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Cqv Jobs in Indiana (NOW HIRING)

Amcor plc

Quality Assurance Engineer

Evansville, IN · On-site

Establish and develop gauges and/or measurement techniques for (new) molds during production and/or mold qualification for both metrological and physical properties. * Assist and/or coordinate CQV ...

Amcor

Quality Assurance Engineer

Evansville, IN · On-site

Establish and develop gauges and/or measurement techniques for (new) molds during production and/or mold qualification for both metrological and physical properties. * Assist and/or coordinate CQV ...

New

Heartland FPG

Sr. Project Engineer

Indianapolis, IN · On-site

$94K - $123K/yr

Skilled in developing DQ, FAT, CQV, Ramp up analysis, and other project management protocols. * PE or SrPE, plus PMP certification preferred. * Proficient in MS Office especially Excel and Microsoft ...

CAI

Validation Engineer

Bloomington, IN

$72K - $80K/yr

Key Responsibilities 1. Technical Responsibilities - Develop documentation for CQV activities - Write and execute protocols (field verification) - Develop summary reports at client sites 2. Areas of ...

CAI

Validation Engineer

Indianapolis, IN

$72K - $80K/yr

Key Responsibilities 1. Technical Responsibilities - Develop documentation for CQV activities - Write and execute protocols (field verification) - Develop summary reports at client sites 2. Areas of ...

CAI

Validation Engineer

Bloomington, IN · On-site

$72K - $80K/yr

Key Responsibilities 1. Technical Responsibilities - Develop documentation for CQV activities - Write and execute protocols (field verification) - Develop summary reports at client sites 2. Areas of ...

CAI

Validation Engineer

Indianapolis, IN · On-site

$72K - $80K/yr

Key Responsibilities 1. Technical Responsibilities - Develop documentation for CQV activities - Write and execute protocols (field verification) - Develop summary reports at client sites 2. Areas of ...

AtkinsRéalis

Lead Scheduler

Indianapolis, IN · On-site

Large capital construction project experience, preferred experience managing Pharma, Heavy Industrial and CQV projects. * Must be site based. * Must be able to understand float and how to tie scope.

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Showing results 41-60

All JobsCqv JobsCqv Jobs in Indiana

Cqv information

See Indiana salary details

$95.2K

$114.6K

$131.8K

How much do cqv jobs pay per year?

As of Aug 9, 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?

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 August 2026, with employment types broken down into 86% Full Time, 1% Part Time, and 13% Contract. Highlights an 92% Physical, 3% Hybrid, and 5% Remote job distribution, with an average salary of $114,567 per year, or $55.1 per hour.

Construction Quality Lead

Dcode Talent LLC

Indianapolis, IN • On-site

Contractor

Re-posted 21 days ago

Job description

Job Title: Construction Quality Lead  
Location: Indianapolis IN

Duration: 12+ months Contract

Description:

  • The Construction QA Lead will provide construction QA oversight and compliance verification.
  • This role will verify construction activities and installed systems with approved drawings, specs, validated submittals, GMP and RA standard.
  • This person will be the authority in the field to verify compliance, identity non-conformances and escalate issues impacting compliance. The role will be working with Mechanical, commissioning, System Turnover and Quality teams.

Day to Day:

  • Provide QA construction oversight across all disciplines to verify compliance
  • Verify contractor QA inspections/documentation are completed and in accordance with inspection testing plans
  • Identify construction non-conformances/ deviations from approved design or specs to escalate
  • Maintain records of field QA observation and communicate findings to project leadership
  • Verify readiness of systems for mechanical completion (inspections, test records, QA documents)
  • Support system walkdowns
  • Confirm QA document turnovers

Skills:

  • 10+ years of experience in construction quality oversight on large capital projects, preferably within pharmaceutical or GMP-regulated environments. Pharmaceutical experience.
  • Strong understanding of construction quality systems, inspection programs, and regulatory compliance requirements.
  • Experience with GMP construction environments and regulatory expectations for pharmaceutical facilities.
  • Familiarity with industry codes and standards including ASME, ASTM, NFPA, ISO, and applicable construction standards.
  • Experience reviewing and supporting Inspection and Test Plans (ITPs), non-conformance management, and quality documentation programs.
  • Strong understanding of Mechanical Completion, commissioning readiness, and turnover documentation requirements.
  • Ability to identify compliance risks and quality deviations within complex multi-disciplined construction environments.
  • Strong collaboration and communication skills with engineering teams, contractor organizations, CQV teams, and project leadership.

Degree: Engineering, Construction Management