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Validation Associate Jobs in New Jersey (NOW HIRING)

DTCC

Model Validation Senior Associate

Jersey City, NJ · On-site

Effective validation helps to ensure that models are sound, identifying potential limitations and assumptions and assessing their possible impact. All model components, inputs, processing, outputs ...

AtlantiCare

Warehouse Associate I

Egg Harbor Township, NJ · On-site

$15.75 - $18.75/hr

Warehouse Associate I Role Description Title: Warehouse Associate I Job Code: 150 Exempt: Non ... Valid New Jersey Driver's License * Good command of the English language * Ability to drive and ...

Momentum Solar

Warehouse Associate

East Brunswick, NJ · On-site

$20 - $22/hr

Warehouse Associate Momentum Solar is a premier residential solar provider with offices in multiple ... Valid driver's license * Warehouse experience * Must be able to operate a sit-down forklift

System One

Warehouse Associate

Parlin, NJ · On-site

$20 - $25/hr

Warehouse Associate Location: Parlin, NJ Type: Contract-to-Hire Compensation: $20 - $25 per hour ... Valid New Jersey driver's license with an acceptable driving record is required. T his requirement ...

System One

Warehouse Associate

Parlin, NJ · On-site

$20 - $25/hr

Warehouse Associate Location: Parlin, NJ Type: Contract-to-Hire Compensation: $20 - $25 per hour ... Valid New Jersey driver's license with an acceptable driving record is required. T his requirement ...

System One Holdings, LLC

Warehouse Associate

Parlin, NJ · On-site

$20 - $25/hr

Warehouse Associate Location: Parlin, NJ Type: Contract-to-Hire Compensation: $20 - $25 per hour ... Valid New Jersey driver's license with an acceptable driving record is required. T his requirement ...

4 Way Logistics, Inc.

Delivery Associate

Linden, NJ · On-site

$23.75 - $24/hr

Delivery Associate Seasonal Driver for 4 Way Logistics LLC Location: Linden, NJ, United States ... Valid Driver's license & Clean driving record. * Drug screening. Highlights: * Competitive pay.

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All JobsValidation Associate JobsValidation Associate Jobs in New Jersey

Validation Associate information

See New Jersey salary details

$22

$52

$79

How much do validation associate jobs pay per hour?

As of Aug 10, 2026, the average hourly pay for validation associate in New Jersey is $52.79, according to ZipRecruiter salary data. Most workers in this role earn between $40.00 and $64.18 per hour, depending on experience, location, and employer.

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

To thrive as a Validation Associate, you need a background in life sciences or engineering, strong analytical skills, and knowledge of regulatory compliance standards such as GMP or FDA guidelines. Familiarity with validation software, laboratory instrumentation, and documentation management systems is typically required, and certifications like Lean Six Sigma can be beneficial. Attention to detail, problem-solving abilities, and effective communication are essential soft skills in this role. These skills ensure that processes, equipment, and systems meet regulatory requirements and quality standards, which is critical for product safety and organizational compliance.

What is the difference between Validation Associate vs Quality Control Analyst?

AspectValidation AssociateQuality Control Analyst
Required CredentialsBachelor's degree in life sciences or related field; certifications like CQE or ASQ often preferredBachelor's degree in chemistry, biology, or related field; certifications like CQE or ASQ common
Work EnvironmentPharmaceutical, biotech, or medical device manufacturing facilities; focus on validation processesLaboratories, manufacturing plants; focus on testing and quality assessment
Employer & Industry UsageUsed in regulated industries requiring validation of processes and systemsCommon in quality testing, inspection, and product release processes

While both roles require a background in science and similar certifications, a Validation Associate primarily focuses on validating processes and systems to ensure compliance, whereas a Quality Control Analyst concentrates on testing products and materials to verify quality. Both roles are essential in regulated industries but serve different functions within the quality assurance framework.

What is a validation associate?

Validation Associates are professionals responsible for ensuring that processes, equipment, and systems in industries like pharmaceuticals, biotechnology, and manufacturing meet required standards and regulations. They plan and execute validation protocols to confirm that products are produced consistently and meet quality specifications. Their work involves documenting procedures, performing tests, analyzing data, and maintaining compliance with regulatory agencies such as the FDA. Validation Associates play a critical role in quality assurance and risk management within their organizations.

