16.04.24 | Vollzeit | Zürich | Mandarin Oriental Savoy, ZurichDuties - Responsible for room-night and revenue production from allocated accounts - Implement agreed rate structure and strategy for the accounts. - Organise and accompany familiarisation trips and hotel site inspections for clients. - To conduct rate negotiations and co-ordinate contracting for key
Später ansehen11.04.24 | Vollzeit | Zürich | gloor & lang ag life science careersCoordinates the conduct of internal audits and regulatory inspectionsYour profile- B.Sc, M.Sc. Life Sciences- 3-5 years of experience in Clinical QA Operations- Experience in CRO and Clinical Vendor Management- Excellent knowledge in GCP and GMP regulationsYour autonomy, your integrity, and your initiative
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
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