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 strong 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:
• Robust 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.
#J-18808-Ljbffr

📌 Documentation Lead for Pharma Projects (Ontario)
🏢 Valspec
📍 Ontario