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Cqv 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

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

SupportFinity™

Market Director

Austin, TX · On-site

$140 - $200/hr

Develop and execute a comprehensive market strategy to position the firm as a leader in CQV services. * Identify emerging trends, client needs, and competitive landscapes to position service ...

Exyte GmbH

Ensure readiness for commissioning, qualification, and validation (CQV) processes Preconstruction & Operational Planning * Partner with commercial and preconstruction teams to support bid strategy ...

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See Texas salary details

$90.8K

$109.3K

$125.7K

How much do cqv jobs pay per year?

As of Aug 24, 2026, the average yearly pay for cqv in Texas is $109,267.00, according to ZipRecruiter salary data. Most workers in this role earn between $100,000.00 and $118,300.00 per year, depending on experience, location, and employer.

What is a CQV?

A CQV (Commissioning, Qualification, and Validation) job involves ensuring that equipment, systems, and processes in industries like pharmaceuticals and biotechnology meet regulatory and operational requirements. CQV professionals develop protocols, execute tests, and document compliance to ensure that facilities maintain safety and efficacy standards. They work closely with engineers, quality teams, and regulatory bodies to achieve validated systems.

What are the key skills and qualifications needed to thrive in the CQV position, and why are they important?

To thrive as a CQV (Commissioning, Qualification, and Validation) specialist, you need a strong background in engineering or life sciences, along with expertise in equipment qualification, validation protocols, and regulatory compliance. Familiarity with industry standards such as cGMP, FDA, and tools like validation software and document management systems is highly valuable. Strong analytical thinking, attention to detail, communication, and teamwork skills are crucial for ensuring project success and regulatory adherence. These skills ensure that pharmaceutical and biotech manufacturing processes meet rigorous quality standards and regulatory requirements.

What are the most common challenges faced by CQV specialists in the pharmaceutical industry?

CQV specialists in the pharmaceutical industry frequently encounter challenges such as managing tight project deadlines, adapting to evolving regulatory requirements, and coordinating across multi-disciplinary teams. Balancing compliance with operational efficiency demands a thorough understanding of documentation and attention to detail. Working with new or complex equipment can also present learning curves that require problem-solving and collaboration with engineering, production, and quality assurance teams. However, overcoming these challenges offers valuable experience and opportunities to build a robust skill set highly regarded in regulated industries.

What does a CQV engineer do?

A CQV (Commissioning, Qualification, and Validation) engineer is responsible for ensuring that manufacturing equipment, systems, and processes meet regulatory standards and quality requirements. They develop and execute validation protocols, perform testing, and document compliance to support product quality and safety in industries like pharmaceuticals and biotech.

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

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

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

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

Cqv jobs near you
Infographic showing various Cqv job openings in Texas as of August 2026, with employment types broken down into 86% Full Time, and 14% Contract. Highlights an 93% In-person, and 7% Remote job distribution, with an average salary of $109,267 per year, or $52.5 per hour.

CQV Engineer

Austin, TX • On-site

Stark Pharma Solutions Inc
See more jobs at Stark Pharma Solutions Incexternal

Contractor

Re-posted 19 days ago

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/