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 Documentation Reviewer will perform quality control activities which are relevant to his/her field of expertise and linked to assigned projects.

Responsibilities

• Review data (tables, forms, calculations, etc.) and reports, as assigned;
• Report findings to immediate supervisor to identify improvement opportunities;
• Help in implementing good quality control practices;
• Prepare the documentation to be transferred to the archives at the end of a project;
• Complete tasks in compliance with GLPs, driving documents, and current procedures.

• B.Sc. in Biosciences (or a related field).

• At least 1 year of equivalent experience / experience in the bio-pharmaceutical industry;
• Strong attention to detail;
• Knowledge of the GLP (Good Laboratory Practices) and GCP (Good Clinical Practices) regulations;
• Basic scientific knowledge in biochemistry and immunology;
• Bilingualism \xe2\x80\x93 Verbal and written in French and English;
• Knowledge of Microsoft Office programs, specifically Word and Excel;
• Good organizational skills and ability to prioritize;
• High degree of initiative, sense of urgency and flexibility.

CellCarta