Din browser (Safari 1.0) er mere end 3 år gammel.
Vi anbefaler at du opgraderer til den nyeste version, da vi ellers ikke kan garantere at alt funktionalitet på Jobindex vil fungere korrekt.
12 jobannoncer matcher din søgning 12 jobannoncer fundet
Vil du modtage denne slags jobannoncer på mail?
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.
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.
Regulatory Affairs & QA Lead
Har du lyst til at blive en del af en spændende arbejdsplads, som opererer globalt med nogle af markedets bedste produkter?
Som vores Regulatory Affairs & QA Lead bliver du en del af et velfungerende team med 5 engagerede kolleger, der hver dag arbejder målrettet og brænder for deres arbejde.
Der kan være mange indgangsvinkler til jobbet men du skal have erfaring med medicinsk udstyr, være omhyggelig, energisk og brænde for det regulatoriske arbejde.
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
PTA-Ingeniør
Kontinuerlig produktudvikling gør, at vi i dag har det største og bedste sortiment indenfor vores felt og det har åbnet en række muligheder for eksport til nye markeder. Det betyder at vi skal have udskilt PTA-funktionen fra udviklingsafdelingen og derfor søger vi en person til at stå i spidsen for dette.
Vi tilbyder et afvekslende job i en moderne virksomhed med en fuld intern værdikæde bestående af produktudvikling, indkøb, produktion og salg.
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.
Project Leader – process/hydrogen safety
Do you want to apply your skills to promote a fast and safe transition of the energy and transportation sectors away from carbon-based fuels?
You will be leading diverse teams of experts to deliver state-of-the-art results to our partners in the hydrogen sector, working on some of our largest fire safety projects.
We have great offices and facilities, and you get good staffing conditions, such as pension scheme, dental insurance, and health insurance. We have an active staff and art association, and our chefs cook delicious food for us daily.
Battery specialist
Do you want to apply your skills to promote a fast and safe transition of the energy and transportation sectors away from carbon-based fuels? Do you have experience working with or developing battery technologies?
As our new Battery Fire Specialist, you will provide expertise on Li-ion batteries and other upcoming technologies to the team. You will be part of projects performing risk analyses, battery fire tests, and fire safety design for clients and in R&D contexts.
Erfaren QA-Specialist – til frigivelse af produkter
Stillingen byder på et bredt udsnit af QA-opgaver og flere kan komme til, så du får gode muligheder for at videreudvikle dine QA-kompetencer.
Opgaverne:
- Selvstændig frigivelse af PKC’s produkter og behandling af afvigelser og håndtering af ændringssager
- Sparringspartner for QA-gruppen, QC-gruppen og produktionen
Du får ansvar for og stor medbestemmelse over dine opgaver. Der er tid til fordybelse, men der er også dage, hvor det går rigtig stærkt, og opgaverne blev andre end dem, du havde planlagt og forventet.
Product Sustainability Specialist
Ønsker du at have fingeren på pulsen indenfor udvikling af bæredygtig maling og serviceydelser relateret til bæredygtige produkter?
Du vil få en spændende og afvekslende hverdag, hvor du vil være ansvarlig for planlægning og udførelse af egne opgaver. Opgaverne er mangeartede og der er stor mulighed for personlig udvikling.
(Senior) Regulatory Product Compliance Specialist to Corporate Quality, Group R&D
Would you like to step into position where you ensure a smooth and efficient market access, making a difference for our end users?
Quality Assurance Associate, Supply Chain Management Unit (SCMU), Copenhagen
The Position: The Quality Assurance Associate position is located in the Product Quality Assurance Team in the UNFPA Supply Chain Management Unit (SCMU).
