15.05.24 | Vollzeit | Neuchâtel | Takeda PharmaceuticalEmployment application is true to the best of my knowledge. Job Description About the role As Product Quality Expert (PQE) you will report directly to the Head of Quality Compliance & Systems and be responsible for compliance/regulatory activities related to biologic products. The PQE is the representative
Später ansehen15.05.24 | Vollzeit | Neuchâtel | Takeda PharmaceuticalMaintaining excellence in laboratory practices and enjoy working in a collaborative environment, this role is perfect for you. How you will contribute You will ensure that all in-process samples, raw material and final products are analyzed in accordance with SOPs and regulatory requirements to applicable
Später ansehen15.05.24 | Vollzeit | Neuchâtel | Takeda PharmaceuticalLaboratories, Warehouse and Engineering/Maintenance/Validation departments as applicable. Ensure quality of information within systems and documentation in respect to current guidelines, compliance and regulatory requirements. Support and work in line with the “QA on the shopfloor” requirements (for example
Später ansehen15.05.24 | Vollzeit | Neuchâtel | Takeda PharmaceuticalThat the processes are effectively established and maintained. Additionally, you'll play a pivotal role in enhancing the overall site capability. Your expertise will be instrumental in enhancing site capabilities, driving diversity, and fostering an inclusive work environment. How you will contribute Regulatory
Später ansehen15.05.24 | Vollzeit | Neuchâtel | LHHInvestigations related to potential quality issues and/or deviations from standards. - Lead work activities involving Change Controls and CAPA’s. - Identify information regarding stability program that may impact lab capacity, product studies or regulatory commitments directly, escalate promptly to management
Später ansehen14.05.24 | Vollzeit | Neuchâtel | RM Group AGWithin quality systems to ensure compliance with standard procedures and regulatory requirements - Overseeing and approving engineering-controlled documentation revisions and requalifications of cleaning/sterilization processes - Performing assessments of change control from a Quality Engineering
Später ansehen14.05.24 | Vollzeit | Neuchâtel | Randstad Schweiz AGHe/she must ensure the quality of information reported within the various systems and documentation with respect to current guidelines, compliance and regulatory requirements. General information - Start date asap - Planned duration of employment 8 months - Workplace Neuchatel - Workload 100
Später ansehen08.05.24 | Vollzeit | Neuchâtel | RM Group AGAnd processes, ensuring alignment with regulatory standards and internal requirements - Executing validation activities, including IQ, OQ, PQ, test method validation, and process validation, utilizing appropriate tools and methodologies - Analyzing validation data and providing insights to optimizing product
Später ansehen16.11.23 | Vollzeit | Neuchâtel | Michael Page InternationalChange Management 2 - Compensation & Benefits 1 - Accounting, Audit & Advisory, Tax and Treasury 2 - Treasury 2 - Consultancy, Strategy & Change 2 - Consulting 2 - Logistics, Procurement & Supply Chain 2 - Operational Excellence 1 - Supply Chain Management 1 - Legal 1 - Regulatory & Compliance 1 - Public
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