7 job matcher din søgning
GE Healthcare, Brøndby
GE is the world's Digital Industrial Company, transforming industry with software-defined machines and solutions that are connected, responsive and predictive. Through our people, leadership development, services, technology and scale, GE delivers better outcomes for global customers by speaking the language of industry.
Responsible for creating and winning sales opportunities for their products/solutions/services in an assigned territory, and/or in a list of named accounts individually or as part of a One GE Healthcare team.
Act as the clinical/technical expert to establish and continuously develop the relationship with departmental and technical decision makers in their assigned accounts and where applicable work in conjunction with Account Executives and Managers to gain access to C-Suite decision makers.
Indrykket 8. december
Jobindex A/S recruiting on behalf of Medicologic A/S, Copenhagen
Join the market leader in introducing new medical devices to market. You take charge of complex core projects from the initial customer contact to the final approval is secured, focusing on speed to market. And you do so for the biggest players in the field and the medical device start-ups.
As our regulatory affairs senior principal advisor, you handle a strong project portfolio. You handle customer contact and project management throughout the project. Providing your deep knowledge of RA throughout each project, you will:
- Provide information and advice to customers on the regulatory pathway for medical devices and function as a RA subject matter expert toward customers
- Establish regulatory strategy documenting the most suitable pathway for regulatory approval
Indrykket 8. december
Chr. Hansen A/S, Hørsholm
Food Culture and Enzymes is the largest Business Unit within Chr. Hansen and work closely with some of the largest global dairy companies providing them with our pioneering product developments.
We are seeking an Indian-speaking top-ten graduate with appreciation of the Indian food and dairy culture to join our Global Application organization in Denmark and France. You must be prepared and committed to continue your career in our application center in India (Mumbai) after around 2-years trainee period in Europe.
- Develop your dairy application skills within the Fresh Dairy, Cheese and BioProtection segments enabling you to provide top-class technical advice and trouble-shooting to our customers
- Plan, perform and report on trials. Hands-on work in the pilot dairy and laboratories will part of your assignments
Indrykket 4. december
Gubra ApS, Hørsholm
To a vacant position in our growing Peptide Chemistry and Formulation group, Gubra is now looking for a Laboratory technician to join the group. The candidate should have a flair and interest for formulation of peptide drug candidates as well as small molecule test compounds. The candidate is self-motivated and can navigate and collaborate in an energetic organization, and is ready to set ambitious high standards for the output of the group.
Your primary tasks are varied, but include:
- Formulation of peptide and/or small molecule drug candidates for in vivo pharmacology experiments
- Stability determination of peptide drug candidates (chemical and physical stability)
- Biopharmaceutical characterization and analysis of peptides by UPLC
- Data processing and documentation
Indrykket 1. december
Coloplast A/S, Humlebæk
Would you like a job where there is a direct connection between your work and our users?
As a biosafety specialist, you make sure that people with intimate and personal medical conditions can live an easier life with confidence in the products they use. This is an opportunity to work and learn about medical devices and product safety. You will have a diverse role in which you collaborate across a company in growth to enable biological product safety.
In this role, you collaborate across many projects as a specialist on biosafety. You work in cross-functional projects to ensure the biological safety of our products and compliance with regulatory demands in relation to biological safety of medical devices.
Indrykket 28. november
Azanta A/S, Valby
Do you want to be the expert we all ask for advice, and who ensures that our quality assurance system is in compliance with applicable regulations for medicinal products and medical devices?
In this role you will be responsible for improving and maintaining the right quality level at Azanta A/S. You will cover all areas of Azanta and collaborate with our warehouse staff, regulatory affairs, sales & marketing, affiliates as well as CROs and CMOs.
We offer a 30 hour a week position with many opportunities within QA and related areas. Competitive compensation package in an exciting growing international company. You will have a very busy, diverse and exciting work day which you will largely be able to plan yourself.
Indrykket 22. november
We are looking for a Senior Research Scientist to join one of our Discovery Chemistry Groups. As an outstanding medicinal chemist with documented results you have the opportunity to become a Senior Research Scientist in Discovery Chemistry (DC) at the Lundbeck Research Centre in Copenhagen Denmark (DK), and join our quest for new medicines to treat Central Nervous System (CNS) diseases.
As a Senior Research Scientist in a Medicinal Chemistry Group you can expect to be involved in all aspects of the Medicinal Chemistry value chain, and to lead the chemistry component of drug discovery projects. You will be working in a strong team environment within Discovery Chemistry and will form strong and effective collaborations with scientists from other disciplines within Research.
Indrykket 13. november