1. FRANCISCA AVILA POPOCA
1321 Columbine Blvd, Colorado Springs, CO 80907 | M: 719-229-5718 | favilap@its.jnj.com
Profile
Dedicated professional with 16+ years’ experience working in a regulated company. I specialize in manufacturing
process procedures, GMP, Quality System Regulations; ISO 9000 and FDA requirements 820 CFR 21 with excellent
communication skills.
Skills
 C#, ASP.NET, Word, Excel, ShowCase,AUTO CAD, MINITAB, INTRALINK, WINDCHILL, Adaptive, CDR,
EtQ, Think-cell
 Familiar with: Microsoft Project and MicrosoftSQL Server
 Solid knowledge of Microsoft Office Products
 Platforms: Microsoft Windows XP, Window7, Windows 10.
 Toastmaster: communication and leadership skills
 Coaching for Supervisor and manager class certificate.
 Fluent in Spanish
Professional Experience
Packaging Engineer Technician 10/2010 to Current
DepuySynthes companies of J&J
 Author of IQ, OQ, and PQ Protocols.
 Perform equipment Validation.
 Author ofWork Instruction and Processprocedures in Adaptive.
 Author ofproduction forms for packaging requirements.
 Knowledgeable with Quality Regulations; ISO 9000 and FDA requirements 820 CFR 21.
 Author of Process procedures that conform to Quality System Regulations.
 Revise Process Sheets to reflect current operationsaccording to Work Instructions in US and EUor new
requirements in compliance to Quality System Regulations.
 Train an audience of operators, supervisors,and managers on newprocess operations and requirements.
 Acquisition purchasesfor production equipment,materials,and production accessories.
 Act as a liaison to vendors in regardsto tools,fixtures,and equipment.
 Experience resolving CAPAs utilizing cause and effectdiagrams.
 Author ofwork instructions.
 Author ofProcess Tests.
 Author ofqualitydocument changes for current proceduresand newprocedures.
 Create,change, and maintain product routers.
 Responsible for investigating and disposition of non-conformances for product and procedures.
 Responsible for preparing audit readiness proceduresand process flows.
 Key player in mislabelKaizen event.
 Knowledgeable with PFMEA process.
 Analyze Statistic data results utilizing Minitab program.
 Author ofprocedures for Cleaning Rooms for ISO class5 and Class7.
 Member of JJOS deployment team.

2. Synthes,USA
Quality Inspector 05/2003-10/2010
 Inspect medicaldevisesper product drawings (blue prints).
 Inspect product with CMM measuring machine, calipers, micrometers,and tensile tester.
 ReviewDocument Mater Records for accuracy and completion.
 Author ofprocess procedure for peel tester machine.
 Design and implemented QualityAssurance database for order completion tracking.
 Write Manufacturing changesto implementprocess procedures.
 Prepare rawmaterial samples for lab testing.
Material Handler 03/2000- 05/2003
 Distribute product to inventory locations.
 Receive product into stocklocations utilizing inventory database system.
Programmer Analyst 01/2010 to 01/2011
District Attorney's Office
 Primary responsibilitiesinclude design and development ofserver code.
 Developed applications using C# in conjunction with ASP.NET.
 Designed and developed relationaldatabasesusing SQL server.
 ConvertMicrosoft Accessdatabases into SQL server databases to be accessed through the server using
ASP.NET applications.
Education
B.S: Computer Science and Information Systems 2010
Regis University Denver, Colorado, USA