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Sr Validation Engineer Jobs in Delaware (NOW HIRING)

Serverless Guru

Senior Frontend Engineer

Wilmington, DE · On-site +1

$118K - $163K/yr

Senior Front-End Developer Frontend Engineering React • TypeScript • TanStack Router • ... Zod Experience building reusable validation schemas and leveraging type inference across APIs ...

Elevance Health

Engineer Senior

Wilmington, DE · On-site +1

$101K - $139K/yr

Engineer Senior Engineer Senior Location: This role requires associates to be in-office 1 - 2 days ... validate results. * Aid in integrating activities with other IT departments for successful ...

Serverless Guru LLC.

Senior Frontend Engineer

Wilmington, DE · On-site

$118K - $163K/yr

Senior Front-End Developer Frontend Engineering React TypeScript TanStack Router TanStack Query ... Zod Experience building reusable validation schemas and leveraging type inference across APIs ...

Elevance Health

Engineer Senior

Wilmington, DE · On-site

$101K - $139K/yr

Engineer Senior Engineer Senior Location: This role requires associates to be in-office 1 - 2 days ... validate results. * Aid in integrating activities with other IT departments for successful ...

Greenman-Pedersen, Inc.

Senior Traffic Engineer

Milford, DE · On-site

$100K - $138K/yr

Description GPI is seeking a Senior Traffic Engineer to grow and lead our traffic engineering ... Maintain a valid driver's license with a clean motor vehicle report (MVR) for final consideration

Serigor, Inc.

Senior Data Engineer (Hybrid)

Wilmington, DE · On-site

$102K - $139K/yr

Senior Data Engineer (Hybrid) Location: Wilmington, DE / Berwyn, PA Duration: 18 Months, quarterly ... Validate data integrations and transformation accuracy. * Data Engineering * Design, develop, and ...

Elevance Health

Engineer Senior

Wilmington, DE · On-site +1

$101K - $139K/yr

Engineer Senior Location: This role requires associates to be in-office 1 - 2 days per week ... validate results. * Aid in integrating activities with other IT departments for successful ...

Elevance Health

Engineer Senior

Wilmington, DE · On-site

$101K - $139K/yr

Engineer Senior Location: This role requires associates to be in-office 1 - 2 days per week ... validate results. * Aid in integrating activities with other IT departments for successful ...

Burris Logistics

Infrastructure, Senior Engineer

Milford, DE · On-site

$104K - $142K/yr

The Senior Engineer, Infrastructure position is core to the implementation and support of all ... Conduct system testing, validate infrastructure changes, and provide quality assurance for newly ...

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All JobsSr Validation Engineer JobsSr Validation Engineer Jobs in Delaware

Sr Validation Engineer information

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How much do sr validation engineer jobs pay per hour?

As of Sep 13, 2026, the average hourly pay for sr validation engineer in Delaware is $64.83, according to ZipRecruiter salary data. Most workers in this role earn between $51.73 and $73.61 per hour, depending on experience, location, and employer.

What is a Sr validation engineer?

Sr Validation Engineers are experienced professionals responsible for ensuring that products, systems, or processes meet regulatory standards and function as intended. They lead validation projects, develop protocols, oversee testing, and document results to confirm compliance with industry regulations, such as those from the FDA or ISO. Their work is essential in industries like pharmaceuticals, biotechnology, and manufacturing, where product quality and safety are critical. Senior validation engineers also mentor junior staff and help improve validation processes within their organizations.

What are the key skills and qualifications needed to thrive as a Sr validation engineer?

To thrive as a Sr Validation Engineer, you need a solid background in engineering or life sciences, extensive experience with validation protocols, and a strong understanding of regulatory standards such as FDA, GMP, or ISO. Expertise in using validation software, risk assessment tools, and familiarity with documentation management systems is typically required, along with certifications like Six Sigma or ASQ CQE being advantageous. Exceptional problem-solving abilities, attention to detail, and effective communication skills help you lead teams and interact with cross-functional departments. These competencies are crucial for ensuring products and processes meet compliance standards, maintain quality, and support organizational success.

What are some common challenges a Sr validation engineer faces when managing multiple validation projects simultaneously?

A Sr Validation Engineer often manages several validation projects at once, which can present challenges such as coordinating timelines, ensuring compliance with regulatory standards, and balancing cross-functional communication. Keeping detailed documentation and staying organized are essential, as unexpected equipment issues or shifting project priorities may arise. Successful engineers proactively communicate with quality, manufacturing, and R&D teams to mitigate risks, maintain project momentum, and deliver results within required deadlines.

What is the difference between Sr Validation Engineer vs Validation Engineer?

AspectSr Validation EngineerValidation Engineer
Required CredentialsBachelor's/Master's in Engineering, certifications like CQE or ASQ, experience in validation processesBachelor's in Engineering or related field, some certifications preferred, less experience required
Work EnvironmentPharmaceutical, biotech, or manufacturing industries; leading validation projectsSupporting validation tasks under supervision, often in similar industries
Employer & Industry UsageUsed by companies requiring compliance with FDA, ISO, or GMP standardsCommonly used in manufacturing and quality assurance roles

The main difference between a Sr Validation Engineer and a Validation Engineer lies in experience, responsibility, and expertise. The Sr Validation Engineer typically leads validation projects, has more advanced certifications, and plays a strategic role in compliance. Validation Engineers support validation activities and often work under supervision. Both roles are essential in regulated industries like pharmaceuticals and manufacturing, but the senior role involves greater leadership and technical oversight.

