Senior, Quality Assurance (m/w/d) Department: Product Research & Development Employment Type: Permanent Location: Germany, Leer Description Als Senior Quality Assurance Engineer (m/w/d) bist du verantwortlich für die Sicherstellung höchster Softwarequalität in komplexen Entwicklungsprojekten. Du entwickelst Teststrategien, führst
Unternehmensbeschreibung Relias, ein Unternehmen der Bertelsmann Education Group, ist weltweit führend im Bereich digitaler Bildung für das Gesundheits- und Sozialwesen. Die intuitive, cloudbasierte Plattform von Relias bietet umfassende Lösungen für E-Learning und Compliance Management und wird
As the leading company in the field of software solutions for healthcare, we operate in 19 countries and employ over 9,000 dedicated staff members. You will work in a dynamic and innovative environment full of opportunities.
About the role: Whats in the BoxAs FSQA Lead (Food Safety & Quality Assurance), you will assume overall responsibility for food safety and quality assurance at the Factor_ production site in Verden. You will drive the
Job DescriptionDrive GMP compliance—lead risk‑based CSV, validate systems, ensure inspection readiness. Unlock your potential with us! Currently we are looking for a Senior CSV QA Specialist (f/m/d) for our site in Burgwedel.About the RoleA great opportunity is
Overview In this role you help life science customers design, implement, and support LIMS within regulated environments, collaborating with cross-functional teams to deliver compliant laboratory solutions. You’ll shape project delivery from analysis to go-live and contribute
Overview As a Salesforce Consultant at KUKA Group, you will manage the global Salesforce platform to support thousands of users across multiple countries. You will advise business units, drive platform development in agile sprints, and optimize processes
Overview In this Principal Consultant role, you guide Regulatory Affairs strategy and growth within NNIT’s Life Sciences practice. You’ll lead client engagements, drive RFP responses, and shape business development initiatives to expand the Regulatory Affairs portfolio. The
Overview In this Site Activation Specialist role, you will oversee site start-up activities at the country level, ensuring timely regulatory submissions, document completeness, and TMF accuracy. You’ll collaborate with country leaders, CSA, and PM/SAM to drive
Overview As a Product Certification Auditor, you will assess and certify products to ensure responsible antibiotic manufacturing practices within the AMR Kitemark program. You will work across Europe, traveling to client sites to perform audits, report