Validation Engineer

Sacramento, California/Southwest/Full Time Key Responsibilities
1. Technical Responsibilities

• Develop documentation for CQV activities
• Write and execute protocols (field verification)
• Develop summary reports at client sites

• Pharmaceutical facilities
• Utilities
• Equipment

• Plan and coordinate work
• Direct small teams in document development and/or execution

• Bachelor’s degree in a science or engineering field (or equivalent experience)
• 2–4 years’ experience in commissioning and qualification in a regulated industry
• Familiarity with ISPE Baseline Guide 5 (Second Edition) is a plus

• Facilities and equipment startup
• Walk-downs and troubleshooting
• Utilities (WFI, RO, HVAC)
• Upstream/downstream processing
• Purification, recovery
• Building automation
• Pharmaceutical manufacturing processes

• Pursues initiatives aligned with organizational strategy
• Identifies strategic, innovative solutions

• Understands and anticipates customer needs
• Delivers high-quality solutions and service
• Proactively maintains satisfaction and loyalty

• Aligns business strategies with actionable plans
• Anticipates risks and builds contingency plans
• Secures resources for goal achievement Pursue Execution
  • Prioritizes time and resources effectively
  • Holds self and others accountable
  • Acts to overcome obstacles and improve quality
  • Communicates clearly and professionally
  • Adjusts style to fit the audience
  • Explains technical concepts effectively
  Build Partnerships
  • Builds networks across functions
  • Encourages collaboration and breaks down silos
  • Involves stakeholders in decisions
  Influence Others
  • Builds support with sound rationale
  • Gains buy‑in from decision makers
  • Encourages innovative thinking
  Develop Self and Others
  • Enhances interpersonal relationships
  • Models integrity and company values
  • Seeks out growth and breakthrough opportunities