...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...
...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...
...System Engineer with a focus on simulation and algorithm to join a dynamic engineering team. In this role, you will contribute to the design, development, and integration of advanced systems used in b...
...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...
...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...
...System Engineer with a focus on simulation and algorithm to join a dynamic engineering team. In this role, you will contribute to the design, development, and integration of advanced systems used in b...
...system interfaces (ERP, LIMS, SCADA) using OPC, SQL, and web services.Support validation activities (URS, FDS, IQ/OQ/PQ).Troubleshoot and optimize MES performance and data integrity.Participate in Agi...
...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...
...system interfaces (ERP, LIMS, SCADA) using OPC, SQL, and web services.Support validation activities (URS, FDS, IQ/OQ/PQ).Troubleshoot and optimize MES performance and data integrity.Participate in Agi...
...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...