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Graduate – Software Automation Program

Cognizant Denmark is currently seeking applications from Graduate Engineers for our Graduate Program in 2024 based in Hillerød, Denmark.

Successful candidates will be part of the Global Graduate Program.

This Program is an intensive 8-week Training Program that consists of Classroom Training, Workshops, Theory, Practical Training, and a Simulation Project.

Nyuddannet laborant til QC-afdeling

Brænder du for kvalitets- og laboratoriearbejde, og vil du være med til at sikre driftssikkerhed og kvalitet af analyser indenfor medicin- og fødevareindustrien?

Vi søger en laborant på fuldtid til vores QC-laboratorie i Birkerød, hvor du vil komme til at indgå i et team af 8 laboranter, 5 kemikere og 1 laboratorieleder.

Afdelingen er kendetegnet ved at have et godt samarbejde, være fagligt dygtige og meget lydhøre overfor forbedringer i arbejdsgange omkring analyse.

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.

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

Care for Potential – Trainee Program – Denmark

We believe that together we can create a sustainable tomorrow by caring for our resources. The Care for Potential Trainee Program, starting September 2nd, 2024, is a unique opportunity to use your potential and build your career while contributing to something of real value.

The purpose of the program is to provide ambitious young professionals with a structured framework and on-the-job training, as well as hands-on education and invaluable experiences. The program is designed to be both a digital and on-the-job experience with occasional travels, both nationally and internationally.

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

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.