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Pharmaceutical Validation Engineer Jobs (NOW HIRING)

PR · On-site

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 ...

PR · On-site

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 ...

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 ...

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 ...

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 ...

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 ...

PR · On-site

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 ...

PR · On-site

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 ...

PR · On-site

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 ...

PR · On-site

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 ...

PR · On-site

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 ...

PR · On-site

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 ...

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 ...

The Validation Engineer will be responsible for developing and executing validation activities for pharmaceutical equipment, systems, and utilities, ensuring compliance with GMP and regulatory ...

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Pharmaceutical Validation Engineer information

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$51

$78

How much do pharmaceutical validation engineer jobs pay per hour?

As of Jun 15, 2026, the average hourly pay for pharmaceutical validation engineer 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 Pharmaceutical Validation Engineer vs Quality Assurance Specialist?

AspectPharmaceutical Validation EngineerQuality Assurance Specialist
CertificationsGMP, Validation certificationsGMP, QA certifications
Work EnvironmentValidation labs, manufacturing plantsQuality control labs, production facilities
Primary FocusValidating equipment, processes, systemsEnsuring product quality, compliance
Industry UsageCommon in manufacturing and validation teamsWidespread across quality departments

While both roles work within the pharmaceutical industry and require GMP knowledge, the Pharmaceutical Validation Engineer primarily focuses on validating equipment and processes to ensure compliance, whereas the Quality Assurance Specialist concentrates on maintaining overall product quality and regulatory adherence.

What are the key skills and qualifications needed to thrive as a Pharmaceutical Validation Engineer, and why are they important?

Pharmaceutical Validation Engineers need a solid background in engineering or life sciences, with knowledge of regulatory standards such as GMP and experience in validation protocols. Familiarity with technical tools like data loggers, validation software, and documentation systems, as well as certifications like Six Sigma or CQE, are commonly required. Excellent problem-solving, project management, and communication skills help them collaborate across departments and address compliance challenges. These skills and qualifications are crucial to ensure pharmaceutical processes meet regulatory requirements and maintain product quality and patient safety.

What does a Pharmaceutical Validation Engineer do?

A Pharmaceutical Validation Engineer is responsible for ensuring that pharmaceutical manufacturing processes, equipment, and systems operate consistently and produce products that meet strict industry standards and regulatory requirements. They design, conduct, and document validation protocols for equipment, processes, and computer systems to confirm their accuracy and reliability. Their work is crucial for maintaining product quality, patient safety, and compliance with agencies such as the FDA and EMA.

What are the most common challenges a Pharmaceutical Validation Engineer faces when working on new equipment qualification projects?

Pharmaceutical Validation Engineers often encounter challenges such as tight project deadlines, managing complex documentation requirements, and ensuring compliance with stringent regulatory standards like FDA or EMA guidelines. Coordinating with cross-functional teams—including production, quality assurance, and maintenance—can also present hurdles, especially when integrating new equipment into existing processes. Proactive communication, strong organizational skills, and a thorough understanding of validation protocols are essential for overcoming these challenges and ensuring successful project outcomes.
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What states have the most Pharmaceutical Validation Engineer jobs? States with the most job openings for Pharmaceutical Validation Engineer jobs include:

Validation Engineer - Upstream

Validation & Engineering Group, Inc

PR • On-site

Full-time

Posted 25 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.