25.04.24 | Vollzeit | Hanau | BioNTech SEGuidance and support to other IT staff in the domain Knowledge of data integrity, audit trails, and electronic signatures, and experience in implementing and validating regulatory compliance systems Ideally, you have a firm understanding of regulatory requirements, such as CLIA, CAP, and HIPAA Knowledge
Später ansehen25.04.24 | Vollzeit | Frankfurt am Main | BioNTech SEGuidance and support to other IT staff in the domain Knowledge of data integrity, audit trails, and electronic signatures, and experience in implementing and validating regulatory compliance systems Ideally, you have a firm understanding of regulatory requirements, such as CLIA, CAP, and HIPAA Knowledge
Später ansehen25.04.24 | Vollzeit | Kaiserslautern | BioNTech SEGuidance and support to other IT staff in the domain Knowledge of data integrity, audit trails, and electronic signatures, and experience in implementing and validating regulatory compliance systems Ideally, you have a firm understanding of regulatory requirements, such as CLIA, CAP, and HIPAA Knowledge
Später ansehen09.04.24 | Vollzeit | Offenbach am Main | BioNTech SECross-functional team with members from other disciplines Provide statistical guidance into clinical development plans, clinical study protocols, clinical study reports, regulatory submission documents, and publications ensuring accurate deliverables Perform and/or verify sample size calculations Lead
Später ansehen09.04.24 | Vollzeit | Kaiserslautern | BioNTech SECross-functional team with members from other disciplines Provide statistical guidance into clinical development plans, clinical study protocols, clinical study reports, regulatory submission documents, and publications ensuring accurate deliverables Perform and/or verify sample size calculations Lead
Später ansehen09.04.24 | Vollzeit | Mainz | BioNTech SECross-functional team with members from other disciplines Provide statistical guidance into clinical development plans, clinical study protocols, clinical study reports, regulatory submission documents, and publications ensuring accurate deliverables Perform and/or verify sample size calculations Lead
Später ansehen21.04.24 | Vollzeit | Rome (IL) | Reemtsma Cigarettenfabriken GmbHAnd manufacturing of innovative products, including brand quality upgrades, product maintenance, regulatory labelling changes, strategic supply chain, and cost-saving initiatives. Being based in either our Amsterdam, Warsaw, Radom, Tarnowo or Bristol office - This integral Product Realisation Project Manager role
Später ansehen24.03.24 | Vollzeit | Rome (PA) | Reemtsma Cigarettenfabriken GmbHIn all analytical techniques undertaken. Principle Accountabilities - Perform routine/non-routine analysis in a safe and timely manner, adhering to current ways of working e.g., GxP/GLP requirements. - Perform research and regulatory non-routine analysis in a safe and timely manner, always adhering
Später ansehen25.02.24 | Vollzeit | Rome (OR) | Reemtsma Cigarettenfabriken GmbHDrive and foster a culture of continuous improvement and best practice within the team and beyond to drive costs down while maintaining quality, drive capability gap analysis. - Control the NGP Approved Vendor List. - Awareness of evolving legislation and collaboration with the Regulatory team required
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