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Join a team of highly-skilled Regulatory Affairs Professionals for 12 months.
ALK offers an exciting opportunity to work in their Global Regulatory Affairs (GRA) department with lots of interdisciplinary collaboration both internally and externally. GRA counts approximately 50 people and we are located in Hørsholm.
As Regulatory Affairs Professional you will be given a range of responsibilities within both regulatory Clinical, Non-Clinical and Procedural activities in ALK. You will work closely together with the top motivated team members of the RA-team. The team consists of 9 people including the manager of the team.
Student assistant, Commercial Excellence (or internship) position at the head office in a world-leading pharmaceutical company.
We are offering a job opportunity for a motivated young professional to join a high performing international team of seven individuals. We strive to deliver value for our markets and top management through commercial projects, data analysis and process optimization.
You will become part of Global Commercial Excellence team. We will support you in developing your skillset within infrastructure development, project management, business intelligence, commercial operations, change management and at the same time allow a degree of responsibility. As part of the job experience you get to collaborate with key business users in our subsidiaries, analysts, BI and development teams to improve global solutions.
We are looking for two new colleagues to our Regulatory CMC department. We are a team of 9 people handling CMC documentation for ALK tablet portfolio. The team is part of Global Regulatory Affairs which counts approximately 50 people in Hørsholm.
We are looking for two team members that are dedicated to communication of complex scientific matters in a written form. We believe you have experience with global regulatory CMC requirements for biological products and Regulatory Life Cycle Management of medicinal products globally. We also hope you enjoy cross-functional interactions.
Field of responsibility
- Responsible for writing and maintaining regulatory CMC documentation for worldwide submissions
- Responsible for having an overview of submitted and approved CMC documentation in different regions