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Validation Jobs (NOW HIRING)

A Brief Overview The Engineer, Validation Technical leads the site validation and contamination control strategy to ensure compliance with cGMP regulations and company quality standards. This role ...

Assists validation efforts in many ways including the following: executes/supports equipment qualifications, cleaning validations and recertifications, chamber (i.e., freezers, refrigerators ...

Catalyx Services, LLC seeks a Validation Engineer reporting to office in Montgomeryville, PA to prepare various control systems validation documents, including user requirement specifications ...

Join our R&D Lab Engineering team as a Validation Engineer and play a critical role in ensuring the performance, durability, and reliability of nextgeneration engine systems. In this role, you will ...

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 ...

Validation Technician Who we are? We are a French pharmaceutical industrial group, recognized for making affordable healthcare products that improve and simplify patients' lives to as many people as ...

Develop, review, and approve validation master plans, protocols, reports, and supporting documentation. * Partner with Manufacturing, Engineering, Quality, Regulatory, and Supply Chain to support new ...

Validation & Engineering Group, Inc. (V&EG) is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the ...

Position Summary The Validation Specialist is responsible for supporting and executing validation and qualification activities for manufacturing processes, equipment, utilities, and facilities in a ...

Zifo is looking for a Validation Consultant to join their team of laboratory IT (lab computing, Lab IT systems, QA, Validation) professionals. **This role will require a 100% on-site presence at the ...

New

Validation Engineer

Elgin, IL · On-site

$85K/yr

Validation Engineer 1st shift E-Verify Location: Elgin, IL | On-Site Duties/Responsibilities: * Participate in projects/program management, review new and existing drawings as received from customers ...

The Validation Engineer will oversee, evaluate, and calibrate equipment, systems, and procedures used in the development and production of products and will ensure safety, quality, and purity ...

As a Validation Engineer, you will work across laboratory, quality, and digital stakeholders to help maintain compliant systems, support instrument lifecycle activities, and strengthen validation ...

The Validation Engineer - Consulting Services will support the Consulting Services team's offerings around shipper, packaging, and shipping lane qualifications across temperature sensitive supply ...

Stefanini is looking for Validation Specialist in Marion, NC (Hybrid) For quick Apply, please reach out to Rachit Rastogi - call: 2489360662/ email: rachit.rastogi@stefanini.com Work Hours: M-F (40 ...

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How much do validation jobs pay per hour?

As of Jun 28, 2026, the average hourly pay for validation in the United States is $52.00, according to ZipRecruiter salary data. Most workers in this role earn between $39.42 and $63.22 per hour, depending on experience, location, and employer.

What is a validation job?

A validation job involves verifying that products, processes, or systems meet specified standards and requirements. It often includes tasks such as testing, documentation, and compliance checks, especially in industries like pharmaceuticals, manufacturing, and technology. Skills in quality assurance, attention to detail, and familiarity with validation protocols are typically required.

What is the difference between Validation vs Quality Assurance?

AspectValidationQuality Assurance
PurposeEnsures products meet specifications and intended usePrevents defects through process improvements
FocusProduct-specific testing and verificationProcess and system quality control
ActivitiesDesign validation, process validation, equipment validationAudits, process reviews, standards compliance
TimingBefore product releaseThroughout production cycle

Validation focuses on confirming that a product or process meets specified requirements before release, while Quality Assurance emphasizes maintaining quality standards throughout the production process to prevent defects. Both roles are essential in industries like pharmaceuticals and manufacturing, but they serve different stages of quality management.

What is the 3 month rule for jobs?

In validation roles, the 3 month rule often refers to a probationary period during which an employee's performance and fit for the position are assessed. This period typically allows employers to evaluate skills, adherence to procedures, and reliability before confirming permanent employment or considering further training. It is common for companies to set this timeframe to ensure quality and compliance in validation processes.

What jobs pay $10,000 a month without a degree?

Validation roles typically do not pay $10,000 a month without specialized skills or experience. High-paying jobs that can reach this level without a degree often include sales, real estate, or certain entrepreneurial ventures, but they usually require strong skills, certifications, or a proven track record. Most roles with such income levels rely on performance-based compensation rather than formal education alone.

What engineers make $500,000?

Senior engineers in specialized fields such as software, petroleum, or aerospace engineering can earn $500,000 or more annually, often through a combination of base salary, bonuses, and stock options. High-level roles typically require extensive experience, advanced skills, and sometimes professional certifications or advanced degrees.

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

To thrive as a Validation Engineer, you need a solid background in engineering or life sciences, with expertise in quality assurance and regulatory compliance. Familiarity with validation protocols, statistical analysis tools, and industry standards such as GMP, FDA, or ISO guidelines is essential. Strong analytical thinking, attention to detail, and effective communication skills help you identify issues and collaborate across teams. These abilities ensure that products and processes meet strict safety and quality requirements, minimizing risks and ensuring regulatory approval.

What are some common challenges faced by professionals in validation roles, and how can they be overcome?

Professionals in validation roles often face challenges such as tight project timelines, evolving regulatory requirements, and the need for meticulous documentation. Balancing thoroughness with efficiency is crucial, as validation processes must be both comprehensive and timely to support product launches or regulatory submissions. Effective communication with cross-functional teams, proactive planning, and staying updated with industry standards can help overcome these challenges and ensure successful validation outcomes.

What are validation jobs?

