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Utilities & Process Validation Engineer (San Diego)

Utilities & Process Validation Engineer (San Diego)

BioTalentSan Diego, CA, US
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Job Title : Utilities & Process Validation Engineer

Location : San Diego, CA

Position Summary

The Utilities & Process Validation Engineer is responsible for planning, executing, and documenting validation activities for facility systems, utilities (e.g. water, steam, HVAC, compressed gases, clean rooms), and process equipment in a regulated environment (medical device / diagnostics). This role ensures systems operate consistently and meet all applicable regulatory, quality, and safety standards (e.g. FDA, ISO 13485, GMP).

Key Responsibilities

  • Develop validation strategy, plans, protocols, and reports (IQ, OQ, PQ, system performance qualification, requalification, periodic reviews) for facility, utilities, process equipment, and support systems.
  • Define acceptance criteria, test methods, sampling plans, and controls for validation.
  • Perform validation execution : install checks, functional testing, challenge testing, monitoring, data collection, calibration, troubleshooting deviations.
  • Lead or support qualification of new or modified equipment or facility systems (e.g. HVAC, clean steam, WFI / RO, compressed air, HVAC zones, utilities, process piping).
  • Conduct risk assessments, gap analyses, and process capability / statistical analysis as needed.
  • Coordinate with cross-functional teams : engineering, project management, quality, manufacturing, maintenance, and facilities.
  • Review design specifications, vendor documentation, and ensure that design meets validation needs.
  • Oversee revalidation / periodic review of systems; monitor for drift or changes over time.
  • Investigate validation failures / deviations, root-cause analysis, CAPA implementation.
  • Maintain validation master plan, document control, and ensure traceability of validation documentation.
  • Support audits / inspections and respond to regulatory / audit queries.
  • Mentor or guide junior validation engineers / specialists.

Qualifications / Requirements

  • Bachelors degree in engineering (Mechanical, Chemical, Biomedical, or equivalent). Advanced degree a plus.
  • 5+ years of experience in process / utilities / facility validation in a regulated industry (pharma, biotech, medical device, diagnostics).
  • Deep knowledge of validation protocols (IQ / OQ / PQ), GMP, regulatory expectations (FDA, ISO 13485, etc.).
  • Experience with utilities : HVAC, clean steam, WFI / RO, compressed air, gases, HVAC zones, etc.
  • Statistical analysis skills (e.g. capability, control charts).
  • Strong skills in documentation, writing protocols and reports, and attention to detail.
  • Ability to lead validation projects, manage time, coordinate among stakeholders.
  • Experience investigating and resolving deviations / CAPAs.
  • Excellent communication skills, ability to present to quality / management / regulatory audiences.
  • Relevant certifications (e.g. ASQ, or validations training) are a plus.
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