Deputy Commissioning Manager CQV

Location: Houston TX

Onsite Flexibility: Onsite

• Position Type: Contract
• Contract Duration: 12 months
• Pay Rate: $76.75$99.61 / Hour (USD)
• Work Authorization: Applicants must be authorized to work for ANY employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.

The Deputy Commissioning Manager supports the Commissioning Manager in planning coordinating and executing all Commissioning Qualification and Validation (CQV) activities for a cGMP pharmaceutical manufacturing facility. The role ensures systems are safely commissioned thoroughly documented and transitioned to Qualification and Validation in compliance with regulatory requirements project procedures and client quality standards.

The Deputy Commissioning Manager serves as a key interface between Engineering Construction Operations Quality Assurance Validation Equipment Vendors and Project Management teams to ensure successful project delivery from Mechanical Completion through Operational Readiness.

This position is designated as part-time telework per the global telework policy and will require at least three days of in-person attendance per week at the assigned office or project. Weekly in-person schedules will be determined by the individual and their supervisor in consultation with functional or project leadership.

Commissioning Management

• Assist the Commissioning Manager in the development and implementation of 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 the project lifecycle.
• Support development of turnover strategies between Construction Commissioning CQV and Operations.
• Verify commissioning documentation supports Qualification requirements and minimizes duplicate testing.
• Participate in CQV planning sessions and readiness reviews.
• Coordinate with Validation teams to ensure documentation packages meet regulatory expectations.

cGMP Compliance

• Ensure all commissioning activities comply with:

- FDA cGMP requirements - EU GMP requirements - ISPE Baseline Guides - GAMP 5 principles - Good Documentation Practices (GDP)

• Support data integrity and controlled documentation processes.
• Promote a quality-by-design and right-first-time approach throughout project execution.

System Turnover & Mechanical Completion

• Support development and management of:

- System Boundary Drawings - System Turnover Packages (STPs) - Mechanical Completion Packages (MCPs) - Commissioning Turnover Packages

• Coordinate successful transition of systems from Construction to Commissioning and ultimately to CQV and Operations.
• Develop and maintain commissioning schedules checklists and test procedures.
• Develop and implement commissioning plans test scripts Energization Plans and acceptance criteria in alignment with project requirements.
• Review and interpret drawings P&ID diagrams control schematics and project specifications.
• Coordinate with engineering construction QA/QC and operations teams to ensure a seamless transition from construction to operations.
• Coordinate with Commissioning Team Design Engineers Construction teams vendors and owner representatives to resolve technical issues.

Performance Metrics

• Safe execution of commissioning activities.
• On-time system turnover and startup milestones.
• Successful CQV integration and regulatory compliance.
• Reduction of rework and duplicate testing.
• Quality and completeness of turnover documentation.
• Effective management of project risks and interfaces.
• Achievement of operational readiness and successful facility startup.

• Excellent communication and stakeholder engagement skills for coordination with engineering operations and client teams.
• Experience in Commissioning or a technical consulting field such as facility design engineering construction management or related area.
• Identifies owners goals needs and expectations for building operation and function; identifies the Commissioning responsibilities.
• Demonstrated background working with multidisciplinary teams.
• Collaborate: Actively seeks out others opinions and input and is open-minded to their views; challenges others appropriately and is also open to being challenged on their own views.
• Communicate: Effective at adapting communication style appropriately to their audience providing context and using the right tone and level of information.
• Customer Focus: Prioritizes the customer needs and puts these at the forefront of all interactions; ensures that others within their team maintain this same approach.
• Deliver: Demonstrates making well thought out timely decisions and prioritization that leads to successful outcomes; includes the right people at the right time.
• Problem Solve: Accurately assesses a situation to find the best solution or way of working in order to resolve the issues; focused on creating a long-term fix rather than a short-term solution.
• Role Model: Contributes to the culture by inspiring and motivating others through a positive approach and attitude; comes to work determined to do a good job for themselves and for their team.

Technical Knowledge Strong understanding of:

• cGMP Regulations
• FDA and EU GMP Requirements
• ISPE Baseline Guides
• GAMP 5
• CQV Methodologies
• Mechanical Completion Processes
• Turnover Management
• Process Utilities
• HVAC Systems
• Building Management Systems (BMS)
• Environmental Monitoring Systems (EMS)

• Bachelors Degree in Engineering Construction Management or related technical discipline required.
• Professional Engineering (PE) registration preferred.

• 10 years of industrial commissioning startup CQV or facility operations experience.
• Minimum 5 years of pharmaceutical biotechnology life sciences or regulated manufacturing experience.
• Demonstrated experience supporting large capital projects (preferred).
• Experience with commissioning through qualification and operational readiness phases.

• Medical Vision and Dental Insurance Plans
• 401k Retirement Fund

This privately held engineering procurement and construction organization has delivered more than 25000 infrastructure and industrial projects across 160 countries on all seven continents over more than 125 years of operation. Its project portfolio spans energy and industrial infrastructure nuclear and environmental remediation government services and mining and metals representing some of the most technically demanding and geographically diverse assignments in the industry. Clients include national governments global energy companies and the worlds largest public agencies and the organization employs civil and structural engineers project controls specialists procurement managers commissioning and CQV professionals and nuclear and environmental remediation experts across its global teams. With a Glassdoor rating of 4.0 stars from nearly 2500 employee reviews and 78 percent of employees recommending the company to a friend including a 4.0-star rating for career opportunities among the highest in its sector this organization offers engineers project managers and technical professionals work at a scale that is nearly impossible to find elsewhere.

GTT is a minority-owned staffing firm and a subsidiary of Chenega Corporation a Native American-owned company in Alaska. We highly value diverse and inclusive workplaces and support Fortune 500 organizations across banking financial services technology life sciences biotech utilities and retail sectors throughout the U.S. and Canada.

Job Number: 26-12982

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