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Vessel Manager - Offshore Wind Industry

Are you passionate about vessel operations and being the link between our colleagues on- & offshore? Then we can offer you this exciting role within the renewable business area.

You will be responsible for overseeing the safe and efficient execution of daily operations and maintenance scopes in close collaboration with vessel management team and shoreside departments.

We are looking for a people leader, who displays strong interpersonal skills and who has the ability to communicate effectively with a variety of stakeholders.

Biocompatibility Specialist

We are looking for a Biocompatibility Specialist to join the Reprocessing and Biocompatibility team for a 12-month project position.

This is a great opportunity if you would like to gain experience with biocompatibility for advanced reusable medical devices, as you will be part of a cross-functional effort on documenting the safety and performance through the lifetime of our ultrasound scanners, transducers, and accessories.

Quality Supervisor til Maintenance Execution

I denne rolle vil du udvikle og implementere kvalitet i planlægning og udførelse af vedligehold, og lave kvalitetskontrol af det udførte vedligehold og dokumentation.

I revisionsperioder vil du agere supervisor på lige fod med afdelingens maintenance supervisorer for de eksterne leverandører på Avedøreværket, H.C. Ørstedværket og Svanemølleværket. Du vil arbejde ambitiøst med kommunikation og dialog med mange interessenter.

Erfaren specialist i kvalitet til globalt team

Vil du være garant for, at kvaliteten er i top på forretningsområderne inden for indvendig og udvendig solafskærmning, vinduer, fjernbetjeninger og elektriske motorer til alle VELUX’s produkter, og har du lyst til at være en del af et globalt team bestående af 6 dedikerede kollegaer?

Dine primære opgaver vil være at:

• Sikre fremdrift og aktivt deltage i kvalitetsaktiviteter/-leverancer i projekter og ændringer
• Sikre design for kvalitet – i produkt og proces
• En central del af teamet som specificerer og godkender emner, nyt udstyr og processer

Creative Assistant

Are you inspired to contribute your expertise to a global leading Flavors Organization? Are you passionate in working in a dynamic team with creative and empowered people?

Your Focus will be:

• Always following correct compounding procedures
• Prepare compounded flavors for evaluation, including preparation and running of difference testing if project requires.
• Coordinate with QC to obtain specifications of all experimental recipes within 24 hours of completion of evaluation.

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.

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

Production/SHE Lead

Unilever is the place where you can bring your purpose to life with the work that you do – creating a better business and a better world. If you are pasionated by working with people and gets your energy from challenging status quo, then this role is just for you!

WHAT WILL YOUR MAIN RESPONSIBILITIES BE

• As a member of the leadership team, you will contribute with continuous ideas for improvements.
• Focusing on the development of your team (including recruitments) to ensure we always have operators with the necessary skills and mindsets.

Application Consultant

You will use your business acumen and collaboration skills to work with both management and shop floor operators to improve production processes and utilizing IT solutions for the manufacturing automation domain.

You will have domain knowledge of shop floor processes, and experience with Manufacturing Execution System (MES), Manufacturing Information Systems (MIS), database operator tasks, and common communication protocols used to interface production equipment.

Grid Installation Coordinator

Together with your colleagues, your main role will be to support the expert teams, Grid Installation and Commissioning, in their daily tasks. You will be the one structuring and coordinating communication with Project Managers, the Document Management Team, HV Procurement and HV Engineering to ensure a documented and structed workflow. We see you have an important role in this mission.

We offer an excellent opportunity for professional and personal development together with like-minded, friendly, and talented colleagues who prioritise delivering the best results while remembering to share a good laugh.

Health, Safety and Environment (HSE) Manager

Are you a seasoned Health & Safety professional seeking an opportunity to thrive in a supportive and dynamic environment?

We have an exciting opportunity to recruit a Health & Safety Manager, you will play a crucial role in maintaining and enhancing the safety standards at our facility. Your responsibilities will include designing training programs, conducting risk assessments, identifying, and controlling hazards.

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

Miljøkoordinator

Evner du at sætte miljøet på dagsordenen, og brænder du for at håndtere miljøopgaver på tværs af organisationen? Formår du at jonglere med kravene fra myndigheder, kunder og kolleger? Nu har du muligheden for at gøre en reel forskel og præge Ticans fremtidige miljøindsats.

Med reference til den tekniske chef bliver du, i denne nyoprettede stilling, ansvarlig for at udvikle organisationens miljøindsats og forberede virksomheden på implementering af et miljøledelsessystem. Du vil indsamle og administrere data relateret til miljømæssige præstationer på tværs af organisationen.

Surveyor

As a surveyor you will be involved in the blade production from beginning to end. Your will be in charge of inspection and optimalisation of the production equipment at the Aalborg plant.

Your responsibilities will include:

• Measuring, verification and quality control
• Optimization and implementing new projects
• Conducting quality control of the production equipment

You will be working in an international team, so good communication skills are a must. Good skills in written and spoken English are needed as well as working knowledge of MS Office.

Operations Engineer

Forestil dig en fremtid, hvor du er med til at sikre driften af værkets anlæg og drive nye innovative og grønne projekter.

I denne rolle vil du være ansvarlig for både drift og overvågning af produktionsanlægget på Asnæsværket. Derudover vil du være med til at drive og deltage i udviklingen af nye, spændende teknologier som carbon capture og derved være med til at fange og lagre 400.000 tons CO2 allerede i 2025.

Senior Process Specialist

Do you want to be part of Process Support in a company with a unique impact on global healthcare? Grab this opportunity to be part of a fast-growing company ready to invest in you.

You will become a process owner of one or more of our production processes in SFI. This means that you will be responsible for, among other things, validation documentation, revalidations, and risk assessments for the specific process.

Process Specialist

Do you want to be part of Process Support in a company with a unique impact on global healthcare? Grab this opportunity to be part of a fast-growing company ready to invest in you.

Together with the rest of the team, you will be responsible for the daily support of our production lines. You will learn our processes in detail and gain a good overview of the documentation used in production.

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.

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.