CQV Engineer jobs in United States
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Ecocareers · 3 months ago

CQV Engineer

Confidential company is a large pharmaceutical company in Los Angeles seeking a CQV Engineer for a 12-month project. The role involves managing project lifecycle documentation, installation, operational commissioning, and qualification, while ensuring compliance with quality standards.

Staffing & Recruiting

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
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
Author and approve
Develop and execute qualification protocols
Assist with any deviation resolution and handling execution
Train personnel on the operation of the Fractionation process, and related procedures
Create comprehensive documentation of all validation activities
Identify and assess potential risks to product quality and patient safety
Develop mitigation strategies and contingency plans
Manage change control for any modifications or updates to the equipment or processes
Conduct internal and external audits to ensure compliance with quality standards and regulations

Qualification

CQV experienceValidation EngineeringTechnical writingInstallationIQOQCleanroom qualificationMulti-taskingCommunication skillsPositive attitude

Required

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
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

Preferred

Facilities CQV experience including EMPO, Vessel IOV and IOPQ including mixing and temp mapping
Cleanroom qualification experience is a plus

Company

Ecocareers

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Funding

Current Stage
Early Stage
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