24.09.24 | Vollzeit | Neuchâtel | Hays AGAnd relevant to your skills and experience. Description - Responsible for supporting commercial manufacturing performance at the external manufacturing site - Represents MS&T external manufacturing team to provide technical support to the biological drug substance tech transfer process including deviation
Später ansehen22.09.24 | Vollzeit | Neuchâtel | Hays AGAnd relevant to your skills and experience. Description Responsible for supporting commercial manufacturing performance at the external manufacturing site Represents MS&T external manufacturing team to provide technical support to the biological drug substance tech transfer process including deviation
Später ansehen22.09.24 | Vollzeit | Neuchâtel | Hays AGAnd relevant to your skills and experience. Description • Responsible for supporting commercial manufacturing performance at the external manufacturing site • Represents MS&T external manufacturing team to provide technical support to the biological drug substance tech transfer process including deviation
Später ansehen23.09.24 | Vollzeit | Couvet | JobLeads GmbH | CHF 80’000 - CHF 100’000 Of the Site RP for the following quality processes activities under his/her responsibility. - Release of batches as RP deputy. - Close out of Critical Complaints. - Approval of Complaints Extension Requests when an escalated approval is required. - Approval of Investigation Reports/Notifications sent
Später ansehen22.09.24 | Vollzeit | Couvet | JobLeads GmbH | CHF 80’000 - CHF 100’000 Of the Site RP for the following quality processes activities under his/her responsibility. - Release of batches as RP deputy. - Close out of Critical Complaints. - Approval of Complaints Extension Requests when escalated approval is required. - Approval of Investigation Reports/Notifications sent to Health
Später ansehen16.09.24 | Vollzeit | Couvet | JobLeads GmbH | CHF 80’000 - CHF 100’000 Requirements. - Demonstrated experience in Regulatory strategies and tactics. - Strong knowledge of all phases from the global drug development process and clinical trial data flow up to analytical/technology transfer to manufacturing/testing site and product launches. - Solid understanding of Oral Solid
Später ansehen15.09.24 | Vollzeit | Boudry | JobLeads GmbH | CHF 80’000 - CHF 100’000 To establish efficient and optimized processes and structures. Key Duties and Responsibilities 1. ExM Quality Project Process & Governance - Support the development, implementation and maintenance of an integrated ExM governance model and forum, aligned with global and local partner functions/forums
Später ansehen15.09.24 | Vollzeit | St-Sulpice (NE) | JobLeads GmbH | CHF 125’000 - CHF 150’000 And clinical studies. - provide leadership for Design Controls compliance and maintenance of Design History Files. - Contribute to and establish product development policies such as the Quality Management System and ensure adherence to it during the design and development processes. - Identify and manage
Später ansehen25.08.24 | Vollzeit | Neuchâtel | JobLeads GmbH | CHF 80’000 - CHF 100’000 Knowledge in SW development and verification tools on PC and embedded systems - Proven experience in Signal processing and control technique - Modelling and simulation of electrochemical storage systems - Experience in Design and implementation of estimation and optimization algorithms - Knowledge
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