Lead CQ Documentation and IV Execution for Global Biopharma Projects

Take charge as a Documentation and IV Execution Lead, focusing on CQ documentation and compliance in a hybrid work environment. Utilize your 10+ years of quality assurance expertise to drive project success and stakeholder collaboration.

This role demands a seasoned leader in Quality Assurance with strong skills in qualification and validation, particularly in the Pharmaceutical Manufacturing sector. You will oversee lifecycle Documentation within the Kneat platform, managing project milestones and liaising with cross-functional teams. Your leadership will ensure adherence to design specifications, client requirements, and quality standards.

Key Responsibilities :

• Implement and support CQ-related Documentation management
• Manage lifecycle CQ Documentation in the Kneat platform
• Develop positive relationships with stakeholders and teams
• Ensure compliance with schedules and quality standards
• Oversee training programs and maintain records

Requirements :

• 10 years of Quality Assurance experience
• Strong knowledge in Qualification and Validation
• Bachelor's degree in a related field
• Experience training team members
• Fluent in English with communication skills

Drive your expertise in quality assurance and documentation management within dynamic biopharmaceutical projects, leading critical execution initiatives.

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