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Validation Engineer Iii Jobs (NOW HIRING)

Validation & Engineering Group, Inc

PR

Minimum of 3 years of experience in direct pharmaceutical, medical device or biotechnology industries. * Proven experience as a Validation Engineer in a manufacturing environment. * Strong knowledge ...

Validation & Engineering Group, Inc

PR

Minimum of 3 years of experience in direct pharmaceutical, medical device or biotechnology industries. * Proven experience as a Validation Engineer in a manufacturing environment. * Strong knowledge ...

Validation & Engineering Group, Inc

PR

Minimum of 3 years of experience in direct pharmaceutical, medical device or biotechnology industries. * Proven experience as a Validation Engineer in a manufacturing environment. * Strong knowledge ...

Validation & Engineering Group, Inc

PR

Minimum of 3 years of experience in direct pharmaceutical, medical device or biotechnology industries. * Proven experience as a Validation Engineer in a manufacturing environment. * Strong knowledge ...

Validation & Engineering Group, Inc

PR

Minimum of 3 years of experience in direct pharmaceutical, medical device or biotechnology industries. * Proven experience as a Validation Engineer in a manufacturing environment. * Strong knowledge ...

Validation & Engineering Group, Inc

PR

Minimum of 3 years of experience in direct pharmaceutical, medical device or biotechnology industries. * Proven experience as a Validation Engineer in a manufacturing environment. * Strong knowledge ...

Validation & Engineering Group, Inc

PR

Minimum of 3 years of experience in direct pharmaceutical, medical device or biotechnology industries. * Proven experience as a Validation Engineer in a manufacturing environment. * Strong knowledge ...

Validation & Engineering Group, Inc

PR

Minimum of 3 years of experience in direct pharmaceutical, medical device or biotechnology industries. * Proven experience as a Validation Engineer in a manufacturing environment. * Strong knowledge ...

Centstone

Validation Engineer

Kenosha, WI · On-site

$50 - $55/hr

Mostly overnight shifts, 12-hour shifts Openings: 5 Experience: 3+ years for Validation Engineer or 5+ years for Senior Validation Engineer About the Role We are hiring experienced Validation ...

Haumiller Engineering Co

Validation Engineer

Belvidere, IL · On-site

$72K - $90K/yr

Validation Engineer Haumiller Engineering is a 100% employee-owned company that designs and builds ... of 3 years' experience writing technical documentation • Ability to develop technical documents ...

JSat Automation

Validation Engineer

Glendale, CA · On-site

The Validation Engineer will be responsible for the following. * Develop, approve, and execute ... Chemical engineers preferred, with a minimum of three (3) years relevant experience. * Experience ...

Automated Systems, Inc.

Be Seen First

Validation Engineer

Chicago, IL · On-site

$45 - $65/hr

Validation Engineer Location: Greater Chicagoland Area Contract: 6+ month duration with potential ... of 3+ years of experience and has a strong understanding of validation principles to support a ...

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How much do validation engineer iii jobs pay per hour?

As of Jun 7, 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 are the key skills and qualifications needed to thrive as a Validation Engineer III, and why are they important?

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 Validation Engineer III roles and responsibilities?

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 some 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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Validation Engineer Iii jobs near you

Validation Engineer - Upstream

Validation & Engineering Group, Inc

PR

Full-time

Posted 17 days ago

Job description

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.

We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position:

  • Validation Engineer - Upstream

Description:
We are seeking a Validation Engineer with experience in upstream equipment to join our team. The Validation Engineer will be responsible for validating equipment, processes, and systems used in the manufacturing process to ensure compliance with industry standards and regulations. Knowledge of common upstream equipment in biotech is a plus.
Qualifications:

  • Bachelor's degree in Engineering or related field.
  • Minimum of 3 years of experience in direct pharmaceutical, medical device or biotechnology industries.
  • Proven experience as a Validation Engineer in a manufacturing environment.
  • Strong knowledge of upstream equipment and processes, including but not limited to: fermenters, bioreactors, centrifuges, filtration systems, and chromatography equipment.
  • Familiarity with industry regulations and standards.
  • Excellent problem-solving skills and attention to detail.
  • Effective communication skills and ability to work in a team environment.
  • Must be fully bilingual (English / Spanish) with excellent oral skills.
  • Must be proficient using MS Windows and Microsoft Office applications.
  • Experience in Design Documentation (URS, DS), IQ, OQ, PQ protocols development and execution, deviations and reports generation.
  • Available to work extended hours, possibility of weekends and holidays.


Responsibilities:

  • Develop and execute validation protocols for equipment and processes.
  • Coordinate with cross-functional teams to ensure validation requirements are met.
  • Analyze validation test results and prepare reports documenting findings.
  • Identify and address deviations or non-conformances during the validation process.
  • Support continuous improvement initiatives related to equipment validation.

At Validation & Engineering Group, people always come first. We believe that when you're empowered to do your best work, bold ideas thrive and real progress happens. This isn't just a job - it's an opportunity to make a meaningful difference by shaping the future of healthcare and technology alongside a purpose-driven, supportive team.
Excited to build something meaningful together? We look forward to hearing from you.
Validation & Engineering Group is an equal opportunity employer. All applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, or disability status.