Your Tasks and Responsibilities
* Review and transfer of reserve, shipping, and stability samples
* Review of retention samples
* Issuance of reserve and stability samples
* Storage of retention samples in accordance with regulations
* Ensuring compliance with quality (SOP and GMP) and safety guidelines
* Support with documentation and reporting in the administrative area
* Communication with QC project managers, shift teams, logistics, and QA
* Processing and responding to correspondence, including confidential information
Required Skills and Qualifications
* Completed training in administration or a comparable qualification
* 1–3 years of professional experience in an administrative environment, ideally in the pharmaceutical or biotech industry
* Good knowledge of GMP and SOP guidelines
* Excellent organizational skills and strong attention to detail
* Strong communication skills in German and English; knowledge of French is an advantage
* Proficiency with MS Office (Word, Excel, Outlook)
* Ability to handle sensitive information confidentially
* Team player with flexibility
Your Opportunity
If you are a dedicated individual who enjoys working in an innovative environment and wants to actively contribute to meaningful research projects, we look forward to receiving your application. Join our dynamic team in Visp and help shape the future of biopharmaceutical innovation
Administrative Assistant I
Our innovative and leading company in the field of biopharmaceutical research and development is committed to improving global health and quality of life. With cutting-edge technology and a strong focus on the personal development of our employees, we create a dynamic work environment where teamwork, dedication, and expertise are highly valued. Become part of our committed team in Visp and actively contribute to the development of groundbreaking therapies.