22.03.24 | Vollzeit | Frauenfeld, Schaffhausen, Dübe | Daiichi Sankyo Europe GmbHAnd report Pharmacovigilance audits including Service Providers, systems and processes, license partners and affiliates to assure that all are in an acceptable state of compliance Document audit conduct, findings, CAPA ensuring supporting documentation, tracking - verification of CAPA commitment
Später ansehen22.03.24 | Vollzeit | Frauenfeld, Schaffhausen, Dübe | Daiichi Sankyo Europe GmbHAnd report Pharmacovigilance audits including Service Providers, systems and processes, license partners and affiliates to assure that all are in an acceptable state of compliance Document audit conduct, findings, CAPA ensuring supporting documentation, tracking - verification of CAPA commitment
Später ansehen22.03.24 | Vollzeit | Frauenfeld, Schaffhausen, Dübe | Daiichi Sankyo Europe GmbHAnd report Pharmacovigilance audits including Service Providers, systems and processes, license partners and affiliates to assure that all are in an acceptable state of compliance Document audit conduct, findings, CAPA ensuring supporting documentation, tracking - verification of CAPA commitment
Später ansehen22.03.24 | Vollzeit | Frauenfeld, Schaffhausen, Dübe | Daiichi Sankyo Europe GmbHAnd report Pharmacovigilance audits including Service Providers, systems and processes, license partners and affiliates to assure that all are in an acceptable state of compliance Document audit conduct, findings, CAPA ensuring supporting documentation, tracking - verification of CAPA commitment
Später ansehen22.03.24 | Vollzeit | Frauenfeld, Schaffhausen, Dübe | Daiichi Sankyo Europe GmbHAnd report Pharmacovigilance audits including Service Providers, systems and processes, license partners and affiliates to assure that all are in an acceptable state of compliance Document audit conduct, findings, CAPA ensuring supporting documentation, tracking - verification of CAPA commitment
Später ansehen22.03.24 | Vollzeit | Frauenfeld, Schaffhausen, Dübe | Daiichi Sankyo Europe GmbHAnd report Pharmacovigilance audits including Service Providers, systems and processes, license partners and affiliates to assure that all are in an acceptable state of compliance Document audit conduct, findings, CAPA ensuring supporting documentation, tracking - verification of CAPA commitment
Später ansehen23.04.24 | Vollzeit | Zug | Randstad Schweiz AGOf the Johnson & Johnson family of companies and encompasses several business units from the pharmaceutical, medical device, and consumer sectors. The Group Campus Switzerland Services is part of the pharmaceutical division and supports several business units in the areas of finance, human resources
Später ansehen23.04.24 | Vollzeit | Visp | Randstad Schweiz AGOn document control processes, systems, and best practices, ensuring adherence to established procedures. - Collaborate with internal and external stakeholders to coordinate document reviews, approvals, and revisions within specified timelines. - Support the preparation and execution of regulatory inspections
Später ansehen22.04.24 | Freelancer, Vollzeit | www.freelance.deSUVA certificate) • 5-10 years of work experience as EHS or Safety Engineer in a Bio-Pharmaceutical - Pharmaceutical - Chemical Manufacturing environment • Proven process understanding of design safety and legal safety demands in the pharmaceutical environment or similar. • Very strong communication
Später ansehen22.04.24 | Vollzeit, Freelancer | Zürich | jobwinner.chThe System Process Specialist has a profound process understanding and is collaborating with the Business Community to continuously improve business processes and underlying IT
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