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Pharma Validation Engineer Jobs (NOW HIRING)

BioPhase Solutions

Validation Engineer

Los Angeles, CA · On-site

$115K/yr

Certifications related to GMP compliance, quality systems, or validation preferred. * 1-3+ years of experience in validation engineering or a closely related field in a cGMP-regulated pharma or ...

Veg Group

Jr Validation Engineer

New Albany, OH · On-site

$60 - $85/hr

Bachelor's degree in Engineering, Science, or related technical field. * 0-3 years of experience in validation, commissioning, or regulated biotech/pharma environments. * Basic knowledge of GMP and ...

Pinnaql

Jr Validation Engineer

New Albany, OH · On-site

Bachelors degree in Engineering, Science, or related technical field. * 03 years of experience in validation, commissioning, or regulated biotech/pharma environments. * Basic knowledge of GMP and ...

Pinnaql

Jr Validation Engineer

New Albany, OH · On-site

Bachelor's degree in Engineering, Science, or related technical field. * 0 3 years of experience in validation, commissioning, or regulated biotech/pharma environments. * Basic knowledge of GMP and ...

Compli

Senior Validation Engineer

Milwaukee, WI · On-site

$110 - $160/hr

... specializing in pharma, biotech, API, Medical Device and laboratory facilities. Compli ... The Senior Validation Engineer is responsible for providing technical leadership and engineering ...

GBA Team

Senior Validation Engineer

Milwaukee, WI · On-site

$110 - $150/hr

... specializing in pharma, biotech, API, Medical Device and laboratory facilities. Compli ... The Senior Validation Engineer is responsible for providing technical leadership and engineering ...

TekWissen LLC

Senior Validation Engineer

Portsmouth, NH · On-site

$35 - $45/hr

Senior Validation Engineer Location: Portsmouth, NH - 03801 Duration: 7 Months Job Type: Temporary ... Prior experience leading or supporting projects in Biotech, Pharma, or Biologics industries

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How much do pharma validation engineer jobs pay per hour?

As of Sep 6, 2026, the average hourly pay for pharma 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 a pharma validation engineer?

A Pharma Validation Engineer ensures that manufacturing processes, equipment, and systems in the pharmaceutical industry comply with regulatory standards such as FDA, GMP, and ISO. They develop validation protocols, conduct tests, analyze data, and generate reports to ensure consistent product quality and safety. Their role is critical in minimizing risks, maintaining compliance, and supporting regulatory audits.

What does a pharma validation engineer do?

A typical day for a Pharma Validation Engineer involves developing and executing validation protocols for manufacturing equipment, laboratory instruments, or processes, ensuring they meet all regulatory and quality standards. You might collaborate closely with QA teams, production staff, and external vendors to troubleshoot issues, review data, and document results for compliance audits. Preparing detailed reports, participating in cross-functional meetings, and staying updated with current regulatory changes are also common responsibilities. This dynamic environment offers opportunities to work on diverse projects and continually expand your technical expertise while supporting product safety and efficacy.

What skills and qualifications are needed to be a pharma validation engineer?

To thrive as a Pharma Validation Engineer, you need a solid background in engineering or life sciences, with expertise in validation protocols, regulatory compliance (such as FDA or EMA guidelines), and Good Manufacturing Practices (GMP). Experience with validation software (like ValGenesis or MasterControl), statistical analysis tools, and relevant certifications (such as Six Sigma or ISPE) is highly valued. Strong attention to detail, project management abilities, and effective communication skills are crucial for this role. These competencies ensure validation activities meet strict regulatory standards, support product quality, and facilitate seamless cross-functional collaboration in the pharmaceutical industry.

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Pharma Validation Engineer jobs near you
Infographic showing various Pharma Validation Engineer job openings in the United States as of August 2026, with employment types broken down into 93% Full Time, 3% Part Time, and 4% 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

BioPhase Solutions

Los Angeles, CA • On-site

$115K/yr

Full-time

Re-posted 25 days ago

Job description

BioPhase Solutions specializes in recruiting top talented professionals for Southern California's Scientific community. We are currently looking for a Validation Engineer to work for a leading Greater Los Angeles area contract development and manufacturing organization.

Salary: $100-115k+/year depending on experience

Responsibilities:
  • Draft and Review User Requirement Specifications (URS): Develop and refine URS for new and existing process equipment, ensuring alignment with manufacturing needs and regulatory standards.
  • Perform Equipment Qualifications (IQ, OQ, PQ): Plan, execute, and document qualification protocols to verify equipment performance meets cGMP requirements and intended use.
  • Execute Process Validation and Cleaning Validation: Identify critical process parameters, establish validation protocols, and conduct cleaning validations to maintain product quality and regulatory compliance.
  • Generate and Maintain Validation Documentation: Prepare, review, and archive validation reports, SOPs, protocols, and related records to ensure clear traceability and audit readiness.
  • Troubleshoot and Investigate Deviations: Collaborate with cross-functional teams to diagnose equipment and process issues, implement corrective actions (CAPA), and address audit observations promptly.
  • Support Scale-Up and Technology Transfer Efforts: Work with manufacturing and development groups to optimize processes, facilitate seamless scale-up, and transfer validated methods across company sites.
  • Coordinate with Cross-Functional Teams: Engage Quality, Process Development, and Manufacturing teams to meet project timelines, drive continuous improvement, and uphold cGMP standards.
Experience/Requirements:
  • Bachelors in engineering, chemistry, or related field
  • Certifications related to GMP compliance, quality systems, or validation preferred.
  • 1–3+ years of experience in validation engineering or a closely related field in a cGMP-regulated pharma or biotech environment.
  • Strong working knowledge of process validation, equipment qualification (IQ/OQ/PQ), and pharmaceutical manufacturing processes.
  • Proficiency in drafting and reviewing validation documents (URS, SOPs, protocols, reports).
  • Familiarity with deviation investigations, CAPA processes, and audit responses.
  • Basic vendor management skills to evaluate and coordinate with external equipment/service providers.
  • Competence in using data analysis tools and MS Office applications to track and report validation results. 
Please send resumes to mia@biophaseinc.com and visit our website at www.biophaseinc.com for additional job opportunities!!!