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Laborant til mikrobiologisk team

Har du lyst til at være med til at sikre vacciner til forebyggelse af infektionssygdomme?

Bavarian Nordic er i en rivende udvikling og derfor søger vi en laborant til det mikrobiologiske team i Kvistgaard. Du vil i stillingen bidrage til test og frigivelse af vacciner mod kritiske sygdomme. QC-mikrobiologi har ansvaret for at udføre analyser af rutine prøver og valideringer af nye produkter. Desuden yder vi support til vores produktion.

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.

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.

Specialist in Organic Coating Processes and Chemicals, Materials & Processes Engineering Department, Terma Aerostructures A/S.

Your role involves overseeing all organic coating processes, ensuring compliance and quality of materials such as epoxy- and polyurethane-based paints. You will also manage the requirements for consumable chemicals, like solvents for surface cleaning.

The responsibility furthermore entails the overall responsibility for REACH surveillance and chemical substitution activities at our Grenå manufacturing site, in close collaboration with other process owners.

QC Laboratory Technician

Har du lyst til en hverdag fyldt med spændende opgaver, fokus på høj produktkvalitet og med en stor grad af ansvar? Synes du, det er sjovt at arbejde med ingredienser til en bred vifte af fødevarer?

Primære arbejdsopgaver:

• Analyser af råvarer, mellemvarer og færdigvarer, herunder kemiske og sensoriske analyser
• Frigivelse af råvarer, mellemvarer og færdigvarer
• Udarbejdelse af analysecertifikater til vores kunder

Laborant til barselsvikariat til vores QC i Avedøre

Har du erfaring med laboratoriearbejde inklusive klassisk mikrobiologi og kemi og kunne du tænke dig et job, hvor der hele tiden sker noget nyt og spændende – og hvor du bidrager aktivt til teamet?

Du bliver en del af en afdeling, hvor vi har et godt socialt miljø, hvor vi hjælper hinanden, værdsætter høj faglighed og har fokus på kunderne. Du vil få et job med en spændende og afvekslende hverdag i en alsidig fabrik, hvor der er fart over feltet.

Senior QA Specialist

The Senior QA Specialist for Radiometer is responsible for ensuring safe, reliable, and compliant products during new product development and maintenance of existing product platforms. This is done by cooperating, supporting, facilitating, training, and communicating towards the best results with partners in R&D.

This position is part of the QA Design Control department, hybrid based and located in Brønshøj. At Radiometer, our vision is to improve global healthcare with reliable, fast, and easy patient diagnoses.

QA Specialist

You will be responsible for ensuring safe, reliable, and compliant products during new product development and maintenance of existing product platforms.

You will have the opportunity to:

• Provide Design Control guidance for QMS and regulatory compliance in an FDA regulated and ISO compliant environment.
• Represent Quality Assurance in design and development projects and in cross-functional teams supporting new product development.

Senior Biochemical Engineer for Process Development and Engineering

We are now looking for a highly motivated Senior Biochemical Engineer to join our Process Development and Engineering Team at FMC’s Pheromones Plant Health Division.

In the Process Development and Engineering Team you´ll take on a key role in upscaling R&D laboratory results to full-scale biomanufacturing reality. You will work with a variety of pilot-scale and industrial fermentation processes – from L-scale to 100+ m3 “real deal” production campaigns, and you will follow downstream processing from fermentation broth to yielding to-specs products.

Manager, Chemical Substance Registration

The Manager, Chemical Substance Registration is accountable for implementing and executing the chemical control compliance programs of IFF in the EAME region (UK, EU REACH, Turkey REACH, EAEU etc.) for the technical enzymes’ portfolio of products (Biofuels, Fabric & Household Care, Textile Processing and Designed Enzymatic Polysaccharides).

The Manager, Chemical Substance Registration is furthermore a key contact for the Enzyme Business in determining strategic business decisions and should be representing IFF in industry work groups to assure IFF’s regulatory interests.

Manufacturing Science & Technology (MS&T) Technical Transfer Project Manager (Sr Specialist)

Join Orifarm and take charge of building strong business relationships with a key portfolio of our suppliers!

As a MS&T Technical Transfer Project Manager, you will be responsible for securing technical support to Supplier Relationship Management functions, and manufacturing sites comprising support, technological transfers between CMOs and own manufacturing sites, analytical method development and validation, external product development at CDMOs and driving continuous technological improvement and innovation.

Laborant til Incoming QC

Vil du bidrage til diagnostik af cancer og gøre en forskel for patienter? Er du detaljeorienteret og lægger vægt på korrekt produktion og dokumentation? Trives du i et spændende produktionsmiljø?

I Incoming Quality Control (IQC) foretager vi kvalitetskontrol af råvarer og Outsourced supplier materials, hvor vi sikrer at den korrekte dokumentation er tilstede, før vi godkender råvarerne til produktion. Desuden foretager vi test af nogle råvarer, ELISA tests, Bioburden og analyser af vandprøver.

Hverdagen består hovedsageligt af grundig kvalitetskontrol af dokumentation og reviews samt laboratoriearbejde, men vi prioriterer også tid til løbende forbedringer af vores arbejdsgange og processer.

PhD scholarship in Fish Bacteriology and Prophylaxis with specific Emphasis on Bacteriophages as a Control Method – DTU Aqua

Join us on our mission to monitor and promote health of fish and shellfish, with special focus on sustainable aquaculture.

You will be working within bacteriology and microbiology with emphasis on host-pathogen interactions and disease prophylaxis in fish. The focus will be the fish pathogen Flavobacterium psychrophilum and bacteriophages as a prophylactic control measure against disease outbreaks with this important pathogen in aquaculture.

Your work will be part of externally funded research projects, among them the IFD Grand Solutions project AQUAPHAGE Towards a sustainable aquaculture: Phage-based solutions for disease prevention in rainbow aquaculture.

Coordinator in Quality

Are you our new coordinator within Quality? Do you enjoy working with Planning & Forecasting, Contract Laboratory Organization (CLO) management, Reference standard & Control management - then join our Data Management team within Quality in our site in Hillerød.

You will be the point of contact for CLO´s used within Quality Control (QC) ensuring the relationship and making sure contracts are in place. Your responsibilities will include monitoring of inventory levels, providing status to management and facilitating the timely delivery of products to customers.

QA Academic CMC Development

Do you want to be part of an agile, inspiring, and competent team while restoring brain health for patients worldwide?

Then join us as our new QA Academic, ensuring product quality while collaborating with multiple stakeholders leveraging your professional and personal competencies. We offer an exciting job with a broad variety in you daily work supporting CMC deliverables from early to late phase pipeline projects.

Production Supporter for Cell culture processes

Do you have experience with aseptic work and cell culture processes (CEF), and do you like to take on a great professional responsibility and always ensure your process is compliant?

This is an exciting position in an international company with a unique technology and manufacturing process within vaccine/biologics production. You will be working in an open culture, where everybody is working in the same direction and where there is room for ideas and independent action.

Drug Substance Production Supporter

Our vaccines make a real difference to people, and no matter your role we all contribute to protecting lives every day. In Virus Production Support team your main area of responsibility will be:

• Trouble shooting in production
• Process confirmation to ensure your processes are running according to written procedures

Senior Data Manager

The Senior Clinical Data Manager is responsible for leading and overseeing data management activities associated with clinical trials, ensuring data accuracy and consistency, and managing data cleaning and quality control processes.

We strongly endorse a flexible working environment around its core working hours of 09:00-15:00 and endorses fair and equal pay practices.