Validation jobs involve ensuring that products, processes, or systems meet specific requirements and function as intended. In industries like pharmaceuticals, biotechnology, and manufacturing, validation specialists test equipment, procedures, and software to guarantee quality and compliance with regulatory standards. These professionals document their findings and help identify areas for improvement, playing a key role in quality assurance. Validation jobs are essential for maintaining product safety, effectiveness, and meeting industry regulations.
More about Validation jobs
What cities are hiring for Validation jobs? Cities with the most Validation job openings:
What are the most commonly searched types of Validation jobs? The most popular types of Validation jobs are:
What states have the most Validation jobs? States with the most job openings for Validation jobs include:
Engineer, Validation

Other

Posted 16 days ago


Job description

Voyant Beauty believes our people are more than just employees; they’re the driving force behind everything we achieve. Our culture fosters teamwork, respect, and camaraderie, ensuring that every individual’s contribution is valued and celebrated. We invest in their growth, providing opportunities for development and advancement within our dynamic team.

Voyant Beauty is a company that specializes in the development and manufacturing, of beauty, personal and home care products. We work with various brands, retailers, and businesses to create customer formulations and products tailored to their needs. This can include skincare, haircare, bath and body products, fragrances, and more. Essentially, Voyant Beauty serves as a one-stop-shop for companies looking to bring their beauty and personal care product ideas to life.

Safety is a core value at Voyant Beauty. We prioritize the well-being of our team members, ensuring a safe and secure environment where everyone can thrive and excel.

If you’re seeking to be part of a team where your talents are valued, your safety is paramount, and your efforts contribute to meaningful change, then Voyant Beauty is the place for you. Come join us and be a part of our journey.


A Brief Overview
The Engineer, Validation Technical leads the site validation and contamination control strategy to ensure compliance with cGMP regulations and company quality standards. This role serves as the subject matter expert (SME) for hygiene systems and validation, driving continuous improvement and standardization across validation programs. This position is responsible for planning, executing, and overseeing validation activities including process, cleaning, equipment, and utility system qualifications for OTC products, cosmetics, and regulated systems. The Engineer, Validation Technical partners closely with Engineering, Quality Assurance, and Operations to ensure validation and hygiene programs meet regulatory and internal requirements. The role also owns audit readiness and supports regulatory inspections, while proactively mitigating contamination risks across the site.
What you will do

  • Lead the validation lifecycle strategy for new equipment, manufacturing processes, and facility changes, including development, standardization, and approval of IQ/OQ/PQ protocols and final reports.
  • Define, implement, and continuously improve site-wide contamination control programs, including cleaning validation, environmental monitoring, and critical utility systems (e.g., USP water, compressed air).
  • Own audit readiness for validation and hygiene systems, serving as the primary SME during internal and external audits and regulatory inspections.
  • Develop, review, and maintain SOPs, validation protocols, and technical documentation to ensure compliance, consistency, and inspection readiness.
  • Provide technical leadership and cross-functional support to Engineering, Quality, and Operations on validation, hygiene, and compliance-related initiatives.
  • Mentor and provide guidance to junior engineers and technicians, supporting development of validation and quality capabilities across the site.
  • Lead environmental monitoring oversight and interface with third-party laboratories; evaluate microbial and analytical data to assess risk and ensure program effectiveness.
  • Provide input into equipment design and purchase decisions with validation and compliance requirements in mind
  • Support quality investigations, deviations, and CAPA related to validation or equipment failures
  • Drive continuous improvement initiatives across validation and contamination control programs
  • Remain current with regulatory guidance, industry best practices, and emerging risks in cGMP environments
  • Some duties may vary slightly by location


Education Qualifications

  • Bachelor's Degree Mechanical Engineering, Chemical Engineering, or related technical field (Required)


Experience Qualifications

  • 4-6 years Validation experience within a cGMP manufacturing environment (OTC, pharmaceutical, cosmetics, or personal care) (Required)
  • 4-6 years Cross-functional project leadership across engineering, quality, and operations (Required)
  • 4-6 years FDA/OTC regulated environments (Preferred)
  • 4-6 years Leading audits, inspections, and regulatory interactions (Preferred)


Skills and Abilities

  • Process, cleaning, equipment, and utility validation (High proficiency)
  • IQ/OQ/PQ protocol development and execution (High proficiency)
  • cGMP compliance and regulatory standards (High proficiency)
  • Regulatory inspection leadership (FDA and customer audits) (High proficiency)
  • Risk-based validation strategy and decision making (High proficiency)
  • Contamination control program ownership (cleaning, EM, utilities) (High proficiency)
  • SOP and technical document development (High proficiency)
  • Cross-functional collaboration and stakeholder influence (High proficiency)
  • Influencing without authority across functions (High proficiency)
  • Project leadership and prioritization across multiple initiatives (High proficiency)
  • Root cause analysis and deviation/CAPA support (Medium proficiency)
  • Environmental monitoring and lab coordination (Medium proficiency)
  • Analytical and microbiological test interpretation (Medium proficiency)


Licenses and Certifications

  • Lean Six Sigma certification or equivalent training (Preferred)

To Staffing and Recruiting Agencies: Our company does not accept unsolicited curriculum vitae’s or applications from agencies. We are not responsible for any fees related to unsolicited curriculum vitae’s or applications and explicitly reserve its right to contact candidates presented in such unsolicited curriculum vitae’s or application.

Our company provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, religion, sex, color, national origin, sexual orientation, age, disability or veteran status. Voyant Beauty will consider requests for accommodations due to a disability impacting a qualified employee's ability to perform the essential functions of their position consistent with applicable laws. In addition to federal law requirements, Voyant Beauty complies with applicable provincial and local laws governing nondiscrimination in employment in every location in which the company has facilities. This policy applies to all terms and conditions of employment, including recruiting, hiring placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training.