30.08.24 | Vollzeit | Zug | JobLeads GmbH | CHF 80’000 - CHF 100’000 Regulatory Affairs International Affiliate Team is seeking a motivated, curious, flexible, and culturally aware experienced Regulatory professional to assume a full-time employment position in Gilead's office in Zug, Switzerland in the capacity of CMC Regulatory Affairs Senior Manager, reporting to the CMC
Später ansehen29.08.24 | Vollzeit | JobLeads GmbH | CHF 80’000 - CHF 100’000 Senior Manager, Regulatory Affairs CMC (m/f/d) Job Description At Gilead, we’re creating a healthier world for all people. For more than 35 years, we’ve tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer - working relentlessly to develop therapies that help improve lives
Später ansehen29.08.24 | Vollzeit | Morges | JobLeads GmbH | CHF 150’000 - CHF 200’000 Familiarity with GCP/ICH/FDA requirements as well as clinical trial design, biostatistics, medical writing, product safety, healthcare compliance and regulatory affairs. - Strong interpersonal, verbal and written communication skills. Strong public speaking skills. - Excellent leadership and management skills
Später ansehen14.08.24 | Vollzeit | Zug | JobLeads GmbH | CHF 125’000 - CHF 150’000 Champion adoption and assure alignment of iNova’s regulatory information management system with other organizational systems. - Provide regulatory leadership to iNova’s European business. - Manage regulatory affairs in alignment with iNova business objectives and statutory obligations, ensuring speed
Später ansehen12.08.24 | Vollzeit | Grens | JobLeads GmbH | CHF 80’000 - CHF 100’000 Clinical Evaluation plans and reports in compliance with applicable regulatory requirements (EU MDR, MEDDEV 2.7/1, MDCG) 4. Write study protocols, safety plans and reports in liaison with Medical and Regulatory Affairs 5. Support Medical Affairs and Regulatory Affairs in development and execution
Später ansehen12.08.24 | Vollzeit | Luzern | JobLeads GmbH | CHF 100’000 - CHF 125’000 Market demand forecast such as major demand events and commercial strategies. 5. Ensure these operations are executed per GxP, Organon Quality standards, policies and procedures, and local regulations. Collaborating with In-Market Quality and Regulatory Affairs. Proactively identifying and reporting
Später ansehen19.09.24 | Teilzeit, Vollzeit | Genève, Sort-en-Chalosse, Base | Michael Page InternationalVerkaufsadministrator (m/w) 1 - Healthcare & Life Sciences 11 - Biotechnologie 3 - Klinischer Betrieb 2 - Medical devices 2 - Pharma-Industrie 2 - Regulatory Affairs 2 - Technologie 8 - IT Business Analyst (m/w) 2 - IT Support 2 - System Adminstrator (m/w) 2 - ERP 1 - IT Projekt & Program Management 1 - Logistik
Später ansehen19.09.24 | Vollzeit | Michael Page Internationalaffairs across multiple countries and will collaborate with finance teams to efficiently handle the period-end closing process. - Save Job - added 10/09/2024 - Modern Workspace and environment - English only needed (German is a plus) About Our Client The client is a renowned, international Hospitality
Später ansehen19.09.24 | Vollzeit | Vaud | Randstad Schweiz AGQuality standards. Main Tasks - Provide expertise in mAbs/protein analytics to deliver high-quality analytical packages supportingthe company's product development that meet Global Health Authority requirements, particularly in the US and EU. - Work closely with CMC Development Teams, Regulatory Affairs
Später ansehen20.04.24 | Vollzeit | JobLeads GmbH | CHF 150’000 - CHF 200’000 Of another jurisdiction with a strong understanding of Swiss law. - Proven track record as a legal counsel, with experience in compliance, licenses and regulatory affairs. - Deep knowledge of the crypto space. - Integrity, humility, intellectual curiosity, honesty, and direct communication. We are a team
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