11.04.24 | Vollzeit | Zürich | gloor & lang ag life science careersAnd coordinates internal training programs. On site presence up to 3 days/week tasks- Oversight for QMS Quality Management System- Provides Quality Oversight prior to/ during/ close-out of clinical trials- Leads GCP/GMP/GLP Vendor Qualifications- Organize and lead audits at GCP/GMP vendors
Später ansehen02.04.24 | Vollzeit | Zürich | LHHOf medical devices and/or pharmaceutical products Degree in Natural science (pharmacy, chemistry, biology) or comparable university degree required. In-depth knowledge of ISO13485 ISO14971, 21CFR 210,211, 820, European MDR and MDSAP. Experience in Global Health Authority (including FDA) inspections. LI
Später ansehen22.03.24 | Vollzeit | Zürich | Daiichi Sankyo Europe GmbHImplementation are conducted within the electronic quality management systems in a timely manner Support all aspects of pharmacovigilance regulatory inspections including preparation, conduct, coordinating responses, evaluating supporting documentation, tracking and verification of CAPA commitment implementation
Später ansehen22.03.24 | Vollzeit | Zürich | Daiichi Sankyo Europe GmbHImplementation are conducted within the electronic quality management systems in a timely manner Support all aspects of pharmacovigilance regulatory inspections including preparation, conduct, coordinating responses, evaluating supporting documentation, tracking and verification of CAPA commitment implementation
Später ansehen22.03.24 | Vollzeit | Zürich | Daiichi Sankyo Europe GmbHImplementation are conducted within the electronic quality management systems in a timely manner Support all aspects of pharmacovigilance regulatory inspections including preparation, conduct, coordinating responses, evaluating supporting documentation, tracking and verification of CAPA commitment implementation
Später ansehen22.03.24 | Vollzeit | Zürich | Daiichi Sankyo Europe GmbHImplementation are conducted within the electronic quality management systems in a timely manner Support all aspects of pharmacovigilance regulatory inspections including preparation, conduct, coordinating responses, evaluating supporting documentation, tracking and verification of CAPA commitment implementation
Später ansehen22.03.24 | Vollzeit | Zürich | Daiichi Sankyo Europe GmbHImplementation are conducted within the electronic quality management systems in a timely manner Support all aspects of pharmacovigilance regulatory inspections including preparation, conduct, coordinating responses, evaluating supporting documentation, tracking and verification of CAPA commitment implementation
Später ansehen22.03.24 | Vollzeit | Zürich | Daiichi Sankyo Europe GmbHImplementation are conducted within the electronic quality management systems in a timely manner Support all aspects of pharmacovigilance regulatory inspections including preparation, conduct, coordinating responses, evaluating supporting documentation, tracking and verification of CAPA commitment implementation
Später ansehen22.03.24 | Vollzeit | Zürich | Daiichi Sankyo Europe GmbHImplementation are conducted within the electronic quality management systems in a timely manner Support all aspects of pharmacovigilance regulatory inspections including preparation, conduct, coordinating responses, evaluating supporting documentation, tracking and verification of CAPA commitment implementation
Später ansehen22.03.24 | Vollzeit | Zürich | Daiichi Sankyo Europe GmbHImplementation are conducted within the electronic quality management systems in a timely manner Support all aspects of pharmacovigilance regulatory inspections including preparation, conduct, coordinating responses, evaluating supporting documentation, tracking and verification of CAPA commitment implementation
Später ansehenVerpassen Sie nie wieder einen passenden Job!
Alle Jobs für It Quality Manager Pharma in Zürich kostenlos abonnieren.