ZipRecruiter

Log In

1

Cleaning Validation Jobs (NOW HIRING)

Gilead

Cleaning Validation Engineer II

La Verne, CA

$99K - $129K/yr

Lead and execute cleaning validation activities for a multiproduct facility , including parenteral and solid dose products . * Execute validation protocols and test plans, including sample collection ...

Validation & Engineering Group, Inc

PR · On-site

The Validation Specialist is responsible for planning, coordinating, and executing all Commissioning, Qualification, and Validation (CQV) activities related to Cleaning-In-Place (CIP) and ...

Validation & Engineering Group, Inc

PR · On-site

The Validation Specialist is responsible for planning, coordinating, and executing all Commissioning, Qualification, and Validation (CQV) activities related to Cleaning-In-Place (CIP) and ...

Validation & Engineering Group, Inc

PR · On-site

The Validation Specialist is responsible for planning, coordinating, and executing all Commissioning, Qualification, and Validation (CQV) activities related to Cleaning-In-Place (CIP) and ...

Validation & Engineering Group, Inc

PR · On-site

The Validation Specialist is responsible for planning, coordinating, and executing all Commissioning, Qualification, and Validation (CQV) activities related to Cleaning-In-Place (CIP) and ...

Validation & Engineering Group, Inc

PR · On-site

The Validation Specialist is responsible for planning, coordinating, and executing all Commissioning, Qualification, and Validation (CQV) activities related to Cleaning-In-Place (CIP) and ...

Validation & Engineering Group, Inc

PR

The Validation Specialist is responsible for planning, coordinating, and executing all Commissioning, Qualification, and Validation (CQV) activities related to Cleaning-In-Place (CIP) and ...

Validation & Engineering Group, Inc

PR · On-site

The Validation Specialist is responsible for planning, coordinating, and executing all Commissioning, Qualification, and Validation (CQV) activities related to Cleaning-In-Place (CIP) and ...

Validation & Engineering Group, Inc

PR

The Validation Specialist is responsible for planning, coordinating, and executing all Commissioning, Qualification, and Validation (CQV) activities related to Cleaning-In-Place (CIP) and ...

Validation & Engineering Group, Inc

PR · On-site

The Validation Specialist is responsible for planning, coordinating, and executing all Commissioning, Qualification, and Validation (CQV) activities related to Cleaning-In-Place (CIP) and ...

Validation & Engineering Group, Inc

PR · On-site

The Validation Specialist is responsible for planning, coordinating, and executing all Commissioning, Qualification, and Validation (CQV) activities related to Cleaning-In-Place (CIP) and ...

Validation & Engineering Group, Inc

PR · On-site

The Validation Specialist is responsible for planning, coordinating, and executing all Commissioning, Qualification, and Validation (CQV) activities related to Cleaning-In-Place (CIP) and ...

Validation & Engineering Group, Inc

PR

The Validation Specialist is responsible for planning, coordinating, and executing all Commissioning, Qualification, and Validation (CQV) activities related to Cleaning-In-Place (CIP) and ...

Validation & Engineering Group, Inc

PR

The Validation Specialist is responsible for planning, coordinating, and executing all Commissioning, Qualification, and Validation (CQV) activities related to Cleaning-In-Place (CIP) and ...

Validation & Engineering Group, Inc

PR

The Validation Specialist is responsible for planning, coordinating, and executing all Commissioning, Qualification, and Validation (CQV) activities related to Cleaning-In-Place (CIP) and ...

next page

Showing results 1-20

All JobsCleaning Validation Jobs

Cleaning Validation information

See salary details

$36

$39

$42

How much do cleaning validation jobs pay per hour?

As of Jun 24, 2026, the average hourly pay for cleaning validation in the United States is $39.42, according to ZipRecruiter salary data. Most workers in this role earn between $37.98 and $40.87 per hour, depending on experience, location, and employer.

How to become a cleaning validation consultant?

