Location: the actual location of this job is in Visp, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed. The Contamination Prevention & Control (CPC) Environmental Monitoring (EM) team delivers critical GMP
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 for manufacturing processes
Join our Mission to Protect Humankind! Vaxcyte is a clinical-stage vaccine innovation company engineering high-fidelity vaccines to protect humankind from the consequences of bacterial diseases, which have serious and costly health consequences when left unchecked. Working
Requistion ID: 83623 Dentsply Sirona est le plus grand fabricant mondial de produits et de technologies dentaires professionnels, avec plus dun siècle dinnovation et de service à lindustrie dentaire et aux patients du monde entier. Dentsply
Requistion ID: 83623 Dentsply Sirona is the world’s largest manufacturer of professional dental products and technologies, with over a century of innovation and service to the dental industry and patients worldwide. Dentsply Sirona develops, manufactures, and
At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.Through our
This is your opportunity to join AXIS Capital – a trusted global provider of specialty lines insurance and reinsurance. We stand apart for our outstanding client service, intelligent risk taking and superior risk adjusted returns for
Be the gatekeeper of quality-safeguard raw material compliance in a dynamic GMP environment. Proclinical is seeking a QA Raw Material Compliance Specialist to join a dynamic team in Switzerland. In this role, you will play a key part
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 control,
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. The QA Specialist (QA On The Floor) is responsible to the Associate Director, Head of QA Operations
In Bern, we’re launching a new production site and introducing innovative ways of working. This role supports our mission of high‑quality pharmaceutical products. Responsibilities Develop, review and approve CSV and QV strategies, plans, protocols and reports
Review & Qualitätssicherung von Dokumenten Abstimmung mit Engineering, QA & Produktion Strukturierung & Verwaltung der Dokumentation (Versionen, Archiv) Sicherstellen von Normen & Aviation-Compliance Erstellen von Schulungsunterlagen Optimierung von Prozessen & Standards Dein Background Studium im technischen Bereich
QA Specialist (f/m/d) – CSV & QV page is loaded# QA Specialist (f/m/d) – CSV & QVlocations: Berntime type: Full timeposted on: Posted Todayjob requisition id: JR In Bern, we’re not just expanding—we’re reaching a major milestone by launching a
Switzerland, Visp Location: Visp, Switzerland. Relocation assistance available for eligible candidates and their families. What You Will Get An agile career and a dynamic work culture. An inclusive and ethical workplace. Compensation programs that recognize high
Tangem AG, based in Zug, Switzerland, is looking for an experienced web tester with a minimum of 3 years in the field. Responsibilities include testing web applications, API testing, and managing test documentation. Candidates should possess a
agap2 Switzerland is seeking a Consultant to support clients in the pharmaceutical, biotechnology, and medical devices sectors. The role focuses on maintaining and improving quality management systems, and involves drafting and reviewing GMP-related documentation. The ideal candidate
IT Systems & Infrastructure Specialist | MedTech Bern Area, Switzerland | Hybrid | Permanent Position Im currently supporting an innovative and fast-growing MedTech company in Switzerland in the search for an experienced IT Systems & Infrastructure Specialist to
CTC is a specialized search and recruitment partner for the Life Sciences industry, serving clients and candidates since 1997. We enable careers by connecting talented professionals with meaningful opportunities, and we support our clients in engaging,
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description The Procurement Specialist is responsible for identifying innovative and leading sourcing solutions and for supporting the development of relationships with clinical trial suppliers; manufacturers and networks of wholesalers. The individual