06.05.24 | Vollzeit | LHHRegistration and regulatory support to product design & development projects; Experience in project management as project team member; Knowledge of EMEA applicable regulations especially for EU market and Middle East or LATAM markets; Fluent in English. Permanent Contract LI-Hybrid
Später ansehen06.05.24 | Vollzeit | Neuchâtel | LHHDiscipline - Expert knowledge and understanding of stability ICH Guidelines (Q1A, Q5C) and associated policies, directives and guidance documents. A thorough knowledge of cGMP regulations as referenced in The Code of Federal Regulations (21CFR) and their specific application to stability programs
Später ansehen29.04.24 | Vollzeit | Zizers | AO FoundationAnd/or revised regulations (Switzerland, EU, USA, any other country as required based on operational activities) Scout for new and/or revised standards and norms (ISO, ICH) Education of employees Ensure compliant introduction of new employees in collaboration with the AO HR and the assigned line manager Ensure
Später ansehen29.04.24 | Vollzeit | Zizers | AO FoundationAnd/or revised regulations (Switzerland, EU, USA, any other country as required based on operational activities) Scout for new and/or revised standards and norms (ISO, ICH) Education of employees Ensure compliant introduction of new employees in collaboration with the AO HR and the assigned line manager Ensure
Später ansehen01.04.24 | Vollzeit | Zürich | LHHRegistration and regulatory support to product design & development projects; Experience in project management as project team member; Knowledge of EMEA applicable regulations especially for EU market and Middle East or LATAM markets; Fluent in English. Permanent Contract LI-Hybrid
Später ansehen25.03.24 | Vollzeit | Neuchâtel | LHHDiscipline - Expert knowledge and understanding of stability ICH Guidelines (Q1A, Q5C) and associated policies, directives and guidance documents. A thorough knowledge of cGMP regulations as referenced in The Code of Federal Regulations (21CFR) and their specific application to stability programs
Später ansehen02.05.24 | Vollzeit | Michael Page InternationalApplicant - Good Knowledge/understanding of the EU Medical Device Regulation (EU) 2017/745 and European Medical Device Directive 93/42/EEC, Swiss Medical Device Regulation (MedDO) - Knowledge of Medical Device registration requirements in Europe and EUDAMED - Knowledge of product EU regulations
Später ansehen02.05.24 | Vollzeit | Michael Page InternationalTo other departments such as R&D, engineering and clinical affairs as needed The Successful Applicant - At least 8+ years of significant experience in regulatory affairs and quality compliance for medical devices according to EU regulation - A Bachelors or Master's degree in engineering, medical technology
Später ansehen02.05.24 | Vollzeit | Vaud | Michael Page InternationalWith vigilance, post-market surveillance and complaint management is required - - Knowledge of medical devices regulations (EU-MDR, ISO 13 485.) - - Audit experience is a plus - - Proficiency in French and English is mandatory. What's on Offer Great opportunity to join an amazing team and work on challenging
Später ansehen28.03.24 | Vollzeit | Lausanne | Randstad Schweiz AGThis position is integral to ensuring compliance with the EU Medical Device Regulation (EU MDR), Swiss Medical Devices Ordinance (Swiss MedDO), and relevant regulatory standards. Key responsibilities include - Supporting the Regulatory Surveillance process to monitor local EU regulations. - Participating
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