5 job matcher din søgning
Coloplast A/S, Espergærde
Do you have the process understanding needed to develop quality assurance processes in our Laboratory? Then we provide you with the freedom to take our processes to the next level and create transparency in our process overview.
You will be part of the QA & EHS organisation consisting of 20 employees in total. Here, you will join our Laboratory and 7 laboratory technicians – a great mix of skills and seniority where we learn from each other. Furthermore, you will be part of the extended management team in Global Quality, and participate in QA team meetings.
“In Coloplast Mørdrup, we are about 250 people on site. The lab is quite busy, so you will have an important role in assessing the processes and taking the team to new heights”.
Indrykket 13. december
Coloplast A/S, Humlebæk
This is a unique opportunity to have a truly global role within regulatory affairs. Acting as a global steer for Coloplast and leading a team of competent specialists, you will pave the way for a very diverse product portfolio of medical devices from the lowest to the highest risk class.
Become part of the world’s fastest growing medical device company to act across borders and legislations.
You join us in Humlebæk, Denmark, to lead the Global Operations team in Regulatory Affairs. The team ranges from seniors to juniors, who support the global product lifecycle for all Coloplast products within ostomy, continence care and wound care products. As such, you assume full responsibility for the regulatory lifecycle management on a global scale.
Indrykket 11. 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
Do you want to be part of the team bringing our GLP-1 tablet to the market?
Novo Nordisk, Måløv
Novo Nordisk, 28. november