Skip to content
Global Category Specialist for Cleanroom and EI&C (w/m/d) - GMP/cold room/management/SAP/English, German, French Project : For our customer a big pharmaceutical company in Visp we are looking for a highly qualified Global Category Specialist for Cleanroom and EI&C. Background : The Clean Room Solutions and EI&C global category specialist, who manages the procurement category management activities in investment projects and coordinates with Capex Lead buyers the planning and execution of projects at the Visp site and all other sites. Tasks and Responsibilities. Execution and updates of overall... more ->
We are currently looking on behalf of one of our important clients for a German Speaking QMS Application Specialist (Medical Device Sector). The role is a permanent position based in Solothurn Canton & comes with some home office allowance. Your Role: Administrate a QMS Application. Act as a contact point for internal customers, specialist departments & expert external consultants. Coordinate between internal departments, IT & external service providers. Identify potential for improvement, definition of requirements & prioritization. Evaluate, implement & document changes in the system (eg... more ->
Ihre Aufgaben zielgerichtete und kundenorientierte Projektierung bei Optimierungen, Umbauten oder Neuinvestitionen von pharmazeutischen Anlagen in der Wirkstoff- und galenischen Produktherstellung Erstellen von Qualifizierungsplanen und -Reports in den Phasen DQ, IQ, OQ, PQ Inbetriebnahme, Kalibrierung, Qualifizierung und Validierung von Prozessen und Anlagen Qualifizierungsreviews im Anlagenlifecycle von bestehenden komplexen Systemen Deviation- und Change Control Arbeit in internen und/oder externen interdisziplinaren Teams Ihr Profil naturwissenschaftliches oder technisches Studium in den... more ->
We are currently looking for a Head of QC Instrumentation. In the role as Head of QC Instrumentation you will lead a team of instrumentation specialist to support laboratory instrumentation and automation infrastructure in an operational testing environment. With your team you are responsible that QC equipment at our site in Bern, Switzerland is qualified and brought into operation in compliance with GxP requirements. With your peers at our sites in Europe, Australia and the United States you collaborate closely to increase process excellence and ensure regulatory compliance. Your... more ->
Quality Control is responsible to support the entire Couvet site to ensure that each analytical and microbiological testing is performed in compliance with the site's Quality Management Systems (QMS), the cGMP, the applicable laws, regulations, and standards, and in compliance with the Product's Dossier managed by the Customer. The position holder is responsible, within the frame of AS&T, of any testing-related topic to ensure the execution of new technology/product method transfer and/or validation, the creation of adequate testing methods and specifications and their associated training... more ->
We are currently looking on behalf of one of our important clients for a Head of Laboratory Test Development & Validation (German Speaking). The role is a permanent position based in Bern Canton & comes with good home office allowance. Your Role: Oversee the personnel & technical management of a specialist group of 4 Engineers & 3 Laboratory Technicians. Develop & validate new physical measurement & testing methods. Provide technical support for Design Verification Laboratories. Hold responsibility for the operation & maintenance of a Development Laboratory. Plan, coordinate & execute... more ->
Technical QA Manager (m/f/d) - Quality Management/Qualification/Validation/CSV of Small Molecules/Data Integrity/GMP/IMP/English & German Project : For our customer a big pharmaceutical company in Basel we are looking for a highly qualified Technical QA Manager (m/f/d). Background : The IMP Quality Operations Unit Switzerland in Global Technical Operations is the Quality partner for all Manufacturing Units and Clinical Packaging in Pharmaceutical Technical Development in Switzerland and responsible for the Quality and GMP-compliance oversight of all Investigational Medicinal Products (IMPs)... more ->
CSL Behring is a global biotherapeutics leader driven by its promise to save lives. In the role as Senior Scientist, QC Excellence Instrumentation you will support laboratory instrumentation and automation infrastructure in the operational QC testing environment. You will carry out equipment qualifications for our site in Bern, Switzerland and collaborate with our sites in Europe, Australia and the United States for global qualification projects. Your responsibilities include, but are not limited to: Support laboratory instrumentation and automation infrastructure in an operational testing... more ->
QA Manager (m/f/d) - GMP/Quality Risk Management/Qualification/Validation/Parentals/English & German Project: For our customer a big pharmaceutical company in Basel we are looking for a highly qualified QA Manager (m/f/d). Background: The IMP Quality Operations Unit Switzerland in Global Technical Operations is the Quality partner for all Manufacturing Units and Clinical Packaging in Pharmaceutical Technical Development in Switzerland and responsible for the Quality, Quality Systems and GMP-compliance oversight of all Investigational Medicinal Products (IMPs) manufactured and packed for... more ->
Hello. We're Haleon. A new world-leading consumer health company. Shaped by all who join us. Together, we're improving everyday health for billions of people. By growing and innovating our global portfolio of category-leading brands - including Sensodyne, Panadol, Advil, Voltaren, Theraflu, Otrivin, and Centrum - through a unique combination of deep human understanding and trusted science. What's more, we're achieving it in a company that we're in control of. In an environment that we're co-creating. And a culture that's uniquely ours. Care to join us. This is an exciting time to join us and... more ->