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Validation Engineer Iii Jobs (NOW HIRING)

CYNET SYSTEMS

Validation Engineer 3

Austin, TX · On-site

$65 - $67/hr

Ability to communicate with a variety of engineering disciplines and management. Responsibilities: * Writes comprehensive electrical & functional test plans for the processor interface validation of ...

Akraya Inc.

Validation Engineer III

Hillsboro, OR

Software testing engineer who will performing day to day validation related activities including: Software building and continuous integration environment maintenance and improvements Validation new ...

Collabera

Software Validation Engineer III

Warsaw, IN · On-site

The Software Validation Engineer will be responsible for performing validation activities as new or implemented software within the operations, quality or other functions. Strong and in-depth ...

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Validation Engineer Iii information

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How much do validation engineer iii jobs pay per hour?

As of Aug 8, 2026, the average hourly pay for validation engineer iii 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 the difference between Validation Engineer Iii vs Validation Engineer Ii?

AspectValidation Engineer IiiValidation Engineer Ii
Required CertificationsGMP, GxP, or industry-specific validation certificationsGMP, GxP, or industry-specific validation certifications
Work EnvironmentPharmaceutical, biotech, or medical device manufacturingPharmaceutical, biotech, or medical device manufacturing
Experience LevelAdvanced, with 3+ years of validation experienceIntermediate, with 1-3 years of validation experience
Job ResponsibilitiesLeading validation projects, complex troubleshooting, mentoringSupporting validation activities, executing protocols

The Validation Engineer Iii typically has more experience and handles complex validation projects, often leading initiatives and mentoring junior staff. In contrast, Validation Engineer Ii focuses on supporting validation tasks and executing protocols under supervision. Both roles are common in regulated industries like pharmaceuticals and biotech, with the Iii level requiring more expertise and responsibility.

What skills and qualifications are needed to thrive as a Validation Engineer III?

To excel as a Validation Engineer III, you need a strong background in engineering or life sciences, extensive knowledge of validation protocols, and experience in regulated industries such as pharmaceuticals or medical devices. Familiarity with technical tools like validation lifecycle management software, statistical analysis packages, and regulatory standards (e.g., FDA, GMP) is typically required, along with relevant certifications such as Six Sigma or CQE. Critical thinking, attention to detail, and effective communication are crucial soft skills for documenting processes and collaborating with cross-functional teams. These competencies ensure compliance, product quality, and the successful execution of complex validation projects.

What are the roles and responsibilities of a Validation Engineer III?

A Validation Engineer III is responsible for ensuring that products, processes, and systems meet regulatory and company standards for quality and safety. This role typically involves planning and executing validation tests, writing protocols and reports, analyzing data, and troubleshooting validation issues. Validation Engineer IIIs often lead validation projects, mentor junior staff, and work closely with cross-functional teams in industries like pharmaceuticals, biotechnology, or manufacturing. They ensure compliance with regulatory requirements such as FDA, GMP, or ISO standards. Strong analytical, documentation, and project management skills are important for success in this position.

What are common challenges faced by a Validation Engineer III, and how can they be addressed?

As a Validation Engineer III, one common challenge is coordinating among cross-functional teams such as manufacturing, quality, and regulatory departments to ensure validation activities meet strict compliance standards and timelines. Managing multiple projects simultaneously while adhering to evolving regulatory requirements can also be demanding. Strong project management, effective communication, and staying updated on industry guidelines help address these challenges and ensure successful validation outcomes.
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What states have the most Validation Engineer Iii jobs? States with the most job openings for Validation Engineer Iii jobs include:
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Validation Engineer Iii jobs near you
Infographic showing various Validation Engineer Iii job openings in the United States as of August 2026, with employment types broken down into 92% Full Time, 2% Part Time, and 6% 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 III

Novartis Pharmaceuticals Corporation

Durham, NC • On-site

$183K/yr

Full-time

Medical, Life, Retirement, PTO

Re-posted 24 days ago

Job description

Band

Level 3


Job Description Summary

Step into a role where your expertise directly enables life-changing therapies to reach patients safely and efficiently. As a Validation Engineer III, you will play a critical role in bringing manufacturing systems to life-leading validation efforts that ensure compliance, quality, and operational excellence in a cutting-edge GMP environment. Your work will help build and sustain the foundation for reliable, high-quality production, making a meaningful impact on patients around the world.


Job Description

Location:

  • This position will be located in Durham, NC and will be an onsite role.
  • Novartis is unable to offer relocation support for this role: please only apply if this location is accessible for you.

Key Responsibilities:

  • Lead commissioning, qualification, and validation activities for manufacturing, laboratory, and utility systems
  • Author, execute, and review validation protocols, reports, and standard operating procedures
  • Oversee user requirement specifications, ensuring compliance, quality, and timely document resolution
  • Perform environmental mapping studies and support specialized validation activities
  • Analyze validation data to confirm accuracy, completeness, and regulatory compliance
  • Develop and support validation strategies and timelines for sustained GMP operations
  • Conduct risk and impact assessments to define system boundaries and validation scope
  • Own validation lifecycle documentation, including plans, assessments, and final reports
  • Support computer systems validation activities for global systems and applications
  • Collaborate with cross-functional teams to support audits, inspections, and project execution

Essential Requirements:

  • Bachelor's or master's degree in engineering or science with five years of relevant pharmaceutical industry experience
  • Proven experience in validation or engineering within a pharmaceutical or biopharmaceutical environment
  • Strong knowledge of GMP requirements and validation lifecycle stages
  • Hands-on experience with installation, operational, and performance qualification activities
  • Familiarity with global regulatory guidelines, including FDA and International Council for Harmonisation standards
  • Experience performing environmental mapping and using validation tools such as Kaye Validator
  • Experience with biosafety cabinet smoke studies
  • Working knowledge of risk-based validation approaches and industry best practices such as ASTM E2500 and GAMP 5
  • Excellent technical writing, communication, and problem-solving skills with attention to detail

Novartis Compensation and Benefit Summary:

The salary for this position is expected to range between $ 98,700 and $183,300 annually.

The final salary offered is determined based on factors like, but not limited to, relevant skills and experience, and upon joining Novartis will be reviewed periodically. Novartis may change the published salary range based on company and market factors.

Your compensation will include a performance-based cash incentive and, depending on the level of the role, eligibility to be considered for annual equity awards.

US-based eligible employees will receive a comprehensive benefits package that includes health, life and disability benefits, a 401(k) with company contribution and match, and a variety of other benefits. In addition, employees are eligible for a generous time off package including vacation, personal days, holidays and other leaves.

#LI-Onsite


EEO Statement:

The Novartis Group of Companies are Equal Opportunity Employers. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status. We strive to create an inclusive workplace that cultivates bold innovation through collaboration and empowers our people to unleash their full potential.


Accessibility and reasonable accommodations

The Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please send an e-mail to tas.nacomms@novartis.com call +1 (877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message.
https://www.novartis.com/careers/careers-research/notice-all-applicants-us-job-openings


Salary Range

$98,700.00 - $183,300.00


Skills Desired

Business Continuity, Change Control, Cost Management, Data Analytics and Digital, Engineering Technical Expertise, GDP Knowledge, gmp knowledge, HSE Knowledge, Knowledge Of Relevant Tools And Systems, Manufacturing Process (Production), Operational Excellence, Quality Compliance, Resilience and Risk Management, Total Productive Maintenance

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