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Pharmaceutical Validation Engineer Jobs in Kansas

Ceva Santé Animale

QA Validation Engineer

Lenexa, KS · On-site

QA Validation Engineer The success of a company depends on the passionate people we partner with ... Knowledge of pharmaceutical development, regulatory requirements, and manufacturing sciences with a ...

Ceva Santé Animale

QA Validation Engineer

Lenexa, KS

Knowledge of pharmaceutical development, regulatory requirements, and manufacturing sciences with a ... Ability to validate Excel file programming according to defined objectives * Proficiency in the use ...

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 ...

Icon plc

GMP Equipment Validation Specialist

Lenexa, KS · On-site

... engineering, or a related technical discipline. * At least one year of GMP equipment validation or qualification experience within the pharmaceutical, laboratory, or clinical research industry, with ...

ICON

GMP Equipment Validation Specialist

Lenexa, KS · On-site

... engineering, or a related technical discipline. * At least one year of GMP equipment validation or qualification experience within the pharmaceutical, laboratory, or clinical research industry, with ...

Argenta

Senior Plant Engineer

Shawnee, KS · On-site

$86K - $117K/yr

Reviews and approves standard operating procedures describing validation principles and activities ... Knowledge in Pharmaceutical regulations. * Bachelors degree in engineering discipline

Argenta

Senior Plant Engineer

Shawnee, KS · On-site

$86K - $117K/yr

Reviews and approves standard operating procedures describing validation principles and activities ... Knowledge in Pharmaceutical regulations. * Bachelors degree in engineering discipline

Argenta

Senior Plant Engineer

Shawnee, KS

$86K - $117K/yr

Reviews and approves standard operating procedures describing validation principles and activities ... Knowledge in Pharmaceutical regulations. * Bachelors degree in engineering discipline

Vytalize Health

Associate Data Engineer

Kansas City, KS · On-site

$110K - $132K/yr

You will learn to think about data quality metrics, testing, and validation as core ... Background in healthcare, pharmaceutical, or other regulated industry * Previous internship or ...

Elanco

Manufacturing Process Engineer

Elwood, KS

$71K - $94K/yr

... validation of major capital projects. This includes defining project scope, evaluating design ... Experience in pharmaceutical, biotechnology, or a related/relevant industry * Self-motivated team ...

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Pharmaceutical Validation Engineer information

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How much do pharmaceutical validation engineer jobs pay per hour?

As of Aug 17, 2026, the average hourly pay for pharmaceutical validation engineer in Kansas is $46.37, according to ZipRecruiter salary data. Most workers in this role earn between $35.14 and $56.39 per hour, depending on experience, location, and employer.

What does a pharmaceutical validation engineer do?

A Pharmaceutical Validation Engineer is responsible for ensuring that pharmaceutical manufacturing processes, equipment, and systems operate consistently and produce products that meet strict industry standards and regulatory requirements. They design, conduct, and document validation protocols for equipment, processes, and computer systems to confirm their accuracy and reliability. Their work is crucial for maintaining product quality, patient safety, and compliance with agencies such as the FDA and EMA.

What are the key skills and qualifications needed to thrive as a pharmaceutical validation engineer?

Pharmaceutical Validation Engineers need a solid background in engineering or life sciences, with knowledge of regulatory standards such as GMP and experience in validation protocols. Familiarity with technical tools like data loggers, validation software, and documentation systems, as well as certifications like Six Sigma or CQE, are commonly required. Excellent problem-solving, project management, and communication skills help them collaborate across departments and address compliance challenges. These skills and qualifications are crucial to ensure pharmaceutical processes meet regulatory requirements and maintain product quality and patient safety.

What are the most common challenges a pharmaceutical validation engineer faces when working on new equipment qualification projects?

Pharmaceutical Validation Engineers often encounter challenges such as tight project deadlines, managing complex documentation requirements, and ensuring compliance with stringent regulatory standards like FDA or EMA guidelines. Coordinating with cross-functional teams—including production, quality assurance, and maintenance—can also present hurdles, especially when integrating new equipment into existing processes. Proactive communication, strong organizational skills, and a thorough understanding of validation protocols are essential for overcoming these challenges and ensuring successful project outcomes.