To become a cleaning validation consultant, professionals typically need a background in pharmaceutical or biotech manufacturing, with knowledge of validation processes and regulatory standards such as FDA or EMA guidelines. Gaining experience in cleaning procedures, validation protocols, and quality assurance is essential, often complemented by certifications like ASQ or ISPE training. Strong analytical skills and familiarity with validation tools and documentation are also important for success in this role.

What is the difference between Cleaning Validation vs Microbiologist?

AspectCleaning ValidationMicrobiologist
Required credentialsGMP, GMP-related certifications, technical trainingBiology, microbiology degrees, certifications
Work environmentPharmaceutical, biotech manufacturing facilitiesLaboratories, research facilities, healthcare settings
Employer and industry usagePharmaceutical, biotech, food industriesHealthcare, research, environmental testing

Cleaning Validation focuses on ensuring that cleaning processes effectively remove contaminants from equipment, primarily in manufacturing settings. Microbiologists study microorganisms, their behaviors, and control methods, often working in labs. While both roles require scientific knowledge and certifications, Cleaning Validation specialists concentrate on process validation in production environments, whereas Microbiologists focus on microbial analysis and research.

How to become a validation specialist?

To become a validation specialist, typically one needs a background in life sciences, engineering, or a related field, along with experience in quality assurance or manufacturing. Certification in validation processes, such as those from ISPE or PDA, can enhance prospects, and familiarity with regulatory standards like GMP is essential. Strong attention to detail and knowledge of validation tools and documentation are also important.

Do validation engineers make good money?

Validation engineers, including those in cleaning validation, typically earn competitive salaries that vary by industry, experience, and location. They often require knowledge of regulatory standards and validation processes, which can lead to higher compensation as they gain expertise. Overall, validation engineering is considered a well-paying field within quality assurance roles.

What does cleaning validation do?

Cleaning validation is a process used in quality assurance roles to ensure that cleaning procedures effectively remove contaminants from equipment, preventing cross-contamination and ensuring product safety. It involves testing and documenting cleaning processes, often requiring knowledge of regulatory standards and analytical methods. Proper cleaning validation helps maintain compliance and product quality in manufacturing environments.
More about Cleaning Validation jobs
What cities are hiring for Cleaning Validation jobs? Cities with the most Cleaning Validation job openings:
What states have the most Cleaning Validation jobs? States with the most job openings for Cleaning Validation jobs include:
What job categories do people searching Cleaning Validation jobs look for? The top searched job categories for Cleaning Validation jobs are:
Cleaning Validation jobs near you
Cleaning Validation Engineer II

Cleaning Validation Engineer II

Gilead

La Verne, CA

$99K - $129K/yr

Full-time

Medical, Dental, Vision, Life, PTO

Posted 2 days ago

Gilead Sciences rating

9.7

Company rating: 9.7 out of 10

Based on 7 frontline employees who took The Breakroom Quiz

1st of 71 rated pharmaceutical

Job description

At Gilead, we're creating a healthier world for all people. For more than 35 years, we've tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer - working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the globe. We continue to fight against the world's biggest health challenges, and our mission requires collaboration, determination and a relentless drive to make a difference.

Every member of Gilead's team plays a critical role in the discovery and development of life-changing scientific innovations. Our employees are our greatest asset as we work to achieve our bold ambitions, and we're looking for the next wave of passionate and ambitious people ready to make a direct impact.

