01.05.25 | Vollzeit | Eysins | JobLeads GmbH | CHF 150’000 - CHF 200’000 FDA and notified body site inspections. Interface with the FDA on Post-Market Activities site inspections, manufacturing complaints, additional information requests. - Assess resource needs to align the required level of quality support provided when needed with suitable competencies, including
Später ansehen27.04.25 | Vollzeit | Eysins | JobLeads GmbH | CHF 80’000 - CHF 100’000 And CP. Main Tasks - Maintain an up-to-date knowledge of cGxP regulation and applicable standards (especially in the US and EU) and implement requirements into locally applicable procedures (SOPs, Guiding Documents, Working Instructions, etc); - Support a GMP compliant transition of Programs from
Später ansehen19.04.25 | Vollzeit | Eysins | JobLeads GmbH | CHF 80’000 - CHF 100’000 Projects and work streams according to agreed deliverables, timelines, and budget. 4. Identifying and executing opportunities to build trust and partnerships with internal and external stakeholders (such as health authorities) leading to early engagement to accelerate development. 5. Working effectively
Später ansehen11.03.25 | Vollzeit | Eysins | JobLeads GmbH | CHF 80’000 - CHF 100’000 Requirements are met along the assigned project development work. - Keep up to date with the latest regulatory CMC requirements through regulatory surveillance. Coordinate timely implementation of any changes or new relevant laws or guidance; provide comments on new laws on behalf of FK-SBS through
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