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Validation Specialist Jobs (NOW HIRING)

We are seeking a Junior Validation Specialist with 1-3 years of experience to support validation and qualification activities in a regulated environment. This role is ideal for a detail-oriented ...

We are seeking a Junior Validation Specialist with 1-3 years of experience to support validation and qualification activities in a regulated environment. This role is ideal for a detail-oriented ...

We are seeking a Junior Validation Specialist with 1-3 years of experience to support validation and qualification activities in a regulated environment. This role is ideal for a detail-oriented ...

We are seeking a Junior Validation Specialist with 1-3 years of experience to support validation and qualification activities in a regulated environment. This role is ideal for a detail-oriented ...

We are seeking a Junior Validation Specialist with 1-3 years of experience to support validation and qualification activities in a regulated environment. This role is ideal for a detail-oriented ...

Validation Specialist Key Responsibilities: * Develop, review, and execute Validation Master Plans (VMPs) and validation protocols, including IQ, OQ, and PQ . * Validate and qualify equipment ...

We are seeking a Junior Validation Specialist with 1-3 years of experience to support validation and qualification activities in a regulated environment. This role is ideal for a detail-oriented ...

We are seeking a Junior Validation Specialist with 1-3 years of experience to support validation and qualification activities in a regulated environment. This role is ideal for a detail-oriented ...

We are seeking a Junior Validation Specialist with 1-3 years of experience to support validation and qualification activities in a regulated environment. This role is ideal for a detail-oriented ...

We are seeking a Junior Validation Specialist with 1-3 years of experience to support validation and qualification activities in a regulated environment. This role is ideal for a detail-oriented ...

Validation Specialist The QC Inspection Specialist (QMCS / Validation Specialist) supports computerized system validations and broader validation activities across pharmaceutical manufacturing ...

New

Validation Specialist

Cidra, PR · On-site

$80 - $110/hr

Cidra, Puerto Rico | Posted on 08/06/2026 Validation Specialist with a strong knowledge of injection molding processes to support the development, execution, and documentation of validation ...

Validation Specialist The Validation Specialist develops, executes, and maintains validation and qualification programs to ensure manufacturing equipment, utilities, processes, and systems meet FDA ...

Position Overview The Validation Specialist ensures that all manufacturing processes, equipment, and products within the health and beauty industry meet regulatory, quality, and safety standards.

Validation Specialist Who we are? As a French pharmaceutical industrial group, we strive to make healthcare solutions that improve and simplify patients' lives accessible to as many people as ...

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Validation Specialist information

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$15

$50

$75

How much do validation specialist jobs pay per hour?

As of Aug 21, 2026, the average hourly pay for validation specialist in the United States is $50.45, according to ZipRecruiter salary data. Most workers in this role earn between $39.66 and $61.30 per hour, depending on experience, location, and employer.

What does a validation specialist do?

A validation specialist handles calibration, temperature mapping, and maintenance for equipment in a lab environment. Your primary responsibilities include measuring software performance to ensure accurate results, preparing equipment, executing studies to validate the product, writing instructions for procedures, and verifying standard operating systems within the industry. Your duties are to develop methods to control processes involved, create protocols for validation, assist with technology transfer, analyze data, make adjustments where needed, support process optimization, ensure products meet regulatory standards, and troubleshoot issues that arise.

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

To thrive as a Validation Specialist, you need a solid understanding of quality assurance, regulatory compliance, and process validation, typically backed by a degree in science, engineering, or a related field. Familiarity with validation protocols, risk assessment tools, and industry standards like GMP or FDA regulations is essential, as well as proficiency in documentation systems. Strong analytical thinking, attention to detail, and effective communication skills help you excel in coordinating validation activities and collaborating across departments. These skills ensure that products and processes consistently meet industry standards, regulatory requirements, and organizational quality goals.

What are some common challenges faced by validation specialists during project timelines, and how can they be managed?

Validation Specialists often encounter tight deadlines and evolving project requirements, which can make it challenging to ensure all validation protocols are meticulously documented and executed. Effective communication with cross-functional teams, proactive planning, and maintaining organized records can help manage these challenges. Additionally, staying updated on regulatory changes and leveraging validation management software can streamline processes and reduce the risk of errors.

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

AspectValidation SpecialistQuality Assurance Specialist
Required CredentialsTypically requires a degree in life sciences, engineering, or related fields; certifications like CQE or CSQE are commonOften requires similar degrees; certifications like CQE or Six Sigma are also common
Work EnvironmentWorks in regulated industries such as pharmaceuticals, biotech, or medical devices, focusing on validation processesWorks across various industries, focusing on process improvement and compliance
Employer & Industry UsageUsed by companies needing validation of equipment, systems, or processes to meet regulatory standardsUsed by organizations aiming to ensure quality standards and process consistency

While both roles focus on quality and compliance, Validation Specialists primarily verify that equipment and systems meet regulatory standards through validation processes. Quality Assurance Specialists oversee overall quality systems and process improvements. The roles often overlap but differ in scope and focus within regulated industries.

What cities are hiring for Validation Specialist jobs?

Cities with the most Validation Specialist job openings:

What are the most commonly searched types of Validation Specialist jobs?

The most popular types of Validation Specialist jobs are:

Who are the top companies hiring for Validation Specialist jobs?

The top employers for Validation Specialist jobs are:

What states have the most Validation Specialist jobs?

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

Infographic showing various Validation Specialist job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 85% Full Time, 12% Part Time, and 2% Contract. Highlights an 79% Physical, 2% Hybrid, and 19% Remote job distribution, with an average salary of $104,945 per year, or $50.5 per hour.

Full-time

Posted 14 days ago


Job description

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 industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.

We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position:

  • Jr. Validation Specialist

Position Overview:
We are seeking a Junior Validation Specialist with 1–3 years of experience to support validation and qualification activities in a regulated environment. This role is ideal for a detail-oriented professional looking to grow their career in validation, with hands-on involvement in testing, documentation, and field execution under supervision.

Key Responsibilities:

  • Support execution of validation and qualification protocols (IQ, OQ, PQ).
  • Assist with testing activities, data collection, and data logging.
  • Perform field verification of systems and equipment under supervision.
  • Assist in the preparation and review of validation documentation, including protocols and reports.
  • Ensure all activities are performed in compliance with GMP and company procedures.
  • Support deviation investigations, CAPAs, and documentation updates as needed.
  • Collaborate with cross-functional teams including Engineering, Quality, and Operations.

Qualifications:

  • Bachelor’s degree in Engineering, Life Sciences, or related field.
  • 1–3 years of experience in validation, CQV, or related technical role in a regulated industry (pharma, biotech, or medical devices).
  • Basic understanding of GMP and regulatory requirements.
  • Familiarity with validation lifecycle concepts (IQ/OQ/PQ).
  • Strong attention to detail and organizational skills.
  • Good communication and teamwork abilities.

Preferred:

  • Exposure to utilities, equipment qualification, or manufacturing processes.
  • Internship or hands-on experience in validation or quality environments.
  • Experience with documentation practices in regulated industries.

At Validation & Engineering Group, people always come first. We believe that when you're empowered to do your best work, bold ideas thrive and real progress happens. This isn't just a job - it's an opportunity to make a meaningful difference by shaping the future of healthcare and technology alongside a purpose-driven, supportive team.
Excited to build something meaningful together? We look forward to hearing from you.
Validation & Engineering Group is an equal opportunity employer. All applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, or disability status.