We believe every employee deserves a great leader. People Leaders are the cornerstone to the employee experience at Gilead and Kite. As a people leader now or in the future, you are the key driver in evolving our culture and creating an environment where every employee feels included, developed and empowered to fulfil their aspirations. Join Gilead and help create possible, together.
Job Description

Knowledge & Skills:
  • Understanding and application of validation principles, concepts, practices, and industry standards.
  • Working knowledge of current Good Manufacturing Practices (cGMPs) and regulatory requirements.
  • Familiarity with equipment, utility systems, facility operations, and automation systems.
  • Strong investigation and troubleshooting skills.
  • Good verbal, written, and interpersonal communication skills.
  • Proficient in Microsoft Office applications.
Key Responsibilities:
  • Perform validation activities for equipment, utilities, facilities, processes, and/or automation systems in accordance with approved SOPs, cGMPs, and regulatory requirements.
  • Lead and execute cleaning validation activities for a multiproduct facility, including parenteral and solid dose products.
  • Execute validation protocols and test plans, including sample collection, data recording, and results documentation.
  • Compile, analyze, and interpret validation data; prepare validation reports and recommend process improvements.
  • Initiate and support investigations and troubleshooting of validation deviations or failures, identifying root cause and corrective actions.
  • Coordinate and execute change control activities related to validation, including drafting protocols, reports, and data summaries.
  • Maintain comprehensive and compliant validation documentation and records.
  • Author and revise validation procedures, protocols, and technical documentation.
  • Coordinate and oversee contractors and external resources to ensure timely completion of validation activities.
  • Collaborate with cross-functional teams (Manufacturing, Quality, Engineering, etc.) to support project execution.
  • Provide day-to-day guidance and training to validation technicians and junior staff as needed.
  • Serve as a technical resource for validation-related inquiries from internal teams, contractors, and vendors.
  • Resolve moderately complex validation issues with limited supervision while ensuring compliance and data integrity.
  • Experience with recovery studies and cleaning validation within GMP-regulated environments
  • Hands-on experience with swabbing execution for cleaning verification and monitoring
  • Occasionally support night, weekend, and off-shift schedules as needed based on business demands
Basic Qualifications:
  • Bachelor's degree in a science or related field with at least 4 years of relevant experience

OR

  • Master's degree (MS/MBA) with at least 2 years of relevant experience.


The salary range for this position is: $99,705.00 - $129,030.00. Gilead considers a variety of factors when determining base compensation, including experience, qualifications, and geographic location. These considerations mean actual compensation will vary. This position may also be eligible for a discretionary annual bonus, discretionary stock-based long-term incentives (eligibility may vary based on role), paid time off, and a benefits package. Benefits include company-sponsored medical, dental, vision, and life insurance plans*.

For additional benefits information, visit:

https://www.gilead.com/careers/compensation-benefits-and-wellbeing

* Eligible employees may participate in benefit plans, subject to the terms and conditions of the applicable plans.


For jobs in the United States:

Gilead Sciences Inc. is committed to providing equal employment opportunities to all employees and applicants for employment, and is dedicated to fostering an inclusive work environment comprised of diverse perspectives, backgrounds, and experiences. Employment decisions regarding recruitment and selection will be made without discrimination based on race, color, religion, national origin, sex, age, sexual orientation, physical or mental disability,genetic information or characteristic, gender identity and expression, veteran status, or other non-job related characteristics or other prohibited grounds specified in applicable federal, state and local laws. In order to ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Era Veterans' Readjustment Act of 1974, and Title I of the Americans with Disabilities Act of 1990, applicants who require accommodation in the job application process may contact ApplicantAccommodations@gilead.comfor assistance.


For more information about equal employment opportunity protections, please view the'Know Your Rights' poster.

NOTICE: EMPLOYEE POLYGRAPH PROTECTION ACT
YOUR RIGHTS UNDER THE FAMILY AND MEDICAL LEAVE ACT


Gilead Sciences will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, (c) consistent with the legal duty to furnish information; or (d) otherwise protected by law.

Our environment respects individual differences and recognizes each employee as an integral member of our company. Our workforce reflects these values and celebrates the individuals who make up our growing team.


Gilead provides a work environment free of harassment and prohibited conduct. We promote and support individual differences and diversity of thoughts and opinion.


For Current Gilead Employees and Contractors:

Please apply via the Internal Career Opportunities portal in Workday.

Apply