4 of 4 TrackWise Jobs in the North of England

trend analysis, and risk-based approaches to assess QMS performance and drive continuous improvement. * Experience with at least one eQMS, such as Veeva, MasterControl, TrackWise, or equivalent. * Working knowledge of Good Documentation Practice and ALCOA+ data integrity principles. * Demonstrated ability to collaborate with cross-functional teams, foster support … Intermediate Microsoft Office skills, including Word, Excel, PowerPoint, and Outlook. Non-Essential Qualifications: * Working familiarity with two or more eQMS systems (e.g., MasterControl, Veeva, TrackWise) * Knowledge of computer systems validation (CSV) in the pharmaceutical/biopharma industry * Knowledge of the clinical trial/drug development process and/ ...

trend analysis, and risk-based approaches to assess QMS performance and drive continuous improvement. * Experience with at least one eQMS, such as Veeva, MasterControl, TrackWise, or equivalent. * Working knowledge of Good Documentation Practice and ALCOA+ data integrity principles. * Demonstrated ability to collaborate with cross-functional teams, foster support … Intermediate Microsoft Office skills, including Word, Excel, PowerPoint, and Outlook. Non-Essential Qualifications: * Working familiarity with two or more eQMS systems (e.g., MasterControl, Veeva, TrackWise) * Knowledge of computer systems validation (CSV) in the pharmaceutical/biopharma industry * Knowledge of the clinical trial/drug development process and/ ...

trend analysis, and risk-based approaches to assess QMS performance and drive continuous improvement. * Experience with at least one eQMS, such as Veeva, MasterControl, TrackWise, or equivalent. * Working knowledge of Good Documentation Practice and ALCOA+ data integrity principles. * Demonstrated ability to collaborate with cross-functional teams, foster support … Intermediate Microsoft Office skills, including Word, Excel, PowerPoint, and Outlook. Non-Essential Qualifications: * Working familiarity with two or more eQMS systems (e.g., MasterControl, Veeva, TrackWise) * Knowledge of computer systems validation (CSV) in the pharmaceutical/biopharma industry * Knowledge of the clinical trial/drug development process and/ ...

Scotland Opportunity: Do you currently work in a pharmaceutical or a related industry as a Master Data Specialist? Have you used JD Edwards or TrackWise? Are you detail-oriented and organized with a strong emphasis on data integrity, quality, and compliance? If yes then this is the role … approving Client Codes and Study Codes within Prisym under established procedures. Generating and approving Customer and Equipment Setup. Raising required Change Controls in Global TrackWise to support approved data revisions under established procedures. Performing assigned master data activities with attention to accuracy, completeness, and required turnaround times. Analysing ...