J O S E S . R E G A L A D O 309 E. Warner Ave. Santa Ana CA, 92707 (714)604-3098 spk23jr@sbcglobal.net

Working in Pharmaceutical Manufacturing for 11 years in different areas have given me the experience to become a leader in the field. I

am looking forward to apply my knowledge, expertise and ideas in the necessary areas.

P R O F E S S I O N A L E X P E R I E N C E

BBRAUN MEDICAL INC. IRVINE , CA

2005 – Present 2005-2006 -Machine Operator PIC Filling

Performed adjustments, setups, production changeovers, and cleaning of filling machine. Notifies supervisor of any problems.

Maintains work area in a clean and orderly condition.

Enters all Filling information into SAP and DPR system.

Complies with all departmental and company policies and procedures.

Measures, inspects, and documents information related to production batch records.

2007-2011 -Mixing Technician

Coordinate with production line schedules Perform confirmations through various systems such as SAP,PLC and EBR(Electronic Batch Record) Following SOP’s, Perform compounding of many different types of solutions for filling areas Perform sanitation of all pumps, slurry mixers, dust collectors, filter housings, stainless stee l plumbing, used in mixing process Perform specific sanitation and general custodial duties in the Mixing complex, Filling and Assembly clean rooms

2011-2013 -Weighing Technician

Following Process Order specifications and procedure, weigh multiple components for various solution types Using SAP System, order sufficient raw material for the following day’s production schedule. Perform chemical inventory for applicable solutions. Work with Quality control and Raw Materials Lab Mettler Toledo Scale balance/HMI Verification for process

2013-Present - Weigh/Mix, Filling Areas Lead

Supervise all hourly personnel in the unit for proper application of company policies and procedures, on the job performance . Coordinate shift production schedules to ensure optimum product flow and maximize equipment, mat erials and manpower.

Monitor manufacturing processes for compliance with quality and GMP requirements.

Produce daily production reports.

Provide on the job training for personnel including safety and emergency response.

Work with support groups (Quality Control, Engineering) on Process, Quality and Cost improvement projects.

Perform/Support quality investigations in a timely and thorough manner per applicable investigation procedures.

Monitor training qualifications for all employees to ensure all employees have completed required training job functions.

Ensure that all areas and equipment are maintained in Good Housekeeping condition.

E D U C A T I O N

HIGH SCHOOL , SANTA ANA CA

Company policies and procedures, GMP, FDA and OSHA regulations

Security Essentials Certified Time and project management skills

B.Braun Certificates in ”Management in Pharmaceutical Manufacturing”

Dale Carnegie Training, PIL (Partners In Leadership) Tools Certificate

A D D I T I O N A L S K I L L S

Microsoft Office, Excel and Powerpoint

Bilingual in Spanish and English

SAP (System, Applications and Products) EBR (Electronic Batch Record)