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Medline

Validation Engineer

Hartland, WI · On-site

$73K - $110K/yr

Job Summary Responsible for the validation of facility utilities, and equipment processes for cGMP products such as pharmaceuticals, medical devices, and cosmetic products to adhere to 21 CFR 211/210 ...

Novartis Group Companies

Validation Lead

Indianapolis, IN · On-site

$114.10K - $211.90K/yr

As our Validation Lead in Indianapolis, you will shape and own the site's end to end validation strategy-process, cleaning, primary packaging, and ongoing process verification-so manufacturing stays ...

Unifin SAS

Validation Technician

Rochester, NY

Assists validation efforts in many ways including the following: executes/supports equipment qualifications, cleaning validations and recertifications, chamber (i.e., freezers, refrigerators ...

Pinnaql

Validation Engineer

Greenville, NC

Validation & Engineering Group, Inc. (V&EG) is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the ...

Unifin SAS

Validation Specialist

Rochester, NY

Position Summary The Validation Specialist is responsible for supporting and executing validation and qualification activities for manufacturing processes, equipment, utilities, and facilities in a ...

Alk Abello

Validations Specialist

Oklahoma City, OK · On-site

Validation Specialist ALK is a forward-thinking allergy company with a long tradition for allergy innovation. We are making a bold move into digital to transform the way consumers, patients, and ...

Unifin SAS

Validation Technician

Rochester, NY · On-site

Validation Technician Who we are? We are a French pharmaceutical industrial group, recognized for making affordable healthcare products that improve and simplify patients' lives to as many people as ...

Validation & Engineering Group, Inc

PR · On-site

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices ...

PharmEng Technology Americas

PR · On-site

We are seeking an experienced Validation Engineer in Dorado, Puerto Rico. Objectives of this Role: * Write and execute, Installation Qualification (IQ), and Operational Qualification (OQ) protocols ...

Validation & Engineering Group, Inc

PR

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices ...

voyant

Engineer, Validation

Holmdel, NJ

A Brief Overview The Engineer, Validation Technical leads the site validation and contamination control strategy to ensure compliance with cGMP regulations and company quality standards. This role ...

OnLogic

Validation Engineer

South Burlington, VT · On-site

$90K - $120K/yr

As a Validation Engineer at OnLogic, you will play a crucial role in ensuring the quality and reliability of our advanced industrial computing products. In this position, you'll be responsible for ...

Validation & Engineering Group, Inc

PR · On-site

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices ...

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How much do validator jobs pay per hour?

As of Jun 3, 2026, the average hourly pay for validator in the United States is $17.17, according to ZipRecruiter salary data. Most workers in this role earn between $13.94 and $19.23 per hour, depending on experience, location, and employer.

What is a Validator job?

A Validator is responsible for reviewing, testing, and verifying data, processes, or systems to ensure accuracy, compliance, and reliability. This role is common in industries like finance, blockchain, pharmaceuticals, and engineering, where precise validation is critical. Validators analyze documentation, run tests, and confirm that systems meet regulatory or operational standards. Their work helps maintain quality control, prevent errors, and ensure that processes function as intended.

What are the key skills and qualifications needed to thrive in the Validator position, and why are they important?

To thrive as a Validator, you need strong analytical skills, keen attention to detail, and an understanding of relevant industry standards, typically supported by a degree in quality assurance, engineering, or a related field. Familiarity with validation software, data analysis tools, and regulatory compliance systems (such as GMP, ISO, or FDA guidelines) is often required. Strong organizational skills, effective communication, and the ability to work independently or within cross-functional teams help set exceptional Validators apart. These skills are crucial for ensuring product or process quality, regulatory compliance, and smooth collaboration in validation projects.

What are the most common challenges Validators face in their daily work?

Validators often encounter challenges such as interpreting complex regulatory requirements, troubleshooting unexpected deviations during validation testing, and maintaining meticulous documentation for audits. They may also need to coordinate with multiple departments, including engineering, quality assurance, and production, to ensure all processes meet standards. Staying current with evolving regulations and industry best practices is essential to success in this role. While the position requires attention to detail and persistence, it also provides valuable opportunities to develop expertise in compliance and quality assurance, which can support career advancement.
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Validator jobs near you
Infographic showing various Validator job openings in the United States as of May 2026, with employment types broken down into 93% Full Time, 6% Part Time, and 1% Contract. Highlights an 86% Physical, 2% Hybrid, and 12% Remote job distribution, with an average salary of $35,722 per year, or $17.2 per hour.
Validation Engineer

