Internship QC support (m/f/d)

<p style="text-align:justify"> </p><p><span style="font-size:12.0px"><span style="font-family:Verdana, Geneva, sans-serif">Work Your Magic with us!  </span></span></p><p> </p><p><span style="font-size:12.0px"><span style="font-family:Verdana, Geneva, sans-serif">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.  </span></span></p><p style="text-align:justify"> </p><br/><p><strong><span style="font-family: verdana, geneva, sans-serif;">Start date: 1st september 2026</span></strong></p><p><strong><span style="font-family: verdana, geneva, sans-serif;">Duration: 12 months </span></strong></p><p><strong><span style="font-family: verdana, geneva, sans-serif;">Location: Corsier-sur-Vevey</span></strong></p><p><strong><span style="font-family: verdana, geneva, sans-serif;">Role level: Internship</span></strong></p><p>As part of the Quality Control lab, you will be supporting the quality control activities as member of the QC Support team, which is mainly responsible for the Compliance activities, the Samples Management and various activities allowing the proper functioning of the lab.<br>Your internship will consist of working closely with the QC Support team and more specifically with an expert of the team that you will support in his/her improvement and compliance activities.</p><p>Your Role:</p><ul><li>Manage and improve the pharmacopoeia update process</li><li>By improving GMP Documentation</li><li>Writing periodic review reports</li><li>By participating in risk analysis process for QC Support activities</li><li>Be part of various project related to continuous improvement</li><li>By helping the different team members in their activities (operational activities, samples management, investigations, training, etc.).</li><li>You will be in contact with others QC teams, external providers, and other Merck’s sites. These activities will be done according to the GMP compliance.</li></ul><p>Your profil:</p><ul><li>Organized and highly autonomous</li><li>Team player</li><li>Strong communication and diplomatic skills</li><li>Fluent in French</li><li>Proficient in English</li><li>Interested in project management topics<br><br></li></ul><br/><p> </p><p><span style="font-size:12.0px"><span style="font-family:Verdana, Geneva, sans-serif"><strong>What we offer: </strong>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 progress!</span></span></p><p> </p><p><span style="font-size:12.0px"><span style="font-family:Verdana, Geneva, sans-serif">Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!</span></span></p><p> </p>