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Pharmaceutical Validation Jobs (NOW HIRING)

Argenta

Validation Specialist

Shawnee, KS · On-site

Bachelor's degree in Engineering, Life Sciences, Pharmaceutical Sciences, or a closely related field, and 2 years of experience in pharmaceutical validation, quality systems, or related GMP-regulated ...

Argenta

Validation Specialist

Shawnee, KS · On-site

Bachelor's degree in Engineering, Life Sciences, Pharmaceutical Sciences, or a closely related field, and 2 years of experience in pharmaceutical validation, quality systems, or related GMP-regulated ...

Actalent

Qa/qc Inspector

Lebanon, IN

Apply pharmaceutical validation practices and validation protocols to inspection and documentation activities where applicable. * Utilize P&IDs and mechanical and piping documentation to verify ...

Actalent

Traveling Qa/qc Inspector

Saint Louis, MO

Apply pharmaceutical validation practices and validation protocols to inspection and documentation activities where applicable. * Utilize P&IDs and mechanical and piping documentation to verify ...

Actalent

Traveling Qa/qc Inspector

Lebanon, IN

Apply pharmaceutical validation practices and validation protocols to inspection and documentation activities where applicable. Utilize P&IDs and mechanical and piping documentation to verify ...

Actalent

Traveling Qa/qc Inspector

Lebanon, IN

Apply pharmaceutical validation practices and validation protocols to inspection and documentation activities where applicable. Utilize P&IDs and mechanical and piping documentation to verify ...

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Pharmaceutical Validation information

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How much do pharmaceutical validation jobs pay per hour?

As of Aug 9, 2026, the average hourly pay for pharmaceutical validation in the United States is $52.00, according to ZipRecruiter salary data. Most workers in this role earn between $39.42 and $63.22 per hour, depending on experience, location, and employer.

What are some of the main challenges encountered in a pharmaceutical validation role?

One of the main challenges in Pharmaceutical Validation is staying updated with constantly evolving regulatory requirements and ensuring that all validation activities meet stringent compliance standards. Professionals often manage multiple concurrent projects, which requires effective prioritization, organization, and close coordination with cross-functional teams such as quality assurance, manufacturing, and engineering. Thorough documentation and meticulous attention to detail are essential, as even minor oversights can lead to compliance issues. However, overcoming these challenges provides valuable problem-solving experience and opportunities for advancement within quality assurance, regulatory affairs, or project management.

What is a pharmaceutical validation?

A Pharmaceutical Validation job involves ensuring that systems, equipment, and processes in the pharmaceutical industry meet regulatory and quality standards. Professionals in this role develop protocols, conduct testing, and document validation activities to ensure compliance with regulations like FDA, EU GMP, and ISO standards. They work with manufacturing processes, laboratory instruments, and software to verify that products are consistently produced and controlled according to required quality standards. This role is critical in maintaining drug safety, efficacy, and regulatory approval.

What are the key skills and qualifications needed to thrive in pharmaceutical validation, and why are they important?

To thrive in Pharmaceutical Validation, you need a strong background in pharmaceutical sciences or engineering, familiarity with regulatory guidelines (such as FDA, GMP, and ICH), and hands-on experience in validation protocols. Proficiency with validation lifecycle documentation tools, quality management systems (QMS), and specialized software like TrackWise or ValGenesis is essential. Attention to detail, analytical thinking, and excellent collaboration and communication skills are highly valued in this role. These competencies ensure that pharmaceutical processes, equipment, and systems meet strict quality standards, supporting product safety and regulatory compliance.

More about Pharmaceutical Validation jobs
What cities are hiring for Pharmaceutical Validation jobs? Cities with the most Pharmaceutical Validation job openings:
What are the most commonly searched types of Pharmaceutical Validation jobs? The most popular types of Pharmaceutical Validation jobs are:
What states have the most Pharmaceutical Validation jobs? States with the most job openings for Pharmaceutical Validation jobs include:
What job categories do people searching Pharmaceutical Validation jobs look for? The top searched job categories for Pharmaceutical Validation jobs are:
Pharmaceutical Validation jobs near you
Infographic showing various Pharmaceutical Validation job openings in the United States as of August 2026, with employment types broken down into 90% Full Time, 3% Part Time, and 7% Contract. Highlights an 87% Physical, 4% Hybrid, and 9% Remote job distribution, with an average salary of $108,152 per year, or $52 per hour.

CQV Engineer - Commissioning, Qualification & Validation

PACIV

Indianapolis, IN • On-site

Full-time

Medical, Retirement, PTO

Re-posted 10 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
PACIV stands for Process Automation, Controls, Instrumentation & Validation.
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
PACIV offers a competitive compensation package designed to support employee well-being and long-term financial success.
  • 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.
  • Direct-hire applicants only
  • C2C, 1099, and third-party agency submissions will not be considered.
  • PACIV does not sponsor H-1B visas or support H-1B transfers.
Also Known As
Commissioning Engineer, Qualification Engineer, Validation Engineer, C&Q Engineer, Commissioning & Qualification Engineer, Pharmaceutical Validation Engineer, GMP Validation Engineer, Capital Projects Validation Engineer.
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