14.06.24 | Vollzeit | Neuchâtel | Takeda PharmaceuticalOf internal management as well as across functions and business units. - Directs organization of 4 to 5 direct reports (Managers) and approximately 70 indirect headcount. Manages overall coaching, training, development and succession plans for the team. - Creates an environment that fosters lifelong learning
Später ansehen14.06.24 | Vollzeit | Neuchâtel | Takeda PharmaceuticalApplication is true to the best of my knowledge. Job Description About the role This position is within the Quality organization at the Neuchâtel facility and is intended for the Quality Assurance department. Within this position, QA Expert is responsible for Quality Assurance in the frame of activities all
Später ansehen13.06.24 | Vollzeit | Neuchâtel | Takeda PharmaceuticalAnd Manage communication and escalation to authorities and global functions. Responsible for maintaining site licenses, renewals and paper inspections and lead the program of Self-Inspection. Be the representative for Halal certification. Quality Governance Report on quality metrics and KPIs. Conduct
Später ansehen14.06.24 | Vollzeit | Neuchâtel | jobwinner.chProtocols and reports for validation documentation (such as process validation, test method validation, validation plan.) - Ensures that risk analysis activities (PFMEA) are performed and documented according to procedures and within the defined timeline - Organize meeting for risk analysis activities
Später ansehen14.06.24 | Vollzeit | Neuchâtel | jobwinner.chWrite protocols and reports for validation documentation (such as process validation, test method validation, validation plan.) - Ensures that risk analysis activities (PFMEA) are performed and documented according to procedures and within the defined timeline - Organize meeting for risk analysis
Später ansehen14.06.24 | Vollzeit | Neuchâtel | jobwinner.chAccording to procedures and within the defined timeline - Write protocols and reports for validation documentation (such as process validation, test method validation, validation plan.) - Ensures that risk analysis activities (PFMEA) are performed and documented according to procedures and within
Später ansehen12.06.24 | Vollzeit | Le Locle | Randstad Schweiz AGRequirements - Ensures that quality activities for validation of new processes/ products are performed and documented according to procedures and within the defined timeline - Write protocols and reports for validation documentation (such as process validation, test method validation, validation plan
Später ansehen12.06.24 | Vollzeit | Le Locle | Randstad Schweiz AGSystems, analyze and report results) - Manage site bioburden and dose audit programs - Carry out microbiology/HPLC laboratory investigation - Review and approve laboratory documents & sterilization certificates - Support equipment qualification affecting cleanliness/sterilization - Review and assess
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
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