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Full Time Validation Engineer Jobs (NOW HIRING)

Agilent

Process Validation Engineer

Frederick, CO · On-site

$105K - $164K/yr

As a Process Validation Engineer within the Process Validation team of Agilent's Advanced ... The full-time equivalent pay range for this position is $105,280.00 - $164,500.00/yr plus ...

Agilent

Process Validation Engineer

Frederick, CO · On-site

$105K - $164K/yr

As a Process Validation Engineer within the Process Validation team of Agilent's Advanced ... The full-time equivalent pay range for this position is $105,280.00 - $164,500.00/yr plus ...

Hitachi, Ltd.

FDA Validation Engineer

Nashville, TN · On-site

Engineering & Science Job Schedule: Full time Remote: No JR Automation, a Hitachi Group Company ... Join us as an FDA Validation Engineer. Location type: This is an onsite position based in Nashville ...

Agilent

Process Validation Engineer

Boulder, CO · On-site

$105K - $164K/yr

As a Process Validation Engineer within the Process Validation team of Agilent's Advanced ... The full-time equivalent pay range for this position is $105,280.00 - $164,500.00/yr plus ...

Quality Agents

Validation Engineer IV

Rockville, MD · On-site

Our Validation Engineers will be involved with the qualification and requalification of equipment ... for full-time employees including: * Health, dental and vision insurance * Life, AD&D and ...

Apply Early

Quality Agents

Validation Engineer II

Rockville, MD · On-site

Our Validation Engineers will be involved with the qualification and requalification of equipment ... for full-time employees including: * Health, dental and vision insurance * Life, AD&D and ...

Apply Early

Hitachi

FDA Validation Engineer

Nashville, TN

Engineering & Science Job Schedule: Full time Remote: No JR Automation, a Hitachi Group Company ... Join us as an FDA Validation Engineer. Location type: This is an onsite position based in Nashville ...

LG Electronics

Sr. Validation Engineer

Aliso Viejo, CA · On-site

$87K - $116K/yr

Lead and guide validation engineers from a project execution perspective * Serves as the primary ... Recruiting Range $87,112-$116,150 USD Benefits Offered Full-Time Employees: * No-cost employee ...

Lancesoft

Validation Engineer 4

San Jose, CA · On-site

$75 - $87.37/hr

... engineers and technicians in the planning, test, & debug processor validation.EXPERIENCE AND ... At LanceSoft, full time regular employees who work a minimum of 30 hours a week or more are ...

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All JobsFull Time Validation Engineer Jobs

Full Time Validation Engineer information

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

As of Jul 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 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 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 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.

What are Full Time Validation Engineers?

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.
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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 June 2026, with employment types broken down into 1% As Needed, 18% Full Time, 77% Part Time, and 4% Contract. Highlights an 88% Physical, 4% Hybrid, and 8% Remote job distribution, with an average salary of $108,152 per year, or $52 per hour.
Process Validation Engineer

Process Validation Engineer

Agilent

Frederick, CO • On-site

$105K - $164K/yr

Full-time

Posted 6 days ago

Agilent Technologies rating

8.1

Company rating: 8.1 out of 10

Based on 40 frontline employees who took The Breakroom Quiz

110th of 527 rated manufacturers

Job description

Job Description

Agilent Technologies Advanced Therapeutics Division (previously Nucleic Acids Solutions Division) is looking for a Process Validation Engineer to join their Process Validation team working at their state-of-the-art, contract Active Pharmaceutical Ingredient manufacturing facility that specializes in oligonucleotide chemistries located in Boulder and Frederick, Colorado.


As a Process Validation Engineer within the Process Validation team of Agilent's Advanced Therapeutics Division (ATD), the candidate will be responsible for executing process validation activities of oligonucleotide Active Pharmaceutical Ingredient (API) manufacturing. The responsibilities may include:

Control Strategies: Contribute knowledge and technical expertise to the development and refinement of manufacturing control strategies for oligonucleotide unit operations (examples: synthesis, deprotection, ultrafiltration, purification, annealing, concentration, lyophilization).


Stage 1 Assessments/Evaluations: Identify, assess, mitigate, and communicate process risks that may impact product quality, process performance, or regulatory compliance. Prepare and/or review process validation documentation including risk assessments, characterization plans/reports, technical assessments, control strategies, protocols, and summary reports.


Stage 1 Characterization: Perform or support process development studies. May include planning, executing, and analyzing Design of Experiments (DOE) and Proven Acceptable Range (PAR) experiments to support design space understanding and process validation as they relate to oligonucleotide upstream and downstream process operations.


Experiment Execution: Support laboratory scale experiment execution (occasional) to assess process risks and/or demonstrate robustness of process conditions. This may include set-up and operation of laboratory equipment. Document bench experiments in accordance with good documentation practices (GDP), analyze results, summarize findings, and provide recommendations based on outcomes.


Stage 2 CGMP Protocol Execution: Lead and/or support execution of process validation studies in a CGMP manufacturing setting.


PPQ and Commercial Support: Evaluate change controls associated with Process Performance Qualification (PPQ) or commercial processes. Evaluate process validation impact of nonconformances. Review commercial batch records to ensure alignment with Process Control Strategies.


Stage 3 CPV: Support continued process verification, which may include but is not limited to leading Continued Process Verification (CPV) plans, authoring CPV reports, and reviewing Product Quality Reports.


Lifecycle: Supports all areas of process validation from FDAs Product Lifecycle's Stages 1, 2, and 3.

Communication: Provide process validation-related updates to clients and project teams in the form of slides, memos, and reports.

Qualifications

  • Bachelor's degree (B. S.) or equivalent in chemistry, chemical engineering or related applied sciences field.

  • 8+ years of experience in a GMP API setting.

  • Knowledge and understanding unit operations and associated control strategy of an oligonucleotide manufacturing process or like process.

  • Knowledge and experience in process validation studies at the bench and in a plant setting.

  • Knowledge and experience in designing, conducting, and statistical interpretation in Design of Experimentation (DOE), preferably using SAS JMP (or similar) software is highly desirable.

Additional Details

This job has a full time weekly schedule. Applications for this job will be accepted until at least July 1, 2026 or until the job is no longer posted.The full-time equivalent pay range for this position is $105,280.00 - $164,500.00/yr plus eligibility for bonus, stock and benefits. Our pay ranges are determined by role, level, and location. Within the range, individual pay is determined by work location and additional factors, including job-related skills, experience, and relevant education or training. During the hiring process, a recruiter can share more about the specific pay range for a preferred location. Pay and benefit information by country are available at: https://careers.agilent.com/locationsAgilent Technologies, Inc. is an Equal Employment Opportunity and merit-based employer that values individuals of all backgrounds at all levels. All individuals, regardless of personal characteristics, are encouraged to apply. All qualified applicants will receive consideration for employment without regard to sex, pregnancy, race, religion or religious creed, color, gender, gender identity, gender expression, national origin, ancestry, physical or mental disability, medical condition, genetic information, marital status, registered domestic partner status, age, sexual orientation, military or veteran status, protected veteran status, or any other basis protected by federal, state, local law, ordinance, or regulation and will not be discriminated against on these bases. Agilent Technologies, Inc., is committed to creating and maintaining an inclusive in the workplace where everyone is welcome, and strives to support candidates with disabilities. If you have a disability and need assistance with any part of the application or interview process or have questions about workplace accessibility, please email job_posting@agilent.com or contact +1-262-754-5030. For more information about equal employment opportunity protections, please visit www.agilent.com/en/accessibility.Travel Required: NoShift: DayDuration: No End DateJob Function: R&D

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