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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.

Senior Project Manager

Are you motivated by being the driver of the implementation of new equipment/facilities or complex upgrading projects) up to EUR 15 million?

You will be responsible for and ensure project execution of all phases in your projects including scope definition, identifying the solution, and mitigating risks, time, budget, and quality. We primarily work with the stage gate model for our larger projects.

Team Lead, Technical Documentation & Support

Brænder du for teknisk dokumentation, og udvikling af intelligente akustikløsninger? Kan du omsætte teknisk viden til praksis og sikre høj kvalitet gennem detaljeret dokumentation? Vil du være en del af et internationalt orienteret firma, med solid erfaring inden for akustik, hvor bæredygtighed er et kernepunkt?

Med udgangspunkt i fremragende bygningsakustik søges en Team Lead til Technical Documentation & Support, der er et team, der varetager en række opgaver indenfor dokumentation, test & certificeringer og compliance.

Ingeniør til validering

Vi har brug for en konsulent til et spændende job indenfor kvalificering og validering. Stillingen byder på mange forskellige opgaver og projekter hos vores kunder på det meste af Sjælland, og du får en spændende, travl og varierende hverdag.

Du vil bl.a. koordinere, planlægge og udføre validerings- og kvalificeringsprojekter, som kan omhandle: rengøringsvalidering, sterilisationsprocesser, procesanlæg, IT-validering, klimafaciliteter, produktions-, måle- og laboratorieudstyr.

Technical Specialist, Product Quality, Nourish (Maternity cover, 12 months)

Are you an enthusiastic, motivated and detail-oriented professional with a desire to work in a team of colleagues with great technical competencies within production, regulation and processes?

Your core responsibilities:

• Handling deviations for products manufactured at our factories.
• Handling of product quality related complaints.
• Coordinate and implement customer-specific requirements. Maintenance of master data in various IT systems, including SAP.

Miljøkonsulent

Har du erfaring inden for miljøområdet, og er du dygtig til at sætte dig ind i kunders behov?

Du skal være med til at omsætte miljøfaglige udfordringer hos vores kunder til funktionelle IT-løsninger, og du skal være drivkraften mellem vores kunder, vores forretning og produktudvikling.

Du bliver en del af en fleksibel og rummelig arbejdsplads i Rødovre, hvor du har mulighed for at tilrettelægge din dag, så det passer godt til dig og dine behov.

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.

QEHS Manager

Unique opportunity to join an innovative biotech company with a proven and sustainable technology on the edge of global expansion.

Do you want to help develop the protein of the future, which will make it possible to feed the world's growing population without damaging our ecosystems?

You will be leading a small team responsible for managing and coordinating all QEHS activities, including certifications, audits, and training. You will ensure that operations are conducted in a safe and efficient manner and in conformance with safety regulations.

Kemiingeniør – byg pilotanlæg, der kan skabe grønnere ammoniak

2 % af de globale CO₂-udledninger stammer fra produktionen af ammoniak. Synes du også, at det er 2 % for meget? Og vil du være hjernen bag de pilotanlæg, der skal opskalere vores prototype til en demonstration unit?

Så kom og få en hverdag med startup-ånd og fleksible arbejdstider.

Vi har potentialet til at gøre produktionen af ammoniak CO₂-neutral. Og du bliver den, der designer og bygger de anlæg, der får os i mål. Så du kan virkelig få virksomheden til at blomstre

Er du kemifagligt stærk – optimér vores processer, når vi øger produktionen

Vil du være med til at videreudvikle vores arbejdsgange, når vi omdanner halm til ethanol, prebiotiske fibre og lignin – og dermed udnytter ressourcer, der ellers kunne være gået op i røg?

Du kommer ind, bedst som vi skal øge vores produktionsmængde. Og med dine inputs vil vi forhåbentlig også kunne nedbringe vores elforbrug og CO₂-udledning undervejs.

Teknologi-entusiastisk QC-medarbejder

Vi søger lige nu en engageret og kvalificeret LIMS Udvikler i AJ Vaccines til at varetage og implementere vores nye Laboratory Information Management System (LIMS) samt sikre overholdelse af regulatoriske krav. Som LIMS Udvikler vil du komme til at spille en afgørende rolle i vores globale mission om at redde liv verden over.

Du vil være ansvarlig for at implementere og understøtte designet af vores LIMS-system ved at oprette og vedligeholde den Masterdata, der udgør rygraden af vores LIMS, og som er i overensstemmelse med vores strategiske målsætning og regulatoriske krav.

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

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.

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.

Genopslag – Naturvidenskabelig kandidat til Jordbrugskontrol

Vil du være med til at kontrollere gødningsregnskaber og gødningsprodukter og herigennem bidrage til at minimere udledningen af næringsstoffer til vores vandmiljø? Kan du formidle faglige problemstillinger og løsninger på en let forståelig måde?

Vi tilbyder dig et spændende og selvstændigt job i et kollegialt miljø med en åben ledelsesstil. Vi lægger vægt på, at det skal være sjovt at gå på arbejde, og vi kan tilbyde fleksible arbejdstider på en familievenlig arbejdsplads

Utility Engineer

Er du klar til at blive en del af en innovativ, international vaccinevirksomhed, som den tekniske specialist?

I rollen vil dine primære arbejdsopgaver være support til teknikere og brugere, herunder hjælp til fejlsøgning på anlæg og udstyr, samt at sikre:

• Robusthed af anlæg ved kontinuerligt at have styr på vedligehold
• At GMP og regulatoriske krav er overholdt

Head of the Department of Virus & Microbiological Special Diagnostics

Do you have solid management experience and deep insight and experience within virology?

As Head of the Department of Virus & Microbiological Special Diagnostics, you are responsible for the daily management of the department to ensure the diagnostic preparedness for infection in a one-health perspective with synergy between laboratory diagnostics in humans and animals.

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.

Department Manager for Histology

We are seeking a dedicated Department Manager to lead our Histology department. The ideal candidate will possess proven leadership abilities and a passion for managing and developing teams, preferably with a background in Histology. 

The Histology department is committed to delivering high-quality histological data within all Gubra’s research areas, including MASH, obesity, metabolic and fibrotic disorders. Our growing team consists of 7 scientists and 5 laboratory technicians who work collaboratively across Gubra and provides valuable, decision-making data for customer studies as well as internal projects.

Department Manager for Molecular Pharmacology

Gubra is seeking a dedicated and experienced Department Manager to lead our Molecular Pharmacology department. The ideal candidate will possess proven leadership abilities and a passion for managing and developing teams, along with a background in molecular pharmacology and drug discovery.

Your tasks include

• Daily management of a team of scientists and lab technicians to ensure high performance, personal development, well-being and engagement.
• Guide the team to accomplish department goals and objectives.
• Oversee the planning, execution, and analysis of experiments to support Gubra’s internal and partnered drug discovery projects.