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Urgently Hiring Pharma Validation Engineer Jobs (NOW HIRING)

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 ...

Pinnaql

Jr Validation Engineer

New Albany, OH

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 ...

Catalent Pharma Solutions

Validation Engineer

Chelsea, MA · On-site

$89K - $110K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

The Validation Engineer is responsible for executing validation activities within a GMP ... hiring process. Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions ...

Adare Pharma

Validation Engineer

Vandalia, OH · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Our Business Adare Pharma Solutions is a global Contract Development and Manufacturing Organization ... Position Validation Engineer Location Vandalia, Ohio Summary In this position, the Engineer will ...

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 urgently hiring pharma validation engineer jobs pay per hour?

As of Aug 17, 2026, the average hourly pay for urgently hiring 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.

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The most popular types of Pharma Validation Engineer jobs are:

Urgently Hiring Pharma Validation Engineer jobs near you

Validation Engineer

BioPhase Solutions

Los Angeles, CA

$115K/yr

Full-time

Re-posted 5 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!!!