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Commissioning Qualification Validation Cqv Jobs in Indiana

Stark Pharma Solutions Inc

CQV Lead

Indianapolis, IN · On-site

CQV Lead Location: Indiana Duration: Long Term Job Overview We are seeking an experienced CQV Lead ... Coordinate equipment installation, startup, commissioning, qualification, and validation activities.

CAI

Senior Validation Engineer

Bloomington, 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 ...

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 ...

CAI

Senior Validation Engineer

Indianapolis, 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 ...

CAI

Senior Validation Engineer

Bloomington, IN

$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

Indianapolis, IN

$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

Carmel, IN

$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

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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Commissioning Qualification Validation Cqv information

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$49

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How much do commissioning qualification validation cqv jobs pay per hour?

As of Aug 28, 2026, the average hourly pay for commissioning qualification validation cqv in Indiana is $49.48, according to ZipRecruiter salary data. Most workers in this role earn between $37.50 and $60.14 per hour, depending on experience, location, and employer.

What is a commissioning qualification validation (CQV) professional?

Commissioning, Qualification, and Validation (CQV) professionals are specialists who ensure that equipment, systems, and processes in industries like pharmaceuticals, biotechnology, and manufacturing meet regulatory standards and function as intended. They are responsible for planning, executing, and documenting activities that demonstrate compliance with quality and safety regulations. CQV experts play a critical role in bringing new facilities and systems into operation, guaranteeing that everything is tested and verified according to industry guidelines. Their work helps prevent failures, enhance product quality, and ensure patient or consumer safety.

What are some typical challenges faced by commissioning qualification validation (CQV) professionals during facility start-up projects?

CQV professionals often encounter challenges such as tight project timelines, evolving regulatory requirements, and coordination among cross-functional teams. During facility start-up, balancing documentation accuracy with rapid progress can be demanding, especially when unexpected technical issues arise. Additionally, aligning the expectations of engineering, quality assurance, and operations departments requires strong communication and adaptability. By proactively addressing these challenges, CQV professionals help ensure a smooth transition from construction to validated production.

What are the key skills and qualifications needed to thrive as a commissioning qualification validation (CQV) professional, and why are they important?

To excel as a CQV professional, you need a solid background in engineering or life sciences, comprehensive knowledge of Good Manufacturing Practice (GMP), and experience with commissioning and validation processes. Familiarity with industry-standard software like ValGenesis, TrackWise, and documentation management systems, as well as certifications such as ISPE CQV or Six Sigma, is often required. Attention to detail, strong problem-solving abilities, and effective communication are crucial soft skills in this field. These competencies ensure equipment and processes meet regulatory standards, guarantee product quality, and support successful project delivery in highly regulated industries.

What is the difference between Commissioning Qualification Validation Cqv vs Equipment Validation Specialist?

AspectCommissioning Qualification Validation CqvEquipment Validation Specialist
CredentialsGMP, FDA, or industry-specific certificationsGMP, FDA, or industry-specific certifications
Work EnvironmentPharmaceutical, biotech, or manufacturing facilities during project startupManufacturing or laboratory environments focusing on equipment performance
Employer & Industry UsageUsed in regulated industries for system and process validationUsed for validating individual equipment and systems

While both roles involve validation processes, Cqv focuses on the overall commissioning, qualification, and validation of systems and processes during facility startup. Equipment Validation Specialists primarily validate specific equipment performance. Both require similar certifications and work in regulated manufacturing environments, but their scope differs in focus and responsibilities.

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For Commissioning Qualification Validation Cqv jobs in Indiana, the most frequently searched job titles are:

What job categories do people searching Commissioning Qualification Validation Cqv jobs in Indiana look for?

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What cities in Indiana are hiring for Commissioning Qualification Validation Cqv jobs?

Cities in Indiana with the most Commissioning Qualification Validation Cqv job openings:

Commissioning Qualification Validation Cqv jobs near you

CQV Engineer - Commissioning, Qualification & Validation

Indianapolis, IN • On-site

Process Automation - Controls.Instruments.Validations, Inc.
See more jobs at Process Automation - Controls.Instruments.Validations, Inc.external

$70 - $90/hr

Other

Medical, Retirement, PTO

Posted 9 days ago

Job description

CQV Engineer (Commissioning, Qualification & Validation)

Location: Indianapolis, IN
Travel: Up to 40% domestic & international travel

Bring Critical Manufacturing Systems to Life

We bring advanced manufacturing to life by delivering world‑class automation, validation, and instrumentation solutions. Our teams solve complex challenges, support industry‑leading facilities, and make a measurable impact on critical manufacturing operations every day.

We are looking for a CQV Engineer to join our Indianapolis, IN team. In this position, you will support the commissioning, qualification, and validation of manufacturing systems, equipment, facilities, utilities, and automation systems within regulated pharmaceutical environments. You will work on high‑impact capital projects that help transform complex systems into operational, compliant, and production‑ready assets.

Responsibilities
  • Develop and drive completion of Commissioning & Qualification (C&Q) deliverables, including validation plans, risk assessments, project strategies, user requirements, functional specifications, design specifications, impact assessments, traceability matrices, test cases, engineering studies, and final summary reports.
  • Apply a strong understanding of commissioning and qualification principles to support project execution and regulatory compliance activities.
  • Support pharmaceutical capital projects for:
    • Active pharmaceutical ingredient (API) manufacturing equipment
    • Filling operations
    • Device assembly systems
    • Packaging equipment
    • Facilities and utilities
    • Automation systems
  • Participate in project review meetings, including design reviews, qualification reviews, testing strategy discussions, execution reviews, and project status meetings.
  • Develop, review, and maintain validation and qualification documentation within electronic lifecycle management systems.
  • Assess, document, and support change management activities resulting from design updates, deviations, and testing outcomes.
  • Participate in Factory Acceptance Testing (FAT) and Site Acceptance Testing (SAT) activities.
  • Complete required client training and site‑specific onboarding requirements.
  • Perform other duties as assigned.
Qualifications
  • Bachelor's degree in Biomedical or Chemical Engineering.
  • Experience with Commissioning & Qualification (C&Q) deliverables, CQV activities, validation documentation, or relevant academic/project experience.
  • Strong understanding of validation principles and deliverables, including requirements development, design, testing, and reporting.
  • Strong interpersonal, verbal, written, and presentation communication skills.
  • Highly motivated, results‑driven mindset with the ability to manage multiple priorities in a fast‑paced environment.
  • Demonstrated project management skills and the ability to independently drive assignments to completion.
  • Ability to travel up to 40% domestically and internationally.
Why Join PACIV
  • Work on pharmaceutical manufacturing and life sciences capital projects.
  • Gain hands‑on experience with commissioning, qualification, validation, FAT, and SAT activities.
  • Collaborate with experienced engineering, automation, and validation professionals.
  • Build expertise working with manufacturing systems, utilities, facilities, and automation technologies.
  • Contribute to projects that support critical manufacturing operations and production readiness.
Compensation & Benefits
  • Generous Paid Time Off: Vacation, Sick Leave, and Company Holidays
  • PACIV pays 90% of yearly health care premiums
  • Health Savings Account (HSA) with Company Contributions
  • 401(k) with Company Match up to 4% and immediate vesting with enrollment

Equal Opportunity Employer

PACIV is an Equal Opportunity Employer and considers all qualified applicants in accordance with applicable federal, state, and local employment laws. Employment is contingent upon successful completion of applicable pre‑employment requirements and verification of authorization to work in the United States.

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