About Our Client For our client, a leading international pharmaceutical company with modern offices in the canton of Lucerne, we are seeking a Batch Record Review Specialist (m/f/d). In this role, you will support clinical biologics
Bist du bereit für eine neue und spannende Herausforderung in einem führenden Schweizer Technologieunternehmen, das innovative High-Tech-Komponenten und -Systeme auf der Basis von Röntgen- und Hochfrequenztechnologie herstellt? Dann habe ich die passende Stelle für dich! Für
Overview Are you passionate about quality, precision, and working in a GMP-regulated environment? We are currently seeking a detail-oriented GMP Documentation Specialist (m/w/d) to join our client’s Manufacturing Operations team in a dynamic, fast-paced biopharmaceutical environment.
Randstad (Schweiz) AG sucht für die Comet AG in Flamatt mehrere Mitarbeiter für die Endmontage innovativer High-Tech-Komponenten. Die Aufgaben umfassen die Endmontage von Vakuumkondensatoren, die Vorbereitung für das Versilbern, elektrische Kontrollen und Dokumentationen im SAP. Notwendig sind
The GMP Documentation Specialist supports clinical biologics manufacturing by performing operational review of executed batch records and ensuring documentation supports ALCOA+ standards and GMP expectations. The role is part of the Operational Excellence team within Manufacturing
Johnson & Johnson is a global health care company that develops medicines, medical devices and consumer products. We are committed to creating solutions that prevent, treat and cure complex diseases and to improving patient outcomes worldwide.
The Batch Record Reviewer supports clinical biologics manufacturing by performing operational review of executed batch records and ensuring documentation meets ALCOA+ , GDP , and GMP expectations. As part of the Manufacturing Operational Excellence team, this