45 job ads match your search 45 job ads found

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.

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.

Controls Engineer

Are you a results-driven problem-solver, eager to positively change the world?

The Controls Engineer is primarily responsible for design, specification, commissioning, and support of prototype and industrial automation equipment and data systems at Biomason’s manufacturing partner site(s).

Join Biomason and help us end the world's dependence on carbon-emitting construction materials.

Systems Design 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?

The Systems Design Engineer is primarily responsible for design, specification, commissioning, and support of prototype and industrial automation equipment and data systems at Biomason’s manufacturing partner site(s).

Join Biomason and help us end the world's dependence on carbon-emitting construction materials.

IT Infrastructure Engineer

As an IT Infrastructure Engineer at Zealand Pharma A/S, you will implement new infrastructure solutions and support existing systems.

Responsibilities include:

• Provides day to day support of overall infrastructure including network, physical and virtual servers, hypervisors, and storage platforms.
• Configures and implement new systems and enhancements to existing systems in support of business needs.

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.

(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.

Senior Scientist, Infectious Disease Vaccine Discovery and Research

You will conduct various laboratory activities with the primary goal of producing reliable test results and optimizing lab procedures while adhering to correct procedures as well as health and safety guidelines. The role also includes documentation and reporting of results both in writing and in different forums.

You will work with dedicated colleagues in an inspiring and fast-moving environment with a collaborative and innovative spirit.

Student Worker in QC Development & Projects

Are you curious about the daily operations of a laboratory? We are seeking a dedicated Student Worker to join our QC Development & Projects team.

In this role you’ll make an impact by: Engaging in a variety of laboratory tasks including producing buffers, maintaining equipment, and managing laboratory supplies. You will also develop and digitize training materials, update and maintain procedural documents and working files, and organize, report, and review study data, focusing on stability studies related to probiotics.

Lab technician Trainee (Immunology)

Gut Immunology lab is a newly established and the home to an enthusiastic, diverse, and international group of researchers in the field of gut microbiology and immunology. The research focuses primarily on immunopathologic mechanisms, novel therapeutics, and the translation of basic science findings for applications in gut health diseases.

As part of our team, you have the chance to learn a wide range of techniques, such as:

• Mammalian cell culture techniques and cell-based in vitro assays
• Bacterial and microbiological techniques (media preparation, identification and bacteria culturing, anaerobic techniques)

Senior Associate Accounting Operations

Are you passionate about biotechnology and quality assurance? Genmab is offering a great opportunity as a Senior Associate Accounting Operations

The Finance area of Genmab is growing and now looking for a Senior Accountant to join the Accounting Operations team in Copenhagen.

This is a key position within the Accounting Operations Teams and a great opportunity for an experienced, motivated, and ambitious accounting professional. You will be working in a highly motivated team of experienced finance professionals in an organization where we value innovation, determination, integrity, and teamwork.

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.

Manager Virus Production

Do you want to play a central and important role in Bavarian Nordic´s manufacturing strategy by setting directions and ensuring smooth daily operation in our production facility?

Our newly established Drug Substance Facility in Kvistgaard will soon start production ramp-up, and we therefore need to strengthen our leadership. You will become responsible for the day-to-day shopfloor management of 15-20 operators.

Senior Medical Writer

Do you want to work in a global context and according to the highest standards of current practice to provide new products to patients with unmet medical needs?

As a Senior Medical Writer, you will be responsible for delivering submission-ready documents and take the role as lead medical writer on specific assignments. In addition, you can look forward to joining a diverse organisation shaped by cross-functional and global collaboration – and a focus on continuous transformation to support the future needs of clinical development.

Technician, EMA Solids Support Team

Welcome to Solid Support Team 13 skilled process engineers and technicians responsible for quality, introducing new products, throughput, and optimizing the products.

In this role you’ll make an impact by:

• Responsible technician for the MG-coating line, ensuring smooth and efficient coating processes for granulating with MnTACN
• Coordinate the steering system changes, bridging the gap between process engineers, technicians, and programmers to optimize operational efficiency.

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