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Equipment Validation Jobs (NOW HIRING)

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 ...

Astrix Inc

Laboratory Validation Specialist

Rensselaer, NY · On-site

$55 - $78/hr

Provide quality review and approval of validation activities related to equipment, systems, and process changes * Develop, execute, and review IQ, OQ, and PQ validation protocols and reports * Review ...

New

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

Fresenius Kabi

Validation Engineer

Wilson, NC · On-site

$60K - $85K/yr

... validation and equipment/system requalification ... Will participate in equipment improvement teams charged with enhancing the compliance and ...

System One

QA Validation Engineer

Bethlehem, PA · On-site

Experience working in equipment validation required * Must come from a regulated environment - food, pharma, chemical * Must have experience working with temperature controlled product * 3-5 years of ...

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Equipment Validation information

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How much do equipment validation jobs pay per hour?

As of Aug 17, 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?

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.
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What states have the most 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 August 2026, with employment types broken down into 1% As Needed, 80% Full Time, 15% 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.

Validation Engineer

Katalyst Healthcares and Lifesciences

Rochester, NY • On-site

Other

Posted 3 days ago

New

Job description

Responsibilities:
  • Client is seeking validation consultants to support a 9-month minimum onsite project in South Carolina. The consultants will support validation execution and gap assessments tied to equipment qualification, tank qualification, mixing studies, smoke studies, aseptic technique, and instrument/equipment qualification.
  • The project is being driven by audit findings and identified gaps in the site's validation program. The primary focus will be equipment validation, especially around tanks used for drug substance mixing and drug product filling. The team needs to assess whether existing IOQ/OQ documentation is robust enough, identify gaps between OQ and PQ, and determine whether current qualifications can support performance qualification expectations.
  • The consultants will also support product-specific mixing study needs, including evaluating mixing from an equipment qualification perspective. This includes understanding tank qualification, viscosity considerations, matrix/bracketing approaches, risk assessment, and how to identify, group, and mitigate validation gaps.
  • The team will also support smoke study execution in an aseptic processing environment. The site has a tunnel and two lyophilizers, so candidates should understand aseptic technique, equipment operation, and how to drive execution as a validation representative.
  • This role is execution-heavy, but the client also needs consultants who can perform gap assessments and provide guidance on validation strategies. The lead consultant should be able to drive the project, guide internal resources, manage execution, and keep the validation effort moving forward.

Requirements:
  • Bachelor's degree in Engineering, Science, Life Sciences, or related technical discipline preferred. Equivalent hands-on validation experience can be considered.
  • Include Must Have:
  • Validation execution experience in a pharmaceutical, biotech, or aseptic manufacturing environment.
  • Equipment qualification experience.
  • Strong understanding of IOQ/OQ/PQ expectations.
  • bility to perform gap assessments.
  • Tank qualification experience.
  • Mixing study experience or strong understanding of equipment-based mixing qualification.
  • septic processing experience.
  • Smoke study experience or strong understanding of smoke study execution.
  • bility to support protocol execution and documentation.
  • bility to assess whether qualification packages are robust enough.
  • bility to identify validation gaps and recommend mitigation strategies.
  • bility to handle a strong personality and drive work forward without being timid.

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