ZipRecruiter

Log In

1

Cqv Jobs (NOW HIRING)

CRB

CQV Engineer III

Raleigh, NC · On-site

The CQV Engineer II will develop and implement commissioning strategies, lead verification activities, and manage deliverables in alignment with project timelines and quality standards. The position ...

Centstone

Validation Engineer (CQV)

Lexington, KY · On-site

Title: Validation Engineer (CQV) Location: Lexington, KY Onsite Duration: Long term Positions: 3 Job Summary We are seeking a Validation Engineer to support Commissioning, Qualification, and ...

Stellent IT LLC

CQV Lead, Upstream

Holly Springs, NC · On-site

$88K - $116K/yr

Title - CQV Lead, Upstream Location: Holly Springs, North Carolina Visa - OPEN NEED LEAD CANDIDATE ONLY WITH LINKEDIN PROFILE seeking a highly experienced CQV (Commissioning, Qualification, and ...

Unicon Pharma Inc.

CQV Lead

Davie, FL · On-site

$45 - $50/hr

CQV Lead Duration: 9 + months (possible extension) Davie, FL Shift Schedule: Monday - Friday 8.00AM to 5.00PM Temp to perm: Possible based on openings and performance Core essential skill sets: 1. ...

CRB

CQV Engineer III

Raleigh, NC · On-site

The CQV Engineer II will develop and implement commissioning strategies, lead verification activities, and manage deliverables in alignment with project timelines and quality standards. The position ...

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

$79K - $104K/yr

CQV Lead Utilities Location: Netherlands Contract Type: Staff or Contract (12-month project) Job Summary We are seeking a CQV Lead - Utilities (Team Lead) to lead a team of engineers and specialists ...

Zifo

Principal CQV Consultant

Cary, NC · On-site

We are seeking a CQV Subject Matter Expert with a dual mandate: (1) Business Development / Pre‑Sales to shape opportunities, lead solutioning, and win new CQV programs; and (2) Delivery Oversight ...

Zifo

Principal CQV Consultant

Cary, NC · On-site

We are seeking a CQV Subject Matter Expert with a dual mandate: (1) Business Development / Pre-Sales to shape opportunities, lead solutioning, and win new CQV programs; and (2) Delivery Oversight to ...

Stark Pharma Solutions Inc

CQV Lead

Indianapolis, IN · On-site

Position: CQV Lead Location: Indiana Duration: Long Term Job Overview We are seeking an experienced CQV Lead to lead the coordination and execution of a large laboratory equipment deployment ...

Zifo

Principal CQV Consultant

Cary, NC · Hybrid

We are seeking a CQV Subject Matter Expert with a dual mandate: (1) Business Development / PreSales to shape opportunities, lead solutioning, and win new CQV programs; and (2) Delivery Oversight to ...

DPS Group

CQV Project Manager

Kenosha, WI · On-site

Arcadis is seeking a CQV PM to manage the entire program for our client in Wisconsin. Role accountabilities: • Refine Program Level Strategy for assigned workstream • Develop detailed activity ...

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 ...

next page

Showing results 1-20

All JobsCqv Jobs

Cqv information

See salary details

$91K

$120K

$147K

How much do cqv jobs pay per year?

As of Aug 12, 2026, the average yearly pay for cqv in the United States is $120,000.00, according to ZipRecruiter salary data. Most workers in this role earn between $108,000.00 and $131,500.00 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 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 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.

More about Cqv jobs
What cities are hiring for Cqv jobs? Cities with the most Cqv job openings:
What are the most commonly searched types of Cqv jobs? The most popular types of Cqv jobs are:
What states have the most Cqv jobs? States with the most job openings for Cqv jobs include:
What job categories do people searching Cqv jobs look for? The top searched job categories for Cqv jobs are:
Cqv jobs near you
Infographic showing various Cqv job openings in the United States as of August 2026, with employment types broken down into 100% Full Time. Highlights an 67% In-person, and 33% Remote job distribution, with an average salary of $120,000 per year, or $57.7 per hour.

CQV Engineer

Stark Pharma Solutions Inc

Philadelphia, PA • On-site

Contractor

Re-posted 22 days ago

Job description

Job Title: CQV Engineer
Location: Philadelphia, PA
Duration: Long Term Contract

Job Summary

We are seeking a highly motivated CQV (Commissioning, Qualification, and Validation) Engineer to support commissioning and qualification activities within a GMP-regulated biopharmaceutical manufacturing environment. The CQV Engineer will be responsible for supporting equipment startup, system qualification, utility validation, and process readiness activities to ensure compliance with FDA, cGMP, and industry standards.

The ideal candidate will work closely with Engineering, Manufacturing, Quality Assurance, Validation, and Automation teams to support capital projects, facility expansion initiatives, and manufacturing operations.

Key Responsibilities

  • Support commissioning and qualification activities for manufacturing equipment, process systems, utilities, and cleanroom environments
  • Develop and execute commissioning and qualification documentation including FAT, SAT, IQ, OQ, and PQ protocols
  • Perform equipment qualification for biopharmaceutical manufacturing systems including upstream and downstream process equipment
  • Support utility qualification activities involving HVAC, purified water systems, clean steam, compressed gases, and environmental monitoring systems
  • Coordinate system walkdowns, punch list management, and turnover documentation activities
  • Ensure all CQV activities comply with FDA, cGMP, GDP, and company quality standards
  • Collaborate with Automation, Engineering, Validation, and Quality teams during equipment installation, startup, and qualification phases
  • Assist with deviation investigations, change control activities, and CAPA implementation related to CQV processes
  • Review P&IDs, engineering drawings, SOPs, and technical documentation to support qualification activities
  • Support technology transfer and facility expansion projects within GMP manufacturing environments
  • Participate in internal audits and regulatory inspections by providing CQV documentation and technical support

Required Qualifications

  • Bachelor’s degree in Chemical Engineering, Mechanical Engineering, Biomedical Engineering, Biotechnology, or related technical field
  • 3+ years of CQV, validation, or qualification experience within biopharmaceutical, pharmaceutical, or regulated manufacturing industries
  • Strong understanding of cGMP, FDA regulations, GDP, and validation lifecycle practices
  • Experience executing IQ/OQ/PQ protocols and commissioning activities
  • Knowledge of clean utilities, HVAC systems, aseptic processing, and GMP facility operations
  • Familiarity with deviation management, CAPA, and change control systems
  • Ability to read and interpret P&IDs, engineering drawings, and technical specifications
  • Strong communication, technical writing, and problem-solving skills