How does a validation associate typically collaborate with other departments during a project?

A Validation Associate frequently works cross-functionally with teams such as Quality Assurance, Manufacturing, and Research & Development. They coordinate to gather essential documents, understand process requirements, and ensure that all validation activities meet regulatory standards. Effective communication and organization are key, as Validation Associates often facilitate meetings, resolve discrepancies, and provide updates to stakeholders. This collaborative approach helps maintain compliance and supports the successful launch or improvement of products and processes.
What are the most commonly searched types of Validation jobs in New Jersey? The most popular types of Validation jobs in New Jersey are:
What are popular job titles related to Validation Associate jobs in New Jersey? For Validation Associate jobs in New Jersey, the most frequently searched job titles are:
What job categories do people searching Validation Associate jobs in New Jersey look for? The top searched job categories for Validation Associate jobs in New Jersey are:
What cities in New Jersey are hiring for Validation Associate jobs? Cities in New Jersey with the most Validation Associate job openings:
Validation Associate jobs near you
Infographic showing various Validation Associate job openings in New Jersey as of August 2026, with employment types broken down into 1% As Needed, 69% Full Time, 27% Part Time, 1% Temporary, and 2% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $109,800 per year, or $52.8 per hour.

Quality Assurance Validation Associate

New Cibo Vita LLC

Totowa, NJ • On-site

$23 - $27/hr

Full-time

Posted 12 days ago

Job description

The QA Validation Associate supports the development, execution, and documentation of validation protocols to ensure that all equipment, manufacturing processes, cleaning procedures,

and systems consistently meet quality and regulatory standards. Working under the guidance of the QA Validation Lead, this role is essential in maintaining Good Manufacturing Practices

(GMP) and ensuring our Totowa facilities remain audit-ready and compliant with food safety regulations.

Key Responsibilities:
    1. Protocol Support & Development
  • Assist in authoring and updating validation protocols for equipment, production processes, and cleaning cycles.
  • Help define acceptance criteria and sampling plans based on technical inputs from

    • Production and Engineering.

  • Ensure all draft protocols align with internal SOPs and regulatory expectations before

    • execution.

      2. Execution of Validation Trials
  • Coordinate and perform onfloor validation activities, including Installation

    • Qualification (IQ), Operational Qualification (OQ), and Performance Qualification

    (PQ).

  • Record raw data, observations, and any deviations in realtime during trials to ensure documentation integrity.
  • Monitor critical control parameters to verify that equipment is operating within validated

    • limits.

      3. Data Analysis & Reporting
  • Compile and organize data from completed trials to assist in the preparation of final validation reports.
  • Identify and escalate any "out of specification" results or failed criteria to the Validation

    • Lead.

  • Maintain the site validation master file and ensure all records are filed according to

    • document control standards.

      4. Compliance & Audit Readiness
  • Support the facility’s "Audit 365" posture by ensuring all validation paperwork is complete and accessible for FDA, SQF, or thirdparty inspections.
  • Participate in internal quality audits to verify that validated states are being maintained on the production floor.
  • Stay updated on current food safety trends and GMP requirements related to equipment

    • and process qualification.

      5. Continuous Improvement
  • Identify opportunities to streamline validation sampling or data collection to improve efficiency.
  • Assist in training production and sanitation personnel on new validated procedures or updated SOPs.
  • Support the QA team in drafting or revising SOPs related to equipment maintenance and

    • calibration.

    Qualifications:
  • Education: Associate degree in a technical field (Food Science, Engineering, Biology) or a bachelor’s degree in progress.
  • Experience: 13 years of experience in a quality or manufacturing role; experience in a regulated environment (Food, Pharma, or MedTech) is preferred.
  • Technical Skills: Basic understanding of GMP, HACCP, and the IQ/OQ/PQ framework.
  • Communication: Strong technical writing skills and the ability to communicate clearly with crossfunctional teams.
  • Software: Proficiency in Microsoft Office (Excel/Word); familiarity with Quality

    • Management Systems (QMS) is a plus.

    Working Conditions
  • Environment: Onsite manufacturing role across multiple Totowa facilities.
  • Physical: Requires standing for extended periods during trials, wearing required PPE, and adhering to strict food safety protocols.
  • Schedule: Primarily day shift, with occasional flexibility required for offshift or

    • weekend validation trials to minimize production downtime.

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