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Cqv Jobs (NOW HIRING)

BlackDiamond Networks

CQV Lead

Indianapolis, IN · On-site

Commissioning & Qualification (CQV) Lead - Manufacturing Expansion Location: IN Start Date: July 15th Duration: 12+ Months Role: We are seeking an experienced Commissioning & Qualification (CQV) Lead ...

Algo Soft Solutions LLC

Pharma CQV Lead

Harvard, MA · On-site

We are seeking a Lead CQV Engineer / CQV Project Manager to serve as the primary CQV technical lead for project scope. This resource will own CQV execution strategy, deliverable approach, reviewer ...

Intellectt INC

CQV Engineer

Bloomington, IN · On-site

CQV Engineer Location: Bloomington, IN (Onsite) Experience: 10+ Years (Pharma Required) Job Summary: Seeking an experienced CQV Engineer with 10+ years of pharmaceutical industry experience to ...

Intellectt INC

CQV Engineer

Holly Springs, NC · On-site

CQV Engineer Location: Holly Springs, NC Duration: Long-Term Contract Summary: We are hiring experienced CQV Engineers for a large greenfield biopharmaceutical manufacturing project in Holly Springs ...

Intellectt INC

CQV Specialist

Framingham, MA · On-site

CQV Specialist Location: Framingham, MA (Onsite) Duration: 6+ months Job Summary: The CQV Specialist will support commissioning, qualification, and validation activities for utilities, equipment, and ...

Intellectt INC

CQV Specialist

Framingham, MA · On-site

CQV Specialist Location: Framingham, MA (Onsite) Duration: 6+ months Job Summary: The CQV Specialist will support commissioning, qualification, and validation activities for utilities, equipment, and ...

Intellectt INC

Sr. CQV Specialist

Raritan, NJ · On-site

Job Title: Sr. CQV Specialist Location: Raritan, NJ Duration: Longterm Job Summary Sr. CQV Specialist needed to manage and execute Commissioning, Qualification, and Validation activities in a cGMP ...

Intellectt INC

CQV Specialist

Framingham, MA · On-site

CQV Specialist Location: Framingham, MA (Onsite) Job Summary: The CQV Specialist will support commissioning, qualification, and validation activities for utilities, equipment, and systems in a ...

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 ...

Intellectt INC

CQV Engineer

Holly Springs, NC · On-site

CQV Engineer Location: Holly Springs, NC We are seeking an experienced CQV Engineer to support a large greenfield biopharmaceutical manufacturing project. The ideal candidate will have strong hands ...

Intellectt INC

CQV Consultant

Los Angeles, CA · On-site

This is Mahaboob from Intellectt INC; we've got an important CQV Consultant - Los Angeles, CA with one of our prestigious clients. Interested candidates can please send your updated resume at ...

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 ...

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 ...

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. ...

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 ...

Intellectt INC

CQV Engineer

Holly Springs, NC · On-site

CQV Engineer Location: Holly Springs, NC Job Summary Seeking experienced CQV Engineers to support a large greenfield biopharmaceutical manufacturing project. Candidates should have strong hands-on ...

Intellectt INC

Sr. CQV Specialist

Raritan, NJ · On-site

Job role: Sr. CQV Specialist Location: Raritan, NJ. Duration: Longterm Job Summary The Sr. CQV Specialist will support Commissioning, Qualification, and Validation activities in a cGMP Clinical and ...

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Cqv information

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How much do cqv jobs pay per year?

As of Jul 2, 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 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.

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Cqv jobs near you

CQV Lead

BlackDiamond Networks

Indianapolis, IN • On-site

Other

Posted 12 days ago

Job description

Title: Commissioning & Qualification (CQV) Lead – Manufacturing Expansion Location: IN Start Date: July 15th Duration: 12+ Months Role: We are seeking an experienced Commissioning & Qualification (CQV) Lead to support a large-scale pharmaceutical manufacturing expansion project within a GMP-regulated environment. This individual will serve as the primary CQV lead for a designated manufacturing, overseeing commissioning, qualification, startup readiness, and CQV execution activities from design through operational handoff. This is a highly visible leadership role responsible for driving CQV strategy, coordinating service providers, managing schedules, supporting FATs, overseeing qualification execution, and ensuring successful turnover of systems to operations.

The CQV Lead will work closely with Engineering, Construction, Automation, Manufacturing, Validation, Quality, and Operational Readiness teams throughout the project lifecycle. Key Responsibilities: • Serve as the primary CQV lead and point of contact for assigned manufacturing systems and facilities • Develop and execute commissioning, qualification, and startup strategies for GMP manufacturing environments • Manage CQV schedules, project milestones, critical path activities, and readiness metrics • Coordinate commissioning and qualification activities across Engineering, Construction, Quality, Validation, Automation, and Operations teams • Support Factory Acceptance Testing (FAT), Site Acceptance Testing (SAT), turnover, and startup activities • Oversee execution of IQ, OQ, PQ, commissioning protocols, and qualification documentation • Manage service providers, contractors, and CQV resources supporting project execution • Coordinate pre-commissioning activities including calibration, automation downloads, utility startup, and system readiness • Review and approve qualification documentation, protocols, test scripts, deviations, and final reports • Lead change management activities and support project governance reviews • Support operational readiness initiatives and system handover to end users • Drive issue resolution, punch-list closure, risk assessments, and continuous improvement initiatives • Ensure compliance with GMP regulations, validation standards, and project quality requirements Preferred Background: • 10+ years of CQV, validation, engineering, or startup experience within pharmaceutical, biotech, or GMP-regulated manufacturing environments • Strong experience supporting large-scale capital projects and facility expansions • Extensive knowledge of commissioning, qualification, validation, and startup methodologies • Experience leading cross-functional teams and managing multiple stakeholders • Hands-on experience with GMP manufacturing facilities, utilities, process equipment, and automation systems • Familiarity with electronic validation systems such as Kneat or similar platforms • Experience supporting API, peptide, biologics, or sterile manufacturing operations preferred • Strong understanding of regulatory requirements, GMP documentation practices, and 21 CFR Part 11 • Ability to manage schedules, project risks, and contractor performance in a fast-paced project environment Skills: • Commissioning, Qualification & Validation (CQV) • IQ / OQ / PQ Protocol Development & Execution • GMP Manufacturing Startup & Operational Readiness • FAT, SAT & System Turnover Management • Facilities, Utilities & Process Equipment Qualification • Change Management & Risk Assessment • Construction, Engineering & CQV Coordination • Capital Project & Facility Expansion Support • Validation Documentation & Regulatory Compliance • Cross-Functional Leadership & Stakeholder Management

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