Juniorspecialist, Regulatory Affairs

Brænder du for den grønne udvikling, og har du en baggrund inden for kemi? Har du lyst til ar­bejde med produktdokumentation og miljømærker?

Dit ansvar er helt overordnet at sikre, at vores produkter lever op til den gældende lovning. Dine daglige arbejdsopgaver vil være at:

• udarbejde kemisk/teknisk dokumentation til vores kunder, f.eks. ingredienslister og varedekla­rationer
• godkende etiketter, herunder claims og brugsanvisninger

Business Support, PtX - Denmark

We are seeking a dynamic candidate to join our team, bringing a blend of professional competencies and personal skills essential for success in a rapidly evolving landscape.

As a Business Support for PtX at Eurowind Energy, you will play a pivotal role in the development and implementation of PtX projects across Eurowind's markets

As a Business Support specialist within our PtX Competence Center, you will be instrumental in driving business development initiatives to support PtX projects across Eurowind markets.

QA-assistent til international producent af kosttilskud og lægemidler

‎Trives du med at arbejde i et GMP-reguleret miljø, og vil du gerne bidrage til at opretholde den høje kvalitet?

Vi tilbyder et alsidigt job i et åbent og dynamisk arbejdsmiljø med muligheder for faglig og personlig udvikling.

Du kommer til at indgå som en del af et tæt tværfagligt samarbejde med bl.a. laboratorie-, kemi- og kvalitetssikringsafdelingen. Du vil være tilknyttet kvalitetssikringsafdelingen, hvor der vil være gode muligheder for udvikling.

Opgaverne kan bl.a. bestå i:

• Gennemgang, kontrol og frigivelse af råvarer, færdigvarer eller emballagedele.
• Arkivering af dokumentation og referenceprøver.
• Supportfunktion for øvrige afdelinger i form af certifikater og øvrig dokumentation.

Compliance Officer til Abacus Medicine Group

Are you looking for a chance to put a human face on compliance in an international company? Do you enjoy communicating compliance to your co-workers in a working environment where your idea book is welcome? Then you might just be the Compliance Officer that Abacus Medicine Group is looking for.

As Compliance Officer you will play a vital role in ensuring that our organization adheres to the highest standards of data protection and regulatory compliance. This requires a solid knowledge of the area, attention to detail and good communication skills as you’ll be helping your colleagues in the organization understand and implement compliance in their work routines.

Software Lead

At TracInnovations we develop and produce a motion tracking system to improve the quality of magnetic resonance scanning images and patient comfort.

As a Software Lead, you will play a pivotal role in leading a team of skilled software developers to drive the development of our cutting-edge motion tracking software. You will be involved in all aspects of the development life cycle, from initial planning and design to implementation, profiling, and testing, ensuring the delivery of high-quality software products.

Maintenance Operations Center Supervisor

Can you maintain overview over multiple tasks, and do you love to coordinate and solve complex challenges?

As a Maintenance Operations Center (MOC) Supervisor at Sunclass Airlines, you play a critical role in ensuring the safety, reliability, and efficiency of our airline's fleet. You are responsible for coordinating and overseeing maintenance and operational activities and responding to technical issues in real-time.

You will of course be given relevant training upon employment, and your CRS (Certificate Release to Service) will be maintained.

Clinical & Product Training Manager (EMEA/Asia) to GE HealthCare Denmark

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 global Clinical and Product training team consists of fifteen dedicated and passionate specialists with a mix of seniority, educational backgrounds, and nationalities.

We are a strong team that values collaboration, support, honesty, and respect. We are driven by making a difference and continually improving training activities across the globe.

Regional Information Security Officer (m/f/d)

Join us in this role where you’ll advise and support our Central Europe countries management teams and regional business leaders in all information security management, cyber risk management, cyber compliance management, and corporate cyber strategy implementation matters.

You’ll act on behalf of our entities as information security focal point to national authorities where and as required by local legislation. In your role, you’ll monitor the national cyber and information security legislation across regions and support the use and local implementation as well as the continues improvement of the global corporate information security management system.

