Senior Project Manager, CQV - Remote

Overview

CRB is seeking a motivated individual for the role of CQV, Sr. Project Manager, responsible for leading and guiding cGMP services for Life Sciences clients, ensuring compliance and timely project delivery.

In Short

• Lead Commissioning, Qualification, and Validation (CQV) services.
• Ensure compliance with cGMP standards.
• Develop and formalize project packages for client approaches.
• Write and approve CQV documents according to regulatory standards.
• Support onsite and offsite CQV activities.
• Prepare and review technical reports.
• Provide training to client staff on CQV processes.
• Collaborate with market leaders for project delivery.
• Travel flexibility is required.
• Mentor and guide project teams in CQV services.

Requirements

• Bachelor’s Degree in Architecture, Engineering, or related field.
• 8+ years of experience in CQV and compliance.
• Strong knowledge of US and global regulatory requirements.
• Effective leadership and collaboration skills.
• Excellent organizational and communication skills.
• Experience with writing commissioning and validation protocols.
• Familiarity with statistical and risk assessment tools.
• Knowledge of FDA and EMEA regulations.
• Ability to manage multiple projects simultaneously.
• Strong interpersonal skills for effective communication.

Benefits

• Competitive salary and benefit package.
• Opportunities for professional development.
• Diverse and inclusive workplace.
• Flexible working arrangements.
• Commitment to corporate responsibility.