Become a key player in Valspec's greenfield pharmaceutical program as a Documentation/Data Lead. You'll oversee critical documentation and data integrity efforts throughout project lifecycles. In this vital role, you will lead CQV documentation governance, ensuring proper management of turnover packages and readiness documentation.

Your expertise in data integrity, metrics, and compliance tracking will be essential. The position is designed for those with solid CSV management experience and a background in document review, resource planning, and quality oversight within large-scale pharma projects. Key Responsibilities:
Oversee turnover packages and manage readiness documentation
Ensure data integrity and uphold reporting standards
Support metrics, dashboards,



and compliance tracking
Manage CQV documentation across project lifecycles
Collaborate with project teams to uphold quality systems

Requirements:
Solid CSV management skills and governance experience
Proven background in quality systems and document review
Experience on large capital pharma or biotech projects
Knowledge of resource planning techniques
Ability to manage documentation effectively

Elevate your career at Valspec by ensuring that life-changing drugs reach those in need.

📌 Documentation Lead For Pharma Projects Toronto
🏢 Valspec
📍 Toronto