...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 in computer system projects: Determine the validation approach and writing of validation plans and reports Coaching of Project engineers in validation Executing functional risks analysis Re...
...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...
...validation in computer system projects: Determine the validation approach and writing of validation plans and reports Coaching of Project engineers in validation Executing functional risks analysis Re...
...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...