Do you adhere to high quality standards and enjoy working in a GMP environment?


We are looking for a reliable person for an exciting position in aseptic manufacturing and the microbiology laboratories in Bern.


**Main Responsibilities**
Your responsibilities will primarily include:



- Creation of process and risk analyses
- Development of work instructions, manufacturing procedures, and training documentation
- Handling of changes, deviations, and actions within the quality management system
- Implementation of global visual inspection guidelines into local processes and work instructions
- Close collaboration with internal and external stakeholders from Maintenance, Automation, Quality, and other interfaces

**Your Profile**
You bring the following qualifications and experience:



- Completed degree in a scientific field (university or university of applied sciences)
- Ideally professional experience in the chemical, pharmaceutical, or food industry within a GMP environment
- Experience in conducting process risk analyses in a GMP setting
- Ability to work independently and quickly grasp new topics, as well as build project-specific knowledge
- Ability to manage multiple projects simultaneously and maintain oversight even in fast-paced environments thanks to strong planning skills
- Proactive personality able to deal with uncertainty, challenge existing processes, and propose improvements
- Strong team player with clear and open communication skills, capable of building relationships with stakeholders from different functions and managing their needs effectively
- Fluent German and good English skills (both written and spoken)

**Additional Information**

- Duration: 12 months
- Workload: 100%
- Start date: ASAP