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 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 role focuses on right‑first‑time
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 manufacturing by
Aristo Group is seeking a Batch Record Reviewer in Luzern, Switzerland. This role supports clinical biologics manufacturing by ensuring compliance with ALCOA+, GDP, and GMP standards through operational reviews and documentation management. The ideal candidate has a degree
Michael Page International (Switzerland) SA is seeking a Batch Record Review Specialist in Luzern, Switzerland. The successful candidate will be responsible for ensuring the accuracy and compliance of batch records in clinical biologics manufacturing. Applicants should have a bachelor’s degree
Quality Assurance Specialist (m/w/d), 50% Einsatzort: Therwil Art(en) der Anstellung: Teilzeit, Temporärstelle Unser Kunde, ein Pharmaunternehmen im Raum Therwil/Reinach , braucht dringend Verstärkung. Für eine langfristige temporäre Anstellung (Krankheitsvertretung) suchen wir per sofort eine motivierte und
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
Novartis in Muttenz sucht einen Documentation Specialist, der die Verwaltung und Übergabe von Herstelldokumentationen in einem GMP-regulierten Umfeld unterstützt. Zu den Aufgaben gehören die Prüfung und Zusammenstellung der Batchdokumentation zur fristgerechten Übergabe an die Qualitätssicherung. Der
Votre profil Créée en 2007, Antaes est une société suisse de conseil en management et technologie classée dans le top 15 des sociétés de conseil en Suisse. Nous comptons plus de 300 ingénieurs expérimentés qui partagent
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
Aristo Group is seeking a GMP Documentation Specialist in Luzern, Switzerland, to support clinical biologics manufacturing. This role involves reviewing executed batch records, ensuring compliance with ALCOA+ standards, and aiding in documentation creation and lifecycle support. The ideal
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
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,