20.05.24 | Vollzeit | Zug | JobLeads GmbH | CHF 150’000 - CHF 200’000 To review requests for grants and sponsorships. Ensures that review and approval processes strictly follow compliance guidelines. TEAM LEADERSHIP AND CROSS-FUNCTIONAL COLLABORATION - Manages and develops the associate Medical Director International TTR and provides support concerning hiring, training
Später ansehen05.05.24 | Vollzeit | Baar | Exact Sciencesbusiness acumen, intellectual curiosity and creativity, and relevant legal, regulatory and industry issues. - Uphold Company mission and values through accountability, innovation, integrity, quality, and teamwork. - Support and comply with the Company's Quality Management System policies and procedures
Später ansehen03.05.24 | Vollzeit | Frauenfeld | Daiichi Sankyo Europe GmbHDocumentation, tracking - verification of CAPA commitment implementation 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
Später ansehen03.05.24 | Vollzeit | Frauenfeld | Daiichi Sankyo Europe GmbHDocumentation, tracking - verification of CAPA commitment implementation 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
Später ansehen03.05.24 | Vollzeit | Frauenfeld | Daiichi Sankyo Europe GmbHDocumentation, tracking - verification of CAPA commitment implementation 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
Später ansehen03.05.24 | Vollzeit | Frauenfeld | Daiichi Sankyo Europe GmbHDocumentation, tracking - verification of CAPA commitment implementation 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
Später ansehen03.05.24 | Vollzeit | Frauenfeld | Daiichi Sankyo Europe GmbHDocumentation, tracking - verification of CAPA commitment implementation 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
Später ansehen03.05.24 | Vollzeit | Frauenfeld | Daiichi Sankyo Europe GmbHDocumentation, tracking - verification of CAPA commitment implementation 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
Später ansehen03.05.24 | Vollzeit | Frauenfeld | Daiichi Sankyo Europe GmbHDocumentation, tracking - verification of CAPA commitment implementation 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
Später ansehen03.05.24 | Vollzeit | Frauenfeld | Daiichi Sankyo Europe GmbHDocumentation, tracking - verification of CAPA commitment implementation 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
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