22.09.24 | Vollzeit | Solothurn | JobLeads GmbH | CHF 80’000 - CHF 100’000 Governance frameworks, compliance standards, and reporting requirements - Conducting project audits, tracking progress, and measuring success based on defined key performance indicators - Identifying areas of improvement in project methodologies, tools, and training - Working closely with project teams
Später ansehen22.09.24 | Vollzeit | Solothurn | JobLeads GmbH | CHF 80’000 - CHF 100’000 The lifecycle management of QC and MFG instruments and equipment. Responsibilities include, but are not limited to, directing the QC labs and MFG areas with respect to knowledge related to equipment maintenance, regulatory compliance, site procedures, and lifecycle for instrumentation. The position
Später ansehen21.09.24 | Vollzeit | Solothurn | JobLeads GmbH | CHF 80’000 - CHF 100’000 compliance and quality systems in the pharmaceutical industry. If you are experienced in QC equipment management and eager to work in a dynamic global team, apply now! #J-18808-Ljbffr
Später ansehen31.08.24 | Vollzeit | Olten | JobLeads GmbH | CHF 80’000 - CHF 100’000 For information security audits, ensuring compliance within your area of responsibility. - Support subsidiaries with information security queries during audits. - Deploy group-wide information security awareness campaigns. Requirements - Higher education (Bachelor's or Master's degree) in information security
Später ansehen14.08.24 | Vollzeit | Olten | JobLeads GmbH | CHF 80’000 - CHF 100’000 2. Defining and ensuring compliance with quality requirements for drug delivery systems and medical devices in development projects. 3. Ensuring the conformity of our products and product documentation over the entire product life cycle - focus on development and industrialization - Design Control
Später ansehen11.08.24 | Vollzeit | Olten | JobLeads GmbH | CHF 80’000 - CHF 100’000 Job Description Role - Interest in the development of complex (electronic, software and mechanic) medical devices - Defining and ensuring compliance with quality requirements for drug delivery systems and medical devices in development projects - Ensuring the conformity of our products and product
Später ansehen18.09.24 | Vollzeit | Solothurn | Randstad Schweiz AGAnd German. - Knowledge of regulatory compliance and quality systems in the pharmaceutical industry. If you are experienced in QC equipment management and eager to work in a dynamic global team, apply now
Später ansehen11.07.24 | Teilzeit | Solothurn | Ypsomed AGIn compliance with ISO 13485 and FDA Medical Device Design Control processes - Contribute to requirements definition, create design documentation and verification test plans - Participate in peer reviewing of the various hardware development artifacts - Support the verification team with HW related
Später ansehen30.08.22 | Vollzeit | Olten | Jobtic SAThe applications and thus ensuring their smooth operation. You support the team with your in-depth expertise and can assume professional leadership. Onboarding new projects is also one of your responsibilities. You also ensure compliance with the service level agreement and inform internal and external
Später ansehen11.11.19 | Vollzeit | Olten | PebEx AGApplikationssupport, Monitoring und Sicherstellen der Verfügbarkeit der Applikationen sowie der Compliance - Aufsetzen und Pflegen der Dokumentation Profil Kooperative, belastbare und verantwortungsbewusste Persönlichkeit- Engagierter und zuverlässiger Teamplayer mit einer methodischen Arbeitsweise - Abgeschlossene
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