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Validation Engineer Ii Jobs (NOW HIRING)

Civica Rx

Validation Engineer II (377)

Petersburg, VA · On-site

$120K - $145K/yr

Position Summary Validation Engineer II will be responsible for leading the commissioning, qualification, and validation (CQV) for a newly announced facility expansion for biologics that includes a ...

Civica Rx

Validation Engineer II (377)

Petersburg, VA · On-site

$120K - $145K/yr

Position Summary Validation Engineer II will be responsible for leading the commissioning, qualification, and validation (CQV) for a newly announced facility expansion for biologics that includes a ...

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How much do validation engineer ii jobs pay per hour?

As of Jul 15, 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 job?

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.

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Validation Engineer Ii jobs near you

0065V6421 CSV Engineer (Laboratory)/Validation Engineer 2 Consultant

Two River Consulting Partners

Summit, NJ • On-site

Contractor

Posted 14 days ago

Job description

0065V6421 CSV Engineer (Laboratory)/Validation Engineer 2 Consultant  
Please contact Amanda Mazza, amanda@tworivercp.com
Job Overview: We are seeking an experienced CSV Engineer to support the implementation and validation of ELLA and Synergy Neo2 laboratory instruments. The ideal candidate should have hands-on experience supporting GxP laboratory instrument implementations and be comfortable managing validation activities for both technologies in parallel.
**Experience with ELLA and Synergy Neo2**
Validation Engineer Responsibilities:
  • Support CSV activities for ELLA and Synergy Neo2 instrument implementation
  • Develop, review, and/or execute validation deliverables including validation plans, risk assessments, test protocols, traceability matrices, summary reports, and related documentation
  • Partner with laboratory, Quality, IT, and project stakeholders to ensure validation activities are completed on schedule
  • Support GxP compliance, data integrity, and 21 CFR Part 11 considerations as applicable
  • Manage validation workstreams for both instruments simultaneously
  • Identify and escalate risks, gaps, delays, or documentation issues
  • Support deviation resolution and documentation updates during protocol execution
Job Requirements:
  • Strong CSV experience in a GxP laboratory or regulated life sciences environment
  • Prior experience with laboratory instrument implementation and validation
  • Experience with ELLA and Synergy Neo2 strongly preferred
  • Ability to manage multiple validation activities or technologies concurrently
  • Familiarity with IQ/OQ/PQ, CSV lifecycle documentation, risk-based validation, data integrity, and Part 11 expectations
  • Strong communication skills and ability to work effectively with cross-functional teams
  • Experience supporting ECQ or lab equipment qualification
  • Experience in biotech, pharma, plasma, or manufacturing laboratory environments
  • Prior experience working in client-facing hybrid/onsite roles
This role can be a local/hybrid setup. At minimum, a 50% on-site presence is required.
LOCATION
50% onsite in Summit, NJ
EMPLOYMENT
Competitive C2C or W2 Contractor
 

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