Aufgabenbereich: Etablieren, kontrollieren und optimieren von qualitätsrelevanten Systemen und Prozessen Sicherstellen einer hochwertigen und termingerechten Bearbeitung der Vorgaben Verantwortlich für Dokumentationsfragen sowie die Einhaltung von GMP Richtlinien Identifizieren von kostensparenden Massnahmen Ansprechpartner für Qualitätsfragen für interne und externe Kunden Als Schnittstelle zur Quality Assurance unterstützen Sie aktiv die Durchführung von Audits und Inspektionen Führen eines Teams von 3 Mitarbeitern


(im Bereich Qualitätssicherung/-management)

The global director Pilot Plants is responsible for the manufacturing of clinical material used in clinical phase II and III trials. Furthermore, he is responsible for the registration and launch of leads that have passed successfully the phase III trials.


(im Bereich Management/Business Development, Produktion, Qualitätssicherung/-management, Projektmanagement)

Harlan Laboratories is a leading global provider of essential non-clinical contract research, research models, animal diets, and services to the pharmaceutical, biotech, medical device, agrochemical and chemical industries, as well as to academic and government research organizations. Our focus is on providing customers with products and services to optimize the discovery and safety of new medicines and compounds. We have over 2,800 employees in 12 countries, but we act locally, understanding the value of close relationship and collaboration with our costumers. For the enhancement of our team in Switzerland we have an opening for a Manager, Safety Assessment. Responsibilities Management of Personnel in the operating unit Safety Assessment (SAS) within Toxicology, i.e. management of study director pool together with team leaders, planning coordination group together with corresponding group leader, reporting assistants. Development of training program for cross training, study governance, customer relation (“program management”, communication) General instruction, training and further education of subordinated staff in cooperation with HR. Wherever necessary and useful building dedicated teams for the clients. Coordination and control of collaboration with other laboratory units and groups, especially Animal House and Clinical Pathology. Responsibility for strict compliance with animal welfare regulations. Responsibility for strict compliance with GLP regulations . Coordination of preparation of offers related to toxicology studies. . Consulting and customer support in collaboration with strategic alliance managers with respect to consulting of study and/or development strategies – practical possibilities at Harlan. Revisions and preparation of SOPs in collaboration with subordinated staff. Profile Education as a Biochemist / Biologist / Toxicologist or Vet More than 10 years of experience as a senior study director Leadership skills (more than 5 years of experience) Worked in a Pharma company or CRO Fluent in German and English


(im Bereich Management/Business Development, Sonstiges/Flexibel)