Student Assistant - Specialty RX

Are you eager to apply your academic knowledge in a real-world context? Can you imagine yourself learning the art of business development within the pharmaceutical industry?

In this role, your responsibility will grow over time as you will be exposed to a variety of tasks and challenges. Initially, you will be responsible for maintaining the systems and tools that we use in our daily work. You will also be exposed to tasks such as: Market Screening, Project Management, and Market Access support.

Clinical Operations Manager

Do you want key operational responsibility in phase 1-4 clinical trials as part of a high performing team?

As Clinical Operations Manager you are indispensable in the trial, leading and executing all the operational aspects throughout the different trial stages. You work closely with the Clinical Project Manager who is responsible for the clinical and strategic deliverables.

IT Business Lead - EMEA

Are you passionate about driving innovation? Do you consider yourself to possess a self-leading, structured, and proactive mindset? If yes, then we would like to hear from you.

You will be a part of a highly qualified and skilled team that will guide you and ensure a smooth and tailored onboarding enabling you to add immediate value to the organisation.

Chemical Engineer – build pilot plants to create green ammonia

2% of the global CO₂ emissions originate from ammonia production. Do you also think that is 2% too much? And do you want to be the mastermind behind the pilot plants that will let us scale up our prototype to a demonstration unit?

Then join us and get your daily dose of entrepreneurial startup spirit while enjoying flexible working hours.

Are you our new CAMO Engineering Manager in Air Greenland?

As CAMO Engineer, you will be a part of Technical Manager Management team who have the highest priority on Flight Safety and LEAN development.

Responsibilities includes

• Ensure compliance of the continuous airworthiness requirements of Continuing Airworthiness Regulation (EU) No 1321/2014
• Ensure compliance with IOSA and BARS requirements within CAMO.
• Ensure updated AMP’s on all Air Greenland operated Aircraft types.

Housing and relocation cost is offered according to company policies.

Process R&D Engineer - Emulsifiers

Do you want to join the global leader in Food Ingredients and help us serve the World with solutions for healthy & nutritious food?

You will be directly responsible for process development, scale up of new emulsifier processes and ensuring that our production sites are delivering products that meet quality, quantity, and cost. You will drive scale-up activities and help transfer product from R&D to full scale manufacturing.

OT Network Specialist – Renewables company

Join our dynamic SCADA team at Eurowind Energy as an OT Network Specialist! If you thrive on ensuring the stability of OT networks and facilitating seamless connections to power plants, this role is tailor-made for you.

You'll be responsible for configuring and commissioning power plant OT networks, maintaining asset inventories, troubleshooting network issues, and ensuring compliance and security.

Senior Environmental Advisor

With over 90 years' combined experience, NES Fircroft (NES) is proud to be the world's leading engineering staffing provider.

Your scope of work will include:

• Manage the preparation and submission of various EIA documentation.
• Prepare and submit small ‘Environmental Statements’.
• Oversee / support ENV team peers who may assist with preparing EIA documentation.

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.

AFC manager

We offer an exciting and unique opportunity to take on the challenge within a global corporation, engaging with customers and stakeholders worldwide. Daily responsibilities encompass a variety of inspiring and complex tasks overseeing analysis and reporting of economic and financial performance of our Engineering Business Line.

The package includes a pension plan, appealing cafeteria benefits, membership in the staff association and more.

Analyst and Project Coordination In Life Science Consultancy

Would you like to work with data analysis and research of worldwide trends in the pharmaceutical and biotechnological industries?

You will get the responsibility of managing and coordinating the day-to-day operations needed to solve our projects and writing reports for our commercial unit.

An academic background in life science (pharmacy, biotechnology etc.), economics or similar is required.

Regulatory Affairs Specialist

We are on an exciting path of growth and are currently seeking a new specialist to join our team and play a crucial role in ensuring that our operations adhere to relevant regulations and industry standards.

A significant part of your role will be to take regulatory ownership of selected product areas, and ensure the required activities take place, to ensure we are following current regulatory standards for medical device development.