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Pharmaceutical Process Validation Engineer Jobs

2T Consulting

We are seeking a Process Validation Engineer with hands-on experience in Test Method Validation (TMV) within a regulated manufacturing environment. The role will be responsible for leading TMV ...

Scorpion Therapeutics

NY · On-site

Applies engineering principles to develop and execute process controls and validation strategies * Uses statistical and engineering methods to assess manufacturing process performance * Supports ...

INCOG

Senior Process Validation Engineer

Fishers, IN · On-site

$97K - $125K/yr

TSMS - Senior Process Validation Engineer The Senior Process Validation Engineer - Technical Services and Manufacturing Sciences (TSMS) will be responsible for leading all facets of Process ...

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How much do pharmaceutical process validation engineer jobs pay per hour?

As of Sep 13, 2026, the average hourly pay for pharmaceutical process validation engineer in the United States is $39.54, according to ZipRecruiter salary data. Most workers in this role earn between $23.08 and $51.44 per hour, depending on experience, location, and employer.

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For Pharmaceutical Process Validation Engineer jobs, the most frequently searched job titles are:

Process Validation Engineer - TMV

Warren, PA

2T Consulting
IT Services • 51 - 200 employees
Learn more about 2T Consultingexternal

Full-time

Posted 24 days ago

Job description

We are seeking a Process Validation Engineer with hands-on experience in Test Method Validation (TMV) within a regulated manufacturing environment. The role will be responsible for leading TMV remediation activities, executing validation protocols, analyzing results, and ensuring validation activities are completed in accordance with quality-system requirements.

Key Responsibilities
  • Lead and execute Test Method Validation (TMV) and remediation activities.
  • Develop, review, execute, and support the approval of TMV protocols and final validation reports.
  • Plan and perform validation testing, including sample preparation, test method execution, and data collection.
  • Analyze validation results and document findings, deviations, and issues identified during execution.
  • Apply statistical methods, including Gage R&R, to assess test method capability and support validation conclusions.
  • Troubleshoot validation issues and collaborate with relevant teams to identify and implement effective resolutions.
  • Support operator training to ensure consistent and compliant execution of validated test methods.
  • Partner cross-functionally with Engineering, Quality, Manufacturing, and other stakeholders to complete validation activities.
  • Maintain accurate validation records and documentation in accordance with quality-system and regulatory requirements.
  • Track TMV remediation activities and timelines and drive assigned activities through successful completion.
  • Support continuous improvement of manufacturing and validation processes as needed.
Required Qualifications & Experience
  • Hands-on experience with Test Method Validation (TMV) activities.
  • Experience with the complete validation lifecycle, including protocol development, execution, data analysis, and final reporting.
  • Strong knowledge of statistical analysis, including Gage R&R and measurement system analysis (MSA).
  • Experience working in a regulated manufacturing environment, preferably within the medical device industry.
  • Strong technical writing, documentation, and validation report-writing skills.
  • Ability to independently plan and execute validation activities while meeting established timelines.
  • Experience working collaboratively with Engineering, Quality, Manufacturing, and Operations teams.
  • Strong analytical, organizational, problem-solving, and communication skills.

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