Job Title: CQV - Validation Engineer

Location: Los Angeles, CA (Onsite)

Overview:

We are seeking an experienced Facilities CQV / Validation Engineer to support a pharmaceutical capital project. The role involves equipment and facilities qualification , on-site construction oversight , and collaboration with cross-functional teams.

Required Experience:

• BS degree in Engineering or related field
• 3+ years of Validation Engineering experience in pharmaceutical manufacturing
• Hands-on experience with IQ/OQ/PQ of vessels, tanks, centrifuges, filter presses
• Experience with EMPQ (Environmental Monitoring Performance Qualification)
• Cleanroom qualification experience is a plus
• Strong technical writing/documentation skills
• Experience performing job walks on construction sites

Key Responsibilities:

• Execute IQ/OQ/PQ protocols for processing equipment and facilities
• Support EMPQ and cleanroom qualifications
• Conduct daily construction site job walks in full PPE
• Collaborate with engineering, utilities, QA, and operations teams
• Maintain accurate and compliant documentation
• Support multiple shifts and respond to project needs as required