What is the difference between Pharmaceutical Validation Engineer vs Quality Assurance Specialist?

AspectPharmaceutical Validation EngineerQuality Assurance Specialist
CertificationsGMP, Validation certificationsGMP, QA certifications
Work EnvironmentValidation labs, manufacturing plantsQuality control labs, production facilities
Primary FocusValidating equipment, processes, systemsEnsuring product quality, compliance
Industry UsageCommon in manufacturing and validation teamsWidespread across quality departments

While both roles work within the pharmaceutical industry and require GMP knowledge, the Pharmaceutical Validation Engineer primarily focuses on validating equipment and processes to ensure compliance, whereas the Quality Assurance Specialist concentrates on maintaining overall product quality and regulatory adherence.

What are popular job titles related to Pharmaceutical Validation Engineer jobs in Kansas?

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What job categories do people searching Pharmaceutical Validation Engineer jobs in Kansas look for?

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What cities in Kansas are hiring for Pharmaceutical Validation Engineer jobs?

Cities in Kansas with the most Pharmaceutical Validation Engineer job openings:

Pharmaceutical Validation Engineer jobs near you
Infographic showing various Pharmaceutical Validation Engineer job openings in Kansas as of August 2026, with employment types broken down into 90% Full Time, 4% Part Time, and 6% Contract. Highlights an 86% Physical, 5% Hybrid, and 9% Remote job distribution, with an average salary of $96,456 per year, or $46.4 per hour.

Validation Engineer

Pioneer Data Systems

Valley Falls, KS • On-site

Contractor

Re-posted 11 days ago

Job description

Job Description

Job Description:    POSITION SUMMARY
Validation engineer with experience in equipment, HVAC, utility and process qualification within a pharmaceutical industry. Previous plant experience is recommended. Background in aseptic processing, microbiology, environmental monitoring, chemistry, and production is recommended. The additional resources are requested for a total of fourteen (14) weeks starting in December 2017 and ending March 2018 to support Winter Shutdown changes. Hours can involve weekend or night shifts. Validation activities including writing system impact assessments, oversight of engineering during shutdown activities, execution of installation qualification, operational qualification, performance qualification, and summarizing qualification results/drafting qualification report summaries. The support staff must act in accordance with plant safety requirements, training and procedures.
POSITION RESPONSIBILITIES
Schedules and executes validations/qualifications per Standard Operating Procedures (SOPs) and regulatory guidelines.
Coordinates and communicates all testing with affected functional groups and evaluates test results.
Executes equipment, facility, utility and computer system, Automated Process Control validation studies to include protocol preparation, scheduling, protocol execution, analyze data and compose a final report.
Oversee and assist Engineers and/or Technicians with their assigned projects.
Provide technical expertise to define approaches and execution of system validation activities in accordance with cGMP, cGXP, CFR 21 Parts, 11, 210 and 211, EU Annex 11, ICH Q7, Q8 and Q9, and other applicable regulations, procedures and industry guidance.
Thorough understanding of risk based validation, industry standards and best practices for validation.
ORGANIZATIONAL RELATIONSHIPS
Will interact with Shutdown stakeholders: Engineering, Operations, Quality, Safety, Planning, Contractors, etc.
Weekly/daily meeting attendance as required.
Will participate in team led by Pfizer group leaders.
EDUCATION AND EXPERIENCE
Education: BS/BA degree in science, engineering, manufacturing technology or closely related field or combination of education and work experience
Experience: Recommended minimum of 4 years pharmaceutical validation experience
TECHNICAL SKILLS REQUIREMENTS
Knowledge of ICH and other regulatory guidelines; demonstrated ability to interpret and apply these guidelines to document writing
PHYSICAL POSITION REQUIREMENTS
Logistics: Requires contractor to be on-site weekly with travel home every other weekend
Must be able and willing to work beyond office hours which may include weekends.
Requires routine sitting, standing, walking, listening and talking
Acute mental and visual attention at all times
Handle multiple projects while managing frequent interruptions
Requires moderate lifting or moving up to 25 pounds (lbs

Additional Information

Anuj Mehta

732-947-3452

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