ZipRecruiter

Log In

1

Validation Scientist Salary Jobs (NOW HIRING)

Nitto Denko Corp.

$89K - $109K/yr

As a Process Development Validation Scientist, you will be responsible for drafting new Process ... The annualized salary range for this role is $89,500.00 - $109,500.00.

Clinical Lab

Clinical Laboratory Scientist

Redding, CA · On-site

$50.67 - $69.36/hr

Clinical Laboratory Scientist Salary Range: $2,128.14 - $2,913.12 per week (base gross), based on a ... and valid California State License. Pay Transparency Premiere Healthcare Staffing offers ...

Performance Validation, Inc

Validation Engineer

Raleigh, NC · On-site

$80K - $83K/yr

Develop a sound understanding of how to properly implement technical, quality, and scientific ... Competitive base salary * Biannual profit share * Employee stock ownership program * 401(k) company ...

next page

Showing results 1-20

All JobsValidation Scientist Salary Jobs

Validation Scientist Salary information

See salary details

$22

$51

$78

How much do validation scientist salary jobs pay per hour?

As of Aug 12, 2026, the average hourly pay for validation scientist salary 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 the difference between Validation Scientist Salary vs Quality Assurance Specialist Salary?

AspectValidation Scientist SalaryQuality Assurance Specialist Salary
Required CredentialsBachelor's degree in life sciences or related field; certifications like CQE or ASQBachelor's degree; certifications like CQE or ISO auditor
Work EnvironmentLaboratories, manufacturing plants, regulated industriesQuality control labs, manufacturing facilities, regulated industries
Employer & Industry UsagePharmaceuticals, biotech, medical devicesPharmaceuticals, manufacturing, food industry

Validation Scientists and Quality Assurance Specialists often share similar credentials and work environments in regulated industries. Validation Scientists focus on validating processes and systems, while QA Specialists oversee quality compliance. Both roles are essential for ensuring product safety and regulatory adherence, but their specific responsibilities differ.

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

To thrive as a Validation Scientist, you need a strong background in life sciences or engineering, experience with validation protocols, and often a relevant bachelor's or master's degree. Familiarity with regulatory standards (such as FDA or EMA), statistical analysis software, and documentation systems is typically required. Attention to detail, problem-solving, and effective communication are critical soft skills for this role. These skills ensure that products and processes meet strict regulatory requirements, maintain quality standards, and support successful audits and inspections.

What are some common challenges faced by validation scientists in the pharmaceutical industry?

Validation scientists in the pharmaceutical industry often encounter challenges such as staying current with evolving regulatory requirements, managing tight project timelines, and ensuring thorough documentation for audits. They may also need to troubleshoot complex equipment or process issues and coordinate with cross-functional teams like quality assurance, manufacturing, and engineering to resolve discrepancies. Effective communication and adaptability are essential, as the role frequently involves balancing multiple projects and responding to shifting priorities.

What does a validation scientist do?

A validation scientist is responsible for developing, executing, and documenting validation protocols to ensure that manufacturing processes, equipment, and systems meet regulatory standards and quality requirements. They analyze data, identify issues, and implement improvements to maintain compliance, often using tools like statistical software and following Good Manufacturing Practices (GMP).

What is the average salary of a validation scientist?

The average salary of a Validation Scientist typically ranges from $60,000 to $100,000 per year in the United States, depending on factors such as education, experience, industry, and geographic location. Entry-level Validation Scientists may earn toward the lower end of this range, while those with several years of experience or who work in high-demand areas such as pharmaceuticals or biotechnology can earn higher salaries. Additional benefits, such as bonuses and healthcare, may also be included in the compensation package.
More about Validation Scientist Salary jobs
What cities are hiring for Validation Scientist Salary jobs? Cities with the most Validation Scientist Salary job openings:
What states have the most Validation Scientist Salary jobs? States with the most job openings for Validation Scientist Salary jobs include:
What job categories do people searching Validation Scientist Salary jobs look for? The top searched job categories for Validation Scientist Salary jobs are:
Validation Scientist Salary jobs near you
Infographic showing various Validation Scientist Salary job openings in the United States as of August 2026, with employment types broken down into 88% Full Time, 10% Part Time, and 2% Contract. Highlights an 91% Physical, 3% Hybrid, and 6% Remote job distribution, with an average salary of $108,152 per year, or $52 per hour.

Process Development Validation Scientist II

Nitto Denko Corp.

$89K - $109K/yr

Full-time

Re-posted 9 days ago

Job description

About this opportunity :

As a Process Development Validation Scientist, you will be responsible for drafting new Process Validation protocol and report documents to support process development, manufacturing, and validation activities.  Responsible for drafting Risk Assessment Spreadsheets. 

Key Responsibilities:  

  • Preparation of Process Validation protocols / reports, CPV protocols and reports, PC&P reports, and VMP / VSR to enable Avecia's process validation programs to be executed efficiently. 
  • Preparation of Manufacturing Study Protocols and associated reports. 
  • Creates new Process Validation document templates. 
  • Drafts Risk Assessment Spreadsheets 
  • Contributes to Initial and Final Risk Assessment activities. 
  • Contributes to investigations of OOT results during CPV and OOS/CAPA results during manufacture of validated products. 
  • Prepares and delivers PPQ training. 
  • Maintain an appropriate level of training on company and departmental procedures as determined by Avecia and Process Validation. 

Required Skills/Abilities: 

  • Bachelor's Degree in science-related discipline and 6+ years related experience, Master's degree and 3+ years related experience in science-related discipline.
  •  Knowledge of ICH guidance related to GMP and Process Validation.
  • Excellent written and verbal communications, including technical writing. 
  • Proficiency in Microsoft Office Software.
  • Knowledge of statistics and its application to such aspects as process sampling and data trending analysis, knowledge of Minitab and SPC preferred. 

The annualized salary range for this role is  $89,500.00 - $109,500.00.

Apply