...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, GAMP, 21 CFR Part 11 and other related regulations. Proven experience as an independent validation proj... Universities, Coordination, Functional Support, GMP, Corporate Cu...
...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...
...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, GAMP, 21 CFR Part 11 and other related regulations. Proven experience as an independent validation proj... Universities, Coordination, Functional Support, GMP, Corporate Cu...
...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, collaborates closely with project stakeholders, and maintains a strong focus on quality. You will join an environment where technology, compliance, and teamwork go hand in ...
...validation and compliance.Qualifications:Bachelor or Master's degree in Engineering, pharmaceutical science, or a related field.Proven experience in Computer System Validation (CSV) within the life sc...
...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, collaborates closely with project stakeholders, and maintains a strong focus on quality. You will join an environment where technology, compliance, and teamwork go hand in ...
...validation and compliance.Qualifications:Bachelor or Master's degree in Engineering, pharmaceutical science, or a related field.Proven experience in Computer System Validation (CSV) within the life sc...