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Technical support to international sales of feed supplements

A central role at R2 Agro, combining the technical knowhow of the products with the commercial value.

Your main responsibility will be technical support to our product portfolio. This requires that you can provide technical support to our distributors and regional managers, and participate in customer meetings and technical fora.

You will have the possibility of working from home sometimes, and you will meet a lot of good, social, and skilled colleagues.

Project Manager – Test & Verification

You get the possibility to be a key person in Foss New Product Development projects by ensuring high quality and product compliance to our world class analytical solutions.

As a member of the R&D Hardware Test & Verification team, you will be one of three Project Managers responsible for overseeing all reliability, environmental, and legal testing of instruments used in analytical solutions. Additionally, you will plan and ensure that our team develops and integrates value-adding production tests, which are crucial for the seamless assembly of the instruments.

Verification Engineer

Do you want to make a difference as an engineer by contributing to maintaining the safety, reliability, and integrity of our clients’ assets throughout their life cycle. Then you should join Bureau Veritas and some of the strongest engineering professionals in the industry in this new role.

As part of our client’s safety procedures, you will verify and check findings on- and offshore, to make sure that the client is adhering to all rules and regulations always maintaining the highest safety level.

You will handle a wide variety of verification assignments from gathering logs, materials, checking structural integrity designs, lifting equipment, electrical systems including UPS etc.

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.

Formulation Operator

As a Formulation Operator, you will operate processing equipment for the production of industrial enzymes. We’re looking for an energetic individual who is ready to tackle challenges in a fast-paced environment.

In this role you’ll make an impact by

• Operating a bridge crane, yard vehicle, and preparing raw materials for use in process equipment
• Taking production samples and analyzing those samples in the production laboratory as well as acting based on the obtained results.

Lab Technician

Med laboratorier i USA, Storbritannien, Tyskland og Danmark har LGC Biosearch Technologies planer om at fortsætte med at vokse.

Vi søger i øjeblikket talentfulde kandidater, der er klar til udfordringen med at arbejde i en formålsdrevet organisation med høj vækst.

Du vil blive en del af et mindre team og indgå i produktionen, hvor der syntetiseres, oprenses, analyseres, kvantificeres samt laves QC kontrol af syntetiserede produkter.

Vi tilbyder en arbejdsplads med gode kolleger, højt humør, en attraktiv frokostordning og muligheden for massage, hvis ønsket er der.

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.

Factory Manager Odense

You will be responsible for the factory and its production, where your most important task will be to support stakeholders – with focus on the Nordic market.

You will contribute with input for improvements that can strengthen Unilever's business and participate in meetings with your colleagues from other European Home Care factories, where learning is shared across the factories.

Automations-/PLC-programmør til specialfremstillede maskiner

Vil du arbejde med den allernyeste teknologi i en af Danmarks førende virksomheder inden for specialfremstillede maskiner? Og har du lyst til at programmere og udvikle maskiner til store danske virksomheder i bl.a. legetøjs- og medico-branchen?

Vi forestiller os, at du er uddannet automationsteknolog, ingeniør, stærkstrømstekniker eller maskinmester – det vigtigste er dog, at du har stor interesse for softwaredesign, indkøring af maskiner og samspillet mellem el og mekanik.

Er du interesseret?

Quality Manager

We are looking for a new hands-on Quality Manager who will continue the development of the Dancop Quality System.

Othe tasks will include internal auditing of our quality system and work processes, and training of employees in quality assurance.

You are offered an attractive workplace with good and skilled colleagues, and an international working environment with an informal and humorous tone.

Automation Project Manager, Airport Engineering

Do you have experience with automation projects, and would you like to manage automation projects within Airport baggage handling systems through a team of highly skilled automation experts?

Join us to put all your project management and technical skills into play as you ensure high-quality automation software on sharp project driven deadlines. Take this unique chance to work in an international company with a wide range of internal and external stakeholders.

Senior Product Test Engineer - Medical Devices

Do you want to design safe and reliable medical devices, bringing our clients' life-changing solutions into the hands of patients and helping patients to get better treatment?

You will be an essential contributor in the development and designing optimal verification methods for requirement confirmation.

We seek to enable the best work environment that helps you and the business work together to produce superior results.

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

Research & Development (R&D) Manager

As our R&D Manager, you will:

• Play a pivotal role in our Technology organization.
• Be part of a collaborative and professional R&D team, driving innovation and improvements at every level.
• Good opportunities for personal and professional development in an international corporate environment.

Embrace this opportunity to become a key player in an international company where your skills in leadership, creativity, and innovation can flourish.

Sustainability Project Assistant

WELCON A/S is looking for a Project Assistant within sustainability to join us in the spring of 2024 on an interim basis until end of 2025, with the possibility of permanent employment afterwards.

You will be involved in processes ranging from ESG-reporting and data collection to the execution of our sustainability strategy.

Expect to work alongside some of the best colleagues in the country, where flexibility is highly valued, and you'll experience an informal work environment with freedom and responsibility.

Lead Business Development Manager

Your primary responsibility is to spearhead business development initiatives aimed at identifying and developing profitable growth opportunities across the company's global operations in the CBS sector.

You will be responsible for crafting and executing growth strategies, translating them into real-world business opportunities that will improve growth and profitability for the company.

Supply Chain Development Manager – Industrial Engineering

Are you ready to make a tangible impact and thrive in a global and collaborative environment?

As part of the Supply Chain Development team, you will join three highly skilled colleagues dedicated to drive optimizations throughout the Supply Chain.

As the Supply Chain Development Manager, you are responsible for driving optimizations by evaluating product designs, standardization, data, and workflows to implement improvements in cooperation with Engineering with the purpose of eliminating waste. Furthermore, you will be Involved in training staff in new processes and provide them with instructions and manuals.

Technical Writer to GE HealthCare Denmark

Join GE HealthCare to help develop high quality instructions for use for our ultrasound scanners, transducers, and reprocessing methods in compliance with rules and legislation in various countries. This is your opportunity to become part of an innovative team where your work has a real impact on people’s lives around the world.

Our Technical Documentation team consists of six dedicated and passionate specialists with a mix of seniority, educational backgrounds, and nationalities. Our Technical Writers develop and maintain the user documentation for our high-performance equipment.

Global Director of Training

FairWind is a leading provider of one-stop solutions for installation and service of onshore and offshore wind turbines throughout the world. Some of your responsibilities will be to:

• Ensure EWA and all future FairWind Group training centres operate at best-in-class safety- and quality levels.
• Drive the global expansion of the FairWind Group training activities.

We offer stable employment with freedom under responsibility, and an agile company structure and short decision-making path.

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.