CQV Project Coordinator

Quanta Consultancy Services Ltd; North Carolina; On-site; USD 60,000 - 80,000; Full time

Job summary

An established industry player in pharmaceutical manufacturing is seeking a CQV Project Coordinator to support their new facility on the East Coast. This role offers a unique opportunity to lead project execution, coordinate multi-functional teams, and drive progress in a dynamic environment. The ideal candidate will have extensive experience in large-scale project coordination, strong communication skills, and a proactive attitude. Join a growing organization where your contributions will have a significant impact on the success of critical projects. If you thrive in collaborative settings and are eager to take on challenges, this position is perfect for you.

Qualifications

• 5+ years of experience in project coordination in a Pharm/cGMP environment.
• Strong communication and analytical skills are essential.

Responsibilities

• Manage schedule execution of selected work packages and ensure material readiness.
• Engage with PMs and other teams to align on best practices.

Skills

Project Coordination

Communication Skills

Analytical Skills

Problem-Solving

Collaboration

Proactive Attitude

Education

BA/BS in a related field

Tools

Lean / Six Sigma

Job description

CQV Project Coordinator - United States, North Carolina - 6-12 Months Contract

Our client, a global pharmaceutical manufacturing organization, is looking for a talented CQV Project Coordinator to join their expanding team. With continued organizational growth and considerable investment across their portfolio and capital programs, this is an extremely exciting opportunity to contribute towards their brand-new manufacturing facility on the East Coast of the United States.

Essential Duties and Responsibilities for this role include, but are not limited to:

• Focus will be on execution, staffing coordination, and area availability.
• Manage schedule execution of selected work packages (exact packages to be defined in coordination with the candidate).
• Drive and support the readiness and availability of materials for start-up and commissioning execution.
• Take on critical projects at the request of, and reporting to, the CQV leadership team.
• Actively engage with PMs/Coordinators in other teams to ensure alignment and sharing of best practices.
• Work with project troubleshooting and EHS teams for field coordination activities.
• Adopt the “one team approach” acting as a partner with our EPCM firm to remove hurdles.

Requirements:

• Extensive experience in project coordination on large-scale projects.
• Extensive experience in a relevant field / greenfield project experience.
• Experience liaising with other departments and building PMs/leads, ensuring streamlined FAT deliverables for all buildings.
• Willingness to take action in a proactive manner for driving progress.
• Strong communication skills.
• BA/BS in a related field and 5+ years’ experience successfully executing complex projects in a Pharm/cGMP environment.
• Experience coordinating field activities bringing together multi-functional teams in a dynamic yet visible way.
• Emphasis for this hire is on attitude (Positive Can-Do attitude) and strong collaboration.
• Excellent analytical and problem-solving capabilities.
• Lean / Six Sigma capabilities highly recommended.
• Acts with detail-driven ownership and follow-through.

If you are interested, please apply now for immediate consideration and further information.