6 job matcher din søgning
Coloplast A/S, Humlebæk
Join Coloplast to become part of a global company that makes a difference every day.
You will work from our Headquarter in Humlebæk, Denmark. Here, you as a senior specialist will ensure appropriate and compliant biocompatibility documentation for Coloplast products applying your insight into regulations and industry trends. You will help grow the team by acting as a mentor through guidance and coaching of junior colleagues, especially with respect to scientific and professional aspects of evaluation of biocompatibility and toxicology.
In addition, you will provide expert toxicological support to the business, initiating and monitoring biocompatibility testing in-house as well as with our suppliers. Supporting cross-functional activities related to biosafety, you will influence our policies, guidelines and attitudes regarding environment and safety for our customers.
As a Sales Manager, you are responsible for supporting and developing your own geographical sales area in close cooperation with the local Tetra Pak market company.
You will work closely with our customers, your colleagues in the market companies, the support functions in the sales team, and your colleagues in other teams.
- Driving sales and actively developing the long-term relations to customers and market companies
- Listening to, understanding and analysing customer needs
- Planning and running customer seminars, trainings, and presentations
Kevin Murphy Europe A/S, Copenhagen
Reporting to the Global Director of Procurement, the Global Regulatory Affairs Manager will be responsible for leading activities of the Regulatory Affairs Department with an emphasis on global regulatory strategy and the preparation, review and submission of documents to any regulatory authorities at a global level.
Oversees the regulation process for products requiring governmental approval, including filing necessary applications and handling all government interactions in the geographical areas where KEVIN.MURPHY Group products are marketed. Coordinates inspection of the organization and contract facilities and develops procedures to ensure regulatory compliance. Requires a Master's degree in the area of specialty.
Would you like to work with aseptic filling and be a part of our Environmental Monitoring-Support Team?
Novo Nordisk, Gentofte