22.09.24 | Vollzeit | Lausanne | JobLeads GmbH | CHF 80’000 - CHF 100’000 For performing and/or overseeing the set-up, maintenance, control, cleaning, validation, and closure of clinical study databases, in compliance with Procedural Documents (e.g., Policies, Standard Operating Procedures (SOP), and regulatory guidelines). He/she works closely with Clinical Trial Managers
Später ansehen19.09.24 | Vollzeit | Aubonne | JobLeads GmbH | CHF 80’000 - CHF 100’000 Transparent communication style will encourage teamwork and support the development of all team members. Your profile - Proven experience in managerial roles within the pharmaceutical or packaging industry. - Higher education degree in pharmacy or a related field, or equivalent experience. - In-depth
Später ansehen17.09.24 | Vollzeit | Gland | JobLeads GmbH | CHF 80’000 - CHF 100’000 And storage solutions. - Implement and manage disaster recovery and business continuity plans. - Identify potential barriers to change and develop strategies to overcome them. - Ensure compliance with relevant regulations, standards, and best practices. - Oversee IT operational concerns, ensure efficiency
Später ansehen16.09.24 | Vollzeit | Lausanne | JobLeads GmbH | CHF 80’000 - CHF 100’000 Perform literature research - Write experimental plans and implement them - Document all results according to guidelines and present results to the team Clinical Research Activities - Perform clinical study site management/monitoring activities in compliance with ICH-GCP, Sponsor SOPs, Local Laws
Später ansehen16.09.24 | Vollzeit | Yverdon-les-Bains | JobLeads GmbH | CHF 80’000 - CHF 100’000 This position regularly works cross-functionally with Manufacturing, Quality, Logistics, Facilities, Drug Product Development, and Vendors. You have - Bachelor's Degree in Engineering, Chemistry, Pharmacy, or Natural Science. - Minimum 4-6 years of experience in the pharmaceutical industry. - Strong problem
Später ansehen15.09.24 | Vollzeit | Lausanne | JobLeads GmbH | CHF 80’000 - CHF 100’000 The QA Engineer CSV will ensure that all computerized systems are validated in accordance with regulatory requirements and industry standards, playing a crucial role in maintaining the quality and compliance of our operations. Main Responsibilities - Validation Management Lead and manage the validation
Später ansehen15.09.24 | Vollzeit | Corsier-sur-Vevey | JobLeads GmbH | CHF 80’000 - CHF 100’000 And managers to forecast activity volumes and plan resources accordingly - Monitor and report on schedule adherence and adjust to ensure alignment with high-level project timelines - Collaborate with cross-functional teams, including production, supply chain, and project management, to integrate QC planning
Später ansehen15.09.24 | Vollzeit | Lausanne | JobLeads GmbH | CHF 80’000 - CHF 100’000 And Qualification activities for HVAC systems in pharmaceutical facilities, including the development of IQ/OQ/PQ protocols. - Oversee functional testing, verifications, and inspections of HVAC systems to ensure proper operation and compliance with technical and regulatory specifications. - Collaborate closely
Später ansehen15.09.24 | Vollzeit | Lausanne | JobLeads GmbH | CHF 125’000 - CHF 150’000 Including at least 3 years within Clinical Quality Management System & Compliance. 3. Experience in managing and conducting GCP audits (CROs, TMF, Investigational Sites and CSR). 4. Excellence knowledge of GCP. Current and strong working knowledge of GCP, CFR Title 21 and regulatory guidance’s including
Später ansehen25.08.24 | Vollzeit | Lausanne | JobLeads GmbH | CHF 125’000 - CHF 150’000 Management System & Compliance - Experience in managing and conducting GCP audits (CROs, TMF, Investigational Sites and CSR) - Excellence knowledge of GCP. Current and strong working knowledge of GCP, CFR Title 21 and regulatory guidance's including, ICH quality, clinical, multidisciplinary guidance
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