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Bechtel Corporation seeks a Deputy Commissioning Manager in Houston to lead CQV activities for a cGMP pharmaceutical facility, ensuring safe commissioning and proper documentation. You will collaborate across Engineering, Construction, Operations, QA, and Validation to achieve on-time turnover.
Ideal candidates have 10+ years in commissioning or startup, pharma/biotech experience, and strong regulatory knowledge, with PE registration preferred and a focus on right‑first‑time delivery.
Requisition ID: 298861
Relocation Authorized: National - Family
Telework Type: Full-Time Office/Project
Work Location: Houston, TX
Since 1898, we have helped customers complete more than 25,000 projects in 160 countries on all seven continents that have created jobs, grown economies, improved the resiliency of the world's infrastructure, increased access to energy, resources, and vital services, and made the world a safer, cleaner place.
Differentiated by the quality of our people and our relentless drive to deliver the most successful outcomes, we align our capabilities to our customers' objectives to create a lasting positive impact. We serve the Infrastructure; Nuclear, Security & Environmental; Energy; Mining & Metals, and the Manufacturing and Technology markets. Our services span from initial planning and investment, through start-up and operations.
Core to Bechtel is our Vision, Values and Commitments . They are what we believe, what customers can expect, and how we deliver. Learn more about our extraordinary teams building inspiring projects in our Impact Report .
Bechtel Manufacturing and Technology (M&T) is an exciting and growing business that serves the increasing demand of EPC services for customers in the Data Centers, Semiconductor, Pharmaceutical and Electric Vehicle (batteries, charging infrastructure, and production), markets.
M&T strives to exceed our customer objectives through utilizing our agility, innovative technologies, and world class talent. M&T will solve the industries toughest challenges, building both our company and the world for the future.
Headquartered in the U.S. with employees in various states, M&T also has colleagues in the United Kingdom, India, and other locations while we actively pursue exciting opportunities in other parts of the world. We are looking for talented people to join our team that are passionate about making a difference and contributing to historical projects that will have a lasting impact on society.
The Commissioning Manager supports 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 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.
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: Is effective at adapting their 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. Ensure 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. It is focused on creating a long term fix rather than a short-term solution.
Role Model: Contributes to the Bechtel culture by inspiring and motivating others through their positive approach and attitude. Comes to work determined to do a good job, for themselves and for their team.
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Assist 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.
Bachelor's Degree in Engineering, Construction Management, or related technical discipline. 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 ($200M+ preferred).
Experience with commissioning through qualification and operational readiness phases.
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 owner’s goals, needs, and expectations for building operation and function; identifies the Commissioning responsibilities.
Demonstrated background working with multidisciplinary teams.
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)
The Deputy Commissioning Manager will be measured by:
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.
For decades, Bechtel has worked to inspire the next generation of employees and beyond! Because our teams face some of the world's toughest challenges, we offer robust benefits to ensure our people thrive. Whether it is advancing careers, delivering programs to enhance our culture, or providing time to recharge, Bechtel has the benefits to build a legacy of sustainable growth. Learn more at Bechtel Total Rewards
As a global company, Bechtel has long been home to a vibrant multitude of nationalities, cultures, ethnicities, and life experiences. This diversity has made us a more trusted partner, more effective problem solvers and innovators, and a more attractive destination for leading talent.
We are committed to being a company where every colleague feels that they belong-where colleagues feel part of "One Team," respected and rewarded for what they bring, supported in pursuing their goals, invested in our values and purpose, and treated equitably. Click here to learn more about the people who power our legacy.
Bechtel is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity and expression, age, national origin, disability, citizenship status (except as authorized by law), protected veteran status, genetic information, and any other characteristic protected by federal, state or local law. Applicants with a disability, who require a reasonable accommodation for any part of the application or hiring process, may e-mail their request to acesstmt@bechtel.com