1

Validation Manager Jobs in Rosenberg, TX (NOW HIRING)

Be Seen First

Commissioning Manager/ Deputy Commissioning Manager/CQV Manager/Validation Manager/Commissioning Superintendent/Commissioning Supervisor Duration: 12 Months Location: Houston, TX 77056/Chandler, AZ ...

This position reports to the Process Validation Manager and is part of the Technical Operations Department located in Fargo, ND and will be fully remote. In this role, you will have the opportunity ...

This position reports to the Process Validation Manager and is part of the Technical Operations Department located in Fargo, ND and will be fully remote. In this role, you will have the opportunity ...

Client- Haliburton FPGA Design & Validation Engineer (Oil & Gas Systems) Houston, TX, USA Long term ... Protocol Management: Develop and test custom and industry-standard communication bridges (e.g ...

Create and manage project timelines and deliverables. * Monitor and review Quality Management ... Validation, Equipment Maintenance, Manufacturing, Quality Control, New Hire Onboarding, external ...

This role supports system validation strategy, audit readiness, CAPA management, and risk-based compliance activities across regulated technology environments. This role helps clients address ...

This role supports system validation strategy, audit readiness, CAPA management, and risk-based compliance activities across regulated technology environments. This role helps clients address ...

This role supports system validation strategy, audit readiness, CAPA management, and risk-based compliance activities across regulated technology environments. This role helps clients address ...

High-Reliability Validation: Lead hardware-in-the-loop (HIL) testing in the lab to simulate harsh ... Protocol Management: Develop and test custom and industry-standard communication bridges (e.g ...

High-Reliability Validation: Lead hardware-in-the-loop (HIL) testing in the lab to simulate harsh ... Protocol Management: Develop and test custom and industry-standard communication bridges (e.g ...

next page

Showing results 1-20

Validation Manager information

See Rosenberg, TX salary details

$42.4K

$94.1K

$143.2K

How much do validation manager jobs pay per year?

As of Sep 8, 2026, the average yearly pay for validation manager in Rosenberg, TX is $94,060.00, according to ZipRecruiter salary data. Most workers in this role earn between $66,500.00 and $117,800.00 per year, depending on experience, location, and employer.

What is a validation manager?

A validation manager works in a manufacturing plant and oversees the proper operation of machinery and equipment. Your job duties include developing operational plans for the entire facility, identifying areas of process improvement, and scheduling periodic auditing reviews of the facility. The qualifications needed for a career as a validation manager include a bachelor’s degree in business, organizational theory, quality control, or a related field. You also need strong communication and computer skills and experience in a management position.

What are the key skills and qualifications needed to thrive as a validation manager, and why are they important?

To thrive as a Validation Manager, you need a strong background in quality assurance, regulatory compliance (such as FDA or EMA guidelines), and validation principles, usually supported by a degree in life sciences or engineering. Familiarity with validation protocols, risk management tools, and systems like GMP documentation platforms is essential. Leadership, attention to detail, and effective communication are crucial soft skills for managing teams and coordinating cross-functional projects. These skills and qualities ensure that products and processes consistently meet regulatory standards, reducing risks and ensuring compliance.

How does a validation manager typically collaborate with other departments during project execution?

Validation Managers frequently work cross-functionally with quality assurance, manufacturing, engineering, and regulatory teams to ensure all systems and processes meet required standards. Effective collaboration involves coordinating validation protocols, sharing critical documentation, and communicating status updates to keep projects on track. A Validation Manager often leads meetings to align stakeholders, addresses compliance concerns, and resolves issues swiftly to prevent delays. Building strong relationships across departments is essential for smooth validation processes and successful project outcomes.

What is the difference between Validation Manager vs Quality Assurance Specialist?

AspectValidation ManagerQuality Assurance Specialist
CertificationsGxP, ISO, or industry-specific validation certificationsISO, Six Sigma, or QA-related certifications
Work EnvironmentRegulated industries like pharmaceuticals, biotech, or medical devicesManufacturing, software, or service industries
Primary FocusEnsuring validation processes for equipment, systems, and processes meet standardsMonitoring and improving overall quality processes and compliance

The Validation Manager primarily oversees validation activities to ensure compliance with industry standards, focusing on equipment and process validation. In contrast, the Quality Assurance Specialist concentrates on maintaining overall quality standards across products and services. Both roles are essential for compliance but differ in scope and responsibilities.

What are popular job titles related to Validation Manager jobs in Rosenberg, TX?

For Validation Manager jobs in Rosenberg, TX, the most frequently searched job titles are:

What cities near Rosenberg, TX are hiring for Validation Manager jobs?

Cities near Rosenberg, TX with the most Validation Manager job openings:

Infographic showing various Validation Manager job openings in Rosenberg, TX as of August 2026, with employment types broken down into 84% Full Time, 14% Part Time, and 2% Contract. Highlights an 83% Physical, 2% Hybrid, and 15% Remote job distribution, with an average salary of $94,060 per year, or $45.2 per hour.

Commissioning Manager/ Validation Manager/CQV Manager

sgsconsulting

Houston, TX • On-site

$85 - $99/hr

Contractor

Posted 4 days ago

Be Seen First

After you apply to this job, you can share why you’re interested to jump to the top of the candidate list.


Job description

Role: Commissioning Manager/ Deputy Commissioning Manager/CQV Manager/Validation Manager/Commissioning Superintendent/Commissioning Supervisor

Duration: 12 Months

Location: Houston, TX 77056/Chandler, AZ 85224


Details:

· 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.

· 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 Client 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.

· "This position is designated as part-time telework per our 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"


Major Responsibilities:

· 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.



Education and Experience Requirements:

· Bachelor’s degree in engineering construction management or related technical discipline. Professional Engineering (PE) registration preferred.

o 10+ years of industrial commissioning, startup, CQV, or facility operations experience.

o Minimum 5 years of pharmaceutical, biotechnology, life sciences, or regulated manufacturing experience.

o Demonstrated experience supporting large capital projects ($200M+ preferred).

o Experience with commissioning through qualification and operational readiness phases.


Required Knowledge and Skills:

· Excellent communication and stakeholder engagement skills for coordination with engineering, operations, and client teams.

o Experience in Commissioning or a technical consulting field such as facility design, engineering, construction management or related area.

o Identifies owner’s goals, needs, and expectations for building operation and function; identifies the Commissioning responsibilities.

o 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.

Company Description

Software Galaxy Systems, LLC (SGS) is an award-winning Contingent Workforce Services firm providing a broad range of integrated suite of services through a global delivery platform. SGS brings innovative talent management strategies to empower its clients to stay focused on growth of their core competencies. SGS has developed a comprehensive process-oriented methodology to manage high-volume contingent labor, payroll services and SOW’s for today’s competitive landscape.

SGS is proud of the partnerships it has built with its clients, MSP’s, and employees which has allowed it to deliver unparalleled service to its wide-ranging customer base. SGS is a certified minority owned enterprise that provides innovative yet practical solutions, from concept through execution. We combine technology with strategy and aim to deliver results today that endure tomorrow. SGS’ client centric approach delivers unparalleled value with vastly responsive, streamlined and highly process oriented workforce solutions.

SGS has been awarded and acknowledged by leading MSP’s (i.e., KellyOCG, TAPFIN, Guidant Global, etc.) for its exemplary performance in the contingent workforce space.