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Pharmaceutical Validation Engineer Jobs (NOW HIRING)

Sterling Engineering Inc.

Validation Engineer

Indianapolis, IN · On-site

$75K - $120K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Validation Engineer - VHP / Aseptic Processing / Pharmaceutical Manufacturing Location : Indianapolis, IN or remote in Northeast US Hire Type : Direct Hire Compensation : $75,000 - $120,000 Benefits

Performance Validation, Inc

Validation Engineer

Raleigh, NC

$80K - $83K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

... pharmaceutical validation * BS degrees in Biomedical Engineering, Chemical Engineering or ... Mechanical Engineering preferred Experience: * Change and Deviation Management * Strong ...

AMRI

Senior Principal Validation Engineer

Albuquerque, NM · On-site

  • Retirement

Senior Principal Validation Engineer in Albuquerque, NM Build your future at Curia, where our work ... Experience with FDA and EU regulations for pharmaceuticals and validation requirements Supervisory ...

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Pharmaceutical Validation Engineer information

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How much do pharmaceutical validation engineer jobs pay per hour?

As of Aug 17, 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?

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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Pharmaceutical Validation Engineer jobs near you
Infographic showing various Pharmaceutical Validation Engineer 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 86% Physical, 5% Hybrid, and 9% Remote job distribution, with an average salary of $108,152 per year, or $52 per hour.

Validation Engineer

Sterling Engineering Inc.

Indianapolis, IN • On-site

$75K - $120K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 9 days ago

Job description

Title: Validation Engineer - VHP / Aseptic Processing / Pharmaceutical Manufacturing
Location: Indianapolis, IN or remote in Northeast US
Hire Type: Direct Hire
Compensation: $75,000 - $120,000
Benefits: Health, Dental, Vision, 401K, PTO
Must have Skill Set:

  • Must have proven Validation Engineering experience in a pharmaceutical, biotech, life sciences, or regulated manufacturing environment.
  • Must have equipment validation experience. Cleanroom validation experience is also acceptable.
  • Must have proven experience developing and executing decontamination cycle development and validation activities.
  • Must have hands-on experience with Vaporized Hydrogen Peroxide (VHP/VPHP) systems.
  • Must have experience with Steris VHP generators or similar VHP generator systems.
  • Must have experience working in aseptic processing environments, including sterilization of equipment prior to production.
  • Must have strong pharmaceutical validation documentation experience, including validation protocols, IQ, OQ, PQ documentation, validation reports, and GMP documentation.
  • Must be willing and able to travel up to 60% to customer sites, including local day trips and overnight travel throughout the Northeastern United States.

Overview:

We are seeking an experienced Validation Engineer to support pharmaceutical, biotech, and advanced therapy manufacturing projects. This is a highly hands-on customer-facing role responsible for equipment validation, commissioning, qualification, and decontamination cycle development for aseptic manufacturing systems.

The ideal candidate will have proven experience in Validation Engineering, equipment validation, VHP (Vaporized Hydrogen Peroxide) systems, VHP cycle development, and aseptic processing environments. This individual will work closely with engineering teams and customers to execute Factory Acceptance Testing (FAT), Site Acceptance Testing (SAT), Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) activities while ensuring compliance with pharmaceutical quality and regulatory requirements.

This position requires regular travel to customer sites. Candidates must be comfortable traveling up to 60%, including both local day trips and overnight travel throughout the Northeast region.

Job Duties:

  • Lead and support validation engineering activities for pharmaceutical and biotechnology manufacturing equipment.
  • Execute and support equipment validation, including FAT, SAT, IQ, OQ, and PQ activities.
  • Develop, optimize, and validate Vaporized Hydrogen Peroxide (VHP/VPHP) decontamination cycles.
  • Perform cycle development and support Performance Qualification activities related to VHP sterilization processes.
  • Work directly with customers and field service teams during equipment installation, commissioning, startup, and qualification.
  • Support validation activities within aseptic processing environments, ensuring proper sterilization of manufacturing equipment prior to production.
  • Prepare, review, and execute pharmaceutical validation documentation, including validation protocols, reports, SOPs, deviations, and change control documentation.
  • Ensure compliance with GMP, regulatory, customer, and internal quality requirements.
  • Support quality investigations, process improvements, inspections, and corrective actions.
  • Collaborate with engineering, quality, manufacturing, and customer teams throughout project execution.
  • Travel to customer facilities for validation, commissioning, startup, and qualification activities (approximately 60% travel).

Qualifications:

  • Bachelor's degree in Engineering, Life Sciences, or a related technical discipline, or equivalent industry experience.
  • Proven experience in Validation Engineering is required.
  • Proven experience with equipment validation is required.
  • Experience with cleanroom validation is acceptable in lieu of equipment validation experience.
  • Proven experience with Vaporized Hydrogen Peroxide (VHP/VPHP) systems is required.
  • Experience with Steris VHP generators is strongly preferred.
  • Proven experience developing decontamination cycles and VHP cycle development is required.
  • Experience working in aseptic processing and sterile pharmaceutical manufacturing environments is required.
  • Strong knowledge of pharmaceutical validation principles, GMP requirements, and regulated manufacturing environments.
  • Experience preparing and executing pharmaceutical documentation, including IQ/OQ/PQ protocols, validation reports, SOPs, and related quality documentation.
  • Excellent communication, problem-solving, and organizational skills.
  • Proficiency with Microsoft Office.
  • Ability and willingness to travel up to 60%, including local day travel and overnight travel throughout the Northeastern United States.


Qualified applicants will receive consideration for employment without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or genetic information.