15.04.24 | Vollzeit | Pontresina | Grand Hotel Kronenhof01.06.2024 - 10 months TLNT1 CH This is what you move with us Serving and clearing dishes Looking after guests Proper handling and cleaning of machines and equipment in service Compliance with hygiene regulations Providing information on the food and drinks menu All preparation and follow-up work
Später ansehen14.04.24 | Vollzeit | Visp | RandstadJobdescription For our client, an international company in Visp, we are looking for a CQV Engineer. The CQV Engineer is primarily responsible for the preparation and the execution of the CQV activities as per below responsibilities. General Information Start date ASAP Latest start date October
Später ansehen14.04.24 | Vollzeit | Visp | RandstadJobdescription For our client, an international company in Visp, we are looking for a CQV Lead. The CQV Lead is primarily responsible for the preparation and the execution of the CQV activities relating to Upstream, Bioconjugation or Downstream Process Equipment. The target area will be assigned
Später ansehen29.04.24 | Vollzeit | JobLeads GmbH | CHF 150’000 - CHF 200’000 Demonstrated success and experience supporting oncology product pre-launch, launch and post-launch activities is essential. - In-depth understanding of how to navigate payer systems without prior experience in the market is critical. - Experience with HTA dossier preparation, submission and negotiation
Später ansehen03.05.24 | Vollzeit | Zug, Dietikon, Frauenfeld, Zür | 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, Uster, Luzern, Schaffh | 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, Emmen, Schaffhausen, U | 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, Luzern, Schaffhausen, E | 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 | Zürich, Uster, Schaffhausen, E | 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 | Zürich, Schaffhausen, Emmen, L | 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
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