18.04.24 | Vollzeit | Luzern | Daiichi Sankyo Europe GmbHSchedule, conduct and 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
Später ansehen15.04.24 | Vollzeit | Luzern | Randstad Schweiz AGFor a clinical packaging job. - Reviewing county-specific label text on accuracy and regulatory requirements. - Handling of randomization schedules for clinical studies. - Reviewing and release of label batch record documents. - Ensuring activities are completed within given timelines and timely escalation when
Später ansehen04.04.24 | Vollzeit | Luzern | Universität LuzernRitz at or . The application deadline is May 31, 2024. We kindly ask you to send your electronic application documents to the Chair of the Appointment Committee and Dean of the Faculty of Health Sciences and Medicine, Prof. Dr. Stefan Boes, and to submit them via in accordance with the instructions
Später ansehen22.03.24 | Vollzeit | Luzern | Daiichi Sankyo Europe GmbHCritical findings from audits and inspection to QA and functional department leadership Support management of Quality Assurance SOPs and policies to ensure that they are current, adhere to laws, regulations, guidance documents and Daiichi-Sankyo standards Support quality documentation and quality system
Später ansehen22.03.24 | Vollzeit | Luzern | Daiichi Sankyo Europe GmbHCritical findings from audits and inspection to QA and functional department leadership Support management of Quality Assurance SOPs and policies to ensure that they are current, adhere to laws, regulations, guidance documents and Daiichi-Sankyo standards Support quality documentation and quality system
Später ansehen22.03.24 | Vollzeit | Luzern | Daiichi Sankyo Europe GmbHCritical findings from audits and inspection to QA and functional department leadership Support management of Quality Assurance SOPs and policies to ensure that they are current, adhere to laws, regulations, guidance documents and Daiichi-Sankyo standards Support quality documentation and quality system
Später ansehen22.03.24 | Vollzeit | Luzern | Daiichi Sankyo Europe GmbHCritical findings from audits and inspection to QA and functional department leadership Support management of Quality Assurance SOPs and policies to ensure that they are current, adhere to laws, regulations, guidance documents and Daiichi-Sankyo standards Support quality documentation and quality system
Später ansehen22.03.24 | Vollzeit | Luzern | Daiichi Sankyo Europe GmbHCritical findings from audits and inspection to QA and functional department leadership Support management of Quality Assurance SOPs and policies to ensure that they are current, adhere to laws, regulations, guidance documents and Daiichi-Sankyo standards Support quality documentation and quality system
Später ansehen22.03.24 | Vollzeit | Luzern | Daiichi Sankyo Europe GmbHCritical findings from audits and inspection to QA and functional department leadership Support management of Quality Assurance SOPs and policies to ensure that they are current, adhere to laws, regulations, guidance documents and Daiichi-Sankyo standards Support quality documentation and quality system
Später ansehen22.03.24 | Vollzeit | Luzern | Daiichi Sankyo Europe GmbHCritical findings from audits and inspection to QA and functional department leadership Support management of Quality Assurance SOPs and policies to ensure that they are current, adhere to laws, regulations, guidance documents and Daiichi-Sankyo standards Support quality documentation and quality system
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