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.
14 jobannoncer matcher din søgning 14 jobannoncer fundet
Vil du modtage denne slags jobannoncer på mail?
Production Engineer, med Proces,- GMP- & maskinteknisk erfaring
Kunne du tænke dig at arbejde for en af markedets førende hudplejeproducenter? Brænder du for processer, kvalitet og optimering?
Du får bl.a. en vigtig rolle i vores nyoprettet ‘Riemann Industrialisation team’, der har ansvar for implementering af nye produkter, - processer og udstyr, Teamet vil også forestå optimeringer, problemløsninger og udarbejdelse af årsagsanalyser. Af øvrige opgaver vil der være koordinering og videndeling tværorganisatorisk mellem R&D, Produktion, QA og tekniskudvikling afdeling.
Continuous Improvement Partner
As a Continuous Improvement Partner in Drug Substance Manufacturing, you will be part of a team of Improvement Partners who develops and sustains systems and tools that enables the organization to consistently increase the level of operational excellence in manufacturing.
Your primary tasks will include but not be limited to:
- Develop and sustain CI systems and tools.
- Coach on ideal behaviour that drives a proactive improvement culture.
QA Tekniker / QA Release
Vi søger en kompetent og initiativrig QA Tekniker, der vil være med til at bidrage til den fortsatte udvikling af Elos Medtech QA-område.
Målrettet træning/uddannelse vil blive gennemført, så lad dig ikke begrænse af, at den ideelle kandidat vil passe til en eller flere af nedenstående forventninger:
- Omhyggelig, struktureret og har øje for helheden samt kommunikerer konstruktivt og sætter en ære i at sikre, at vores produkter efterlever de høje kvalitetskrav
- Erfaring med Axapta eller andet ERP-system
- Kendskab til GMP-regler, ISO 13485 og/eller ISO 9000
- IT-kyndig og rutineret bruger af MS Office pakken
Coordinator in Quality
Are you our new coordinator within Quality? Do you enjoy working with Planning & Forecasting, Contract Laboratory Organization (CLO) management, Reference standard & Control management - then join our Data Management team within Quality in our site in Hillerød.
You will be the point of contact for CLO´s used within Quality Control (QC) ensuring the relationship and making sure contracts are in place. Your responsibilities will include monitoring of inventory levels, providing status to management and facilitating the timely delivery of products to customers.
Microbiologist in Quality Control - Maternity Cover (12 months)
Are you eager to join a fast-growing pharmaceutical company?
Adv QA Professional in Device Development
Are you looking for an exciting opportunity to advance your career in Quality Assurance?
Operational Responsible for Storage Facilities
Are you motivated by working in a changing environment?
Safety Risk Manager - Medical Device Development
Are you ready to make a significant impact on Novo Nordisk's medical device development projects and contribute to enhancing the lives of our patients?
Clean Utility Engineer
Are you ready to be a part of Novo Nordisk's most significant expansion project in Hillerød?
Validation Specialist
Are you experienced in validation of Finished Product processes within the pharmaceutical industry?
Validation Support & Responsible
Are you ready for a unique opportunity to shape the validation direction for Novo Nordisks Raw Materials warehouse?
Product Responsible
Are you ready to harness your skills in design control and to take up responsibility for some of the largest products in the market?
Scientist for QC Raw Materials Analytical Management Team
We are looking for a scientist that understands the quality setup of a QC laboratory in a GMP environment.
Instrument Maintenance Coordinator for QC Instrument Support
Are you a good coordinator with a big picture mind-set and “can-do” attitude who thrives in an environment where close collaboration involving multiple stakeholders is key?