04.06.24 | Vollzeit | Sempach | B. Braun Medical AGRegulatory Affairs Manager (f/m/d)The Global Regulatory Affairs department of the B. Braun Avitum division has an opportunity for a Regulatory Affairs Managerlocated at our site in Sempach, Switzerland. In our plant in Sempach, we develop and produce a broad range of products for cleaning
Später ansehen01.06.24 | Vollzeit | Sempach | B. Braun Medical AGRegulatory Affairs Manager (f/m/d)The Global Regulatory Affairs department of the B. Braun Avitum division has an opportunity for a Regulatory Affairs ManagerLocated at our site in Sempach, Switzerland. In our plant in Sempach, we develop and produce a broad range of products for cleaning
Später ansehen03.05.24 | Vollzeit | Schaffhausen | Daiichi Sankyo Europe GmbHManager, GvP Audits is responsible to support all aspects of pharmacovigilance audits and regulatory inspections including preparation, conduct, tracking and verification of CAPA commitment implementation to assure all are in an acceptable state of compliance. The position will report to the Head
Später ansehen03.05.24 | Vollzeit | Uster | Daiichi Sankyo Europe GmbHManager, GvP Audits is responsible to support all aspects of pharmacovigilance audits and regulatory inspections including preparation, conduct, tracking and verification of CAPA commitment implementation to assure all are in an acceptable state of compliance. The position will report to the Head
Später ansehen03.05.24 | Vollzeit | Kriens | Daiichi Sankyo Europe GmbHManager, GvP Audits is responsible to support all aspects of pharmacovigilance audits and regulatory inspections including preparation, conduct, tracking and verification of CAPA commitment implementation to assure all are in an acceptable state of compliance. The position will report to the Head
Später ansehen03.05.24 | Vollzeit | Schaffhausen | Daiichi Sankyo Europe GmbHManager, GvP Audits is responsible to support all aspects of pharmacovigilance audits and regulatory inspections including preparation, conduct, tracking and verification of CAPA commitment implementation to assure all are in an acceptable state of compliance. The position will report to the Head
Später ansehen03.05.24 | Vollzeit | Schaffhausen | Daiichi Sankyo Europe GmbHManager, GvP Audits is responsible to support all aspects of pharmacovigilance audits and regulatory inspections including preparation, conduct, tracking and verification of CAPA commitment implementation to assure all are in an acceptable state of compliance. The position will report to the Head
Später ansehen03.05.24 | Vollzeit | Luzern | Daiichi Sankyo Europe GmbHManager, GvP Audits is responsible to support all aspects of pharmacovigilance audits and regulatory inspections including preparation, conduct, tracking and verification of CAPA commitment implementation to assure all are in an acceptable state of compliance. The position will report to the Head
Später ansehen03.05.24 | Vollzeit | Uster | Daiichi Sankyo Europe GmbHManager, GvP Audits is responsible to support all aspects of pharmacovigilance audits and regulatory inspections including preparation, conduct, tracking and verification of CAPA commitment implementation to assure all are in an acceptable state of compliance. The position will report to the Head
Später ansehen03.05.24 | Vollzeit | Kriens | Daiichi Sankyo Europe GmbHManager, GvP Audits is responsible to support all aspects of pharmacovigilance audits and regulatory inspections including preparation, conduct, tracking and verification of CAPA commitment implementation to assure all are in an acceptable state of compliance. The position will report to the Head
Später ansehenVerpassen Sie nie wieder einen passenden Job!
Alle Jobs für Product Manager Pharma in Luzern Kanton kostenlos abonnieren.