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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.

Supporter til produktionsforbedringer og drift

Vil du være med til at bekæmpe kræft?

Brænder du for at lave forbedringer af processer og produktionsfaciliteter, samtidig med, at produktionen holdes kørende?

Dine opgaver vil være at stå for store og små procesforbedringer. Det kan være mindre tilretninger af SOP’er eller store forandringer som fundamentalt ændrer vores måde at arbejde på.

Vi tilbyder masser af ansvar og indflydelse på dine arbejdsopgaver.

Akademiker til daglig support og procesforbedringer

Vil du være med til at bekæmpe kræft? Brænder du for at lave forbedringer der sikrer høj kvalitet? Er du klar til at gøre en forskel for dine kolleger og forbedre produktionsfaciliteterne til gavn for Agilents kunder?

Dit hovedansvar vil være at sikre GMP-niveauet i produktionen. Du vil i den forbindelse skulle afklare GMP-spørgsmål samt udarbejde Non-Conformance Reports (NCRs).

QA Assistant, GS-5, QAC

This position is embedded in the Quality Assurance Centre (QAC), where teams have coreresponsibilities around quality assurance and quality control of supply processes and the productswe procure and deliver.

The incumbent will beresponsible for assisting the Quality Assurance Specialist (non-pharma) in the management of all aspects of Pre-Delivery Inspection (PDI) arrangements for non-pharma items from initial request tofinal invoice certification.

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.

Formulation Scientist

Are you looking to use and grow your experience in formulation development in a broad role with independent responsibilities? Do you want to drive formulation projects and contribute to the strategic development of future products?

In this role, your overall focus will be formulation development of drug products. Your responsibilities will cover formulations used for toxicology and clinical studies through the development phases and all the way to the commercial drug product.

Communicative and collaborative Lubrication Oil Senior Research Engineer

Are you an experienced and dedicated lubrication expert? Are you interested in making a vital impact on the decarbonization of the maritime industry?

Would you like to close the circle between lubrication, materials and combustion, and thereby make ship engines run better on our green fuels? Then we might have the right position for you.

Experienced Scientist for validating QC methods in Novonesis

Do you want to work in an environment where great collaboration is valued as highly as scientific excellence?

Working as Scientist in our team, you will be responsible for validating and optimizing analytical methods for Human Health products in our QC labs. You will work closely with other scientists and laboratory technicians to plan and implement efficient microbiological methods.

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.

TotalEnergies Exploration & Production Graduate Program – join our E&P Graduate Program at TotalEnergies Denmark now!

Are you a recent graduate from an engineering school or a technical university? Are you looking for an experience in an international energy company and willing to tackle new challenges? Our E&P Graduate Program is just right for you!

During the 2-to-2,5-year program, you will firstly join our affiliate in Denmark to anchor your career within a local context, but after approximately 1 year you will undertake your first mission with an exchange to the OneTech Branch in France. It gives you the opportunity to strengthen your technical, scientific, and organizational knowledge, develop your competencies and discover how the company operates in various energy domains.

PhD scholarships on “Live” Visualizations of Single Nanoparticle Catalysts at the Atomic-Scale - DTU Physics

Could you envision “seeing” chemical reactions being catalyzed at the atomic-scale? Two or more scholarships are now open for experimental research in nanoparticle catalysis using advanced operando electron microscopy at the Center for Visualizing Catalytic Processes (VISION).

VISION is developing and applying a new unique platform for visualizing catalytic nanoparticles and reactions at the atomic-level by integrating cutting-edge electron microscopy, microfabricated nanoreactors, nanoparticle synthesis and computational modelling. This approach enables new, direct operando observations that are urgently needed to advance mechanistic insight into catalytic processes at the atomic-scale.

Inside Sales Representative - Analytical Instruments – Danish

Have you ever considered using your scientific background in a different way? Looking for a new challenge where you can apply your skills in a commercial environment? Then this position is for you!

As our new Inside Sales Representative you will have the responsibility for selling Agilent Technologies products, solutions, and services to our valued customers across Chromatography and Spectroscopy.

We offer an independent job among good colleagues, in a growth orientated conglomerate. You will become part of a caring and fast paced environment, built on integrity, information, and trust.

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.

Laboratory Technician - Food Chemistry - Aarhus

We are looking for a Laboratory Technician with a passion for research and innovation with analytical interests within chromatography to join the Food Chemistry Team at Arla Innovation Centre, Aarhus. If this is you then don’t hesitate to apply.

A typical task covers the following:

• Taking in a request, coordinating and planning laboratory trials and analyses.
• Executing and reporting trials and analysis.

PhD scholarship in Bioinformatics of the Glycosylation Machinery of Archaea - DTU Bioengineering

DTU Bioengineering seeks a qualified candidate for a fully funded 3-year PhD position within Bioinformatics Based Mapping of N-Glycosylation of Proteins in Archaea. The PhD project is part of a Marie Sklodowska-Curie doctoral training Program, GLYCO-N, funded by the EU (MSCA Doctoral Network).

The PhD project is thus part of a bigger interdisciplinary research effort that aims to 1) Understand the diversity and structural complexity of archaeal, microalgal and viral N-glycosylation and 2) Harness this knowledge for new solutions in biomedicine and biotechnology.

Global Business Leader - Sweeteners

IFF is very excited to welcome a new Global Business Leader – Sweeteners to our team, and we hope it’s you!

Your primary responsibility will be to set the commercial strategic direction and build strong execution plans with the sales regions. You will work in a competitive market but with interesting opportunities for driving profitable growth. You will be responsible for revenue and profit growth for the assigned portfolio, you will create and oversee the implementation of the Product Strategy.

Manufacturing Supporter

We are looking for a talented Manufacturing Supporter for the Drug Substance Production to join the DS Documentation and Support Department in Hillerød.

The work we do at FUJIFILM Diosynth Biotechnologies (FDB) has never been more important—and we are looking for talented candidates to join us.

You will be part of a team, consisting of 14 people, with a great sense of humor and a high willingness to support where needed.

Application Scientist

In this role, you’ll make impact by becoming our go-to cheddar cheese authority, spearheading the development of innovative cultures and solutions. Working alongside a diverse group of scientists, technicians, and project teams, you will be instrumental in our R&D and commercial initiatives.

Based in our contemporary Dairy Application & Technology Centre, you will be at the forefront of expanding our capabilities and pioneering innovations with our partners.

Senior LIMS Specialist for Global QC Development

In this role you’ll make an impact by working as a Senior LIMS Specialist in our team, where you will take part in management of projects for LIMS changes across QC laboratories and other stakeholders including implementation, documentation and communication.

Future projects could be introducing and validating LIMS solutions on new equipment or technologies, new LIMS functionalities, improving and aligning existing processes.

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.