Overview
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. Responsibilities
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
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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. Responsibilities
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
#J-18808-Ljbffr
Quality control Analyst Arbeitgeber: Lee Hecht Harrison Nederland B.V.
Lee Hecht Harrison Nederland B.V. ist ein hervorragender Arbeitgeber, der seinen Mitarbeitern in Bern, Schweiz, eine dynamische und unterstützende Arbeitsumgebung bietet. Mit einem starken Fokus auf Qualität und kontinuierlicher Verbesserung fördert das Unternehmen die berufliche Weiterentwicklung und bietet zahlreiche Schulungs- und Entwicklungsmöglichkeiten. Die Unternehmenskultur ist geprägt von Teamarbeit und Innovation, was es zu einem idealen Ort macht, um in der aseptischen Fertigung und Mikrobiologie einen bedeutenden Beitrag zu leisten.
Kontaktdaten:
Lee Hecht Harrison Nederland B.V. Recruiting-Team
