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Full Time Validation Engineer Jobs (NOW HIRING)

Inteva Products

Senior Validation Engineer

Troy, MI · On-site

... Coordinate validation readiness activities across Program Management, Product Engineering ... Education Requirement Full-Time/Part-Time Full-Time Shift -not applicable- Location Inteva Products ...

Rivian

Validation Engineer - Powertrain

Plymouth, MI · On-site

$85K - $107K/yr

Define Engineering Requirements: Formulate clear validation methods and technical requirements ... Full-time employee coverage is effective on their first day of employment. Part-time employee ...

Rivian

Validation Engineer - Powertrain

Plymouth, MI · On-site

$85K - $107K/yr

Define Engineering Requirements: Formulate clear validation methods and technical requirements ... Full-time employee coverage is effective on their first day of employment. Part-time employee ...

Valspec

Process Validation Engineer

Raleigh, NC

Contract | Full-Time (40 Hours/Week) Duration: Approximately 9 Months Position Summary Our client is seeking an experienced Process Engineer to support process validation and Process Performance ...

Valspec

Process Validation Engineer

Durham, NC · On-site

Contract | Full-Time (40 Hours/Week) Duration: Approximately 9 Months Position Summary Our client is seeking an experienced Process Engineer to support process validation and Process Performance ...

Valspec

Process Validation Engineer

Sanford, NC · On-site

Contract | Full-Time (40 Hours/Week) Duration: Approximately 9 Months Position Summary Our client is seeking an experienced Process Engineer to support process validation and Process Performance ...

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How much do full time validation engineer jobs pay per hour?

As of Sep 1, 2026, the average hourly pay for full time validation engineer 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 is a full time validation engineer?

Full Time Validation Engineers are professionals who work to ensure that products, systems, or processes meet specified requirements and function as intended. They design and execute tests, analyze data, and document results to demonstrate compliance with regulatory standards and internal quality guidelines. Validation Engineers are commonly employed in industries such as pharmaceuticals, biotechnology, manufacturing, and electronics, where product safety and consistency are critical. Their role is crucial in preventing defects and ensuring that products are safe and effective for their intended use.

What are some common challenges faced by full time validation engineers, and how can they be addressed?

Full Time Validation Engineers often encounter challenges such as tight project deadlines, evolving regulatory requirements, and the need to coordinate with cross-functional teams. Managing documentation and ensuring thorough testing while maintaining compliance can also be demanding. To address these challenges, it's important to stay organized, communicate proactively with colleagues in quality assurance, manufacturing, and R&D, and keep up-to-date with industry standards and regulations. Leveraging project management tools and regular team meetings can help streamline validation activities and minimize potential bottlenecks.

What are the key skills and qualifications needed to thrive as a full time validation engineer, and why are they important?

To thrive as a Full Time Validation Engineer, you need a solid background in engineering principles, quality assurance, and validation processes, typically supported by a degree in engineering or a related field. Familiarity with industry standards (such as GMP or FDA regulations), data analysis tools, and validation software like ValGenesis or TrackWise is commonly required. Strong attention to detail, analytical thinking, and effective communication skills set top performers apart in this role. These capabilities ensure that products and processes consistently meet regulatory standards and quality expectations, which is critical for compliance and operational success.

What is the difference between Full Time Validation Engineer vs Validation Technician?

AspectFull Time Validation EngineerValidation Technician
CredentialsBachelor's in Engineering or related field, certifications like GxP or IQ/OQ/PQAssociate's or Bachelor's, often with on-the-job training
Work EnvironmentDesigning validation protocols, analyzing data, overseeing validation processesExecuting validation tests, collecting data, supporting validation activities
Industry UsagePharmaceutical, biotech, medical device manufacturingSimilar industries, often as support staff
Search & ComparisonOften compared for roles involving validation planning and oversightCompared for hands-on testing and data collection roles

The Full Time Validation Engineer typically leads validation projects, requiring more technical expertise and planning skills, while the Validation Technician focuses on executing validation tests and supporting validation activities. Both roles are essential in regulated industries like pharmaceuticals and biotech, but they differ in responsibilities and required credentials.

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Full Time Validation Engineer jobs near you
Infographic showing various Full Time Validation Engineer job openings in the United States as of August 2026, with employment types broken down into 93% Full Time, 3% Part Time, and 4% Contract. Highlights an 86% Physical, 5% Hybrid, and 9% Remote job distribution, with an average salary of $108,152 per year, or $52 per hour.

