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Senior Validation Engineer Jobs in Indiana (NOW HIRING)

You will work closely with data scientists, MLOps engineers, system owners, risk stakeholders, and ... Experience leading small teams or workstreams and interfacing directly with senior stakeholders ...

You will work closely with data scientists, MLOps engineers, system owners, risk stakeholders, and ... Experience leading small teams or workstreams and interfacing directly with senior stakeholders ...

Our client is seeking a Senior CSV Validation Specialist dedicated to Building Management System ... The role supports the Site Automation Engineering organization and works closely with automation ...

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Senior Validation Engineer information

See Indiana salary details

$33

$61

$94

How much do senior validation engineer jobs pay per hour?

As of Jul 15, 2026, the average hourly pay for senior validation engineer in Indiana is $61.64, according to ZipRecruiter salary data. Most workers in this role earn between $49.18 and $70.00 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Senior Validation Engineer, and why are they important?

To thrive as a Senior Validation Engineer, you need a solid background in engineering, quality assurance, and regulatory compliance, typically supported by a relevant degree and experience in validation within regulated industries. Familiarity with validation protocols (IQ, OQ, PQ), statistical analysis tools, and systems like FDA 21 CFR Part 11 is crucial. Strong problem-solving, attention to detail, and effective communication skills help ensure successful project outcomes and cross-functional collaboration. These skills and qualifications are essential to maintain product quality, meet regulatory standards, and drive continuous improvement.

What does a Senior Validation Engineer do?

A Senior Validation Engineer is responsible for ensuring that products, systems, or processes meet regulatory standards and function as intended. They develop and execute validation protocols, analyze test data, and document results to confirm compliance with industry and company standards. Senior Validation Engineers often lead validation projects, collaborate with cross-functional teams, and mentor junior staff. Their work is critical in industries like pharmaceuticals, biotechnology, and manufacturing, where product safety and efficacy are essential.

What are some typical challenges faced by Senior Validation Engineers when leading validation projects?

Senior Validation Engineers often encounter challenges such as managing tight project timelines, ensuring compliance with evolving regulatory standards, and coordinating cross-functional teams. Balancing the needs of production, quality assurance, and regulatory affairs requires strong communication and project management skills. Additionally, troubleshooting unexpected validation failures and documenting results thoroughly are key aspects that demand both technical expertise and attention to detail.

What is the difference between Senior Validation Engineer vs Validation Specialist?

AspectSenior Validation EngineerValidation Specialist
CredentialsBachelor's or Master's in Engineering, Life Sciences, or related fields; often with certifications like GxP or CSVSimilar educational background; certifications like GxP or CSV are common
Work EnvironmentDesigns and oversees validation protocols in manufacturing, biotech, or pharmaceutical settingsExecutes validation tasks, tests, and documentation in similar environments
Employer & IndustryPharmaceutical, biotech, medical device companiesSame industries, often working under validation teams
Search & ComparisonOften compared for experience level and responsibilitiesCommonly searched together for validation roles

The main difference is that a Senior Validation Engineer typically leads validation projects, designs protocols, and oversees validation activities, while a Validation Specialist focuses on executing validation tests and documentation. Both roles require similar credentials and work in comparable environments, but the Senior Validation Engineer has more responsibility for planning and oversight.

What are the most commonly searched types of Validation Engineer jobs in Indiana? The most popular types of Validation Engineer jobs in Indiana are:
What are popular job titles related to Senior Validation Engineer jobs in Indiana? For Senior Validation Engineer jobs in Indiana, the most frequently searched job titles are:
What cities in Indiana are hiring for Senior Validation Engineer jobs? Cities in Indiana with the most Senior Validation Engineer job openings:
Infographic showing various Senior Validation Engineer job openings in Indiana as of July 2026, with employment types broken down into 91% Full Time, 7% Part Time, and 2% Contract. Highlights an 87% Physical, 4% Hybrid, and 9% Remote job distribution, with an average salary of $128,201 per year, or $61.6 per hour.
Senior Quality Engineer, Validation

Senior Quality Engineer, Validation

Cardinal Health

Indianapolis, IN

$84K - $114K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 28 days ago


Cardinal Health rating

7.8

Company rating: 7.8 out of 10

Based on 329 frontline employees who took The Breakroom Quiz

132nd of 885 rated healthcare providers


Job description

At Cardinal Health, we're developing the innovative products and services that make healthcare safer and more productive. Join a growing, global company genuinely committed to making a difference for our customers and communities.

What a Sr. Quality Engineer contributes to Cardinal Health

  • Schedule, execute, and evaluate scientifically and statistically sound qualification experiments complying with all regulatory requirements.

  • Assure entire process and required inputs function in a consistent and repeatable manner, and comply with regulatory requirements, product license requirements, and policies affecting final product integrity. 

  • Coordinates schedules involving manufacturing equipment to maximize equipment utilization.

  • Prepares documentation dossiers on completed studies that summarize the experimental results, specifications, and conformance to defined acceptance criteria.

  • Provides technical support to various departments as needed.

  • Develops policies, programs, SOPs, and Quality standards to meet current industry, corporate Quality, and external Regulatory requirements.

Accountabilities

  • Conducts & develops validation and qualification protocols, projects and studies supporting manufacturing facility start-up and operation. Validation documentation to ensure products are manufactured in accordance with cGMP, pharmaceutical regulatory agencies, manufacturer, and Cardinal Health specifications/requirements.