Validation Engineer

Medline

Hartland, WI • On-site

$73K - $110K/yr

Full-time

Medical, Life, Retirement, PTO

Posted 12 days ago

Medline Industries rating

7.6

Company rating: 7.6 out of 10

Based on 244 frontline employees who took The Breakroom Quiz

217th of 515 rated manufacturers

Job description

Job Summary
Responsible for the validation of facility utilities, and equipment processes for cGMP products such as pharmaceuticals, medical devices, and cosmetic products to adhere to 21 CFR 211/210, 21 CFR 820, and other applicable regulatory requirements. Assist in authoring and executing protocols to demonstrate that manufacturing processes are executed with consistent quality and results within a controlled environment. Responsible for managing and or performing revalidation, engineering studies to evaluate new products or components, change control assessments, and coordination of computer and test method validations of applicable products.
Job Description
  • Validate new and revalidate as appropriate existing equipment used in OTC/Cosmetic and medical device manufacturing.
  • Perform engineering studies to determine if projects are feasible.
  • Assist with measurement system analysis including Gage R&R.
  • Support product/design transfer activities including validations and creation of updates to documentation needed to manufacture OTC cosmetic and medical devices.
  • Support Change Assessment activities including assessment and qualification of changes to existing product components and implementation of products into manufacturing lines.
  • Support root cause investigations for non-conformances related to manufacturing validations.
  • Develop, prepare and install equipment and revise test validation procedures/protocols to ensure that a product is manufactured in accordance with appropriate regulatory agency validation requirement and current industry practices.
  • Responsible for IQ/OQ and PQ phases and implementation of validated SOPs.
  • Coordinate projects directly with vendors and service providers to ensure that all validation and installation requirements are being satisfied during the execution of protocols.
  • Develop timelines for all projects and ensure that deadlines and goals are being met. Frequently update management and team on progress.
  • Proactively work with members of the division or project team to identify issues that might delay the project; make recommendations to improve time lines for project completion.
  • Compile and analyze validation data, prepare reports, and make recommendations for changes and/or improvements.
  • Maintain all of the documentation pertaining to qualification and validation of assigned projects and equipment/systems.

REQUIRED EXPERIENCE
Education
  • Bachelor of Science Degree in Biology, Chemistry, or Engineering.

Work Experience
  • At least 2 years of validation experience in a cGMP Device or Drug environment.
  • Experience with validations of controlled environments or equipment validations in a regulated environment.
  • Experience with validation documentation and related change control.
  • Strong ability to manage multiple priorities, self-starter attitude, good oral and writing skills and the ability to work independently and as a team in an efficient manner.

PREFERRED QUALIFICATIONS
  • Masters of Science in Chemistry, Biology, Biotechnology, Chemical Manufacturing, Biomedical Engineering, or Engineering.
  • Six Sigma certification.
  • 3 years of validation experience in a cGMP Device or Drug environment.
  • Process validation experience in a pharmaceutical or Medical Device manufacturing environment.
  • Experience with validation of various product types such as liquid products, solid dosage products, and multi-component products.
  • Experience in FDA regulated environment.
  • Experience with ISO 13485 and ISO 11607 standards.
  • Experience with Measurement System Analysis.
  • Experience with Minitab statistical analysis software.
  • Experience with root cause analysis.

Medline Industries, LP, and its subsidiaries, offer a competitive total rewards package, continuing education & training, and tremendous potential with a growing worldwide organization.
The anticipated salary range for this position:
$73,000.00 - $110,000.00 Annual
The actual salary will vary based on applicant's location, education, experience, skills, and abilities. This role is bonus and/or incentive eligible. Medline will not pay less than the applicable minimum wage or salary threshold.
Our benefit package includes health insurance, life and disability, 401(k) contributions, paid time off, etc., for employees working 30 or more hours per week on average. For roles where employees work less than 30 hours per week, benefits include 401(k) contributions, paid time off, as well as access to the Employee Assistance Program, Employee Resource Groups and the Employee Service Corp. For a more comprehensive list of our benefits please click here.
We're dedicated to creating a Medline where everyone feels they belong and can grow their career. We strive to do this by seeking diversity in all forms, acting inclusively, and ensuring that people have tools and resources to perform at their best. Explore our Belonging page here.
Medline Industries, LP is an equal opportunity employer. Medline evaluates qualified individuals without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, age, disability, neurodivergence, protected veteran status, marital or family status, caregiver responsibilities, genetic information, or any other characteristic protected by applicable federal, state, or local laws.

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About Medline

Sourced by ZipRecruiter

Medline Industries, LP is the leading nationwide supplier of medical, surgical and pharmaceutical products to hospitals, nursing homes, HME providers, surgery centers, physician offices and home care/hospice settings.

Industry

Medical equipment and supplies manufacturing

Company size

10,000+ Employees

Headquarters location

Winnetka, IL, US

Year founded

1966

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