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Quality Validation Jobs (NOW HIRING)

A role where craftsmanship and quality truly matter What You'll Do * Provide validation experience and guidance during equipment design, software design, build, debug, qualification and improvement ...

Title : Quality Validation Engineer Location: North of Puerto Rico (Open to Puerto Rico Residents) Positions : 1 6 months contract Objective Support multiple new line development projects by ...

Validation Engineer III

San Diego, CA · On-site

$35 - $39.02/hr

The end goal is to deliver consistent and high-quality validation and supporting documentation for design and development organization. This role requires strong technical, communication ...

The end goal is to deliver consistent and high-quality validation and supporting documentation for design and development organization. This role requires strong technical, communication ...

PR · On-site

We are seeking a Project Manager to lead and coordinate capital, engineering, manufacturing, quality, validation, automation, and operational improvement projects within a regulated pharmaceutical ...

PR · On-site

We are seeking a Project Manager to lead and coordinate capital, engineering, manufacturing, quality, validation, automation, and operational improvement projects within a regulated pharmaceutical ...

PR · On-site

We are seeking a Project Manager to lead and coordinate capital, engineering, manufacturing, quality, validation, automation, and operational improvement projects within a regulated pharmaceutical ...

PR · On-site

We are seeking a Project Manager to lead and coordinate capital, engineering, manufacturing, quality, validation, automation, and operational improvement projects within a regulated pharmaceutical ...

PR · On-site

We are seeking a Project Manager to lead and coordinate capital, engineering, manufacturing, quality, validation, automation, and operational improvement projects within a regulated pharmaceutical ...

PR · On-site

We are seeking a Project Manager to lead and coordinate capital, engineering, manufacturing, quality, validation, automation, and operational improvement projects within a regulated pharmaceutical ...

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Quality Validation information

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$22

$51

$78

How much do quality validation jobs pay per hour?

As of Jul 2, 2026, the average hourly pay for quality validation 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 some common challenges faced in a Quality Validation role and how can they be addressed?

Professionals in Quality Validation often encounter challenges such as managing tight project deadlines, ensuring compliance with ever-evolving regulatory standards, and effectively communicating with cross-functional teams. Addressing these challenges involves strong organizational skills, continuous learning about industry regulations, and fostering collaboration between departments like manufacturing, R&D, and quality assurance. Staying proactive and maintaining thorough documentation also helps mitigate risks and improve validation processes.

What is Quality Validation?

Quality Validation is a process used in various industries, especially in manufacturing, pharmaceuticals, and software development, to ensure that products, processes, or systems meet predefined quality standards and regulatory requirements. It involves planned and systematic activities such as testing, documentation, and reviews to confirm that the final output consistently meets the intended purpose. Quality Validation helps organizations minimize errors, enhance reliability, and build customer trust by ensuring that products are both safe and effective before they reach the market.

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

To excel as a Quality Validation Specialist, you need a solid understanding of quality assurance principles, regulatory compliance, and validation methodologies, often supported by a degree in a scientific or engineering field. Familiarity with validation protocols, statistical analysis software, and quality management systems (QMS) is typically required, along with certifications like Six Sigma or GMP training. Attention to detail, problem-solving, and effective communication are crucial soft skills for identifying issues and ensuring compliance across teams. These competencies are vital for maintaining product safety, regulatory adherence, and continuous improvement within quality-driven industries.

What is the difference between Quality Validation vs Quality Assurance?

AspectQuality ValidationQuality Assurance
Primary FocusEnsuring products meet user needs and specifications through testing and validationImplementing processes to prevent defects and improve quality systems
ActivitiesValidation testing, product verification, compliance checksProcess audits, quality system development, preventive measures
CredentialsOften requires technical certifications and testing experienceQuality management certifications like ISO, Six Sigma
Work EnvironmentLaboratories, testing facilities, production linesQuality departments, process improvement teams

While both roles aim to ensure product quality, Quality Validation focuses on testing and verifying that products meet specifications, whereas Quality Assurance emphasizes establishing processes to prevent defects and improve overall quality systems.

