagues?

As experienced Clinical Project Manager, you naturally know that your success is built on your ability to generate high quality data at high pace and within agreed budgets – without jeopardizing the good relationship to the people and partners involved. Another vital part of your road to success is your ability to think outside the box and handle (unforeseen) challenges on the way.

Scientist, New Product Development, Arla Foods Ingredients - Videbaek

Are you a skilled and passionate Protein Scientist eager to apply your expertise in developing cutting-edge ingredients for sports, medical, and infant nutrition?

Your primary objective will be to conduct trials aimed at progressing new product ideas. Your responsibilities will include:

• Collaborating with NPD teams to develop innovative ingredients.
• Planning and executing trials across laboratory, pilot, and production scales, in collaboration with laboratory technicians and operators.

Ambitious Project Manager to lead key strategic projects

Are you an experienced Project Manager motivated by making a difference? Then look no further – Pharmacosmos is looking for a Project Manager who can solve complex problems across our value chain and deliver impact to the organisation.

As Project Manager, you will become a key member of a small project management team in Pharmacosmos. You will be allocated to important strategic projects that you will lead and drive to completion to the satisfaction of all involved stakeholders using your existing toolbox and competencies for managing projects.

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.

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.

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.

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

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