Elevate pharmaceutical standards with a Lead Consultant role focusing on GMP expertise. Apply your skills in project management and compliance in a energetic, contract-based position.

Join the GMP Consulting team as a Lead/Senior Consultant in Quality Assurance. This six-month contract requires extensive knowledge in quality systems, deviation investigations, and auditing within the pharmaceutical industry. You will prioritize and execute compliance projects, ensuring that client needs are met systematically while navigating complex regulatory frameworks.

Key Responsibilities:
• Establish comprehensive project plans for quality initiatives
• Manage and prioritize compliance projects effectively
• Conduct critical assessments of documentation and data




• Communicate monthly project milestones to stakeholders
• Develop and review required project documentation

Requirements:
• Bachelor's degree in a related field
• 4-7 years of Quality Assurance experience
• Expertise in deviation investigations and change management
• Knowledge of batch record review and lot release
• Experience with Health Canada audits

Bring your quality assurance expertise to enhance compliance in the pharmaceutical industry as a Lead Consultant.
#J-18808-Ljbffr

📌 Lead Consultant in Quality Assurance (Ontario)
🏢 q&
📍 Ontario