More about Quality Validation jobs
What are the most commonly searched types of Quality Validation jobs? The most popular types of Quality Validation jobs are:
What states have the most Quality Validation jobs? States with the most job openings for Quality Validation jobs include:
Infographic showing various Quality Validation job openings in the United States as of June 2026, with employment types broken down into 67% Full Time, and 33% Contract. Highlights an 100% In-person job distribution, with an average salary of $108,152 per year, or $52 per hour.
Principal/Senior Principal, Quality Engineer Validation

Principal/Senior Principal, Quality Engineer Validation

Genentech, Inc.

Hillsboro, OR • On-site

$112K - $209K/yr

Full-time

Posted 13 days ago


Genentech rating

8.8

Company rating: 8.8 out of 10

Based on 22 frontline employees who took The Breakroom Quiz

10th of 73 rated pharmaceutical


Job description

Hillsboro Technical Operations (HTO) is a drug product & finished goods manufacturing organization responsible for the reliable delivery of Roche's commercial portfolio & pipeline products. The Operations organization at HTO is divided into 2 operations: aseptic operations and finished goods operations, which combine to produce millions of units of life-saving medicine every year to patients around the world.
Please note there are two roles available
The Opportunity:
In this exciting role, you will apply knowledge of qualification and validation principles, manufacturing processes, quality systems, engineering design fundamentals, health authority expectations and industry standards, review and approve qualification and validation documents. You will perform quality oversight of the equipment, facility and utility systems, GMP computerized systems, drug product manufacturing processes, cleaning processes, sterilization processes, and analytical methods. This is inclusive of tech transfer oversight, new facility expansions and large construction projects and the scale up/adoption of digital technology.
  • You have specialized depth and/or breadth of expertise in own specialized area and have good knowledge of own Quality function
  • You will work independently within broad guidelines and policies, with guidance in only the most complex situations
  • You will serve as a best practices/quality resource on highly significant matters relating to policies, programs, capabilities, and long-range goals and objectives.
  • You will lead sub streams or participate in cross-functional project teams to solve complex problems by using analytical thinking, tools and judgment to identify innovative solutions for Roche (or an identified area within the company)
  • You will work on complex issues where analysis of situations or data requires an in-depth evaluation of variable factors, including inter-organizational impact.
  • You will exercise judgment based on the analysis of multiple sources of information and interactions with peers and cross-functional squads.

Who you are:
  • You hold a Bachelor's degree (Masters Preferred) with 8 years (Principal) or 12 years (Senior Principal) industry experience
  • You have industry experience in technical validation or quality validation
  • You have an in-depth specialist knowledge of own job discipline and broad knowledge of related disciplines in the field
  • You are recognized internally as an expert in your own job discipline. Has deep skills and expertise across multiple disciplines in the field.
  • Combination Product Manufacturing Experience (single-use autoinjector platforms) is preferred.

The expected salary range for this position based on the primary location for this position of Hillsboro, OR is $93,000 - $172,000 (Principal) or $112,700 - $209,300 (Senior Principal). Actual pay will be determined based on experience, level, qualifications, geographic location, and other job-related factors permitted by law. A discretionary annual bonus may be available based on individual and Company performance. This position also qualifies for the benefits detailed at the link provided below.
Link to Roche/Genentech Benefits
Relocation benefits are available for this position.
Genentech is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company's policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws.
If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form Accommodations for Applicants.

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About Genentech

Sourced by ZipRecruiter

A member of the Roche Group, Genentech has been at the forefront of the biotechnology industry for more than 40 years, using human genetic information to develop novel medicines for serious and life-threatening diseases. Genentech has multiple therapies on the market for cancer & other serious illnesses. Please take this opportunity to learn about Genentech where we believe that our employees are our most important asset & are dedicated to remaining a great place to work.

Industry

Scientific research and development services

Company size

10,000+ Employees

Headquarters location

South San Francisco, CA, US

Year founded

1976

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