Internship - cleaning validation (m/f/d)

vor 2 Wochen

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Work Your Magic with us Ready to explore, break barriers, and discover more? We know you've got big plans – so do we Our colleagues across the globe love innovating with science and technology to enrich people's lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us. United As One for Patients, our purpose in Healthcare is to help create, improve and prolong lives. We develop medicines, intelligent devices and innovative technologies in therapeutic areas such as Oncology, Neurology and Fertility. Our teams work together across 6 continents with passion and relentless curiosity in order to help patients at every stage of life. Joining our Healthcare team is becoming part of a diverse, inclusive and flexible working culture, presenting great opportunities for personal development and career advancement across the globe.Start date: february / marchDuration: 6 monthsLocation: Corsier-sur-VeveyRole level: Internship Your role: As an intern, you will contribute to the cleaning validation strategy definition, execution and reporting for GMP (Good Manufacturing Practices) manufacturing equipment. The success of this study will ensure the absence of contamination of the New Biological Entities produced for clinical trials.Define the strategy: you will begin by confirming the cleaning validation strategy in accordance with internal and external standards/guidelines as well as quality phase appropriateness. This involves understanding the requirements of such study and apply it to BDC (Biotech Development Center) GMP manufacturing suites.Design protocols study: your task will include designing protocols that meet regulatory and operational requirements.Execute validation study: participate in executing parts of the cleaning validation study, ensuring compliance with GMP.Data Analysis and report writing: analyse the data collected during the study and derive conclusions that will contribute to the final report.Collaborate in writing the report summarizing the methodology, results, and recommendations. Your profile: Master/engineer student in Biotechnology or related fields Highly motivated Autonomous Previous experience in Up Stream Process/Down Stream Process is a plus Good written and oral knowledge in EnglishFrench is a plusWhat we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progressApply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity

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