Validation Engineer (Computer Systems)

Fresenius Kabi

Melrose Park, IL • On-site

$65K - $80K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 21 days ago

Fresenius Kabi rating

8.3

Company rating: 8.3 out of 10

Based on 43 frontline employees who took The Breakroom Quiz

25th of 86 rated pharmaceutical

Job description

Job Summary
THIS JOB IS A FULL-TIME ONSITE POSITION, NO CONTRACT WORK AVAILABLE.
THIS JOB IS NOT ELIGIBLE FOR VISA SPONSORSHIP NOW OR IN THE FUTURE.
Salary: $65,000 to $80,000
Final pay determinations will depend on various factors, including, but not limited to experience level, education, knowledge, skills, and abilities.
Our benefits and programs are comprehensive and thoughtfully crafted to ensure our colleagues live healthy lives and have support when it matters most. Benefits offered include a 401(k) plan with company contributions, paid vacation, holiday and personal days, employee assistance program, and health benefits to include medical, prescription drug, dental and vision coverage. Read more about our benefits here.
Responsibilities
The Validation Engineer is specialized in computerized systems validation and knowledgeable in MES (EBR) , historian(QMIB), LAB -X and other manufacturing applications. Provides technical & documentation support for manufacturing process and associated computer systems. Also compliance knowledge on various aseptic manufacturing processes (sterilization, isolator technology, clean rooms, computerized systems, etc). Uses his/her expertise to maintain industry standards within the company.
The focus of the Validation Engineer is on technical and documentation aspects of the department and typically does not have direct report. The Validation Engineer must have excellent verbal and written communication skills as this position interacts directly with multiple departments at the site, regional and global levels.
Job Responsibilities:
  • Schedules and executes computer system qualifications per Standard Operating Procedures (SOPs). Coordinates and communicates all testing with affected functional groups and evaluates test results. Assembles and composes the final report and circulates for approval.
  • Executes validation studies (utility, equipment, cleaning, process, computer, and new products) to include protocol preparation, scheduling, protocol execution, and final report preparation. Presents results to Regulatory Agency when necessary.
  • Participates in dry running the manufacturing system applications and develops the test scenarios, test environments, test scripts.
  • Develops and updates full life cycle documents includes, URS, FDS, DS, risk assessments, impact assessment, FMEAs and test and qualification protocols.
  • Develops/improves validation programs as needed to remain current with cGMPs and industry standards
  • Represents Technical Services in teams assembled to specify, install, validate, troubleshoot and maintain systems, equipment and processes.
  • Conducts and/or participates in deviation investigations to identify root causes and define corrective and/or preventative actions (CA/PA).
  • Authors validation master plans and validation project plans outlining qualification requirements
  • Authors the documentation needed for MES(EBR), Historian(QMIB), manufacturing applications and infrastructure like industrial data center, etc.
  • Provides technical support for Investigations, Action Plans, Change Controls and Risk Assessments as required. Generates innovative solutions to solve difficult problems that may impact multiple disciplines
  • Additional projects and tasks as assigned.
  • All employees are responsible for ensuring the compliance to company documents, programs and activities related to the Health, Safety, Environment, Energy, and Quality Management Systems, as per your roles and responsibilities

Job Requirements:
  • Bachelor's Degree in a Science or Engineering field of study
  • Minimum of one year of related experience in a cGMP facility, including experience with FDA regulations, medical, drug and device products.
  • Installation, Operational and Performance Qualification protocol generation and execution experience
  • Knowledge and understanding of cGMPs, industry guidance, and aseptic techniques
  • Excellent technical writing and verbal communication skills. Experienced in negotiating.
  • Understanding of MES(EBR), historian, oee, and other manufacturing applications.
  • PC literate with standard office application (Word, Excel, PowerPoint, Project, Access) competency
  • Good communication skills and leadership skills.
  • Good judgment and decision skills.
  • Problem solving and multi-tasking.
  • Project supervision and project management skills.
  • Ability to work independently.
  • Ability to adapt and handle change.
  • Knowledge of cGMP Process and Product Validation requirements and techniques.

The Company's primary business language is English. The successful candidate must be able to effectively speak, read, write, and understand English to perform the essential functions of the position, including independently understanding policies, procedures, training materials, and workplace communications written in English due to our heavily regulated work environment.
Additional Information
We offer an excellent salary and benefits package including medical, dental and vision coverage, as well as life insurance, disability, 401K with company contribution, and wellness program.
Please note that joining our team does not create a guaranteed or permanent employment arrangement. All employment is at-will, meaning both the employee and Fresenius Kabi have the right to end the employment relationship at any time, in accordance with applicable federal and state laws.
Fresenius Kabi is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, citizenship, immigration status, disabilities, or protected veteran status.

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