QC Reviewer, Sample Management & SOPs

Altasciences Company; Laval; On-site; CAD 65,000 - 90,000; Full time

Benefits offered by this job

Training and development programs

Employee orientation bonus program

Annual performance reviews

Job summary

Altasciences is seeking a QC Reviewer in the Sample Management Department to perform quality control reviews of documentation and conduct internal audits to ensure regulatory compliance. The role includes drafting and revising SOPs for sample management and glass washing, as well as updating training materials.

The candidate should have a health sciences background with at least 3 years of experience, strong knowledge of FDA-GLP, GCP and TPD regulations, and be fluent in French and English.

Qualifications

• 3+ years of experience in health sciences or related field.
• In-depth knowledge of FDA-GLP, GCP and TPD regulations.
• Experience in medical/pharma field is an asset.
• Strong GLP/GCP focus and attention to detail.
• Bilingual in French and English.

Responsibilities

• Perform 100% quality control on documentation generated by the sample management team.
• Conduct audits within the team and write reports.
• Draft/revise SOPs for sample management and glass washing.
• Maintain and archive documentation and train materials.

Skills

Management

Organizational skills

Communication

Leadership

Decision making

Problem solving

Customer oriented

Bilingual French/English

Education

Health sciences degree or higher

Tools

Access

Outlook

MS-Office

Watson

Job description

Altasciences is seeking a QC Reviewer in the Sample Management Department to perform quality control reviews of documentation and conduct internal audits to ensure regulatory compliance. The role includes drafting and revising SOPs for sample management and glass washing, as well as updating training materials.

The candidate should have a health sciences background with at least 3 years of experience, strong knowledge of FDA-GLP, GCP and TPD regulations, and be fluent in French and English.