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Validation Engineer Ii Jobs (NOW HIRING)

Validation Engineer II Location: Carlsbad, CA Type: W2 Contract Industry: Medical Devices / Healthcare We are actively hiring a Validation Engineer II in the Medical Devices / Healthcare industry.

The Validation Engineer II is a mid-level role responsible for creating, planning, and executing software verification activities, and contributing to continuous improvement and validation processes.

Validation Engineer II (Onsite) Location: Bothell, WA Overview: We are looking for a CQV / Validation Engineer with 5-8 years of experience in GMP-regulated pharma/biotech environments. This role ...

The Validation Engineer II is a mid-level role responsible for creating, planning, and executing software verification activities, and contributing to continuous improvement and validation processes.

The Validation Engineer II is a mid-level role responsible for creating, planning, and executing software verification activities, and contributing to continuous improvement and validation processes.

The Validation Engineer II is a mid-level role responsible for creating, planning, and executing software verification activities, and contributing to continuous improvement and validation processes.

The Validation Engineer II ensures the reliability, consistency, and compliance of our processes, equipment, and systems to meet regulatory requirements and quality standards. This role mainly drives ...

The Validation Engineer II ensures the reliability, consistency, and compliance of our processes, equipment, and systems to meet regulatory requirements and quality standards. This role mainly drives ...

Description The Validation Engineer II ensures the reliability, consistency, and compliance of our processes, equipment, and systems to meet regulatory requirements and quality standards. This role ...

Validation Engineer II 10/24/2016 - 10/1/2017 780 Plantation Drive, Burlington, NC 27215 United States $40/hr on W2 Qualifications: Bachelor's degree in a science or engineering related field OR an ...

The Validation Engineer II works on many phases/sub-tasks of projects of moderate complexity and working under general supervision or mostly independently with minimal supervision. Essential ...

Validation Engineer II

Framingham, MA ยท On-site

$137K - $177K/yr

Summary of The Validation Engineer II will work as part of a larger validation team to ensure the biotech facility equipment, utilities, instrumentation and computerized systems are qualified and ...

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How much do validation engineer ii jobs pay per hour?

As of Aug 5, 2026, the average hourly pay for validation engineer ii 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 are the key skills and qualifications needed to thrive in the Validation Engineer II position, and why are they important?

To thrive as a Validation Engineer II, you need a strong background in engineering principles, quality assurance methodologies, and experience with validation protocols, typically supported by a bachelor's degree in engineering or a related field. Proficiency with industry-specific tools such as statistical analysis software, ERP systems, and knowledge of regulatory standards like GMP or ISO is highly valued, and certifications like ASQ are advantageous. Excellent problem-solving, attention to detail, and effective communication are key soft skills for this role. These competencies are essential to ensure products and processes meet rigorous compliance and quality standards, minimizing risks and ensuring project success.

What are the typical responsibilities of a Validation Engineer II?

A Validation Engineer II is responsible for planning, executing, and documenting validation activities for equipment, systems, and processes to ensure compliance with industry and regulatory standards. This includes developing and reviewing protocols, analyzing test data, troubleshooting issues, and supporting audits or inspections. You can expect to work closely with cross-functional teams such as quality assurance, manufacturing, and R&D to coordinate validation efforts and implement continuous improvements. The role offers opportunities to expand both technical expertise and project management skills, making it a strong stepping stone for career advancement in engineering and quality fields.

What is a Validation Engineer II?

A Validation Engineer II is responsible for ensuring that processes, systems, and products meet regulatory and quality standards. They develop and execute validation protocols, perform testing, analyze data, and document results to maintain compliance with industry regulations. This role typically requires experience in validation methods, technical problem-solving, and collaboration with cross-functional teams. Validation Engineers II work in industries such as pharmaceuticals, medical devices, and manufacturing to ensure product reliability and safety.

More about Validation Engineer Ii jobs
What are the most commonly searched types of Validation Engineer Ii jobs? The most popular types of Validation Engineer Ii jobs are:
Infographic showing various Validation Engineer Ii job openings in the United States as of July 2026, with employment types broken down into 95% Full Time, 2% Part Time, and 3% Contract. Highlights an 87% Physical, 4% Hybrid, and 9% Remote job distribution, with an average salary of $108,152 per year, or $52 per hour.

Validation Engineer II

Intellectt INC

Carlsbad, CA โ€ข On-site

Contractor

Posted 20 days ago


Job description

Hiring: Validation Engineer II
Location: Carlsbad, CA
Type: W2 Contract
Industry: Medical Devices / Healthcare
We are actively hiring a Validation Engineer II in the Medical Devices / Healthcare industry. This is an excellent opportunity for professionals with experience in validation, quality systems, and regulated manufacturing environments.
 
Key Responsibilities:
• Validation Protocol Development & Execution
• Process, Equipment & System Validation
• Validation Master Plans (VMP)
• Change Control & Validation Assessment
• Validation Documentation & Final Reports
• Internal & External Audit Support
• Quality Systems & Regulatory Compliance
• Cross-Functional Project Coordination
 
Requirements:
• Bachelor's Degree in Engineering or related field (Master's preferred)
• 2–3+ years of Validation Engineering experience
• Experience in Medical Device or regulated manufacturing
• Knowledge of Validation Lifecycle & Documentation
• Experience with Change Management and Quality Systems
• Strong technical writing, communication, and analytical skills
• Ability to execute and manage validation projects independently