Cezar Lucki Email & Phone Number

Validation Specialist and CSV Project Manager @ Edge For Life

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Cezar Lucki Location

Irvine, CA, US

Cezar Lucki Work

2018 -now Validation Specialist and CSV Project Manager @
2018 -now Validation Specialist @
2003 -now Proprietor, CEO, Quality and Validation Engineer @
2016 -now Sr. Validation Consultant @
now Validation Specialist @ OncoTracker
2015 -2016 Facility | Utility Validation specialist (now RxSight) @ Calhoun Vision
now Sr. Validation Engineer consultant @
now Quality Engineer Lead Consultant @
now Quality Engineer (Abbott Medical Optics now part of J and J) @
2012 -2012 CSV Consultant @
2011 -2012 Quality Systems Engineer II consultant @
2010 -2011 CSV Consultant @
now Validation and Safety Consultant @
2007 -2009 Business Analyst (consultant) @
2006 -2009 CSV Validation Engineer (consultant) @
now Quality Engineer (consultant) @
2000 -2006 Validation Engineer (consultant) @ Intralase (acquired by AMO/Abbott now split between Johnson & Johnson and Alcon|
2005 -2006 Quality Engineer (consultant) @
now Production and Tech. Transfer Consultant @
now CSV Validation Eng. (consultant) @
2002 -2003 Business Analyst and CSV Eng and Global ERES Compliance Consultant @
now CSV Engineer (consultant) @
1998 -2000 Quality Engineer and Product Support Lead @ Qualisys Diagnostics
1997 -1998 Quality Engineer Associate II @
1996 -1997 Environmental Monitoring Technician and Media and Sterility Technician @
now Environmental Monitoring and Micro and Chemistry Technician @ Allergan

Cezar Lucki Education

Instititue of Validation Technology (IVT) 2001-2001
Irvine Valley College 2000-2001
University of California, Irvine 1990-1995
UC Irvine 1990-1995

Cezar Lucki Skills

Informatics
APIs
IVD
FDA
Parenteral
Validation
Medical Devices
CAPA
GMP
Quality System
21 CFR Part 11
Biotechnology
ISO 13485
21 CFR Part 820 (QSR)
Pharmaceutical Industry
Computer System Validation
Installation Qualification
Operational Qualification
Performance Qualification
Process Validation
Equipment Validation
Computerized System Validation
Facility and Utility Validation
Process Capability
Six Sigma
Statgraphics
Statistica
Quality Engineering
CQE
21 CFR Part 211
21 CFR Part 111 (Neutraceuticals)
V&V
Quality Assurance
Manufacturing
Quality Control
Sop
Change Control
Cleaning Validation
LIMS
Root Cause Analysis
Cross-functional Team Leadership
Technology Transfer
R&D
ISO
Minitab
Testing
Lifesciences
Clinical Trials
GxP
Design of Experiments
Traceability Matrix
CSV
Planning
RF
Suppliers
Specifications
Technical Reviews
Mp2
SCADA
Chemistry
Technical Training
Insurance
Manufacturing Resource Planning
Datastream
SAN
Product Life Cycle
PLC
Protocol
Contract Manufacturing
NDA
Particle
Deviations
Cross Functional Team Leadership
Recorder
SME
Dionex
Regulatory Compliance
Assessment
Databases
Film
Hazardous Materials
Design
Adherence
SPC
Enterprise Systems
Science
Cfr
GLP
Landscape Design
Sampling Plans
Statistics
TOC
Integration
IC
Optics
GAP
System Requirements
Technology
Compliance Support
21 Cfr Part 820 Qsr
SDLC
Budget Analysis
Algorithms
Structures
HPLC
Observation
Data Validation
Manuals
Preventive Actions
Education
Bioscience
Process Flow
Hygiene
Tests
Standards Compliance
Fds
Engineering
Lake
Strategy
Trace
Inventory
Corporate Insurance
Budgeting
Risk Analysis
Medicine
Compounding
Approval Process
Training
Editing
Computerized Systems
Supplements
Policy
R&r
21 Cfr Part 111 Neutraceuticals
Sds
Gage R&r
Root Cause
Neuromodulation
Documentation
Mitigation
Project Management
Eastern Europe
Manufacturing Processes
Investigation
Empower
Chemstation
Molecular
Inspection
Drawing
Hardware
Environmental Monitoring
Industrial Hygiene
GUI
Laboratory
Leica
Gap Analysis
UV
Turbidity
Emergency
SAP
Endotoxin
C
Management System
GAMP
Controllers
MDS
Specs
Product Safety
Data Collection
Stress Testing
Business Analysis
Engineering Support
Schedules
GDP
LAN
System Administration
TGA
FMEA
Total Quality Management
Ivt
User Requirements
QC
Product Support
Presentation
Regulatory Audits
Operations
OOS
Dimension
Maintenance
Bioburden
SD
Curing
Change Management
CERCLA
Forest
Remediation
Performing
House
ASTM
Mass Spec
WLAN
Data Migration
ANSI
Material Review Board
OSHA
Presentations
Deliverables
Change Requests
Catsweb
Functional Design
Regulations
Purchasing
Nexus
Heat
Resources
Laser
Forms
Oven
Reviews
Spreadsheets
Cosmeceuticals
Software
Charter
Technical Architecture
Commitments
Satellite
Agilent
Test Scripts
Database Development
Analytical Skill
Agents
Administration
Biologics
Blueprint
IR
Vaccines
Contingency
Discount
EPA
Legacy Systems
Sealers
Firmware
Vitek
Sampling
Technician
Immunotherapy
Filing
Software Development
Metrology
Vendor Audit
Calibration
EMEA
Chart
Architecture
Kiosk
Software Validation
Commercialization
Product Quality
DBMS
21 Cfr Part 111
21 CFR Part 820

Cezar Lucki Summary

Cezar Lucki, based in Irvine, CA, US, is currently a Validation Specialist and CSV Project Manager at The HydraFacial Company. Cezar Lucki brings experience from previous roles at Validation Professionals, Inc., CL Tech Inc., Illumina and OncoTracker. Cezar Lucki holds a 2001 - 2001 Instititue of Validation Technology (IVT). With a robust skill set that includes Informatics, APIs, IVD, FDA, Parenteral and more. Cezar Lucki has 3 emails and 3 mobile phone numbers on RocketReach.