Your responsibilities Working together with the team, your main duties include:
- Be responsible for the manufacturing of Active Pharmaceutical Ingredients (APIs) regulated by Swissmedic
- Project-specific practical work in the cleanroom including associated documents
- Creates and revise GMP-relevant documents
- Follow the instructions of the quality management system
- Participate in internal training course
- Coordination with researchers for organization of experiments
- General laboratory management, ordering, organization of biologicals and chemicals, as well as maintenance of laboratory equipment
Your profile The position requires training as a Laboratory Technician or Master of Science and preferably at least 2-year experience in the lab, including skills for human T cell expansion and culture. We are looking for someone with excellent organization and writing skills, reliability, and the ability to perform tasks with strict adherence to GMP principles. Additional skills: dependable and able to work well within a team, possesses a high attention to detail. Prior hands-on experience with basic laboratory equipment and practices will be highly valued. The job requires proficient German skills and a good level of communication in English.
What we offer You will be working in an international, dynamic and young team, and will gain exposure to a fascinating research field with concrete application of novel, safe and effective therapies.
