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Cqv Jobs in Raleigh, NC (NOW HIRING)

CAI

CQV Senior Project Manager

Raleigh, NC · On-site

$120K - $175K/yr

The CQV Senior Project Manager is responsible for leading services delivered to life sciences clients in all aspects of CQV-project execution and capital project Operational Readiness. Skills and ...

CAI

CQV Senior Project Manager

Raleigh, NC

The CQV Senior Project Manager is responsible for leading services delivered to life sciences clients in all aspects of CQV-project execution and capital project Operational Readiness. Skills and ...

Valspec

Project Manager - North Carolina

Raleigh, NC

CQV Project Manager - Life Sciences (NC) 📍 Raleigh-Durham, NC About the Role We are hiring a CQV Project Manager to lead commissioning, qualification, and validation projects within pharmaceutical ...

Valspec

Project Manager - North Carolina

Raleigh, NC

CQV Project Manager - Life Sciences (NC) 📍 Raleigh-Durham, NC About the Role We are hiring a CQV Project Manager to lead commissioning, qualification, and validation projects within pharmaceutical ...

Intellectt INC

"cleaning validation"

Holly Springs, NC · On-site

Role:CQV Engineer - Cleaning Validation Location: Holly Springs, NC Key Responsibilities: * Execute and document cleaning validation protocols per FDA/ICH guidelines (ALCOA principles). * Apply ...

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Cqv information

See Raleigh, NC salary details

$87.2K

$115K

$140.9K

How much do cqv jobs pay per year?

As of Jul 2, 2026, the average yearly pay for cqv in Raleigh, NC is $115,026.00, according to ZipRecruiter salary data. Most workers in this role earn between $103,500.00 and $126,000.00 per year, depending on experience, location, and employer.

What is a CQV job?

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.

What are popular job titles related to Cqv jobs in Raleigh, NC? For Cqv jobs in Raleigh, NC, the most frequently searched job titles are:
What job categories do people searching Cqv jobs in Raleigh, NC look for? The top searched job categories for Cqv jobs in Raleigh, NC are:
What cities near Raleigh, NC are hiring for Cqv jobs? Cities near Raleigh, NC with the most Cqv job openings:
Cqv jobs near you
Infographic showing various Cqv job openings in Raleigh, NC as of June 2026, with employment types broken down into 84% Full Time, and 16% Contract. Highlights an 95% In-person, and 5% Hybrid job distribution, with an average salary of $115,026 per year, or $55.3 per hour.
6244 - CIP (Clean-in-Place) CQV Engineer / Lead Validation Engineer

6244 - CIP (Clean-in-Place) CQV Engineer / Lead Validation Engineer

Verista, Inc.

Apex, NC • On-site

Other

Posted 22 days ago

Job description

We are seeking a Clean-in-Place (CIP) CQV Engineer with hands-on experience overseeing the commissioning and qualification of Clean-In-Place (CIP) systems. This role ensures that all systems are designed, tested, and documented in alignment with project requirements and safety standards.

Clean-in-Place (CIP) CQV Engineer Responsibilities:CIP System Leadership
  • Serve as the commissioning and qualification (C&Q) lead for CIP systems (responsibilities described below).
  • Develop and optimize CIP cleaning cycles to meet operational and quality standards.
  • Supervise the safe introduction and handling of caustic solutions during cleaning cycle development.
C&Q Lead ResponsibilitiesCommissioning and Qualification Documentation
  • Gain a thorough understanding of system design by reviewing engineering documentation, P&IDs, and design specifications.
  • Develop User Requirement Specifications (URS) and Quality Risk Assessment for Equipment and Automated Systems (QRAES).
  • Engage with design engineers and SMEs to clarify system intent and operational requirements.
  • Ensure alignment with quality, automation, and engineering teams on critical parameters and documentation.
  • Create Commissioning Test Plans that translate design intent into testable steps.
  • Coordinate with the Automation Team to incorporate all automation functional testing.
  • Collaborate with SMEs to ensure system requirements are accurately reflected in test plans.
  • Develop Installation, Operational, and Qualification (IOQ) protocols.
  • Prepare and submit summary reports documenting commissioning and qualification activities.
System Ownership and Execution
  • Take custody of the system post-construction and maintain ownership through C&Q completion.
  • Perform Lockout/Tagout (LOTO) for system safety.
  • Conduct pre-startup safety checks and risk assessments.
  • Prepare daily pre-task plans and verify team readiness for safe execution.
  • Attend daily commissioning meetings to coordinate activities.
  • Execute commissioning and IOQ protocols.
  • Resolve issues arising during execution.
  • Participate in Factory Acceptance Tests (FATs) and Site Acceptance Tests (SATs) as required.
Requirements:
  • Bachelor's degree in Engineering, Biotechnology, Life Sciences, or a related technical discipline
  • 10+ years of role-specific experience
  • Experience supporting CQV activities within GMP-regulated pharmaceutical or biotechnology environments
  • Hands-on experience with CIP systems and automated cleaning processes
  • Strong understanding of CQV lifecycle documentation (IQ/OQ/PQ protocols and reports)
  • Ability to work independently while coordinating with cross-functional project teams
  • Strong technical documentation and communication skills
  • Experience using digital validation platforms such as Kneat
  • Experience supporting FAT/SAT, commissioning, and equipment startup
  • Familiarity with automated process systems and PLC-based equipment
  • Experience in biologics or large-scale biopharmaceutical manufacturing environments
  • Onsite job requirement in Apex, NC

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