Deputy CQV Commissioning Manager for GMP Facilities

Bechtel Global Corporation; Houston (TX); On-site; USD 140,000 - 180,000; Full time

Job summary

Bechtel Global Corporation is seeking a Deputy Commissioning Manager to lead CQV activities for a cGMP pharmaceutical manufacturing facility. You will coordinate cross-discipline teams, ensure regulatory compliance, and drive operational readiness from Mechanical Completion through CQV and startup.

The role requires a strong background in cGMP, FDA/EU GMP, ISPE, and GAMP 5, with a focus on delivering safe, well-documented turnover packages and a right-first-time approach.

Qualifications

• Bachelor's degree in engineering, Construction Management, or related technical discipline.
• Professional Engineering (PE) registration preferred.
• Experience in industrial commissioning, startup, CQV, or facility operations.

Responsibilities

• Develop and implement commissioning strategies, procedures, and project execution plans.
• Coordinate day-to-day commissioning activities across process, mechanical, electrical, instrumentation, controls, utilities, and automation systems.
• Lead commissioning teams and discipline engineers to achieve project milestones safely and efficiently.
• Support development and management of commissioning schedules, resource plans, and system turnover priorities.
• Facilitate commissioning meetings and provide regular status updates to project leadership.
• CQV Integration: ensure alignment between Commissioning and CQV activities throughout project lifecycle.

Skills

Communication

Stakeholder management

Team leadership

Regulatory knowledge

CQV knowledge

Project management

Education

Bachelor's degree in engineering

PE registration preferred

Job description

Bechtel Global Corporation is seeking a Deputy Commissioning Manager to lead CQV activities for a cGMP pharmaceutical manufacturing facility. You will coordinate cross-discipline teams, ensure regulatory compliance, and drive operational readiness from Mechanical Completion through CQV and startup.

The role requires a strong background in cGMP, FDA/EU GMP, ISPE, and GAMP 5, with a focus on delivering safe, well-documented turnover packages and a right-first-time approach.