04.06.24 | Vollzeit | Neuchâtel | Takeda PharmaceuticalQuality issues and implement corrective action plans Responsible for the effective management of the quality systems operating in his/her scope, including deviations (events), CAPA, batch review, change control, documentation, etc. Effectiveness is demonstrated through KPIs and management reviews in line
Später ansehen04.06.24 | 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 ansehen04.06.24 | Vollzeit | Neuchâtel | Takeda PharmaceuticalIn Neuchâtel (clinical phase III and commercial). Manage/prepare the necessary supportive documentation for regulatory submissions and for major change projects in Neuchâtel facility. Prepare/Review documentation for change controls, audit observations and regulatory agency questions. Support/Write
Später ansehen15.05.24 | Vollzeit | Boudry | INTERIMANAnd manage the "project cockpit" activities liaise with project leads and core teams consolidate documentation to deliver an integrated project reporting system (SCoPE) collect data - prepare reporting and correspondence. centralizing - orchestrating flow of information keeping key indicators and registers
Später ansehen14.05.24 | Vollzeit | Neuchâtel | RandstadGMP operations. He/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
Später ansehen13.05.24 | Vollzeit | Le Locle | RandstadAnd regulatory requirements 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 ansehen06.06.24 | Vollzeit | Neuchâtel | Michael Page InternationalJob Description - Develop and optimize HR processes. - Conduct reviews and updates of company regulations and internal documents. - Enhance workplace tools, such as competency management systems. - Lead the implementation of new HR software solutions. The Successful Applicant - Has at least 10 years
Später ansehen31.05.24 | Vollzeit | Bern | SYSMEX EUROPE GmbHAlternate alternate - Search Sysmex Europe Company Back Sysmex in EMEA Back Newsroom Back Contacts Back Products Back Diagnostics Back Life Science Back Integrated Solutions Back Services Back QC & Online Services Back Document Centre Back Academy Back Knowledge Centre Back Clinic & Laboratory
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 ansehen13.05.24 | 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
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