...computer system validation, GAMP, 21 CFR Part 11 and other related regulations. Proven experience as an independent validation proj... Protocols, Universities, Functional Support, Pharmaceuticals, GMP...
...computer system validation, GAMP, 21 CFR Part 11 and other related regulations. Proven experience as an independent validation project leader in the pharmaceutical industry, preferably GMP GLP. SPECIF...
...computer system validation, GAMP, 21 CFR Part 11 and other related regulations. Proven experience as an independent validation project leader in the pharmaceutical industry, preferably GMP GLP. SPECIF...
...computer system validation, GAMP, 21 CFR Part 11 and other related regulations. Proven experience as an independent validation proj... Protocols, Universities, Functional Support, Pharmaceuticals, GMP...
...computer system validation, GAMP, 21 CFR Part 11 and other related regulations. Proven experience as an independent validation project leader in the pharmaceutical industry, preferably GMP GLP. SPECIF...
...computer system validation, GAMP, 21 CFR Part 11 and other related regulations. Proven experience as an independent validation project leader in the pharmaceutical industry, preferably GMP GLP. SPECIF...
...validation studies and documentation (protocols/reports) for computerized systems. Manage validation documentation through approval and implementation. Perform system validation where industry precede...
...Computer System Validation (CSV) with a passion for quality, compliance, and innovation in the pharmaceutical industry? At Prothya Biosolutions, we’re looking for a Global Lead IT CSV to drive validat...
...Validation Engineer, as part of the project Validation team, will be responsible for the timely validation of cleaning processes. This includes a large variety of CIP processes on the typical biopharm...
...Validation Engineer, as part of the project Validation team, will be responsible for the timely validation of cleaning processes. This includes a large variety of CIP processes on the typical biopharm...
...systems ( ERP, MES, ELN ) Validation & Compliance Develop and execute Computer System Validation (CSV)protocols ( IQ/OQ/PQ ) Ensure compliance with 21 CFR Part 11, GAMP 5, and Annex 11 Maintain audi...
...system and sub-system specifications, architectures, and interface requirements Contributing to system adaptation in collaboration with development and software teams Ensuring requirement traceability...
...systems Ensure and maintain the regulatory system Your tasks Validation and probation of the functional and technical specifications Design test plan: procedures, scenarios, components Organize and ex...
...systems. Prepare and execute integration and validation activities at different system levels. Configure and maintain integration environments and related tools. Contribute to test automation and inte...
...Computer System Validation (CSV) with a passion for quality, compliance, and innovation in the pharmaceutical industry? At Prothya Biosolutions, we’re looking for a Global Lead IT CSV to drive validat...