Job Description

About CellCarta

CellCarta is a leading provider of specialized precision medicine laboratory services to the biopharmaceutical industry. Leveraging its integrated analytical platforms in immunology, histopathology, proteomics, and genomics, as well as related specimen collection and logistics services, CellCarta supports the entire drug development cycle, from discovery to late-stage clinical trials. The company operates globally with over 1,000 employees in its 11 facilities located in Canada, USA, Belgium, Australia, and China.

Position Summary

The In-Life Documentation Reviewer will perform in-life review of experimental documentation in the laboratory based on approved driving documents and SOPs.

Responsibilities

• Reviews experimental documentation in real-time in the laboratory;
• Reviews data (tables, forms, calculations, etc.) and reports, as assigned;
• Reports findings to immediate supervisor to identify improvement opportunities;
• Helps in implementing good quality control practices;
• Works in collaboration with the study teams to deliver quality data on time;
• Trains personnel on QC review, as needed.

• B.Sc. in life sciences (or a related field).

• At least 1 year of equivalent experience in the bio-pharmaceutical industry;
• Knowledge of GLP and GCLP regulations;
• Strong attention to details;
• Excellent organizational skills and ability to prioritize;
• Basic scientific knowledge in biochemistry and immunology;
• High degree of initiative, sense of urgency and flexibility;
• Bilingualism - verbal and written French and English an asset.

CellCarta