  • Maintains close contact with various functions to assure effective communication on challenges and opportunities related to validation.

  • Provides technical support as needed.

  • Develops policies, programs, SOPs, and Quality standards to meet current industry, corporate Quality, and external Regulatory requirements regarding validation.

  • Supports the facility in internal and external regulatory inspections.

  • Works directly with management, contract customers, and/or contract engineers.

  • Maintain effectiveness of the Quality System components relevant to this position.

  • Works autonomously with minimal supervision.

  • Develops, maintains, and enforces Cardinal Health compliance standards.

  • Learns and carries out laboratory procedures or operate equipment as needed to perform qualification testing.

  • Performs other job duties as assigned.

Qualifications

  • Bachelor’s degree in Chemical Engineering, Mechanical Engineering, Chemistry, Metrology or related science field, or equivalent work experience preferred

  • 2 or more years of relevant work experience as a Validation Engineer, Quality Assurance Engineering, or Quality Validation Consultant working with 21 CFR 210, 211 in the FDA regulated industry (Pharmaceutical or Medical Device).   

  • Experience with equipment qualification, software validation, test method validation, and/or process validation.  

  • Validation and Technology Transfer process and experience with writing procedures/ reports and execution of laboratory test. 

  • Must be detail oriented, organized, able to multi-task, a self-starter, and self-motivated.  

  • Must be proficient in Microsoft Word and Microsoft Excel and possess strong technical writing skills.  

  • Preferred: Experience working with radiopharmaceuticals

Performance Expectations

  • Demonstrates a commitment to the organization’s mission, vision and values supporting organizational decisions and behaviors. Contributes to the development and implementation of systems and processes ensuring strategic goal attainment.

  • Works as part of a team with others and shows respect and values diversity toward others.

  • Demonstrates efforts to discovering, meeting and advocating for the customer’s needs.

  • Takes actions to continually improve quality and safety in daily work. Actively participates in improving work processes to meet and exceed expectations. Identifies opportunities for improvement based on process observations, outcome measures, and feedback.

  • Reports errors in a timely and appropriate manner. Takes initiative and is accountable for areas of responsibility meeting regulatory requirements including but not limited to maintaining required trainings as appropriate to position requirements.

  • The ability to act calmly and patiently when working under pressure and/conditions of stress. Maintains integrity, composure, communicates with honesty, transparency, clarity and promotes alternative perspectives.

What is expected of you and others at this level

  • Develops processes and procedures to implement functional strategies.

  • Role models Cardinal Health's high ethical standards and code of conduct.

  • Builds confidence and respect of others through a positive and energizing style.

  • Interprets internal/external business issues and adapts work priorities in own area.

  • Strives for operational excellence by continually challenging old methods or ways of thinking and taking responsible risks to maximize results; serves as a role model in innovative thinking and in focusing on quality within work.

  • Effectively solicits and explains difficult concepts and persuades others to adopt a point of view; states own point of view.

  • Responsible for being a culture champion by participating in the development, monitoring and sustainment of the culture that is an integral part of the Indy manufacturing site philosophy and vision. The incumbent is responsible for embracing and demonstrating the culture of energy, passion and positive atmosphere while delivering superb customer service.

Anticipated salary range: $68,500.00-$97,800.00

Bonus eligible: No

Benefits: Cardinal Health offers a wide variety of benefits and programs to support health and well-being.

  • Medical, dental and vision coverage

  • Paid time off plan

  • Health savings account (HSA)

  • 401k savings plan

  • Access to wages before pay day with myFlexPay

  • Flexible spending accounts (FSAs)

  • Short- and long-term disability coverage

  • Work-Life resources

  • Paid parental leave

  • Healthy lifestyle programs

Application window anticipated to close: 8/17/2026

*if interested in opportunity, please submit application as soon as possible.

The salary range listed is an estimate. Pay at Cardinal Health is determined by multiple factors including, but not limited to, a candidate’s geographical location, relevant education, experience and skills and an evaluation of internal pay equity.

Candidates who are back-to-work, people with disabilities, without a college degree, and Veterans are encouraged to apply.

Cardinal Health supports an inclusive workplace that values diversity of thought, experience and background. We celebrate the power of our differences to create better solutions for our customers by ensuring employees can be their authentic selves each day. Cardinal Health is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, ancestry, age, physical or mental disability, sex, sexual orientation, gender identity/expression, pregnancy, veteran status, marital status, creed, status with regard to public assistance, genetic status or any other status protected by federal, state or local law.


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About Cardinal Health

Sourced by ZipRecruiter

Cardinal Health Innovative Delivery Solutions With over 45 years of experience in helping hundreds of hospital and outpatient pharmacies, we provide access to best practice strategies and tactics to control costs, improve workflow and enhance safety. Cardinal Health Innovative Delivery Solutions is one of the largest employers of acute-care pharmacist in the United States. Cardinal Health is the employer of choice for pharmacists because we offer a variety of career opportunities in pharmacy leadership, clinical specialties, remote order entry, business management, medication therapy management and more.

Industry

Medical equipment and supplies manufacturing

Company size

10,000+ Employees

Headquarters location

Dublin, OH, US

Year founded

1971

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