What are popular job titles related to Sr Validation Engineer jobs in Delaware?

For Sr Validation Engineer jobs in Delaware, the most frequently searched job titles are:

What job categories do people searching Sr Validation Engineer jobs in Delaware look for?

The top searched job categories for Sr Validation Engineer jobs in Delaware are:

What cities in Delaware are hiring for Sr Validation Engineer jobs?

Cities in Delaware with the most Sr Validation Engineer job openings:

Sr Validation Engineer jobs near you
Infographic showing various Sr Validation Engineer job openings in Delaware as of August 2026, with employment types broken down into 90% Full Time, 6% Part Time, and 4% Contract. Highlights an 85% Physical, 5% Hybrid, and 10% Remote job distribution, with an average salary of $134,842 per year, or $64.8 per hour.

Validation - Engineer (m/f/d) (Remote)

Dover, DE • On-site

Frontwell Solutions
See more jobs at Frontwell Solutionsexternal

Other

Posted 9 days ago

Job description

Join FrontWell Solutions, a leader in Laboratory Information Management Systems, Manufacturing IT, and Quality Assurance solutions for the life sciences sector. As a trusted consulting partner, we deliver advanced, compliant, and innovative digital solutions that drive operational excellence and regulatory success for our clients. Our expertise spans the full spectrum of pharmaceutical and biotech IT, with a focus on quality, compliance, and digital transformation.
Position Overview

FrontWell Solutions is seeking a highly skilled Senior Validation Engineer to join our growing team. In this role, you will lead and execute validation projects for computerized systems and manufacturing processes in regulated environments, ensuring compliance with GMP, GLP, GxP, and GCP standards. You will play a pivotal role in modernizing quality management systems, implementing Pharma 4.0 methodologies, and driving paperless validation initiatives using leading platforms such as Kneat, Valgenesis, Polarion, DevOps, and Jira. Your expertise will help bridge the gap between regulatory requirements and digital innovation, supporting both consulting and in-house projects.

Customer Relationship Personal Evolution Autonomy Administrative Work Technical Expertise Key Responsibilities
  • Lead the planning, execution, and documentation of validation activities for computerized systems, equipment, and processes in compliance with GAMP5, CSV/CSA, and relevant regulatory standards.
  • Generate and review validation deliverables, including validation plans, user requirements, specifications, risk assessments, test protocols (IQ/OQ/PQ), and summary reports.
  • Implement and support paperless validation solutions (e.g., Kneat, Valgenesis, Polarion, DevOps, Jira), driving efficiency and data integrity in validation processes.
  • Advise on and execute strategic validation QA initiatives, including QMS modernization and adoption of new methodologies aligned with Pharma 4.0.
  • Provide quality control and QA IT support, ensuring robust compliance in pharmaceutical manufacturing and laboratory environments.
  • Collaborate with cross-functional teams, including MES/LIMS/SAP specialists, to ensure seamless integration and validation of enterprise systems.
  • Mentor and train team members and clients on validation best practices, regulatory requirements, and digital validation tools.
  • Support audits and inspections, providing expert guidance on validation documentation and compliance strategies.
Qualifications
  • Bachelor’s or Master’s degree in Engineering, Life Sciences, Computer Science, or a related field.
  • 3+ years of experience in validation engineering within the pharmaceutical, biotech, or regulated life sciences industries.
  • Deep knowledge of GMP, GLP, GxP, GCP, and GAMP5 standards, with a proven track record in computer system validation (CSV/CSA).
  • Hands-on experience with paperless validation platforms (Kneat, Valgenesis, Polarion, DevOps, Jira, Kneat GxP, Automated Testing tools).
  • Familiarity with MES, LIMS, and SAP systems as secondary skills.
  • Strong technical writing skills and experience generating validation documentation and deliverables.
  • Demonstrated ability to lead validation projects, modernize QMS, and implement new validation methodologies.
  • Excellent communication skills, with the ability to work effectively in both consulting and in-house environments.
  • Solid understanding of pharmaceutical manufacturing processes, quality control, and regulatory requirements.
Why Join FrontWell Solutions?

At FrontWell Solutions, we offer more than just a competitive salary. We are committed to fostering a transparent, supportive, and innovative work environment where your expertise is valued and your career can thrive. With us, you will benefit from:

  • Fair Work Conditions: Transparent and equitable policies for all employees.
  • Remote Work Infrastructure: Advanced tools and support for seamless remote collaboration.
  • Innovative Culture: A start-up spirit that encourages creativity, continuous learning, and the adoption of cutting-edge technologies.
  • Empowerment and Feedback: A culture built on trust, empowerment, and constructive feedback to support your personal and professional growth.
  • Career Growth: Tailored career development plans, early responsibility, and opportunities to lead impactful projects.
  • Work-Life Harmony: Flexible arrangements to support your work-life balance and personal preferences.
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