ZipRecruiter

Log In

1

Pharmaceutical Validation Jobs in Indiana (NOW HIRING)

Genovice

Validation Engineer (Contract)

Indianapolis, IN · Hybrid

$80K - $150K/hr

Overview Our client, an innovative and fast-growing pharmaceutical manufacturing company, is seeking an experienced Equipment Validation Engineer to support validation efforts across its cGMP ...

next page

Showing results 1-20

All JobsPharmaceutical Validation JobsPharmaceutical Validation Jobs in Indiana

Pharmaceutical Validation information

See Indiana salary details

$21

$49

$74

How much do pharmaceutical validation jobs pay per hour?

As of Aug 1, 2026, the average hourly pay for pharmaceutical validation 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 the highest paying job in pharmaceuticals?

In pharmaceutical validation, senior roles such as Validation Director or Quality Assurance Director tend to be the highest paying, often earning six-figure salaries. These positions require extensive experience, leadership skills, and knowledge of regulatory standards like GMP and FDA requirements.

What are the 4 types of validation in pharma?

In pharmaceutical validation, the four main types are Installation Qualification (IQ), Operational Qualification (OQ), Performance Qualification (PQ), and Process Validation. These ensure that equipment, systems, and processes consistently produce quality products and meet regulatory standards, which is essential for validation specialists working in regulated environments. Proper documentation and adherence to guidelines like GMP are critical components of these validation types.

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 job?

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 the Pharmaceutical Validation position, 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.

How much does a validation engineer make?

A validation engineer in the pharmaceutical industry typically earns between $70,000 and $100,000 annually, depending on experience, location, and certifications. Salaries can vary based on the complexity of validation tasks and the company's size, with some roles offering additional benefits such as bonuses or overtime pay.

How to become a validation specialist?

To become a validation specialist in pharmaceuticals, candidates typically need a bachelor's degree in a science or engineering field, along with experience in quality assurance or manufacturing. Gaining knowledge of validation processes, regulatory requirements (such as GMP and FDA standards), and validation tools is essential. Certifications like ASQ Certified Quality Auditor or specific validation training can enhance job prospects.
What are the most commonly searched types of Pharmaceutical Validation jobs in Indiana? The most popular types of Pharmaceutical Validation jobs in Indiana are:
What are popular job titles related to Pharmaceutical Validation jobs in Indiana? For Pharmaceutical Validation jobs in Indiana, the most frequently searched job titles are:
What job categories do people searching Pharmaceutical Validation jobs in Indiana look for? The top searched job categories for Pharmaceutical Validation jobs in Indiana are:
Pharmaceutical Validation jobs near you
Infographic showing various Pharmaceutical Validation job openings in Indiana as of July 2026, with employment types broken down into 1% As Needed, 78% Full Time, 18% Part Time, and 3% Contract. Highlights an 91% Physical, 2% Hybrid, and 7% Remote job distribution, with an average salary of $102,914 per year, or $49.5 per hour.

CQV Engineer - Commissioning, Qualification & Validation

PACIV

Indianapolis, IN • On-site

Full-time

Medical, Retirement, PTO

Re-posted yesterday

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.
#LI-DNI

Powered by JazzHR

N6WHo2RaJP