The Batch Record Review Intern supports the Quality Assurance team (QA OPS) by assisting in the review, verification, and organization of electronic GMP manufacturing documentation. This role provides hands‑on exposure to regulated industry practices, including data integrity, documentation
Today, Lonza is a global leader in life sciences operating across three continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together,
The Batch Record Review Intern supports the Quality Assurance team (QA OPS) by assisting in the review, verification, and organization of electronic GMP manufacturing documentation. This role provides hands‑on exposure to regulated industry practices, including data integrity, documentation
For our site in Visp we are looking for a dedicated Batch Record Reviewer 80 - 100% (f/m/d) to extend our team. If you are passionate about applying your expertise to optimize drug product manufacturing and truly make
Lonza in Visp is seeking a dedicated Batch Record Reviewer (80 - 100%) to join their team. The role involves planning and documenting manufacturing campaigns for drug products while ensuring compliance with GMPs and quality requirements. The ideal
Today, Lonza is a global leader in life sciences operating across three continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is dedicated people working together,
The actual location of this job is in Visp, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed. As our operations continue to expand, we are looking for motivated MSAT Data Managers
We’re expanding our team in Visp and are currently seeking a motivated Intern for QA Documentation Support (m/f/d). In this role, you’ll report directly to the QA Operations Group Leader and collaborate closely with cross-functional teams
Location: the actual location of this job is in Visp, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed. This role offers the opportunity to lead and shape a comprehensive contamination control
Location: the actual location of this job is in Visp, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed. We are looking for a Senior QA Specialist (m/f/d) to join multifunctional QA
Um unser kontinuierliches organisches Wachstum voranzutreiben, suchen wir ständig nach hochqualifizierten Fachkräften. Zur Verstärkung unseres Teams in der Herstellung von Vor- und Endstufen suchen wir eine/n engagierte/n Chemie-& Pharmatechnologe (w/m/d), in Vollzeit im Schichtbetrieb. Ihre Aufgaben:
At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are,
General information Reference 2026-178 Information about Molecular Partners AG Founded in 2004 by a group of PhD students as a spin-off from the University of Zurich, Molecular Partners AG is a thriving and steadily growing clinical
Für unser MES-Team in der Abteilung Digital Manufacturing suchen wir eine/n MES Specialist zur Unterstützung bei der Implementierung des Manufacturing Execution Systems (MES) in neue und bestehende Produktionsprozesse. Ihre Aufgaben Aufnahme, Analyse und Umsetzung von Produktions-
Overview In this exciting role the successful candidate will contribute to CMC tasks from discovery/preclinical stage to clinical and potentially commercial stage. This includes managing outsourcing activities for development and manufacturing of drug substance from early
Job Description The Global Clinical Supply (GCS) organization manages the “end-to-end” clinical supply for the company’s portfolio. GCS is accountable for the planning, sourcing, labelling, packaging and delivery of clinical supplies to clinical sites across more
Für unser MES-Team in der Abteilung Digital Manufacturing suchen wir eine/n MES Specialist zur Unterstützung bei der Implementierung des Manufacturing Execution Systems (MES) in neue und bestehende Produktionsprozesse. Ihre Aufgaben Aufnahme, Analyse und Umsetzung von Produktions-
Location: The actual location of this job is in Visp, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed. The role: The Senior QA Specialist (f/m/d) for QA Projects specifies quality requirements
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
Zur Verstärkung des bestehenden Teams in unserer Wirkstoffproduktion suchen wir zum nächstmöglichen Zeitpunkt eine/n engagierte/n Technical Author Peptide Manufacturing (a), 100% (temporär für 12 Monate mit Aussicht auf Übernahme). Sie sind verantwortlich für das Schreiben produktionsrelevanter