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:
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Creation of process and risk analyses
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Development of work instructions, manufacturing procedures, and training documentation
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Handling of changes, deviations, and actions within the quality management system
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Implementation of global visual inspection guidelines into local processes and work instructions
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Close collaboration with internal and external stakeholders from Maintenance, Automation, Quality, and other interfaces
Your Profile
You bring the following qualifications and experience:
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Completed degree in a scientific field (university or university of applied sciences)
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Ideally professional experience in the chemical, pharmaceutical, or food industry within a GMP environment
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Experience in conducting process risk analyses in a GMP setting
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Ability to work independently and quickly grasp new topics, as well as build project-specific knowledge
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Ability to manage multiple projects simultaneously and maintain oversight even in fast-paced environments thanks to strong planning skills
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Proactive personality able to deal with uncertainty, challenge existing processes, and propose improvements
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Strong team player with clear and open communication skills, capable of building relationships with stakeholders from different functions and managing their needs effectively
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Fluent German and good English skills (both written and spoken)
Additional Information
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Duration: 12 months
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Workload: 100%
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Start date: ASAP
#LI-KK1 #LI-Hybrid
