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QA Specialist for Environmental Support

In this role, you will join Bavarian Nordic's QA Organization as a QA Specialist tasked with establishing strong relationships with stakeholders, effectively communicating GxP requirements, and handling crucial Quality Events in the Quality Management System (QMS).

This is in the context of environmental monitoring, aseptic performance, and sterile & low bioburden processes in Drug Substance and Drug Product Production. Additionally, you will contribute to the ongoing improvement of QA processes to elevate overall quality standards.

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.

Manufacturing Support Documentation Associate

Do you have a flair for compliance and can handle many stakeholders? Are you looking for a position where you can take on responsibility?

About the position:

• Create and maintain records and procedures by collecting information from stakeholders to supply manufacturing with compliant documents.
• Start-up events and support investigations by giving input as procedural SME.
• Support the change process by writing SME assessment to ensure procedural alignment. Perform timely closure of action items to ensure reliable execution of production.
• Continuously improve the department processes and support stakeholder improvement projects.

Senior Project Manager

As part of our decarbonization journey we are looking for an experienced EPC/EPCM project managers to run projects in the Power-to-X area as well as highly challenging demonstration projects of our new technologies in cooperations with strategic partners and customers around the globe and in our own plant production facilities.

We can offer a global project portfolio, exciting new technologies and a customer base containing many global players.

Process and Innovation Lead

We are hiring a Process and Innovation Lead for our factory in Odense, where we produce detergents under our strong Home Care brands such as Neutral, Biotex, and OMO.

In this position you will be the owner of our fabric wash manufacturing processes in the factory. A critical part of this role will be ensuring an effective link with R&D, planning, and factory for innovation, capacity, and project delivery. You will be responsible for mapping potential sustainability projects.

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.

Senior QA Specialist

You will be part of our QA Business Support Team, consisting of 12 QA Specialists and Senior QA Specialists, allocated to projects including innovation projects, capacity projects and strategic QA/QC projects. We participate in projects both as quality and compliance experts to ensure compliance with the requirements for Class III Medical Devices.

We are driven by improving patient outcomes and we take our values to work every day – we care about each other, our environment and our customers and we win for patients with innovative high-quality solutions.

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)

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.

Business Developer with a background in Science

Do you want to be at the forefront of Targeted Radiopharmaceuticals and Molecular Imaging?

We are looking for a professional Business Developer with a background in life sciences and the ambition to contribute to further strengthening Minerva Imaging as the trusted partner for targeted radiopharmaceuticals and molecular imaging.

What truly matters is your passion for the advancement and know-how of our scientific studies and your ability to foster long-term relationships with our collaborators.

Test & Reliability Engineer - Sustaining Engineering, Medical Devices

Do you have a keen eye for Physical Testing, Product Quality, Reliability, Validation, and Documentation? Are you looking for an opportunity to merge your passion with our expertise in the Test and Verification of Infusion Care Medical Devices, for the treatment of chronic diseases such as Diabetes and Parkinson’s Disease?

As a Test Engineer, you will be involved in developing and working with a diversity of physical test methods. Planning and coordinating tests in our laboratory in Osted near Roskilde, and partners within Global Convatec and external. Most of your time, you will be part of a project team in SEG.

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.

Creative Assistant

Are you inspired to contribute your expertise to a global leading Flavors Organization? Are you passionate in working in a dynamic team with creative and empowered people?

Your Focus will be:

• Always following correct compounding procedures
• Prepare compounded flavors for evaluation, including preparation and running of difference testing if project requires.
• Coordinate with QC to obtain specifications of all experimental recipes within 24 hours of completion of evaluation.

Training Partner

Are you passionate about designing high impact training to improve ways of working?

The role will focus on re-designing the training related to onboarding our professionals working directly with our operation, our Operators, and our Laboratory Technicians.

You will meet a DK rooted company growing in number of international colleagues and a way of working, where hybrid, digital, learning and innovation are key words.

Laborant/Lab Technician

Do you want to help our customers with developing their future or existing products? The Innovation Center in Silkeborg, are conducting a lot of different tests from customer all around the world, within food & beverage.

The laboratory technician will be responsible for the laboratory in the innovation center in Silkeborg, providing the needed analysis for our customers during the different trials we conduct in the test center, be responsible for keeping the laboratory fully equipped, take care of the customers questions, and to ensure that the laboratory always stays presentable.

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.

Procesingeniør

Har du lyst til at starte din karriere med at arbejde inden for farmaceutisk produktion? Og har du mod på at bevæge dig ud i tværfaglige udfordringer, der ligger lidt uden for din uddannelse?

Vi er en virksomhed i vækst, og produktionsvolumenerne vokser – så derfor har vi et stort behov for at styrke vores ingeniørgruppe med et nyt medlem, der kan medvirke til, at vi får moderniseret vores udstyr, som produktionen vil få stor gavn af.

QC-laborant med varierende opgaver

Har du lyst til at sikre kvaliteten af vores API’er i en QC-funktion, hvor du får lov at løse en palet af forskellige opgaver? Har du lyst til at blive en del af en velfungerende gruppe, hvor du løbende bliver trænet i nye opgaver af dine erfarne kolleger?

Så er det måske dig, der er vores kommende QC-laborant. Vi er i en proces, hvor vi vokser, og derfor søger vi en laborant, der trives med fleksibilitet og gerne vil udvikle sig.

Vi vil altid være lydhøre over for den enkelte laborant. Hvis du har interesse for en opgave, så lytter vi og sørger for, at du bliver trænet i den og får lov til at løse den