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Validation Specialist Jobs (NOW HIRING)

Stark Pharma Solutions Inc

MD · On-site

Validation Engineer / Validation Specialist Location: Maryland Duration: Long-Term Contract Job Overview We are seeking an experienced Validation Engineer/Validation Specialist to support equipment ...

Argenta

Validation Specialist

Shawnee, KS · On-site

Execute validation lifecycle documents including Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) for both manufacturing and laboratory systems.

The Secant Group

Validation Specialist II

Telford, PA · On-site

The Validation Specialist II coordinates and implements various activities for compliant and effective support of the Secant Group Validation functions conforming to ISO 13485, internal, and customer ...

RXinsider LTD.

System Validation Specialist

Dallas, TX · On-site

$55 - $85/hr

As a System Validation Specialist, you have hands on experience with installing, troubleshooting, repairing, calibrating, and inspecting monitoring equipment used in healthcare facilities. The System ...

New

Secant Group, LLC

Validation Specialist II

Telford, PA · On-site

$80 - $110/hr

The Validation Specialist II coordinates and implements various activities for compliant and effective support of the Secant Group Validation functions conforming to ISO 13485, internal, and customer ...

New

FITS LLC

Validation Specialist

Dorado, PR · On-site

$70 - $90/hr

For Validation services WHAT MAKES YOU A FIT The Technical Part: * Bachelor's in Life Sciences with five (5) years of experience in Validation activities within the Medical Devices Industry.

Argenta

Validation Specialist

Shawnee, KS · On-site

Execute validation lifecycle documents including Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) for both manufacturing and laboratory systems.

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Validation Specialist information

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How much do validation specialist jobs pay per hour?

As of Sep 3, 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.

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Validation Specialist jobs near you
Infographic showing various Validation Specialist job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 83% Full Time, 14% Part Time, and 2% Contract. Highlights an 85% Physical, 2% Hybrid, and 13% Remote job distribution, with an average salary of $104,945 per year, or $50.5 per hour.

Validation Specialist (Cleaning-In-Place)

Validation & Engineering Group, Inc.

Juncos, PR • On-site

Full-time

Re-posted 20 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:
  • Validation Specialist - CIP

Summary:
The Validation Specialist is responsible for planning, coordinating, and executing all Commissioning, Qualification, and Validation (CQV) activities related to Cleaning-In-Place (CIP) and Sterilization-In-Place (SIP) systems within a biotech manufacturing environment. This role ensures that cleaning and sterilization systems are installed, tested, and qualified in compliance with GMP, FDA, EMA, and ASTM E2500 standards, supporting readiness for process validation and commercial manufacturing.
Key Responsibilities:
Commissioning & Qualification Execution:
  • Review and approve vendor FAT/SAT protocols for CIP/SIP equipment.
  • Execute IOQ and PQ protocols for CIP/SIP systems, including cleaning recipe verification, steam sterilization cycle qualification, and temperature mapping.
  • Oversee the qualification of utilities supporting CIP/SIP systems (Clean Steam, WFI, Process Air).
  • Collaborate closely with Automation, Process, and QA Validation for recipe verification and data integrity.

Documentation & Compliance:
  • Generate and review URS, FAT/SAT, IOQ, and PQ documentation in compliance with ASTM E2500 and GAMP 5.
  • Ensure traceability from design specifications through executed testing.
  • Assist in managing deviations, non-conformances, and change controls related to CIP/SIP systems.
  • Prepare summary reports for Quality Assurance approval.

Cross-functional Collaboration:
  • Collaborate with Process Engineers, Automation, QA, and Manufacturing to ensure successful integration of CIP/SIP operations with process equipment.
  • Support operations during process validation batches and cleaning validation campaigns.
  • Provide training and technical guidance to CQV engineers and contractors executing test protocols.

Qualifications:
  • Bachelor's degree in Chemical, Mechanical, or Biochemical Engineering (or equivalent).
  • Minimum 7�10 years of experience in CQV within biotech or pharmaceutical manufacturing environments.
  • Experience in generating and executing documentation for CQV activities.
  • Strong knowledge of cleaning validation, sterilization principles, and automation integration.
  • Familiarity with DeltaV, SCADA, or PLC systems for CIP/SIP recipe management.
  • Expertise in ASTM E2500, ISPE Baseline Guides, GAMP 5, and FDA/EMA guidelines.
  • Proficiency in reviewing P&IDs, piping isometrics, and functional design specifications.
  • Experience executing or overseeing FAT/SAT, IOQ, PQ activities.
  • Knowledge of data integrity, 21 CFR Part 11, and electronic validation systems (e.g., Kneat, ValGenesis).
  • Must be fully bilingual (English / Spanish) with excellent oral skills.
  • Available to work extended hours, possibility of weekends and holidays.

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.

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