26.08.24 | Vollzeit | Lausanne | JobLeads GmbH | CHF 125’000 - CHF 150’000 Measures to maintain optimal oral health. - Collaborate with dental specialists and other healthcare professionals as needed to coordinate comprehensive patient care. - Maintain accurate and up-to-date patient records in compliance with regulatory standards and clinic protocols. - Stay abreast
Später ansehen25.08.24 | Vollzeit | Lausanne | JobLeads GmbH | CHF 125’000 - CHF 150’000 Development Activities. Your responsibilities will be but not limited to - Develop a "risk-based" compound-specific compliance program contributing to document - data accuracy, ultimately resulting in "dossier acceptability" by respective out-licensing partners (emphasis on eCTD Module 5) - Contribute to CRO
Später ansehen24.07.24 | Vollzeit | Aubonne | Randstad Schweiz AGNous sommes à la recherche d’un.e Compliance Specialist Biotech pour notre client, Merck, pour une mission d’une durée de 12 mois. Votre rôle Le/la Compliance Specialist Biotech aide à assurer la compliance au sein de l’équipe Compliance au Manufacturing Operational Support, en respectant
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 | Vevey | JobLeads GmbH | CHF 80’000 - CHF 100’000 Members of the team 1. Advise R&D colleagues on key external collaboration agreements; 2. Contribute to the implementation of template agreements, best practices and guidelines regarding the management of R&D contracts; 3. Collaborate on compliance matters relevant to R&D (data privacy, biodiversity
Später ansehen20.09.24 | Vollzeit | Corsier-sur-Vevey | Randstad Schweiz AGAnd/or approve qualification/validation documents, risk assessment, SOPs and take quality decisions according to company standards The activities of the QA Expert cover all qualification/validation phases from Basic Design until 1st use of equipment/raw material.10. You ensure GMP compliance during all phases
Später ansehen19.09.24 | Teilzeit, Vollzeit | Basel (Basel-Stadt) | Michael Page InternationalDuring the contract period. - Diverse Responsibilities in a Financial Environment - Flexible Part-Time Contract with a 50% workload over 2 months Save Job - Geneva Interim Handling the day-to-day Tax Compliance spectrum for existing and new client relationships (onboarding, change in circumstances, etc
Später ansehen19.09.24 | Teilzeit, Vollzeit | Genève | Michael Page InternationalFertigung 4 - Qualität, Technik 1 - Public Sector & Not for Profit 5 - Projekt Assistent (m/w) 4 - Büro & Geschäftsunterstützung 1 - Bank- & Finanzwesen 3 - Steuern 2 - Compliance - Legal 1 - Beratung, Strategie & Change management 2 - Corporate 2 - Legal 2 - IP & Trademark 1 - Vertragsadministrator
Später ansehen19.09.24 | Vollzeit | Vaud | Randstad Schweiz AGThe analytical CMC sections of regulatory submissions from source documents, ensuring cGMP compliance and data integrity in alignment with the company's quality standards. Collaborate with CROs and CMOs to ensure the analytical life cycle management and secure supply of licensed products, meeting the approved
Später ansehen17.09.24 | Vollzeit | Aubonne | Randstad Schweiz AGIn compliance with specifications, registration and GMP requirements. To evolve in this environment, we are looking for our next Process Validation Expert to ensure the coordination of production troubleshooting and Annex 1 project related. You will be responsible for - Contribute to strategy elaboration
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