Ronald Wright
*** * ****** **. #***, Anaheim, CA 92805
562-***-****, **********@*****.***
Professional Profile
Career Objective
To obtain a position with a company where I can excel and further enhance
my ability to succeed in the workplace.
Skills Summary
Good knowledge of Manufacturing Practices and Standard Operating Procedures
Strong written, verbal, and communication skills
Ability to work safely with materials and equipment
Professional Experience:
Environmental Monitoring Technician 1:
Aerotek/ Gilead Inc. San Dimas, CA 04/2013- 04/2013
Using Aseptic technique for taking viable and nonviable samples of
production areas.
Manufacturing Technician 2:
HireGenics@Baxter Bioscience, Glendale, CA 11/2011 - 03/2013
Aseptic GMP manufacturing of clinical and commercial human blood
therapeutics in a clean-room environment in Clean rooms that are considered
class ISO 8 or class 100,000.
Maintain standard operating procedures (SOP's), batch records, and other
applicable documentation to comply with regulatory requirements and good
manufacturing practices (GMP's).
Act as manufacturing troubleshooter to resolve and communicate issues
related to equipment, process and compliance to the lead technician and
supervisor.
Manual activities include weighing and addition of chemicals, suspending
solid paste, equipment cleaning, room cleaning, and equipment assembly.
Participate in training and mentoring other operators on the floor.
Laboratory Technician 2:
Cedars Sinai Medical Center, Los Angeles, CA 10/2010 - 03/2012
Followed EPA and OSHA mandates to ensure the proper, safe disposal of
hazardous samples and waste.
Assist pathologists by retrieving specimens from operations and cleaning
and arranging of gross area.
Senior Laboratory Technologist:
Idexx Reference Laboratory, Irvine, CA 09/2006 - 03/2010
Perform routine laboratory procedures and assays in multiple departments
including Urinalysis, Serology, and Parasitology to ensure accurate results
to clients within a certain TAT (turn around times.)
Sterility Technician 2:
NAMSA, Irvine, CA 01/2006-06/2007
Performing USP Sterility testing of medical devices using Biological
Indicators, Product Immersion, Membrane Filtration (open filter), Membrane
Filtration (closed Steritest).
Following guidelines of SOP's provided by manufactures specifications.
cGMP documentation of each individual product tested, using aseptic
technique.
Preparation of ISO 8 clean room for testing by cleaning and environmental
monitoring of testing room and walk in incubators.
Following regulations governed by FDA, EU Medical Device Directives and
ISO, AAMI/ANSI
and USP.
Bioburden testing of product design and validation studies.
Education:
Newbridge College, Santa Ana, CA 05/2003:
Medical Laboratory Technician Assistant
Phlebotomy Technician