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Cqv Jobs in Indiana (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 ...

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 ...

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Turner & Townsend

Senior Scheduler - CQV

Lebanon, IN · On-site

Senior CQV Scheduler to join our team to support scheduling as a project controls function on a large-scale project. The ideal individual will have a proven track record of successfully delivering ...

Novartis

Site Equipment & CQV Lead

Indianapolis, IN · On-site

$124K - $186K/yr

Act as Equipment & CQV Workstream Lead on a major site capital project with responsibility for commissioning, qualification and start-up of the GMP production equipment through to operational ...

Turner & Townsend

Senior Scheduler - CQV

Lebanon, IN · On-site

Turner & Townsend is seeking an experienced Senior CQV Scheduler to join our team to support scheduling as a project controls function on a large-scale project. The ideal individual will have a ...

CAI

CQV Senior Project Manager

Indianapolis, IN

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 ...

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CAI

CQV Senior Project Manager

Indianapolis, IN

$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

Senior Validation Engineer

Carmel, IN · On-site

Key Responsibilities CQV Execution & Safety - Perform Commissioning, Qualification, and Validation (CQV) activities with a strong focus on safety - Deliver C&Q activities in alignment with project ...

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CAI

Senior Validation Engineer

Bloomington, IN · On-site

$87K - $94K/yr

Key Responsibilities CQV Execution & Safety - Perform Commissioning, Qualification, and Validation (CQV) activities with a strong focus on safety - Deliver C&Q activities in alignment with project ...

CAI

Senior Validation Engineer

Bloomington, IN

Key Responsibilities CQV Execution & Safety - Perform Commissioning, Qualification, and Validation (CQV) activities with a strong focus on safety - Deliver C&Q activities in alignment with project ...

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Cqv information

See Indiana salary details

$95.2K

$114.6K

$131.8K

How much do cqv jobs pay per year?

As of Jul 2, 2026, the average yearly pay for cqv in Indiana is $114,567.00, according to ZipRecruiter salary data. Most workers in this role earn between $104,800.00 and $124,100.00 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 Indiana? For Cqv jobs in Indiana, the most frequently searched job titles are:
What job categories do people searching Cqv jobs in Indiana look for? The top searched job categories for Cqv jobs in Indiana are:
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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