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Cqv Jobs in Indiana (NOW HIRING)

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 ...

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 ...

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

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 ...

Syner-G

Sr. Project Manager

Lebanon, IN · On-site

Coordinate daily activities of CQV engineers, contractors, vendors, and third-party service providers to ensure successful project execution. * Develop and maintain integrated C&Q schedules aligned ...

Syner-G

Sr. Project Manager

Indianapolis, IN · On-site

Coordinate HVAC scope with construction, CQV, automation, facilities, and manufacturing teams * Oversee cleanroom implementation including airflow design, pressurization cascades, and environmental ...

CAI

Senior Validation Engineer

Carmel, 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 ...

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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 25, 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
Infographic showing various Cqv job openings in Indiana as of July 2026, with employment types broken down into 89% Full Time, 5% Part Time, and 6% Contract. Highlights an 90% Physical, 3% Hybrid, and 7% Remote job distribution, with an average salary of $114,567 per year, or $55.1 per hour.
CQV Engineer

CQV Engineer

Intellectt INC

Bloomington, IN • On-site

Contractor

Posted 12 days ago

Job description

Hello,

I hope you’re doing well.

My name is Vyshu, and I’m reaching out from Intellectt Inc. regarding an exciting contract opportunity for CQV Engineer based in Bloomington, IN with one of our prestigious clients.

I would love to connect and discuss this opportunity in more detail. Please feel free to share your updated resume at vyshnavi.t@intellectt.com

Job Title: 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 support a CDMO client in Bloomington, IN. The ideal candidate will have strong expertise in commissioning, qualification, and validation of large-scale manufacturing equipment.

Key Responsibilities:

  • Develop and execute CQV documentation (IQ/OQ/PQ protocols, reports).
  • Support commissioning and qualification of manufacturing equipment.
  • Work with fill/finish lines and lyophilizers.
  • Ensure compliance with GMP and regulatory standards.
  • Coordinate with cross-functional teams to meet project timelines.

Requirements:

  • 10+ years of CQV experience in pharmaceutical manufacturing.
  • Hands-on experience with fill/finish equipment and lyophilizers.
  • Strong documentation and execution skills.
  • CDMO experience preferred.

Thanks & Regards,
Vyshnavi
Recruiter
Intellectt Inc 
vyshnavi.t@intellectt.com
Direct: 732 204 6550
Desk number: 732 412 6999 - Ext: 225