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CQV Engineer

Job in Glendale, Los Angeles County, California, 91222, USA
Listing for: Katalyst CRO
Full Time position
Listed on 2025-12-21
Job specializations:
  • Engineering
    Quality Engineering, Validation Engineer
Job Description & How to Apply Below

A large pharmaceutical company in Los Angeles is in immediate need of a CQV Engineer for a 12-month onsite project, 40 hours per week.

Responsibilities
  • Generation and Modification of project lifecycle documentation for LA Plant Site.
  • User Requirement Specifications.
  • Functional Specifications.
  • Design Specifications.
  • SOPs.
  • Management of Change (MOC).
  • FMEA.
  • HAZOPs.
  • Risk Assessments.
  • Gap Assessments.
  • Project Closeout Documentation.
  • Turnover Package Generation.
  • Project Change Requests.
  • Construction Activities.
  • Generate and Manage Safety Management Plans and Documentation.
  • Disruptive Construction Activity Requests.
  • Job Hazard Analysis.
  • Lockout Tag Out Plan.
  • Hot Work Permitting.
  • Permit to Work.
  • Detour Plans.
  • Construction Signage.
  • Plant-wide Communications.
  • Generate and Manage Quality Management Plans and Documentation.
  • Construction Control Plan.
  • Assist in site supervision of construction personnel.
Manage Installation and Operational Commissioning
  • Author and approve.
  • Execution.
  • Function Testing.
  • BOM Updates.
  • PM Generation.
  • Asset Lifecycle.
  • Drawing Updates.
  • Support site acceptance testing to review system documents and functions during SAT.
  • Summary Report.
Manage Installation, Operational, and Performance Qualification
  • Author and approve.
  • Develop and execute qualification protocols.
  • Assist with any deviation resolution and handling execution.
Summary Report Training and Documentation
  • Train personnel on the operation of the Fractionation process, and related procedures.
  • Create comprehensive documentation of all validation activities.
Risk Assessment and Mitigation
  • Identify and assess potential risks to product quality and patient safety.
  • Develop mitigation strategies and contingency plans.
  • Change Control:
  • Manage change control for any modifications or updates to the equipment or processes.
Quality Audits
  • Conduct internal and external audits to ensure compliance with quality standards and regulations.
Requirements
  • BS degree minimum.
  • 2-10 years of Validation Engineering experience in pharmaceutical industry.
  • Strong skill set in installation and IQOQ of equipment like centrifuges, filter presses, and processing tanks.
  • Cleanroom qualification experience is a plus.
  • Very strong technical writing/documentation skills.
  • Very strong communication skills and ability to coordinate with cross-functional teams.
  • Experience doing job walks with engineers for capital projects.
  • Must have a positive attitude and ability to multi-task.
  • Must be committed to supporting a long-term project that could go for 2 years.
  • Must be available to support other shifts as requested by the client, this could happen on short notice.
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