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Cqv Engineer Jobs in Texas (NOW HIRING)

Stark Pharma Solutions Inc

CQV Engineer

Austin, TX · On-site

CQV Engineer Location: Austin, TX Duration: Long Term Position Overview We are seeking an experienced CQV Engineer to support Commissioning, Qualification, and Validation (CQV) activities for ...

CAI

CQV Engineer

Milano, TX · On-site

The CQV Engineer develops the documentation to support Commissioning, Qualifications, and Validation. These people are responsible for protocol writing and execution, field verification, and ...

CYNET SYSTEMS

Deputy Commissioning Manager CQV

Houston, TX · On-site

$76 - $99/hr

Bachelor's Degree in Engineering, Construction Management, or related technical discipline. * 10+ years of industrial commissioning, startup, CQV, or facility operations experience. * Minimum 5 years ...

New

sgsconsulting

Be Seen First

Commissioning Manager/ Validation Manager/CQV Manager

Houston, TX · On-site

$85 - $99/hr

Coordinate with engineering, construction, QA/QC, and operations teams to ensure a seamless ... Successful CQV integration and regulatory compliance. * Reduction of rework and duplicate testing.

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Cqv Engineer information

See Texas salary details

$30.7K

$83.1K

$132.3K

How much do cqv engineer jobs pay per year?

As of Sep 5, 2026, the average yearly pay for cqv engineer in Texas is $83,088.00, according to ZipRecruiter salary data. Most workers in this role earn between $62,000.00 and $101,600.00 per year, depending on experience, location, and employer.

What is a CQV engineer?

A CQV (Commissioning, Qualification, and Validation) Engineer is responsible for ensuring that equipment, systems, and processes within regulated industries, such as pharmaceuticals or biotechnology, meet regulatory and operational requirements. They develop and execute test protocols, troubleshoot issues, and document compliance with industry standards (e.g., FDA, GMP). Their role ensures that manufacturing facilities produce safe and effective products. CQV Engineers often collaborate with cross-functional teams, including quality, engineering, and operations.

What are the key skills and qualifications needed to thrive as a CQV engineer?

To thrive as a CQV (Commissioning, Qualification, and Validation) Engineer, you need a solid background in engineering principles, GMP regulations, and life sciences or pharmaceutical processes, often supported by a relevant degree. Familiarity with quality management systems, risk assessment tools, and software for documentation and validation such as TrackWise or Veeva is commonly required, and certifications like Six Sigma or CQV-specific credentials are valuable. Strong analytical thinking, attention to detail, effective communication, and collaboration skills set top performers apart. These competencies are essential to ensure compliance, project success, and seamless interaction with cross-functional teams in highly regulated environments.

What are some common challenges faced by CQV engineers in the pharmaceutical industry?

CQV Engineers in the pharmaceutical industry often encounter challenges such as managing strict timelines while ensuring full compliance with regulatory standards and adapting to evolving project requirements. They must coordinate with multiple departments including QA, production, and engineering to align project goals and documentation. Additionally, troubleshooting unexpected technical issues and staying updated with the latest industry guidelines can be demanding. However, overcoming these challenges is rewarding, as it directly contributes to the safe and effective delivery of life-saving products.

How much do CQV engineers make in the US?

CQV (Commissioning, Qualification, and Validation) engineers in the US typically earn between $80,000 and $130,000 annually, depending on experience, location, and industry. Senior or specialized engineers with certifications and extensive expertise can earn higher salaries, often exceeding $150,000. The role often requires knowledge of regulatory standards and validation tools.

What are popular job titles related to Cqv Engineer jobs in Texas?

For Cqv Engineer jobs in Texas, the most frequently searched job titles are:

What job categories do people searching Cqv Engineer jobs in Texas look for?

The top searched job categories for Cqv Engineer jobs in Texas are:

What cities in Texas are hiring for Cqv Engineer jobs?

Cities in Texas with the most Cqv Engineer job openings:

Cqv Engineer jobs near you
Infographic showing various Cqv Engineer job openings in Texas as of August 2026, with employment types broken down into 73% Full Time, and 27% Contract. Highlights an 100% In-person job distribution, with an average salary of $83,088 per year, or $39.9 per hour.

CQV Engineer

Stark Pharma Solutions Inc

Austin, TX • On-site

Contractor

Re-posted yesterday

Job description

Hi,

My name is Sravani Dasari from Stark Pharma Solutions Inc. We are hiring talent for our client and are currently working on a CQV Engineer position. Please send me your updated resume if you have relevant experience and are interested in this opportunity. The detailed job description is as follows.

Job Title: CQV Engineer
Location: Austin, TX
Duration: Long Term

Position Overview

We are seeking an experienced CQV Engineer to support Commissioning, Qualification, and Validation (CQV) activities for pharmaceutical and medical device manufacturing facilities. This role will focus on equipment qualification, utility validation, process validation, and ensuring compliance with GMP, FDA, and industry regulations. The ideal candidate will have extensive experience with IQ/OQ/PQ execution, validation documentation, deviation investigations, and cross-functional collaboration throughout the validation lifecycle.

Key Responsibilities

  • Execute Commissioning, Qualification, and Validation (CQV) activities for manufacturing equipment, utilities, facilities, and process systems.
  • Develop, review, approve, and execute Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) protocols and reports.
  • Perform equipment, utility, and system qualification activities in accordance with GMP, FDA, and company standards.
  • Support commissioning activities for new manufacturing equipment and facility expansions.
  • Ensure compliance with GMP, FDA regulations, cGMP guidelines, and internal quality management systems.
  • Analyze validation data, investigate deviations, support root cause analysis, and implement CAPA activities.
  • Collaborate with Engineering, Manufacturing, Validation, Quality Assurance, and Regulatory teams to ensure successful project execution.
  • Prepare, review, and maintain validation documentation, traceability matrices, SOPs, and technical reports.
  • Support internal audits, regulatory inspections, and client audits by providing validation documentation and technical expertise.
  • Drive continuous improvement initiatives to enhance validation processes, compliance, and operational efficiency.

Required Qualifications

  • Bachelor's degree in Mechanical Engineering, Chemical Engineering, Electrical Engineering, Biotechnology, Pharmaceutical Engineering, or a related engineering discipline.
  • 5+ years of experience in Commissioning, Qualification & Validation (CQV), Equipment Qualification, or Validation Engineering within the pharmaceutical, biotechnology, or medical device industry.
  • Strong hands-on experience with Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ).
  • Thorough understanding of GMP, cGMP, FDA regulations, ISPE guidelines, and validation lifecycle methodologies.
  • Experience preparing and executing validation protocols, reports, risk assessments, and technical documentation.
  • Hands-on experience with equipment commissioning, qualification, and process validation activities.
  • Knowledge of deviation management, change control, CAPA, and quality systems.
  • Strong analytical, troubleshooting, documentation, and problem-solving skills.
  • Excellent communication and interpersonal skills with the ability to work effectively in cross-functional teams.
  • Experience supporting regulatory audits and inspections is preferred.
  • Familiarity with clean utilities, HVAC systems, computerized systems validation (CSV), cleaning validation, or facility qualification is an added advantage.

I am actively connecting with professionals for current and upcoming opportunities. If you are open to exploring new roles or would like to stay informed about relevant positions, please send me your updated resume along with the best number and time to reach you.

Please follow Stark Pharma Solutions on LinkedIn for the latest job updates: https://www.linkedin.com/company/99455976/