03.09.24 | Vollzeit | Montreux | Pharmaplan AGKnowledge of GMP regulations and industry standards with at least 5 years of relevant job experience. You have worked on pharmaceutical projects within the area of biopharmaceutical process (USP/DSP or support area) with disposable knowledge. You have work experience either within a pharmaceutical
Später ansehen03.09.24 | Vollzeit | Montreux | Pharmaplan AGKnowledge of GMP regulations and industry standards with at least 3 years of relevant job experience - You have worked on projects within the pharmaceutical area (formulation, fill & finish, wash and sterilization, freeze-drying) or biopharmaceutical (USP/DSP) process with disposable knowledge - You have
Später ansehen19.09.24 | Vollzeit | Aubonne | JobLeads GmbH | CHF 80’000 - CHF 100’000 For ensuring compliance and process support across six packaging lines. Your role The successful candidate will play a pivotal role in ensuring that all packaging operations adhere to Good Manufacturing Practice (GMP) requirements. You will be responsible for investigating deviations and complaints, defining
Später ansehen15.09.24 | Vollzeit | Lausanne | JobLeads GmbH | CHF 80’000 - CHF 100’000 From the early stages of the project. - Ensure adherence to Good Manufacturing Practices (GMP) and quality standards in the pharmaceutical industry. - Identify risks and propose solutions to ensure the reliability and efficiency of HVAC systems. About you - Engineering degree in HVAC, energy
Später ansehen15.09.24 | Vollzeit | Lausanne | JobLeads GmbH | CHF 80’000 - CHF 100’000 For the project. 5. Ensure compatibility with client's standards (GMP, GAMP5, etc.). About you 1. Academic degree(s) with a focus on engineering or any other related field. 2. 5 years of experience in engineering projects in the pharmaceutical, biotech, chemical, or similar industries. 3. Fluency in English
Später ansehen06.08.24 | Vollzeit | Clarens | Pharmaplan AGKnowledge of GMP regulations and industry standards with at least 5 years of relevant job experience. You have worked on pharmaceutical projects within the area of biopharmaceutical process (USP/DSP or support area) with disposable knowledge. You have work experience either within a pharmaceutical
Später ansehen06.08.24 | Vollzeit | Clarens | Pharmaplan AGSupport from proposal (scope definitions, cost calculations, staffing), project execution (reporting) until project handover to the client Contribute to Standards and Guidelines development on your area Your profile You have a life science or bio engineering graduation and have a solid knowledge of GMP
Später ansehen16.09.24 | Vollzeit | Yverdon-les-Bains | JobLeads GmbH | CHF 80’000 - CHF 100’000 Actions. - Contribute to all relevant audit inspections and ensure inspection readiness for the site. Ensure compliance with relevant regulatory requirements, GMP, and other industry standards. - Initiate, drive, and implement continuous improvement initiatives to optimize processes, enhance product
Später ansehen15.09.24 | Vollzeit | Corsier-sur-Vevey | JobLeads GmbH | CHF 80’000 - CHF 100’000 Or manufacturing environment, preferably in the pharmaceutical or biotech industry - Strong understanding of QC processes and regulatory requirements in a GMP environment - Proficient in MS Office and planning software (e.g., Microsoft Project, SAP, BINOCS, GLIMS) - Excellent organizational, communication
Später ansehen15.09.24 | Vollzeit | Lausanne | JobLeads GmbH | CHF 80’000 - CHF 100’000 Development best practices of embedded software and eHealth application. - Proven experience with the definition of Validation strategy. - Proven experience with the development of the validation environment on-premise, cloud or hybrid solutions. - Familiar with FDA, GMP, and ISO 13485. - Experience
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