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Pharma Validation Jobs (NOW HIRING)

Medline

Engineer Pharma Validation

$73K - $110K/yr

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

Stark Pharma Solutions Inc

MD · On-site

Hi, My name is Karthik Mutyala, from Stark Pharma Solutions Inc, we are hiring talents for our client. I am working on Validation Engineer right now. Please send me your updated resume if you have ...

SCA Pharma

Validation Engineer

Windsor, CT

SCA Pharma is an FDA 503B outsourcing facility providing customized medications for hospitals and ... The Validation Engineer oversees the aseptic process simulations (media fills), equipment ...

New

SCA Pharma

Validation Engineer

Windsor, CT · On-site

SCA Pharma is an FDA 503B outsourcing facility providing customized medications for hospitals and ... The Validation Engineer oversees the aseptic process simulations (media fills), equipment ...

Stark Pharma Solutions Inc

IL · On-site

Hi, My name is Sravani Dasari from Stark Pharma Solutions Inc. We are hiring talent for our client and are currently working on a Manufacturing Validation Engineer position. Please send me your ...

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Pharma Validation information

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$22

$51

$78

How much do pharma validation jobs pay per hour?

As of Aug 17, 2026, the average hourly pay for pharma 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 is pharma validation?

Pharma validation is the process of ensuring that pharmaceutical manufacturing processes, equipment, and systems consistently produce products meeting predetermined quality standards and regulatory requirements. This process involves documenting and verifying each step in the manufacturing process to ensure safety, efficacy, and compliance. Validation activities include installation qualification (IQ), operational qualification (OQ), and performance qualification (PQ). Proper validation helps minimize risks, ensures patient safety, and is a critical requirement for regulatory approval by agencies like the FDA.

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

To thrive in Pharma Validation, you need a strong background in pharmaceutical sciences, regulatory compliance, and validation protocols, often supported by a relevant degree such as pharmacy, chemistry, or engineering. Familiarity with validation tools, Good Manufacturing Practice (GMP) guidelines, and quality management systems is essential, along with certifications like Six Sigma or Lean Manufacturing being advantageous. Attention to detail, analytical thinking, and effective communication are crucial soft skills for ensuring thorough documentation and collaboration with cross-functional teams. These skills ensure all processes and products meet stringent regulatory standards, safeguarding product quality and patient safety.

What is the difference between Pharma Validation vs Quality Assurance Specialist?

AspectPharma ValidationQuality Assurance Specialist
CertificationsGMP, Validation certificationsGMP, QA certifications
Work EnvironmentValidation labs, manufacturing plantsQuality departments, production sites
Industry UsageEnsures equipment, processes meet standardsMaintains quality systems, audits

Pharma Validation focuses on verifying that equipment, processes, and systems meet regulatory standards through validation protocols. Quality Assurance Specialists oversee overall quality systems, conduct audits, and ensure compliance. While both roles aim to ensure product quality, Validation is more technical and process-specific, whereas QA Specialists handle broader quality management and compliance activities.

What are some typical challenges faced by professionals in pharma validation, and how can they be addressed?

Pharma validation professionals often encounter challenges such as keeping up with ever-evolving regulatory requirements, managing tight project timelines, and ensuring thorough documentation throughout the validation process. Addressing these challenges requires ongoing training on current Good Manufacturing Practices (cGMP), effective project management skills, and close collaboration with cross-functional teams such as quality assurance and production. Proactively communicating with stakeholders and staying organized can help mitigate risks and ensure compliance.
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What states have the most Pharma Validation jobs?

States with the most job openings for Pharma Validation jobs include:

What job categories do people searching Pharma Validation jobs look for?

The top searched job categories for Pharma Validation jobs are:

Pharma Validation jobs near you
Infographic showing various Pharma Validation job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 88% Full Time, 3% Part Time, 1% Temporary, and 7% Contract. Highlights an 86% Physical, 5% Hybrid, and 9% Remote job distribution, with an average salary of $108,152 per year, or $52 per hour.

Engineer Pharma Validation

Medline

Remote

$73K - $110K/yr

Full-time

Medical, Life, Retirement, PTO

Posted 17 days ago

Medline Industries rating

7.5

Company rating: 7.5 out of 10

Based on 249 frontline employees who took The Breakroom Quiz

261st of 540 rated manufacturers

Job description

Job Summary

Responsible for the validation of facility utilities, equipment processes and cleaning 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 and cleaning 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 method validations of applicable products. This position requires up to 40% travel both international and domestic.

Job Description

Responsibilities:
  • Validate new and revalidate as appropriate existing equipment used in OTC/Cosmetic manufacturing.
  • Perform engineering studies to determine if projects are feasible.
  • 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.
  • Develop and execute cleaning validations.
  • Responsible for IQ/OQ and PQ phases.
  • 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.
Qualifications:
  • Bachelor of Science Degree in Biology, Chemistry or Engineering.
  • At least 2 year of validation experience in a cGMP Device or Drug environment. Experience with validations of USP water, 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, or other related field.
  • Six Sigma certification.
  • 3 years of validation experience in a cGMP Device or Drug environment. 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.

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 pagehere.

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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