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Equipment Validation Jobs (NOW HIRING)

Nestle

Senior Validation Engineer

Lower Gwynedd, PA · On-site

This role will be a key subject matter expert in GMP equipment validation and shipping validation and will own the equipment validation, requalification, and shipping validation programs. This role ...

Validation & Engineering Group, Inc

PR · On-site

We are seeking a Validation Engineer with experience in upstream equipment to join our team. The Validation Engineer will be responsible for validating equipment, processes, and systems used in the ...

Validation & Engineering Group, Inc

PR · On-site

We are seeking a Validation Engineer with experience in upstream equipment to join our team. The Validation Engineer will be responsible for validating equipment, processes, and systems used in the ...

Validation & Engineering Group, Inc

PR · On-site

We are seeking a Validation Engineer with experience in upstream equipment to join our team. The Validation Engineer will be responsible for validating equipment, processes, and systems used in the ...

DPS Group

CQV Engineer

Framingham, MA · On-site

Equipment validation protocol development, including drafting documents, managing review cycles and protocol approval. * Support Validation Master Plan development * Execution of equipment validation ...

BoehringerPRD

Description This position manages all equipment, process, systems and product related validation activities, except GXP related computerized systems for both Pharmaceuticals and Vaccines at the site

SOKOL GxP Services

Validation Engineer

Devens, MA · On-site

Equipment validation experience is a plus. * Eligible to work in the United States. Benefits * Competitive pay rate, $ per hour: 46 - 51 (W2 only, no C2C option) * Health insurance; * Holiday pay ...

Lancesoft

QA Validation Specialist 3

Portsmouth, NH · On-site

$80 - $84.41/hr

Notes from intake - Role is Equipment validation and Cleaning Validation Experience with Kneat is absolutely required. Experience with Ellab for Temp Mapping is a plus Manager is looking for ...

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Equipment Validation information

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How much do equipment validation jobs pay per hour?

As of Jul 21, 2026, the average hourly pay for equipment validation in the United States is $63.77, according to ZipRecruiter salary data. Most workers in this role earn between $52.64 and $69.71 per hour, depending on experience, location, and employer.

What is equipment validation?

Equipment validation is the process of ensuring that machinery and equipment used in manufacturing or laboratory settings perform as intended and meet regulatory standards. This process typically involves documented testing, calibration, and qualification procedures to verify that the equipment consistently produces reliable and accurate results. Equipment validation is critical in industries such as pharmaceuticals, biotechnology, and medical devices, where product quality and patient safety are paramount. Proper validation helps organizations comply with regulatory requirements and avoid costly errors or recalls.

What is the difference between Equipment Validation vs Equipment Calibration?

AspectEquipment ValidationEquipment Calibration
PurposeTo ensure equipment performs as intended and meets regulatory requirementsTo adjust and verify equipment accuracy and precision
ProcessComprehensive testing and qualificationRoutine measurement and adjustment
FrequencyTypically during installation, qualification, or as requiredRegular intervals based on manufacturer or industry standards
DocumentationValidation protocols and reportsCalibration certificates and logs

Equipment Validation ensures that equipment functions correctly within regulated environments, confirming suitability for use. Equipment Calibration focuses on maintaining measurement accuracy over time. Both are essential for compliance and quality assurance but serve different purposes in equipment management.

What are some common challenges faced in an Equipment Validation role and how can they be managed?

One of the main challenges in Equipment Validation is ensuring compliance with strict regulatory standards while meeting tight project timelines. Professionals in this role often coordinate with cross-functional teams, such as engineering, quality assurance, and production, to gather technical documentation and execute validation protocols. Managing unexpected equipment failures or documentation gaps can also be demanding. Staying organized, maintaining clear communication, and proactively addressing potential issues are key strategies for overcoming these challenges and ensuring successful validation outcomes.

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

To excel in Equipment Validation, you need a strong background in engineering or life sciences, knowledge of regulatory compliance (such as GMP or FDA standards), and experience in validation protocols. Familiarity with validation software, data analysis tools, and systems like LIMS or TrackWise is commonly required, along with certifications like Six Sigma or CQV being advantageous. Attention to detail, problem-solving ability, and effective communication are crucial soft skills for this role. These competencies ensure validated equipment consistently meets quality and regulatory requirements, minimizing risks and supporting safe, compliant operations.
More about Equipment Validation jobs
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Equipment Validation jobs near you
Infographic showing various Equipment Validation job openings in the United States as of July 2026, with employment types broken down into 1% As Needed, 78% Full Time, 17% Part Time, 1% Temporary, 2% Contract, and 1% Nights. Highlights an 99% Physical, and 1% Remote job distribution, with an average salary of $132,650 per year, or $63.8 per hour.
"cleaning validation"

"cleaning validation"

Intellectt INC

Holly Springs, NC • On-site

Contractor

Re-posted 7 days ago

Job description

Role:CQV Engineer – Cleaning Validation 
Location: Holly Springs, NC 
Key Responsibilities:

  • Execute and document cleaning validation protocols per FDA/ICH guidelines (ALCOA principles).

  • Apply expertise with bioreactors, autoclaves, parts washers, and filling machines.

  • Perform MACO calculations to support cleaning limit determinations.

  • Use Kneat for electronic validation documentation and tracking.

  • Work on fill-finish processes and equipment validation.

  • Coordinate with cross-functional teams including manufacturing, QC, QA, and engineering.

  • Review and contribute to analytical method development related to cleaning and residue testing.

Required Skills & Experience:

  • 5–8+ years in CQV/Validation within biologics/pharmaceutical manufacturing.

  • Strong understanding of FDA cGMP, ALCOA, and data integrity principles.

  • Experience with Kneat or other electronic validation tools.

  • Familiarity with MACO, analytical methods, and technical documentation.

  • Must have experience with fill-finish processes, bioreactors, and cleaning equipment.